Pubmed
ID | Gene
symbols | Title |
16445568 | ABCA8A,ABCA8B | Acute digoxin loading reduces ABCA8A mRNA expression in the mouse liver.
|
12532264 | ABCA8A,ABCA8B | Evolutionary analysis of a cluster of ATP-binding cassette (ABC) genes.
|
20797428 | ACTA2,TAGLN | Resveratrol induces p53 and suppresses myocardin-mediated vascular smooth muscle
cell differentiation.
|
20190033 | ACTA2,COL1A1,COL1A2,TAGLN | Autocrine production of TGF-beta1 promotes myofibroblastic differentiation of
neonatal lung mesenchymal stem cells.
|
20155481 | ACTA2,COL3A1 | Spontaneous arterial dissection: phenotype and molecular pathogenesis.
|
20096952 | ACTA2,TAGLN | Proliferation of human primary vascular smooth muscle cells depends on serum
response factor.
|
20089806 | ACTA2,TAGLN,MMP3 | Cyclosporine up-regulates Kruppel-like factor-4 (KLF4) in vascular smooth muscle
cells and drives phenotypic modulation in vivo.
|
19956410 | ACTA2,BMP4 | Evaluation of differentially expressed genes identified in keratoconus.
|
19639654 | ACTA2,COL3A1 | Mutation of ACTA2 gene as an important cause of familial and nonfamilial
nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD).
|
19635739 | ACTA2,COL3A1,TAGLN,POSTN | Progesterone and interferon tau-regulated genes in the ovine uterine endometrium:
identification of periostin as a potential mediator of conceptus elongation.
|
1675193 | ACTA2,PLAT | A linkage map of mouse chromosome 8: further definition of homologous linkage
relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19.
|
20889195 | C1S,C1R | Enzymatic pathways in the pathogenesis of hereditary angioedema: The role of C1
inhibitor therapy.
|
20693203 | C1S,C1R | Cutaneous manifestations of complement deficiencies.
|
20682770 | C1S,C1R | Identification of the Matriptase Second CUB Domain as the Secondary Site for
Interaction with Hepatocyte Growth Factor Activator Inhibitor Type-1.
|
20666732 | C1S,C1R | Self-association and domain rearrangements between complement C3 and C3u provide
insight into the activation mechanism of C3.
|
20592021 | C1S,C1R | Mapping surface accessibility of the C1r/C1s tetramer by chemical modification
and mass spectrometry provides new insights into assembly of the human C1
complex.
|
20580091 | C1S,C1R | The plasma bradykinin-forming pathways and its interrelationships with
complement.
|
20542571 | C1S,C1R | New insights into the molecular mechanisms of classical complement activation.
|
20351192 | C1S,C1R | Functional characterization of the recombinant human C1 inhibitor serpin domain:
insights into heparin binding.
|
20237569 | C1S,C1R | Structural basis for receptor recognition of vitamin-B(12)-intrinsic factor
complexes.
|
20178990 | C1S,C1R | Calcium-dependent conformational flexibility of a CUB domain controls activation
of the complement serine protease C1r.
|
20153898 | C1S,C1R | Molecular mechanisms involved in the inactivation of the first component of human
complement by Trypanosoma cruzi calreticulin.
|
20118239 | C1S,C1R | Engineering novel complement activity into a pulmonary surfactant protein.
|
20008834 | C1S,C1R | Analysis of human C1q by combined bottom-up and top-down mass spectrometry:
detailed mapping of post-translational modifications and insights into the
C1r/C1s binding sites.
|
19896716 | C1S,C1R | Human astrovirus coat protein binds C1q and MBL and inhibits the classical and
lectin pathways of complement activation.
|
19874244 | C1S,C1R | Anti-complementary effect of polysaccharide B3-PS1 in Herba Scutellariae Barbatae
(Scutellaria barbata).
|
19843402 | C1S,C1R | Pathogenesis and laboratory diagnosis of hereditary angioedema.
|
19807696 | C1S,C1R | Complement activation and disease: protective effects of hyperbilirubinaemia.
|
19806892 | C1S,C1R | [Anti-complement activity of polysaccharide B3-PS2 purified from Herba
Scutellariae Barbatae]
|
19783065 | C1S,C1R | Paths reunited: Initiation of the classical and lectin pathways of complement
activation.
|
19627250 | C1S,C1R | Anti-complementary effect of polysacchride B3-PS1 in Herba Scutellariae Barbatae
(Scutellaria barbata).
|
19564340 | C1S,C1R | MASP-1, a promiscuous complement protease: structure of its catalytic region
reveals the basis of its broad specificity.
|
19522701 | C1S,SERPING1 | Modulation of the proteolytic activity of the complement protease C1s by
polyanions: implications for polyanion-mediated acceleration of interaction
between C1s and SERPING1.
|
19505678 | C1S,C1R | A protein-bound polysaccharide from the stem bark of Eucommia ulmoides and its
anti-complementary effect.
|
19494305 | C1S,C1R | Scabies mite inactivated serine protease paralogs inhibit the human complement
system.
|
19494295 | C1S,C1R | Analogous interactions in initiating complexes of the classical and lectin
pathways of complement.
|
19477526 | C1S,C1R | Early complement proteases: C1r, C1s and MASPs. A structural insight into
activation and functions.
|
19473974 | C1S,C1R | Identification of the C1q-binding Sites of Human C1r and C1s: a refined
three-dimensional model of the C1 complex of complement.
|
19357398 | C1S,C1R | Molecular mechanisms of the defective hepcidin inhibition in TMPRSS6 mutations
associated with iron-refractory iron deficiency anemia.
|
19243221 | C1S,C1R | Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for
synaptic plasticity and learning.
|
19150444 | C1S,C1R | Unconjugated bilirubin inhibits C1 esterase activity.
|
19025126 | C1S,C1R | Human astrovirus coat protein: a novel C1 inhibitor.
|
18977695 | C1S,C1R | C1, MBL-MASPs and C1-inhibitor: novel approaches for targeting
complement-mediated inflammation.
|
18760304 | C1S,C1R | Evolutionary origin of the vertebrate blood complement and coagulation systems
inferred from liver EST analysis of lamprey.
|
18758157 | C1S,SERPING1,C1R | Mutational spectrum of the C1INH (SERPING1) gene in patients with hereditary
angioedema.
|
20476965 | C1S,C1R | Complement deficiency and systemic lupus erythematosus: consensus and dilemma.
|
18674818 | C1S,C1R | Biological activities of C1 inhibitor.
|
18664565 | C1S,C1R | Molecular determinants of Xolloid action in vivo.
|
18602068 | C1S,C1R | Isolation and characterization of an anti-complementary protein-bound
polysaccharide from the stem barks of Eucommia ulmoides.
|
18561091 | C1S,SERPING1,C1R | Transcriptome studies of bovine endometrium reveal molecular profiles
characteristic for specific stages of estrous cycle and early pregnancy.
|
18510966 | C1S,C1R | Plasma concentration of SCUBE1, a novel platelet protein, is elevated in patients
with acute coronary syndrome and ischemic stroke.
|
18369152 | C1S,C1R | Regulation of tumor necrosis factor receptor-1 and the IKK-NF-kappaB pathway by
LDL receptor-related protein explains the antiinflammatory activity of this
receptor.
|
18164932 | C1S,C1R | Procollagen C-proteinase enhancer-1 (PCPE-1) interacts with beta2-microglobulin
(beta2-m) and may help initiate beta2-m amyloid fibril formation in connective
tissues.
|
18160218 | C1S,C1R | Complement activation in the peripheral nervous system following the spinal nerve
ligation model of neuropathic pain.
|
18062908 | C1S,C1R | Genetic analysis of complement C1s deficiency associated with systemic lupus
erythematosus highlights alternative splicing of normal C1s gene.
|
18054386 | C1S,C1R | Studies on the haemolytic activity of circulating C1q-C3/C4 complexes.
|
18048067 | C1S,C1R | Human postmortem brain-derived cerebrovascular smooth muscle cells express all
genes of the classical complement pathway: a potential mechanism for vascular
damage in cerebral amyloid angiopathy and Alzheimer's disease.
|
17850949 | C1S,C1R | The initiating proteases of the complement system: controlling the cleavage.
|
17608619 | C1S,C1R | Human alpha2-macroglobulin is composed of multiple domains, as predicted by
homology with complement component C3.
|
17544813 | C1S,C1R | Assembly of C1 and the MBL- and ficolin-MASP complexes: structural insights.
|
17544812 | C1S,C1R | Serine proteases of the classical and lectin pathways: similarities and
differences.
|
17442284 | C1S,C1R | Transgenic overexpression of the secreted, extracellular EGF-CUB
domain-containing protein SCUBE3 induces cardiac hypertrophy in mice.
|
17356516 | C1S,MGP,TGFB2 | Microarray reveals complement components are regulated in the serum-deprived rat
retinal ganglion cell line.
|
17244723 | C1S,C1R | Alterations of the classic pathway of complement in adipose tissue of obesity and
insulin resistance.
|
17244159 | C1S,C1R | Studies on the interactions between C-reactive protein and complement proteins.
|
17178384 | C1S,C1R | Isolation and characterization of an anti-complementary polysaccharide D3-S1 from
the roots of Bupleurum smithii.
|
17143562 | C1S,C1R | Conformationally altered hyaluronan restricts complement classical pathway
activation by binding to C1q, C1r, C1s, C2, C5 and C9, and suppresses WOX1
expression in prostate DU145 cells.
|
17137866 | C1S,C1R | First case of homozygous C1 inhibitor deficiency.
|
17071722 | C1S,C1R | Complement levels and activity in the normal and LPS-injured lung.
|
17051152 | C1S,C1R | The structure of complement C3b provides insights into complement activation and
regulation.
|
17005253 | C1S,C1R | Synthesis of complement proteins in the human chorion is differentially regulated
by cytokines.
|
16906756 | C1S,C1R | Existence of different but overlapping IgG- and IgM-binding sites on the globular
domain of human C1q.
|
16845603 | C1S,C1R | Gene expression profiling in Salmonella Choleraesuis-infected porcine lung using
a long oligonucleotide microarray.
|
16753137 | C1S,C1R | Localization and characterization of a novel secreted protein SCUBE1 in human
platelets.
|
16716085 | C1S,C1R | The interaction of recombinant subdomains of the procollagen C-proteinase with
procollagen I provides a quantitative explanation for functional differences
between the two splice variants, mammalian tolloid and bone morphogenetic protein
1.
|
16707773 | C1S,C1R | Identification and characterization of novel and unknown mouse
epididymis-specific genes by complementary DNA microarray technology.
|
16697920 | C1S,C1R | Lectin complement system and pattern recognition.
|
16227207 | C1S,C1R | Functional characterization of complement proteases C1s/mannan-binding
lectin-associated serine protease-2 (MASP-2) chimeras reveals the higher C4
recognition efficacy of the MASP-2 complement control protein modules.
|
16217168 | C1S,C1R | Hereditary angioedema.
|
16177097 | C1S,C1R | Functional role of the linker between the complement control protein modules of
complement protease C1s.
|
16167883 | C1S,C1R | Immune function of C1q and its modulators CD91 and CD93.
|
16003522 | C1S,C1R | Cloning of a quail homologue of hatching enzyme: its conserved function and
additional function in egg envelope digestion.
|
15988036 | C1S,C1R | Platelet-derived growth factor D is activated by urokinase plasminogen activator
in prostate carcinoma cells.
|
15866474 | C1S,C1R | Identification of an astacin-like metallo-proteinase transcript from the
infective larvae of Strongyloides stercoralis.
|
15774619 | C1S,C1R | Cleavage of ultralarge multimers of von Willebrand factor by C-terminal-truncated
mutants of ADAMTS-13 under flow.
|
15705970 | C1S,C1R | High throughput substrate specificity profiling of serine and cysteine proteases
using solution-phase fluorogenic peptide microarrays.
|
15670912 | C1S,C1R | Inhibition of classical pathway of complement activation with negative charged
derivatives of bisphenol A and bisphenol disulphates.
|
15609759 | C1S,C1R | Complement determinations in human disease.
|
15596403 | C1S,C1R | The pathophysiology of hereditary angioedema.
|
15527420 | C1S,C1R | A novel human complement-related protein, C1r-like protease (C1r-LP),
specifically cleaves pro-C1s.
|
15514703 | C1S,C1R | Biological effects of C1 inhibitor.
|
15464227 | C1S,C1R | Expression of Btcl2, a novel member of Btcl gene family, during development of
the central nervous system.
|
15385675 | C1S,C1R | Prohaptoglobin is proteolytically cleaved in the endoplasmic reticulum by the
complement C1r-like protein.
|
15358180 | C1S,C1R | A novel human dendritic cell-derived C1r-like serine protease analog inhibits
complement-mediated cytotoxicity.
|
15262284 | C1S,C1R | Cloning and molecular characterization of a cubilin-related serine proteinase
from the hard tick Haemaphysalis longicornis.
|
15225624 | C1S,C1R | VIGR--a novel inducible adhesion family G-protein coupled receptor in endothelial
cells.
|
15218103 | C1S,C1R | Origin of the classical complement pathway: Lamprey orthologue of mammalian C1q
acts as a lectin.
|
15159063 | C1S,C1R | cC1q-R (calreticulin) and gC1q-R/p33: ubiquitously expressed multi-ligand binding
cellular proteins involved in inflammation and infection.
|
14996732 | C1S,C1R | A potential oncogenic activity of platelet-derived growth factor d in prostate
cancer progression.
|
14748705 | C1S,C1R | Proteases of the complement system.
|
14674770 | C1S,C1R | Importance of the prime subsites of the C1s protease of the classical complement
pathway for recognition of substrates.
|
14644096 | C1S,C1R | Microglial activation and increased synthesis of complement component C1q
precedes blood-brain barrier dysfunction in rats.
|
14628103 | C1S,C1R | Complete sequencing and expression of three complement components, C1r, C4 and C1
inhibitor, of the classical activation pathway of the complement system in
rainbow trout Oncorhynchus mykiss.
|
14499584 | C1S,C1R | Interaction of fucoidan with the proteins of the complement classical pathway.
|
12914573 | C1S,C1R | The human complement component C1R gene: the exon-intron structure and the
molecular basis of allelic diversity.
|
12887296 | C1S,C1R | Biochemistry and genetics of mannan-binding lectin (MBL).
|
12818633 | C1S,C1R | Expansion of genes encoding complement components in bony fish: biological
implications of the complement diversity.
|
12805391 | C1S,C1R | High expression of complement components in omental adipose tissue in obese men.
|
12788922 | C1S,C1R | X-ray structure of the Ca2+-binding interaction domain of C1s. Insights into the
assembly of the C1 complex of complement.
|
12746311 | C1S,C1R | Control of insulin-like growth factor binding protein-5 protease synthesis and
secretion by human fibroblasts and porcine aortic smooth muscle cells.
|
12744720 | C1S,C1R | Mouse matriptase-2: identification, characterization and comparative mRNA
expression analysis with mouse hepsin in adult and embryonic tissues.
|
12730962 | C1S,C1R | Expression of complement messenger RNAs and proteins by human oligodendroglial
cells.
|
12708315 | C1S,C1R | [The mechanism of inhibition of the activation of the complement first component
by polyanions and polycations ]
|
20937261 | COL1A1,COL3A1 | Combined use of bFGF and GDF-5 enhances the healing of medial collateral ligament
injury.
|
20922862 | COL1A1,COL1A2 | [Osteogenesis imperfecta and achievements in cell and gene therapy]
|
20869473 | COL1A1,DCN,LOX | Selective isolation and differentiation of a stromal population of human
embryonic stem cells with osteogenic potential.
|
20855225 | COL1A1,COL1A2 | Genetics of bone diseases: Paget's disease, fibrous dysplasia, osteopetrosis, and
osteogenesis imperfecta.
|
20842701 | COL1A1,COL3A1 | Impact of Smad3 loss of function on scarring and adhesion formation during tendon
healing.
|
20839322 | COL1A1,COL3A1 | Cycle-dependent matrix remodeling gene expression response in fatigue-loaded rat
patellar tendons.
|
20839288 | COL1A1,COL1A2 | Mutations in FKBP10 cause recessive osteogenesis imperfecta and type 1 bruck
syndrome.
|
20824135 | COL1A1,COL3A1 | The effects of aging on the molecular and cellular composition of the prostate
microenvironment.
LID - e12501 [pii]
|
20820878 | COL1A1,HAS2 | Lactoferrin promotes hyaluronan synthesis in human dermal fibroblasts.
|
20807599 | COL1A1,BMP2 | Deficiency of vitamin A delays bone healing process in association with reduced
BMP2 expression after drill-hole injury in mice.
|
20736093 | COL1A1,COL1A2 | Collagen gene polymorphisms influence fracture risk and bone mass acquisition
during childhood and adolescent growth.
|
20724489 | COL1A1,COL1A2 | Dietary fluoride restriction does not alter femoral biomechanical strength in
col1a2-deficient (oim) mice with type I collagen glomerulopathy.
|
20721936 | COL1A1,COL1A2 | Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic
determinants.
|
20705404 | COL1A1,COL3A1 | Analysis of mRNA from human heart tissue and putative applications in forensic
molecular pathology.
|
20698769 | COL1A1,COL1A2 | Optimization of genetic engineering and homologous recombination of collagen type
I genes in rat bone marrow mesenchymal stem cells (MSC).
|
20697743 | COL1A1,COL1A2,COL3A1,MGP | Antler development and coupled osteoporosis in the skeleton of red deer Cervus
elaphus: expression dynamics for regulatory and effector genes.
|
20675929 | COL1A1,COL1A2 | [The genetic basis for skeletal disease. Osteogenesis imperfecta and genetic
abnormalities]
|
20660018 | COL1A1,COL1A2 | A sensitive short-term evaluation of antifibrotic effects using newly established
type I collagen reporter transgenic rats.
|
20646442 | COL1A1,SFRP1 | [Microarray analysis of gene expression profiles in pelvic organ prolapse.]
|
20546554 | COL1A1,COL3A1 | Monitoring the healing of combat wounds using Raman spectroscopic mapping.
|
20543949 | COL1A1,COL1A2,COL3A1,COL6A3,PRRX1 | Switch from stress response to homeobox transcription factors in adipose tissue
after profound fat loss.
|
20483354 | COL1A1,COL3A1 | Morphological and proteomic analysis of early stage of osteoblast differentiation
in osteoblastic progenitor cells.
|
20479531 | COL1A1,COL3A1 | In vivo low-intensity pulsed ultrasound (LIPUS) following tendon injury promotes
repair during granulation but suppresses decorin and biglycan expression during
remodeling.
|
20473581 | COL1A1,IGFBP3 | Hepatic Gene Networks in Morbidly Obese Patients With Nonalcoholic Fatty Liver
Disease.
|
20456365 | COL1A1,COL3A1 | Extracellular matrix in multiple sclerosis lesions: Fibrillar collagens, biglycan
and decorin are upregulated and associated with infiltrating immune cells.
|
20433912 | COL1A1,COL3A1,GDF10,VEGFC,MGP | Gene expression profiling of primary human articular chondrocytes in high-density
micromasses reveals patterns of recovery, maintenance, re- and dedifferentiation.
|
20429888 | COL1A1,COL1A2 | Transcriptional regulation of matrix metalloproteinase-1 and collagen 1A2
explains the anti-fibrotic effect exerted by proteasome inhibition in human
dermal fibroblasts.
|
20362275 | COL1A1,COL1A2 | Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive
osteogenesis imperfecta.
|
20338150 | COL1A1,COL1A2 | Reprogramming of somatic cells induced by fusion of embryonic stem cells using
hemagglutinating virus of Japan envelope (HVJ-E).
|
20301472 | COL1A1,COL1A2 | Osteogenesis Imperfecta
BTI - GeneReviews
|
20219212 | COL1A1,COL1A2,COL3A1,MMP3,LTBP1 | Cellular phenotype transformation occurs during thoracic aortic aneurysm
development.
|
20194304 | COL1A1,COL3A1 | Renal medullary microRNAs in Dahl salt-sensitive rats: miR-29b regulates several
collagens and related genes.
|
20191437 | COL1A1,COL3A1 | Analysis of correlation between the process of thyroid fibrosis and TGFB1 gene
expression level in fine-needle aspiration biopsy (FNAB) thyroid specimens
collected from patients with Hashimoto's thyroiditis and non-toxic goitre.
|
20188343 | COL1A1,COL1A2 | Homozygosity for a missense mutation in SERPINH1, which encodes the collagen
chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.
|
20154713 | COL1A1,COL3A1 | Protective action of tetramethylpyrazine phosphate against dilated cardiomyopathy
in cTnT(R141W) transgenic mice.
|
20117381 | COL1A1,COL3A1 | Growth differentiation factor 5 regulates cardiac repair after myocardial
infarction.
|
20092892 | COL1A1,COL1A2,COL6A3,CYP1B1 | Effect of maternal tobacco smoke exposure on the placental transcriptome.
|
20083223 | COL1A1,PLAT | Periostin expression distinguishes between light and dark hypertrophic
chondrocytes.
|
20063114 | COL1A1,COL3A1,COL6A2 | Vascular gene expression patterns are conserved in primary and metastatic brain
tumors.
|
20051715 | COL1A1,COL3A1 | Identification of novel in vitro test systems for the determination of
glucocorticoid receptor ligand-induced skin atrophy.
|
20043993 | COL1A1,FSTL1,THBS2 | Downregulated expression of the secreted glycoprotein follistatin-like 1 (Fstl1)
is a robust hallmark of preadipocyte to adipocyte conversion.
|
20034948 | COL1A1,COL1A2 | Leg pain in an infant.
|
19956414 | COL1A1,COL1A2,COL3A1,ADAM12 | Role of miR-29b on the regulation of the extracellular matrix in human trabecular
meshwork cells under chronic oxidative stress.
|
19929435 | COL1A1,COL1A2 | Relationship between genotype and skeletal phenotype in children and adolescents
with osteogenesis imperfecta.
|
19913322 | COL1A1,COL1A2 | Upregulation of hepatoma-derived growth factor is involved in murine hepatic
fibrogenesis.
|
19907330 | COL1A1,COL1A2 | Osteogenesis imperfecta: questions and answers.
|
19875360 | COL1A1,COL3A1 | Accelerated healing of the rat Achilles tendon in response to autologous
conditioned serum.
|
19862557 | COL1A1,COL1A2 | Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis
imperfecta.
|
19839042 | COL1A1,COL1A2 | Calvarial doughnut lesions and osteoporosis: a new three-generation family and
review.
|
19833228 | COL1A1,BMP4,BMP2 | Atlantic salmon (Salmo salar) muscle precursor cells differentiate into
osteoblasts in vitro: polyunsaturated fatty acids and hyperthermia influence gene
expression and differentiation.
|
19822105 | COL1A1,COL1A2 | Influence of an extract from kudzu symbiosomes containing leghemoglobin on in
vitro cutaneous procollagen production.
|
19790048 | COL1A1,COL1A2,COL3A1 | Hypoxia-inducible factor 1alpha inhibits the fibroblast-like markers type I and
type III collagen during hypoxia-induced chondrocyte redifferentiation: hypoxia
not only induces type II collagen and aggrecan, but it also inhibits type I and
type III collagen in the hypoxia-inducible factor 1alpha-dependent
redifferentiation of chondrocytes.
|
19772464 | COL1A1,CXCL1,IGFBP3 | Induction of cytokine gene expression in human thyroid epithelial cells
irradiated with HZE particles (iron ions).
|
19767743 | COL1A1,BMP2 | Signalling mediated by the endoplasmic reticulum stress transducer OASIS is
involved in bone formation.
|
19748963 | COL1A1,MGP | Identification of phenotypic discriminating markers for intervertebral disc cells
and articular chondrocytes.
|
19723327 | COL1A1,COL3A1,POSTN,BGN | Chondrogenic differentiation potential of osteoarthritic chondrocytes and their
possible use in matrix-associated autologous chondrocyte transplantation.
|
19714363 | COL1A1,COL1A2 | Novel quantitative trait loci for central corneal thickness identified by
candidate gene analysis of osteogenesis imperfecta genes.
|
19696512 | COL1A1,MMP3 | Genetic risk factors for musculoskeletal soft tissue injuries.
|
19678759 | COL1A1,BMP2 | Insight into the molecular pathophysiology of delayed bone healing in a sheep
model.
|
19675075 | COL1A1,COL1A2,PTN | Aggressive inherited and sporadic medullary thyroid carcinomas display similar
oncogenic pathways.
|
19649655 | COL1A1,COL1A2 | Regulation of bone development and extracellular matrix protein genes by RUNX2.
|
19629171 | COL1A1,COL1A2 | A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis
imperfecta.
|
19594296 | COL1A1,COL1A2 | Variable bone fragility associated with an Amish COL1A2 variant and a knock-in
mouse model.
|
19533842 | COL1A1,COL1A2 | Osteogenesis imperfecta: recent findings shed new light on this once
well-understood condition.
|
19491628 | COL1A1,COL1A2 | Mutations in COL1A1 of type I collagen genes in Chinese patients with
osteogenesis imperfecta.
|
19404930 | COL1A1,COL1A2 | Altered mineralization of human osteoarthritic osteoblasts is attributable to
abnormal type I collagen production.
|
19317096 | COL1A1,COL1A2 | [Osteogenesis imperfecta]
|
19283684 | COL1A1,COL1A2 | A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with
osteogenesis imperfecta.
|
19250650 | COL1A1,COL1A2 | Reactive nitrogen species switch on early extracellular matrix remodeling via
induction of MMP1 and TNFalpha.
|
19228264 | COL1A1,MMP3 | Current evidence for a modulation of low back pain by human genetic variants.
|
19201335 | COL1A1,COL3A1 | Expression of extracellular matrix genes during myocardial recovery from heart
failure after left ventricular assist device support.
|
19170097 | COL1A1,COL3A1,MMP3 | Temporal growth factor release from platelet-rich plasma, trehalose lyophilized
platelets, and bone marrow aspirate and their effect on tendon and ligament gene
expression.
|
19152976 | COL1A1,COL1A2,COL3A1,TNXB,ADAMTS2 | Connective tissue and related disorders and preterm birth: clues to genes
contributing to prematurity.
|
19145252 | COL1A1,DCN,FBLN1,POSTN | Differential global and extra-cellular matrix focused gene expression patterns
between normal and glaucomatous human lamina cribrosa cells.
|
19082484 | COL1A1,COL1A2,BGN | Combination of microarray profiling and protein-protein interaction databases
delineates the minimal discriminators as a metastasis network for esophageal
squamous cell carcinoma.
|
19021896 | COL1A1,COL1A2 | Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
|
19015742 | COL1A1,COL1A2 | Allele dependent silencing of COL1A2 using small interfering RNAs.
|
18996919 | COL1A1,COL1A2 | Mutation and polymorphism spectrum in osteogenesis imperfecta type II:
implications for genotype-phenotype relationships.
|
20534718 | COL1A2,COL3A1,LUM | Estradiol replacement alters expression of genes related to neurotransmission and
immune surveillance in the frontal cortex of middle-aged, ovariectomized rats.
|
20150539 | COL1A2,COL3A1,SERPING1 | Integrative urinary peptidomics in renal transplantation identifies biomarkers
for acute rejection.
|
20048181 | COL1A2,BGN | Hypoxia-inducible factor-1 {alpha} expression predicts superior survival in
patients with diffuse large B-cell lymphoma treated with R-CHOP.
|
19949890 | COL1A2,COL3A1 | Secreted phosphoprotein 1 upstream invasive network construction and analysis of
lung adenocarcinoma compared with human normal adjacent tissues by integrative
biocomputation.
|
19741209 | COL1A2,COL3A1 | Reactive oxygen species mediate mitogenic growth factor signaling pathways in
human leiomyoma smooth muscle cells.
|
19531580 | COL1A2,MGP | Retinoic acid cross-talk with calcitriol activity in Atlantic salmon (Salmo
salar).
|
19401702 | COL1A2,COL6A3,POSTN | Analysis of differential gene expression in colorectal cancer and stroma using
fluorescence-activated cell sorting purification.
|
18816857 | COL1A2,COL3A1 | Temporal and spatial expression of collagens during murine atrioventricular heart
valve development and maintenance.
|
18815441 | COL1A2,COL3A1 | Expression of collagen types I, II and III in juvenile angiofibromas.
|
18602130 | COL1A2,LUM | Gene expression profiles following exposure to a developmental neurotoxicant,
Aroclor 1254: pathway analysis for possible mode(s) of action.
|
18579462 | COL1A2,SMOC2 | Microarray analysis of perichondral and reserve growth plate zones identifies
differential gene expressions and signal pathways.
|
18514395 | COL1A2,COL6A1 | Se-methylselenocysteine alters collagen gene and protein expression in human
prostate cells.
|
18499699 | COL1A2,COL6A3,COL6A2 | Sulindac treatment alters collagen and matrilysin expression in adenomas of
ApcMin/+ mice.
|
18272325 | COL1A2,COL3A1 | Natural variation in four human collagen genes across an ethnically diverse
population.
|
18254958 | COL1A2,MMP3 | Transcriptomic dissection of tongue squamous cell carcinoma.
|
17982090 | COL1A2,COL3A1,LUM | Differential expression of inflammatory and fibrogenic genes and their regulation
by NF-kappaB inhibition in a mouse model of chronic colitis.
|
17938000 | COL1A2,COL3A1,LUM | Cartilage gene expression correlates with radiographic severity of canine elbow
osteoarthritis.
|
17852852 | COL1A2,COL3A1,TGFB2 | Multiple inflammatory-, tissue remodelling- and fibrosis genes are differentially
transcribed in the livers of Abcb4 (-/ - ) mice harbouring chronic cholangitis.
|
17822560 | COL1A2,PTN,MGP | The effect of novel nitrogen-rich plasma polymer coatings on the phenotypic
profile of notochordal cells.
|
17666000 | COL1A2,COL3A1,COL6A1 | Downregulation of extracellular matrix-related gene clusters during osteogenic
differentiation of human bone marrow- and adipose tissue-derived stromal cells.
|
17601708 | COL1A2,COL6A3,THBS2 | Molecular basis of the differences between normal and tumor tissues of gastric
cancer.
|
17552940 | COL1A2,MSX1 | Developmental biology and genetics of dental malformations.
|
17306970 | COL1A2,COL3A1 | Type III collagen is essential for growth acceleration of human osteoblastic
cells by ascorbic acid 2-phosphate, a long-acting vitamin C derivative.
|
17133596 | COL1A2,COL3A1 | SPARC, an upstream regulator of connective tissue growth factor in response to
transforming growth factor beta stimulation.
|
17032449 | COL1A2,COL3A1,LUM,BGN | Analysis of normal and osteoarthritic canine cartilage mRNA expression by
quantitative polymerase chain reaction.
|
17014321 | COL1A2,COL3A1,COL6A3 | Assessment of collagen genes involved in fragmented medial coronoid process
development in Labrador Retrievers as determined by affected sibling-pair
analysis.
|
16871529 | COL1A2,COL3A1 | Attenuation of collagen production with small interfering RNA of SPARC in
cultured fibroblasts from the skin of patients with scleroderma.
|
16583319 | COL1A2,COL3A1 | Extracellular matrix containing mutated fibrillin-1 (Fbn1) down regulates Col1a1,
Col1a2, Col3a1, Col5a1, and Col5a2 mRNA levels in Tsk/+ and Tsk/Tsk embryonic
fibroblasts.
|
20864640 | COL3A1,COL6A3 | Altered Spatiotemporal Expression of Collagen Types I, III, IV, and VI in
Lpar3-Deficient Peri-Implantation Mouse Uterus.
|
19424605 | COL3A1,MMP3 | Association of gene polymorphisms with chronic kidney disease in high- or
low-risk subjects defined by conventional risk factors.
|
18467551 | COL3A1,COL6A3 | Effects of leptin deficiency on postnatal lung development in mice.
|
17931229 | COL3A1,COL6A3,COL6A1 | Polymorphic microsatellite markers for genetic analysis of collagen genes in
suspected collagenopathies in dogs.
|
17389037 | COL3A1,ASPN | Novel markers for differentiation of lobular and ductal invasive breast
carcinomas by laser microdissection and microarray analysis.
|
17218422 | COL3A1,COL6A3 | Variation in senescent-dependent lung changes in inbred mouse strains.
|
19455257 | COL3A1,MME | Germinal Center B Cell-Like (GCB) and Activated B Cell-Like (ABC) Type of Diffuse
Large B Cell Lymphoma (DLBCL): Analysis of Molecular Predictors, Signatures, Cell
Cycle State and Patient Survival.
|
16980845 | COL3A1,PTN | Differential gene expression between juvenile and adult dura mater: a window into
what genes play a role in the regeneration of membranous bone.
|
16856881 | COL3A1,POSTN | Expression profiling analysis of the CD5+ diffuse large B-cell lymphoma subgroup:
development of a CD5 signature.
|
16556917 | COL3A1,ADAMTS2 | Regulation of procollagen amino-propeptide processing during mouse embryogenesis
by specialization of homologous ADAMTS proteases: insights on collagen
biosynthesis and dermatosparaxis.
|
16251498 | COL3A1,LUM,POSTN | Identification of endometrial genes regulated by early pregnancy, progesterone,
and interferon tau in the ovine uterus.
|
16035617 | COL3A1,COL6A3,LOXL1,COL6A1,COL6A2,FBLN1,BGN | Caffeine suppresses metastasis in a transgenic mouse model: a prototype molecule
for prophylaxis of metastasis.
|
15716609 | COL3A1,COL6A1 | Gene expression analysis of cultured amniotic fluid cell with Down syndrome by
DNA microarray.
|
15054833 | COL3A1,TNXB,ADAMTS2,COL6A1,COL6A2 | Exclusion of candidate genes in a family with arterial tortuosity syndrome.
|
11917104 | COL3A1,IGFBP5 | In vitro cartilage formation by human adult stem cells from bone marrow stroma
defines the sequence of cellular and molecular events during chondrogenesis.
|
11283408 | COL3A1,COL6A1,COL6A2 | Molecular anatomy of an intracranial aneurysm: coordinated expression of genes
involved in wound healing and tissue remodeling.
|
11279127 | COL3A1,COL6A3,COL6A1,COL6A2 | Identification of novel TGF-beta /Smad gene targets in dermal fibroblasts using a
combined cDNA microarray/promoter transactivation approach.
|
20882040 | COL6A3,COL6A1,COL6A2 | Expression of the Collagen VI alpha5 and alpha6 Chains in Normal Human Skin and
in Skin of Patients with Collagen VI-Related Myopathies.
|
20576434 | COL6A3,COL6A1,COL6A2 | Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related
myopathies using a specific CT scanner pattern.
|
20301676 | COL6A3,COL6A1,COL6A2 | Collagen Type VI-Related Disorders
BTI - GeneReviews
|
20225280 | COL6A3,COL6A1,COL6A2 | Muscle magnetic resonance imaging involvement in muscular dystrophies with
rigidity of the spine.
|
20106987 | COL6A3,COL6A1,COL6A2 | Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular
dystrophy: role of the C2a splice variant.
|
19884007 | COL6A3,COL6A1,COL6A2 | Autosomal recessive inheritance of classic Bethlem myopathy.
|
19015158 | COL6A3,COL6A1,COL6A2 | Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular
study of mitochondrial dysfunction and its rescue.
|
18761340 | COL6A3,COL6A1,COL6A2 | An enhancer required for transcription of the Col6a1 gene in muscle connective
tissue is induced by signals released from muscle cells.
|
18378883 | COL6A3,COL6A1,COL6A2 | A refined diagnostic algorithm for Bethlem myopathy.
|
18366090 | COL6A3,COL6A1,COL6A2 | Exon skipping mutations in collagen VI are common and are predictive for severity
and inheritance.
|
18219255 | COL6A3,COL6A1,COL6A2 | Muscle interstitial fibroblasts are the main source of collagen VI synthesis in
skeletal muscle: implications for congenital muscular dystrophy types Ullrich and
Bethlem.
|
18086302 | COL6A3,POSTN | Human periostin gene expression in normal tissues, tumors and melanoma: evidences
for periostin production by both stromal and melanoma cells.
|
17886299 | COL6A3,COL6A1,COL6A2 | Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
|
17785673 | COL6A3,COL6A1,COL6A2 | Primary collagen VI deficiency is the second most common congenital muscular
dystrophy in Japan.
|
17602442 | COL6A3,COL6A1,COL6A2 | Quantitative evaluation of collagen type VI and SOD gene expression in the nuchal
skin of human fetuses with trisomy 21.
|
17163796 | COL6A3,LAMA2,COL6A1,COL6A2 | The congenital muscular dystrophies: recent advances and molecular insights.
|
16447767 | COL6A3,COL6A1,COL6A2 | [Collagenopathy (Ullrich congenital muscular dystrophy, Bethlem myopathy)]
|
16142353 | COL6A3,NDN,GPC4 | Gene expression profiling of a clonal isolate of oxaliplatin-resistant ovarian
carcinoma cell line A2780/C10.
|
16141002 | COL6A3,COL6A1,COL6A2 | Collagen VI related muscle disorders.
|
16075202 | COL6A3,COL6A1,COL6A2 | A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and
nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular
dystrophy.
|
15955946 | COL6A3,COL6A1,COL6A2 | Detection of common and private mutations in the COL6A1 gene of patients with
Bethlem myopathy.
|
15882279 | COL6A3,COL6A1,COL6A2,FBLN1 | Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and
contractures: a novel syndrome.
|
15689448 | COL6A3,COL6A1,COL6A2 | Automated genomic sequence analysis of the three collagen VI genes: applications
to Ullrich congenital muscular dystrophy and Bethlem myopathy.
|
15642389 | COL6A3,IGFBP5,BGN | Characterization of gene expression in major types of salivary gland carcinomas
with epithelial differentiation.
|
15563506 | COL6A3,COL6A1,COL6A2 | Dominant collagen VI mutations are a common cause of Ullrich congenital muscular
dystrophy.
|
15127309 | COL6A3,COL6A1,COL6A2 | Collagen VI status and clinical severity in Ullrich congenital muscular
dystrophy: phenotype analysis of 11 families linked to the COL6 loci.
|
12840783 | COL6A3,COL6A1,COL6A2 | New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous
in-frame deletion in the COL6A1 gene causes a severe phenotype.
|
12011280 | COL6A3,COL6A1 | Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and
immunohistochemical study.
|
11992252 | COL6A3,COL6A2 | Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital
muscular dystrophy.
|
11707460 | COL6A3,COL6A1,COL6A2 | Kinked collagen VI tetramers and reduced microfibril formation as a result of
Bethlem myopathy and introduced triple helical glycine mutations.
|
10419498 | COL6A3,COL6A1,COL6A2 | Bethlem myopathy and engineered collagen VI triple helical deletions prevent
intracellular multimer assembly and protein secretion.
|
9536084 | COL6A3,COL6A1,COL6A2 | Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI)
collagen gene (COL6A3) in a family with Bethlem myopathy.
|
9497154 | COL6A3,COL6A1 | Morphological classification of nuchal skin in human fetuses with trisomy 21, 18,
and 13 at 12-18 weeks and in a trisomy 16 mouse.
|
9491853 | COL6A3,COL6A1,COL6A2 | Collagen type VI gene expression in the skin of trisomy 21 fetuses.
|
8782832 | COL6A3,COL6A1,COL6A2 | Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy
with contractures.
|
8817344 | COL6A3,COL6A1,COL6A2 | Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
|
19438813 | CRYAB,POSTN | Derivation of a novel undifferentiated human foetal phenotype in serum-free
cultures with BMP-2.
|
19401404 | CRYAB,OGN,PDPN | Individual molecular response to elevated intraocular pressure in perfused
postmortem human eyes.
|
19080366 | CRYAB,DCN,IGFBP3 | Identification of differential gene expression profiles of radioresistant lung
cancer cell line established by fractionated ionizing radiation in vitro.
|
20699749 | CXCL12,LEPR | Application of the chemokine CXCL12 expression plasmid restores wound healing to
near normal in a diabetic mouse model.
|
20602768 | CXCL12,PCOLCE | Hind limb unloading of mice modulates gene expression at the protein and mRNA
level in mesenchymal bone cells.
|
20585037 | CXCL12,CCL11 | Role of the CXCR4/CXCL12 axis in lymphangioleiomyomatosis and angiomyolipoma.
|
20538476 | CXCL12,LIF,CXCL1 | The expression pattern of inflammatory mediators in cerebrospinal fluid
differentiates Guillain-Barre syndrome from chronic inflammatory demyelinating
polyneuropathy.
|
20516641 | CXCL12,CXCL1 | CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone
marrow.
|
20432237 | CXCL12,CCL19 | Epidermis-to-dermis migration of immature Langerhans cells upon topical irritant
exposure is dependent on CCL2 and CCL5.
|
20421491 | CXCL12,CCL19 | Requirement of CCL17 for CCR7- and CXCR4-dependent migration of cutaneous
dendritic cells.
|
20376612 | CXCL12,CXCL1 | The Chemokine Network in Acute Myelogenous Leukemia: Molecular Mechanisms
Involved in Leukemogenesis and Therapeutic Implications.
|
20369317 | CXCL12,CCL19 | Role of Chemokines in the Biology of Natural Killer Cells.
|
20145264 | CXCL12,CCL19 | CXCL12-induced chemotaxis is impaired in T cells from patients with
ZAP-70-negative chronic lymphocytic leukemia.
|
20073989 | CXCL12,PTN | Hypoxic/normoxic preconditioning increases endothelial differentiation potential
of human bone marrow CD133+ cells.
|
20042073 | CXCL12,CCL19 | The chemokine CXCL13 is a key regulator of B cell recruitment to the
cerebrospinal fluid in acute Lyme neuroborreliosis.
|
20360993 | DCN,LUM,OGN | Candidate gene study to investigate the genetic determinants of normal variation
in central corneal thickness.
|
20357198 | DCN,LUM | Linkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and
exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.
|
19652764 | DCN,MFAP5,FBLN1 | Pathway analysis of differentially expressed genes in patients with acute aortic
dissection.
|
19631729 | DCN,MGP,BMP2 | Microarray analysis of senescent vascular smooth muscle cells: A link to
atherosclerosis and vascular calcification.
|
19616852 | DCN,LUM | The association of haplotype at the lumican gene with high myopia susceptibility
in Taiwanese patients.
|
19571260 | DCN,NDN | Characterization of conserved and nonconserved imprinted genes in swine.
|
19379665 | DCN,BGN | Genetic evidence for key roles of decorin and biglycan in dentin mineralization.
|
19292938 | DCN,SDC2,MGP | Evaluation of differentially expressed genes by shear stress in human
osteoarthritic chondrocytes in vitro.
|
19036156 | DCN,LUM | Genetic variation in stromal proteins decorin and lumican with breast cancer:
investigations in two case-control studies.
|
18723084 | DCN,MGP | Gene expression profile of rabbit cartilage by expressed sequence tag analysis.
|
18479593 | DCN,ASPN | [Differentially expressed genes between upward and downward progressing types of
nasopharyngeal carcinoma]
|
18245265 | DCN,BGN | Effects of decorin and biglycan on human airway smooth muscle cell proliferation
and apoptosis.
|
18162102 | DCN,POSTN | Mapping of the porcine FBN2, YWHAQ, CNN3, DCN, POSTN, SPARC, RBM39 and GNAS
genes, expressed in foetal skeletal muscles.
|
18049164 | DCN,PTGES | DNA methyltransferase 1 knockdown induces silenced CDH1 gene reexpression by
demethylation of methylated CpG in hepatocellular carcinoma cell line SMMC-7721.
|
17977755 | DCN,LUM | Undifferentiated human mesenchymal stem cells (hMSCs) are highly sensitive to
mechanical strain: transcriptionally controlled early osteo-chondrogenic response
in vitro.
|
17662275 | DCN,CCL19,SMOC2,OGN | Disease susceptibility of the human macula: differential gene transcription in
the retinal pigmented epithelium/choroid.
|
17558846 | DCN,LUM | Autosomal dominant cornea plana is not associated with pathogenic mutations in
DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
|
17555561 | DCN,ASPN,LUM | Molecular response to aromatase inhibitor treatment in primary breast cancer.
|
17395685 | DCN,BGN | Differences in mRNA and protein expression of small proteoglycans in vaginal wall
tissue from women with and without stress urinary incontinence.
|
17188951 | DCN,BGN | Impaired posterior frontal sutural fusion in the biglycan/decorin double
deficient mice.
|
16908595 | DCN,LUM,BGN | Mitotic arrest, apoptosis, and sensitization to chemotherapy of melanomas by
methionine deprivation stress.
|
20555348 | DPT,IGFBP5,MMP3,SFRP1 | Epigenetically altered wound healing in keloid fibroblasts.
|
19250647 | FHL1,ALDH1A1 | Transcriptional activation by TLX1/HOX11 involves Gro/TLE corepressors.
|
18073142 | FHL1,ALDH1A1 | Transcriptional regulation of FHL1 by TLX1/HOX11 is dosage, cell-type and
promoter context-dependent.
|
17150988 | FHL1,SFRP1 | Genetic analysis of anterior posterior expression gradients in the developing
mammalian forebrain.
|
17061120 | FHL1,MGP | Intra- and interindividual variation in gene expression in human adipose tissue.
|
15910245 | FHL1,ALDH1A1 | Differential gene expression profiling of CD34+ CD133+ umbilical cord blood
hematopoietic stem progenitor cells.
|
20739664 | IGFBP5,IGFBP3,GATA6 | GATA Depletion Impacts Insulin-like Growth Factor 1 mRNA and Protein Levels in
Luteinizing Porcine Granulosa Cells.
|
20739512 | IGFBP5,IGFBP3 | Impact of viral mediated IGF-I gene transfer on skeletal muscle following cast
immobilization.
|
20389077 | IGFBP5,IGFBP3 | Differential modulation of Sonic-hedgehog-induced cerebellar granule cell
precursor proliferation by the IGF signaling network.
|
20186495 | IGFBP5,IGFBP3 | Inhibitor of differentiation 1 (ID1) promotes cell survival and proliferation of
prostate epithelial cells.
|
19933427 | IGFBP5,IGFBP3 | Effect of polymorphisms in candidate genes on reproduction traits in Finnish pig
populations.
|
19665134 | IGFBP5,IGFBP3 | Regulatory effects of biomechanical strain on the insulin-like growth factor
system in human periodontal cells.
|
19557575 | IGFBP5,MGP | FOS proliferating network construction in early colorectal cancer (CRC) based on
integrative significant function cluster and inferring analysis.
|
19378418 | IGFBP5,IGFBP3 | MRNA expression of members of the IGF system in the organ of Corti, the modiolus
and the stria vascularis of newborn rats.
|
19132093 | IGFBP5,TGFB2 | Identification of pax6-dependent gene regulatory networks in the mouse lens.
|
18997086 | IGFBP5,IGFBP3 | Quantification and localization of the IGF/insulin system expression in retinal
blood vessels and neurons during oxygen-induced retinopathy in mice.
|
18936297 | IGFBP5,IGFBP3 | The genomic response of a human uterine endometrial adenocarcinoma cell line to
17alpha-ethynyl estradiol.
|
18608519 | IGFBP5,IGFBP3 | mRNA expression of members of the IGF system in the organ of Corti, the modiolus
and the stria vascularis of newborn rats.
|
18276763 | IGFBP5,IGFBP3 | Gender-specific changes in bone turnover and skeletal architecture in
igfbp-2-null mice.
|
18222913 | IGFBP5,MSX1 | Altered expression of muscle- and cytoskeleton-related genes in a rat strain with
inherited cryptorchidism.
|
18204794 | IGFBP5,IGFBP3 | Cancer genes induced by malathion and parathion in the presence of estrogen in
breast cells.
|
17697390 | IGFBP5,FSTL1 | Gene expression studies of developing bovine longissimus muscle from two
different beef cattle breeds.
|
17695985 | IGFBP5,IGFBP3 | Regulatory effects of biophysical strain on rat TMJ discs.
|
16249290 | IGFBP5,FBLN1 | Endometriosis-specific genes identified by real-time reverse
transcription-polymerase chain reaction expression profiling of endometriosis
versus autologous uterine endometrium.
|
15512944 | IGFBP5,TNFAIP6 | Microarray analysis identified differentially expressed genes in keratocytes from
keratoconus patients.
|
14755496 | LAMA2,COL6A2 | EMG and nerve conduction studies in children with congenital muscular dystrophy.
|
20809277 | LIF,BMP4 | Enhanced effects of secreted soluble factor preserve better pluripotent state of
embryonic stem cell culture in a membrane-based compartmentalized
micro-bioreactor.
|
20713452 | LOX,BMP4,BMP2 | Involvement of cytoskeleton-associated proteins in the commitment of C3H10T1/2
pluripotent stem cells to adipocyte lineage induced by BMP2/4.
|
20606470 | LOX,LOXL1 | Role of Lysyl Oxidases in Neointima Development in Vascular Allografts.
|
20569695 | LOX,PDGFRA | CNS-resident glial progenitor/stem cells produce Schwann cells as well as
oligodendrocytes during repair of CNS demyelination.
|
20559617 | LOX,LOXL1 | LOX family enzymes expression in vaginal tissue of premenopausal women with
severe pelvic organ prolapse.
|
20482627 | LOX,CCL19 | Aggregatibacter actinomycetemcomitans accelerates atherosclerosis with an
increase in atherogenic factors in spontaneously hyperlipidemic mice.
|
20420713 | LOX,SFRP1 | Identifying mRNA targets of microRNA dysregulated in cancer: with application to
clear cell Renal Cell Carcinoma.
|
19565266 | LOXL1,SFRP1 | Hypermethylated SFRP1, but none of other nine genes "informative" for western
countries, is valuable for bladder cancer detection in Mainland China.
|
18158636 | LOXL1,MGP | Decreased endopelvic fascia elastin content in uterine prolapse.
|
20196644 | MFAP5,MFAP2 | Parameters in three-dimensional osteospheroids of telomerized human mesenchymal
(stromal) stem cells grown on osteoconductive scaffolds that predict in vivo
bone-forming potential.
|
19801232 | MME,BMP2 | Stem cell regulatory gene expression in human adult dental pulp and periodontal
ligament cells undergoing odontogenic/osteogenic differentiation.
|
18827820 | MME,DCBLD2 | Identification of novel neuroendocrine-specific tumour genes.
|
16319984 | MME,TGFB2 | High-resolution mapping of molecular events associated with immortalization,
transformation, and progression to breast cancer in the MCF10 model.
|
20505979 | MYL9,COL6A1,HAS2 | The transcription factor EGR1 regulates metastatic potential of v-src transformed
sarcoma cells.
|
17341888 | MYL9,TAGLN | Methylation status of genes upregulated by demethylating agent
5-aza-2'-deoxycytidine in hepatocellular carcinoma.
|
20434574 | NBL1,COL6A2 | Analysis of early changes in the articular cartilage transcriptisome in the rat
meniscal tear model of osteoarthritis: pathway comparisons with the rat anterior
cruciate transection model and with human osteoarthritic cartilage.
|
16596263 | NBL1,BMPR1A | CER1 is a common target of WNT and NODAL signaling pathways in human embryonic
stem cells.
|
20889717 | PDGFRA,EGFR | PDGFRA gene rearrangements are frequent genetic events in PDGFRA-amplified
glioblastomas.
|
20826533 | PDGFRA,GATA6 | A role for PDGF signaling in expansion of the extra-embryonic endoderm lineage of
the mouse blastocyst.
|
20548289 | PDGFRA,DACT1 | A molecular portrait of gastrointestinal stromal tumors: an integrative analysis
of gene expression profiling and high-resolution genomic copy number.
|
19968631 | PDGFRA,CXCL1 | Gene-gene and gene-environment interactions on IgE production in prenatal stage.
|
18773962 | PENK,NDN | Carbamazepine protects against neuronal hyperplasia and abnormal gene expression
in the megencephaly mouse.
|
15239838 | PENK,SFRP4,SAT2,BGN | Microarray profiling of progesterone-regulated endometrial genes during the
rhesus monkey secretory phase.
|
17117407 | PRELP,LUM | Novel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP)
genes in high myopia.
|
12054597 | PRELP,LUM | Molecular analysis of expansion, differentiation, and growth factor treatment of
human chondrocytes identifies differentiation markers and growth-related genes.
|
20840765 | TAGLN,IGFBP3 | Transcriptional profiling of ErbB signalling in mammary luminal epithelial
cells--interplay of ErbB and IGF1 signalling through IGFBP3 regulation.
|
20540360 | TAGLN,IGFBP3 | [A study of the single nucleotide polymorphism in seven genes (GHR, IGFBP3,
IGFR1, IRS1, FMN1, ANXA2, TaGLN) in ethnic Russians and in patients with prostate
cancer]
|
18782851 | TAGLN,RARRES2 | Putative direct and indirect Wnt targets identified through consistent gene
expression changes in APC-mutant intestinal adenomas from humans and mice.
|
18241852 | TAGLN,NDN | CYP26A1 knockout embryonic stem cells exhibit reduced differentiation and growth
arrest in response to retinoic acid.
|
20702851 | TNFAIP6,HAS2 | Does Bone Morphogenetic Protein 6 (BMP6) Affect Female Fertility in the Mouse?
|
20308529 | TNFAIP6,HAS2 | The nuclear receptor cofactor receptor-interacting protein 140 is a positive
regulator of amphiregulin expression and cumulus cell-oocyte complex expansion in
the mouse ovary.
|
20168049 | TNFAIP6,HAS2 | Progesterone is essential for maintenance of Tace/Adam17 mRNA expression, but not
EGF-like factor, in cumulus cells, which enhances the EGF receptor signaling
pathway during in vitro maturation of porcine COCs.
|
20034375 | TNFAIP6,HAS2 | Activation of PKA, p38 MAPK and ERK1/2 by gonadotropins in cumulus cells is
critical for induction of EGF-like factor and TACE/ADAM17 gene expression during
in vitro maturation of porcine COCs.
|
19651638 | TNFAIP6,HAS2 | Stable expression and characterization of N-terminal tagged recombinant human
bone morphogenetic protein 15.
|
19450457 | TNFAIP6,MATN2,EFEMP1,LTBP1 | Gene expression profiling of TGFbeta2- and/or BMP7-treated trabecular meshwork
cells: Identification of Smad7 as a critical inhibitor of TGF-beta2 signaling.
|
18951380 | TNFAIP6,HAS2 | Targeted suppression of Has2 mRNA in mouse cumulus cell-oocyte complexes by
adenovirus-mediated short-hairpin RNA expression.
|
18417710 | TNFAIP6,HAS2 | Identification of potential markers of oocyte competence expressed in bovine
cumulus cells matured with follicle-stimulating hormone and/or phorbol myristate
acetate in vitro.
|
17901238 | TNFAIP6,HAS2 | Hormone-induced expression of tumor necrosis factor alpha-converting enzyme/A
disintegrin and metalloprotease-17 impacts porcine cumulus cell oocyte complex
expansion and meiotic maturation via ligand activation of the epidermal growth
factor receptor.
|
16908014 | TNFAIP6,HAS2 | The preantral granulosa cell to cumulus cell transition in the mouse ovary:
development of competence to undergo expansion.
|
16707453 | TNFAIP6,DACT1 | Progression-specific genes identified by expression profiling of matched ductal
carcinomas in situ and invasive breast tumors, combining laser capture
microdissection and oligonucleotide microarray analysis.
|
16650051 | TNFAIP6,HAS2 | Towards profiling the gene expression of fibroblasts from atopic dermatitis
patients: human 8K complementary DNA microarray.
|
16453284 | TNFAIP6,ADAM12 | Reproducible genetic associations between candidate genes and clinical knee
osteoarthritis in men and women.
|
19184239 | ADAM12,ALDH1A1 | Differential gene expression analysis of subcutaneous fat, fascia, and skin
overlying a Dupuytren's disease nodule in comparison to control tissue.
|
19121738 | ADAM12,POSTN,ALDH1A1 | Identification of biomarkers in Dupuytren's disease by comparative analysis of
fibroblasts versus tissue biopsies in disease-specific phenotypes.
|
19036616 | ADAM12,ASPN | Attempt to replicate published genetic associations in a large, well-defined
osteoarthritis case-control population (the GOAL study).
|
18790654 | ADAM12,ADAMTS2 | Association of a nsSNP in ADAMTS14 to some osteoarthritis phenotypes.
|
17355265 | ADAM12,ADAMTS5 | ADAMs in cancer cell proliferation and progression.
|
15910695 | ADAM12,ASPN | The genetic epidemiology of human primary osteoarthritis: current status.
|
15280379 | ADAM12,SH3D19 | ADAM binding protein Eve-1 is required for ectodomain shedding of epidermal
growth factor receptor ligands.
|
14730609 | ADAMTS12,ADAMTS2,ADAMTS5 | Expression profiling of metalloproteinases and their inhibitors in cartilage.
|
20555395 | ADAMTS2,P4HA2 | Endoplasmic reticulum stress inhibits collagen synthesis independent of
collagen-modifying enzymes in different chondrocyte populations and dermal
fibroblasts.
|
18762113 | ADAMTS2,ADAMTS5 | Metalloproteinase gene expression correlates with clinical outcome in Dupuytren's
disease.
|
16470729 | ADAMTS2,SFRP4 | Evidence of genetic underexpression in chorionic villi samples of euploid fetuses
with increased nuchal translucency at 10-11 weeks' gestation.
|
12697333 | ADAMTS2,ADAMTS5 | Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived
cell line ARPE-19: transcriptional regulation by TNFalpha.
|
11167130 | ADAMTS2,ADAMTS5 | ADAMTS: a novel family of extracellular matrix proteases.
|
20109188 | ADAMTS5,PTGES | Analysis of meniscal degeneration and meniscal gene expression.
|
19922873 | ADAMTS5,FBLN1,BMP4 | ADAMTS metalloproteases generate active versican fragments that regulate
interdigital web regression.
|
19840795 | ADAMTS5,MMP3 | Matrilin-3 activates the expression of osteoarthritis-associated genes in primary
human chondrocytes.
|
19223608 | ADAMTS5,POSTN | Muscle genome-wide expression profiling during disease evolution in mdx mice.
|
19040300 | ADAMTS5,MMP3 | Telomerase transduced osteoarthritis fibroblast-like synoviocytes display a
distinct gene expression profile.
|
17966030 | ADAMTS5,MMP3 | Detection of gene expression in synovium of patients with osteoarthritis using a
random sequencing method.
|
17530714 | ADAMTS5,PTGES | Global analyses of gene expression in early experimental osteoarthritis.
|
16601225 | ADAMTS5,AOX1 | Thrombin and NAD(P)H oxidase-mediated regulation of CD44 and BMP4-Id pathway in
VSMC, restenosis, and atherosclerosis.
|
20397748 | ADAMTSL3,EFEMP1 | Genome-wide association study of height and body mass index in Australian twin
families.
|
18391952 | ADAMTSL3,EFEMP1 | Genome-wide association analysis identifies 20 loci that influence adult height.
|
18840552 | AEBP1,ANGPTL4,PRRX1 | Gene expression profile of the bone microenvironment in human fragility fracture
bone.
|
20230802 | ANGPTL4,CYGB | Neuroglobin, cytoglobin, and transcriptional profiling of hypoxia-related genes
in the rat cerebellum after prenatal chronic very mild carbon monoxide exposure
(25 ppm).
|
18505769 | ANGPTL4,EFEMP1 | Serial analysis of the vascular endothelial transcriptome under static and shear
stress conditions.
|
18457598 | ANGPTL4,IGFBP3 | The role of the small intestine in the development of dietary fat-induced obesity
and insulin resistance in C57BL/6J mice.
|
17033689 | ANGPTL4,PRRX1 | Vascular response to hypoxic preconditioning in the immature brain.
|
16685428 | ANGPTL4,THBS2 | Comparative integromics on Angiopoietin family members.
|
19885562 | AOX1,FBLN1 | Microarray gene expression profiling in meningiomas: differential expression
according to grade or histopathological subtype.
|
19781675 | AOX1,PTN | A microarray based identification of osteoporosis-related genes in primary
culture of human osteoblasts.
|
16879361 | ASPN,OGN | Porcine OGN and ASPN: mapping, polymorphisms and use for quantitative trait loci
identification for growth and carcass traits in a Meishan x Pietrain intercross.
|
20680026 | CCL11,CCL19 | Expression of chemokine decoy receptors and their ligands at the porcine
maternal-fetal interface.
|
20656925 | CCL11,CXCL1 | The migration of T cells in response to influenza virus is altered in neonatal
mice.
|
20625511 | CCL11,IL33 | Gene transcription changes in asthmatic chronic rhinosinusitis with nasal polyps
and comparison to those in atopic dermatitis.
|
20502518 | CCL11,CCL19,CXCL1 | Co-ordinated gene expression in the liver and spleen during Schistosoma japonicum
infection regulates cell migration.
|
20335622 | CCL11,CCL19 | Chemokine levels in subretinal fluid obtained during scleral buckling surgery
after rhegmatogenous retinal detachment.
|
20187767 | CCL11,CXCL1 | Associations of four circulating chemokines with multiple atherosclerosis
phenotypes in a large population-based sample: results from the dallas heart
study.
|
20161726 | CCL11,CXCL1 | Temporal expression of chemokines dictates the hepatic inflammatory infiltrate in
a murine model of schistosomiasis.
|
19893035 | CCL11,CXCL1 | Treatment with a novel chemokine-binding protein or eosinophil lineage-ablation
protects mice from experimental colitis.
|
19845793 | CCL11,CXCL1 | Eosinophils infiltrate thyroids, but have no apparent role in induction or
resolution of experimental autoimmune thyroiditis in interferon-gamma(-/-) mice.
|
19473542 | CCL11,IL7 | Potential plasma markers of Type 1 and Type 2 leprosy reactions: a preliminary
report.
|
19428942 | CCL11,CXCL1 | Cytokine and chemokine expression patterns in lung epithelial cells exposed to
components characteristic of particulate air pollution.
|
18286574 | CCL11,CCL19 | Immunomodulation by herpesvirus U51A chemokine receptor via CCL5 and FOG-2
down-regulation plus XCR1 and CCR7 mimicry in human leukocytes.
|
17982926 | CCL11,CCL19 | Complementary DNA microarray analysis of chemokines and their receptors in
allergic rhinitis.
|
20139367 | CCL19,CXCL1 | Mouse aorta smooth muscle cells differentiate into lymphoid tissue organizer-like
cells on combined tumor necrosis factor receptor-1/lymphotoxin beta-receptor
NF-kappaB signaling.
|
19800444 | CCL19,CXCL1 | Local cytokine and inflammatory responses to candidate vaginal adjuvants in mice.
|
19737877 | CCL19,PDPN | Expression of podoplanin and other lymphatic markers in the human anterior eye
segment.
|
19164539 | CCL19,IL7 | Characterization of the thymic IL-7 niche in vivo.
|
20060954 | CLEC3B,MSX1 | Genome-wide expression profiling reveals new candidate genes associated with
osteoarthritis.
|
20302629 | COL6A1,COL6A2 | Identification of a deep intronic mutation in the COL6A2 gene by a novel custom
oligonucleotide CGH array designed to explore allelic and genetic heterogeneity
in collagen VI-related myopathies.
|
19777066 | COL6A1,SLIT3 | Regulation of adipose tissue stromal cells behaviors by endogenic Oct4 expression
control.
|
19309692 | COL6A1,COL6A2 | Identification and characterization of novel collagen VI non-canonical splicing
mutations causing Ullrich congenital muscular dystrophy.
|
16317594 | COL6A1,COL6A2 | [Myopathy with trabecular fibers associated with familiar autoimmune
polyglandular syndrome type 1]
|
15372526 | COL6A1,COL6A2 | Dilated ascending aorta in a child with ring chromosome 21 syndrome.
|
19078680 | COL6A1,COL6A2 | Bethlem myopathy in a black creole pedigree.
|
11865138 | COL6A1,COL6A2 | Novel mutations in collagen VI genes: expansion of the Bethlem myopathy
phenotype.
|
11331940 | COL6A1,COL6A2 | Physical mapping of mouse collagen genes on chromosome 10 by high-resolution
FISH.
|
9107679 | COL6A1,COL6A2 | Human COL6A1: genomic characterization of the globular domains, structural and
evolutionary comparison with COL6A2.
|
8812475 | COL6A1,COL6A2 | Fine genetic map of mouse chromosome 10 around the polycystic kidney disease
gene, jcpk, and ankyrin 3.
|
8575781 | COL6A1,COL6A2 | Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH.
|
7486833 | COL6A1,COL6A2 | Genetic variation in the COL6A1 region is associated with congenital heart
defects in trisomy 21 (Down's syndrome).
|
7782083 | COL6A1,COL6A2 | Structure of the terminal 300 kb of DNA from human chromosome 21q.
|
8188291 | COL6A1,COL6A2 | Cloning of cDNA and genomic DNA encoding human type XVIII collagen and
localization of the alpha 1(XVIII) collagen gene to mouse chromosome 10 and human
chromosome 21.
|
8094066 | COL6A1,COL6A2 | Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster:
novel DNA polymorphisms in the region of a candidate gene for congenital heart
defects in Down's syndrome.
|
1837533 | COL6A1,COL6A2 | Fine structure physical mapping of the region of mouse chromosome 10 homologous
to human chromosome 21.
|
1676701 | COL6A1,COL6A2 | The COL6A1 and COL6A2 genes exist as a gene cluster and detect highly informative
DNA polymorphisms in the telomeric region of human chromosome 21q.
|
1979060 | COL6A1,COL6A2 | Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region
on human chromosome 2.
|
19073771 | DACT1,SFRP1 | Dact1, a nutritionally regulated preadipocyte gene, controls adipogenesis by
coordinating the Wnt/beta-catenin signaling network.
|
17943183 | DACT1,SFRP4 | Increased expression of Wnt2 and SFRP4 in Tsk mouse skin: role of Wnt signaling
in altered dermal fibrillin deposition and systemic sclerosis.
|
17873379 | DACT1,SFRP1 | Networking of WNT, FGF, Notch, BMP, and Hedgehog signaling pathways during
carcinogenesis.
|
19955106 | DKK2,SFRP4 | Excessive ovarian stimulation up-regulates the Wnt-signaling molecule DKK1 in
human endometrium and may affect implantation: an in vitro co-culture study.
|
19815336 | DKK2,MSX1,SFRP1 | MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in
neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3.
|
19562778 | DKK2,SFRP4 | Wnt antagonist gene polymorphisms and renal cancer.
|
19185060 | DKK2,SFRP1 | Comprehensive expression analysis of all Wnt genes and their major secreted
antagonists during mouse limb development and cartilage differentiation.
|
18021006 | DKK2,SFRP1 | Genetic analyses in a sample of individuals with high or low BMD shows
association with multiple Wnt pathway genes.
|
17392486 | DKK2,SFRP1 | Gene expression change in the Mullerian duct of the mouse fetus exposed to
diethylstilbestrol in utero.
|
17143565 | DKK2,SFRP4,SFRP1 | WNT antagonist, DKK2, is a Notch signaling target in intestinal stem cells:
augmentation of a negative regulation system for canonical WNT signaling pathway
by the Notch-DKK2 signaling loop in primates.
|
16328026 | DKK2,SFRP4,SFRP1 | WNT antagonist, SFRP1, is Hedgehog signaling target.
|
16077992 | DKK2,SFRP4 | Comparative genomics on SFRP2 orthologs.
|
16077939 | DKK2,SFRP4 | Comparative genomics on SFRP1 orthologs.
|
16778180 | EFEMP2,UNC5C,TGFB2 | Silencing of Peroxiredoxin 2 and aberrant methylation of 33 CpG islands in
putative promoter regions in human malignant melanomas.
|
10982184 | EFEMP2,EFEMP1 | Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the
multiple retinopathy critical region on 11q13.
|
19347865 | EPHA3,ROBO2 | Characterization of the 3p12.3-pcen region associated with tumor suppression in a
novel ovarian cancer cell line model genetically modified by chromosome 3
fragment transfer.
|
17185612 | EPHA3,TMEM45A | Transcriptional profiling of human cord blood CD133+ and cultured bone marrow
mesenchymal stem cells in response to hypoxia.
|
20722018 | FBLN1,GDF10 | Characterisation of the human nucleus pulposus cell phenotype and evaluation of
novel marker gene expression to define adult stem cell differentiation.
|
19924294 | FSTL1,BMP4 | Correlating global gene regulation to angiogenesis in the developing chick
extra-embryonic vascular system.
|
19017814 | GDF10,MMP3 | Identification of uterine leiomyoma genes developmentally reprogrammed by
neonatal exposure to diethylstilbestrol.
|
18703560 | GDF10,MGP | Retinoic acid receptor gamma-induced misregulation of chondrogenesis in the
murine limb bud in vitro.
|
19941983 | GPC6,GPC4 | An interstitial duplication of chromosome 13q31.3q32.1 further delineates the
critical region for postaxial polydactyly type A2.
|
19259985 | GPC6,SDC2 | The osteogenic transcription factor Runx2 regulates components of the fibroblast
growth factor/proteoglycan signaling axis in osteoblasts.
|
11566272 | GPC6,GPC4 | A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene
cluster on chromosome 13q32.
|
10480909 | GPC6,GPC4 | Glypican-6, a new member of the glypican family of cell surface heparan sulfate
proteoglycans.
|
10329016 | GPC6,GPC4 | GPC6, a novel member of the glypican gene family, encodes a product structurally
related to GPC4 and is colocalized with GPC5 on human chromosome 13.
|
19265796 | LEPR,LUM | Hepatic gene expression in morbidly obese women: implications for disease
susceptibility.
|
17069581 | LUM,PHLDA1 | Identification of transcripts modulated by ETV6 expression.
|
11092399 | LUM,BGN | A comparison of the expression pattern of five genes of the family of small
leucine-rich proteoglycans during mouse development.
|
18407260 | MEIS2,SFRP1 | Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways
for early limb and skeletal patterning.
|
15735049 | MRC2,P4HA2 | Gene expression profile of papillary thyroid cancer: sources of variability and
diagnostic implications.
|
20845426 | MSX1,BMP4 | Regulation of Tbx22 during facial and palatal development.
|
20702560 | MSX1,BMP4 | BMP-mediated inhibition of FGF signaling promotes cardiomyocyte differentiation
of anterior heart field progenitors.
|
20672350 | MSX1,BMP2 | Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic
cleft palate.
|
20505756 | MSX1,BMP4 | A data integration approach to mapping OCT4 gene regulatory networks operative in
embryonic stem cells and embryonal carcinoma cells.
|
20493240 | MSX1,BMP4,BMP2 | The expression of twisted gastrulation in postnatal mouse brain and functional
implications.
|
20392740 | MSX1,BMPR1A | Opposing Fgf and Bmp activities regulate the specification of olfactory sensory
and respiratory epithelial cell fates.
|
20339300 | MSX1,BMP4 | Nicotine promotes cardiomyocyte apoptosis via oxidative stress and altered
apoptosis-related gene expression.
|
20123092 | MSX1,BMP4,BMP2 | Genetic interactions between Pax9 and Msx1 regulate lip development and several
stages of tooth morphogenesis.
|
19913004 | MSX1,BMP4 | Requirement for Lmo4 in the vestibular morphogenesis of mouse inner ear.
|
19766620 | MSX1,BMP2 | Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell
death during limb development.
|
19622795 | MSX1,SCARA5,PTN | Gene expression profiles of bovine caruncular and intercaruncular endometrium at
implantation.
|
19117070 | MSX1,SFRP1 | Sfrp1, Sfrp2, and Sfrp5 regulate the Wnt/beta-catenin and the planar cell
polarity pathways during early trunk formation in mouse.
|
18836915 | MSX1,POSTN | The effect of type I collagen on osteochondrogenic differentiation in
adipose-derived stromal cells in vivo.
|
18667074 | MSX1,HAS2 | Msx1 and Msx2 are required for endothelial-mesenchymal transformation of the
atrioventricular cushions and patterning of the atrioventricular myocardium.
|
18990770 | NPAS2,IGFBP3 | Correlation between circadian gene variants and serum levels of sex steroids and
insulin-like growth factor-I.
|
19864897 | PDZRN3,ROBO2 | Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl
with 46,XX,inv(7)dn karyotype and phenotypic abnormalities.
|
20634963 | PLA2R1,ROBO2,PDPN | Systematic analysis of a novel human renal glomerulus-enriched gene expression
dataset.
|
19204725 | PLAT,SFRP1 | Chromosome 8p as a potential hub for developmental neuropsychiatric disorders:
implications for schizophrenia, autism and cancer.
|
18492260 | PLAT,POSTN,PDPN | Anaplastic oligodendrogliomas with 1p19q codeletion have a proneural gene
expression profile.
|
19723774 | POSTN,PTN | Lack of periostin leads to suppression of Notch1 signaling and calcific aortic
valve disease.
|
18490578 | POSTN,MMP3 | Examination of oral cancer biomarkers by tissue microarray analysis.
|
18076769 | POSTN,PTN | Unravelling the molecular control of calvarial suture fusion in children with
craniosynostosis.
|
16360395 | RARRES2,ALDH1A1 | Expression profiling of adrenocortical neoplasms suggests a molecular signature
of malignancy.
|
20651036 | ROBO2,SLIT3 | Expression of the repulsive SLIT/ROBO pathway in the human endometrium and
Fallopian tube.
|
20631173 | ROBO2,SLIT3 | Collaborative and specialized functions of Robo1 and Robo2 in spinal commissural
axon guidance.
|
20123755 | ROBO2,SLIT3 | Prefrontal-enriched SLIT1 expression in Old World monkey cortex established
during the postnatal development.
|
19900988 | ROBO2,SLIT3 | Involvement of the SLIT/ROBO pathway in follicle development in the fetal ovary.
|
19114000 | ROBO2,SLIT3 | Quantification of SLIT-ROBO transcripts in hepatocellular carcinoma reveals two
groups of genes with coordinate expression.
|
18566128 | ROBO2,SLIT3 | Novel regulated expression of the SLIT/ROBO pathway in the ovary: possible role
during luteolysis in women.
|
17581972 | ROBO2,SLIT3 | Dual branch-promoting and branch-repelling actions of Slit/Robo signaling on
peripheral and central branches of developing sensory axons.
|
12471613 | ROBO2,SLIT3,UNC5C,NEO1 | Quantification of expression of netrins, slits and their receptors in human
prostate tumors.
|
11804569 | ROBO2,SLIT3 | Pathfinding and error correction by retinal axons: the role of astray/robo2.
|
11755787 | ROBO2,SLIT3 | Role of Slit proteins in the vertebrate brain.
|
11754167 | ROBO2,SLIT3 | Spatiotemporal expression patterns of slit and robo genes in the rat brain.
|
11472852 | ROBO2,SLIT3 | Expression patterns of Slit and Robo family members during vertebrate limb
development.
|
10864956 | ROBO2,SLIT3 | Slit inhibition of retinal axon growth and its role in retinal axon pathfinding
and innervation patterns in the diencephalon.
|
10842075 | ROBO2,SLIT3 | Expression of the vertebrate Slit gene family and their putative receptors, the
Robo genes, in the developing murine kidney.
|
20863401 | SDC2,SNAI2 | Runx2 transcriptome of prostate cancer cells: insights into invasiveness and bone
metastasis.
|
20824703 | SFRP4,SFRP1 | Integrated genetic and epigenetic analysis of bladder cancer reveals an additive
diagnostic value of FGFR3 mutations and hypermethylation events.
|
20795789 | SFRP4,SFRP1 | Acute myeloid leukemia is characterized by Wnt pathway inhibitor promoter
hypermethylation.
|
20364027 | SFRP4,SFRP1 | Methylation of cyclin-dependent kinase inhibitors, XAF1, JUNB, CDH13 and soluble
Wnt inhibitors in essential thrombocythaemia.
|
20145299 | SFRP4,SMOC2 | Transcriptomic signature of cell lines isolated from canine mammary
adenocarcinoma metastases to lungs.
|
20097210 | SFRP4,SFRP1 | Isorhamnetin-induced anti-adipogenesis is mediated by stabilization of
beta-catenin protein.
|
20030932 | SFRP4,SFRP1 | [Methylation status of CpG islands in secreted frizzled-related protein gene
promoter region of malignant hematopoietic cell lines]
|
19874621 | SFRP4,SFRP1 | Wnt pathway reprogramming during human embryonal carcinoma differentiation and
potential for therapeutic targeting.
|
19847810 | SFRP4,SFRP1 | Frequent promoter hypermethylation of Wnt pathway inhibitor genes in malignant
astrocytic gliomas.
|
19730886 | SFRP4,SFRP1 | SFRP4 was overexpressed in colorectal carcinoma.
|
19513747 | SFRP4,SFRP1 | Methylation analysis of SFRP genes family in cervical adenocarcinoma.
|
19387464 | SFRP4,SFRP1 | Wnt signaling pathway is epigenetically regulated by methylation of Wnt
antagonists in acute myeloid leukemia.
|
19299079 | SFRP4,SFRP1 | Epigenetic dysregulation of secreted Frizzled-related proteins in multiple
myeloma.
|
19038436 | SFRP4,SFRP1 | Promoter methylation of SFRPs gene family in cervical cancer.
|
18765431 | SFRP4,SFRP1 | Epigenetic dysregulation of the Wnt signalling pathway in chronic lymphocytic
leukaemia.
|
18716850 | SFRP4,SFRP1 | Epigenetic regulation of WNT signaling pathway genes in inflammatory bowel
disease (IBD) associated neoplasia.
|
18592156 | SFRP4,SFRP1 | Frequent epigenetic inactivation of SFRP genes in hepatocellular carcinoma.
|
18549404 | SFRP4,SFRP1 | Methylation status of Wnt signaling pathway genes affects the clinical outcome of
Philadelphia-positive acute lymphoblastic leukemia.
|
18542073 | SFRP4,SFRP1 | Profiling CpG island field methylation in both morphologically normal and
neoplastic human colonic mucosa.
|
18537968 | SFRP4,SFRP1 | Epigenetic inactivation of secreted Frizzled-related proteins in acute myeloid
leukaemia.
|
18519763 | SFRP4,SFRP1 | Aneuploidy predicts outcome in patients with endometrial carcinoma and is related
to lack of CDH13 hypermethylation.
|
17882284 | SFRP4,SFRP1 | Epigenetic dysregulation of Wnt signaling pathway in multiple myeloma.
|
17462603 | SFRP4,SFRP1 | Wnt3a binds to several sFRPs in the nanomolar range.
|
17443492 | SFRP4,SFRP1 | SFRP1 suppressed hepatoma cells growth through Wnt canonical signaling pathway.
|
17314492 | SFRP4,SFRP1 | Wnt signaling pathway in mammary gland development and carcinogenesis.
|
17148581 | SFRP4,SFRP1 | Epigenetic regulation of Wnt-signaling pathway in acute lymphoblastic leukemia.
|
16708382 | SFRP4,SFRP1 | Epigenetic inactivation of the SFRP genes is associated with drinking, smoking
and HPV in head and neck squamous cell carcinoma.
|
16423993 | SFRP4,SFRP1 | CpG island methylation and expression of the secreted frizzled-related protein
gene family in chronic lymphocytic leukemia.
|
16093361 | SFRP4,VEGFC | Mice null for Frizzled4 (Fzd4-/-) are infertile and exhibit impaired corpora
lutea formation and function.
|
15579438 | SFRP4,TGFB2 | CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in
WT1-mutant Wilms' tumors.
|
20298552 | SLIT3,MMP3 | Slit3 inhibits Robo3-induced invasion of synovial fibroblasts in rheumatoid
arthritis.
|
17942002 | SRPX,SRPX2 | Molecular evolution of the human SRPX2 gene that causes brain disorders of the
Rolandic and Sylvian speech areas.
|
20236627 | SRPX2,SVEP1 | Characterization of SVEP1, KIAA, and SRPX2 in an in vitro cell culture model of
endotoxemia.
|
17616930 | UNC5C,NEO1 | Analysis of Netrin 1 receptors during inner ear development.
|
20215856 | VEGFC,IGFBP3 | Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with
osteonecrosis of the femoral head.
|
19827050 | VEGFC,CXCL1 | Microarray analysis reveals potential target genes of NF-kappaB2/p52 in LNCaP
prostate cancer cells.
|
19778204 | VEGFC,FIGF | Existence of the lymphatic system in the primate corpus luteum.
|
19279691 | VEGFC,MMP3 | Alterations in gene expression induced by cyclic mechanical stress in trabecular
meshwork cells.
|
16685460 | VEGFC,FIGF | Comparative integromics on VEGF family members.
|
15614775 | VEGFC,FIGF | Vascular gene expression and phenotypic correlation during differentiation of
human embryonic stem cells.
|
20949628 | BMP4,BMP2 | Evaluation of germline BMP4 mutation as a cause of colorectal cancer.
|
20926645 | BMP4,BMP2 | Severe polyposis in Apc1322T mice is associated with submaximal Wnt signalling
and increased expression of the stem cell marker Lgr5.
|
20886619 | BMP4,BMP2 | BMP2 expression in the adult rat brain.
|
20861306 | BMP4,BMP2 | Heparan Sulfate Acts as a BMP Co-receptor by Facilitating Ligand-induced Receptor
Hetero-oligomerization.
|
20830741 | BMP4,BMP2 | Low-level laser irradiation enhances BMP-induced osteoblast differentiation by
stimulating the BMP/Smad signaling pathway.
|
20739376 | BMP4,BMP2,BMPR1A | Changes in expression of bone morphogenetic proteins, their receptors and inhibin
co-receptor betaglycan during bovine antral follicle development: inhibin can
antagonise the suppressive effect of BMPs on thecal androgen production.
|
20727875 | BMP4,BMP2 | Modulation of BMP signaling by Noggin is required for the maintenance of palatal
epithelial integrity during palatogenesis.
|
20691278 | BMP4,BMP2 | Highly efficient osteogenic differentiation of human mesenchymal stem cells by
eradication of STAT3 signaling.
|
20679827 | BMP4,BMP2 | Divergent modulation of adipose-derived stromal cell differentiation by TGF-beta1
based on species of derivation.
|
20665672 | BMP4,TGFB2 | Chondro/osteoblastic and cardiovascular gene modulation in human artery smooth
muscle cells that calcify in the presence of phosphate and calcitriol or
paricalcitol.
|
20660069 | BMP4,IGFBP3 | Identification of early response genes and pathway activated by androgens in the
initial segment and caput regions of the regressed rat epididymis.
|
20546278 | BMP4,BMP2 | Investigation of the association of BMP gene variants with nephropathy in Type 1
diabetes mellitus.
|
20506112 | BMP4,BMP2 | BMP signaling in the human fetal ovary is developmentally regulated and promotes
primordial germ cell apoptosis.
|
20505824 | BMP4,BMP2 | Agrin binds BMP2, BMP4 and TGFbeta1.
|
20376510 | BMP4,BMP2 | Identification of oxytetracycline as a chondrogenic compound using a cell-based
screening system.
|
20303683 | BMP4,BMP2 | Differential expression of mRNAs encoding BMP/Smad pathway molecules in antral
follicles of high- and low-fecundity Hu sheep.
|
20230640 | BMP4,BMP2 | Nuclear variants of bone morphogenetic proteins.
|
20175188 | BMP4,BMP2 | Expression patterns of hormones, signaling molecules, and transcription factors
during adenohypophysis development in the chick embryo.
|
20155803 | BMP4,BMP2 | Tieg1/Klf10 is upregulated by NGF and attenuates cell cycle progression in the
pheochromocytoma cell line PC12.
|
20130285 | BMP4,BMP2 | Regulation of retinal progenitor cell differentiation by bone morphogenetic
protein 4 is mediated by the smad/id cascade.
|
20124834 | BMP4,BMP2 | Human adipose-derived stromal cells respond to and elaborate bone morphogenetic
protein-2 during in vitro osteogenic differentiation.
|
20063299 | BMP4,BMP2 | Role of bone morphogenetic proteins on cochlear hair cell formation: analyses of
Noggin and Bmp2 mutant mice.
|
20042692 | BMP4,BMP2 | Bmp2 and Bmp4 exert opposing effects in hypoxic pulmonary hypertension.
|
20034106 | BMP4,BMP2 | Retinoic acid controls expression of tissue remodeling genes Hmgn1 and Fgf18 at
the digit-interdigit junction.
|
20019778 | BMP4,BMP2 | [Effect of icariin on the mRNA expressions of Cbfalpha1, BMP2, BMP4 in rat
osteoblasts]
|
20001953 | BMP4,BMP2 | Regulation of oligodendrocyte progenitor cell maturation by PPARdelta: effects on
bone morphogenetic proteins.
|
19937756 | BMP4,GATA6 | Heparan sulfation-dependent fibroblast growth factor signaling maintains
embryonic stem cells primed for differentiation in a heterogeneous state.
|
19923894 | BMP4,BMP2 | Interplay between BMP4 and IL-7 in human intrathymic precursor cells.
|
19900834 | BMP4,BMP2 | Control of BMP gene expression by long-range regulatory elements.
|
19879168 | BMP4,BMP2 | A common SNP near BMP2 is associated with severity of the iron burden in HFE
p.C282Y homozygous patients: a follow-up study.
|
19861972 | BMP4,BMP2 | Iba1(+)/NG2(+) macrophage-like cells expressing a variety of neuroprotective
factors ameliorate ischemic damage of the brain.
|
19860666 | BMP4,SNAI2 | Hedgehog target genes: mechanisms of carcinogenesis induced by aberrant hedgehog
signaling activation.
|
19846762 | BMP4,HAS2,BMP2 | T-box 2, a mediator of Bmp-Smad signaling, induced hyaluronan synthase 2 and
Tgfbeta2 expression and endocardial cushion formation.
|
19846600 | BMP4,BMP2 | Defining the window of germline genesis in vitro from murine embryonic stem
cells.
|
19786120 | BMP4,BMP2 | Interaction between bone morphogenetic proteins and endothelin-1 in human
pulmonary artery smooth muscle.
|
19786029 | BMP4,BMP2 | Iron-induced expression of bone morphogenic protein 6 in intestinal cells is the
main regulator of hepatic hepcidin expression in vivo.
|
19763374 | BMP4,BMP2 | Marrow stromal cell-based cyclooxygenase 2 ex vivo gene-transfer strategy
surprisingly lacks bone-regeneration effects and suppresses the bone-regeneration
action of bone morphogenetic protein 4 in a mouse critical-sized calvarial defect
model.
|
19737815 | BMP4,BMP2 | Axin2 controls bone remodeling through the beta-catenin-BMP signaling pathway in
adult mice.
|
19733655 | BMP4,BMP2 | Spemann's organizer and the self-regulation of embryonic fields.
|
19729534 | BMP4,BMP2 | Bone morphogenetic proteins.
|
20688128 | HAS2,MMP3 | Chondrotoxicity and toxicokinetics of novel quinolone antibacterial agents
DC-159a and DX-619 in juvenile rats.
|
18572299 | HAS2,MMP3 | Gene expression profiles in the articular cartilage of juvenile rats receiving
the quinolone antibacterial agent ofloxacin.
|
17980161 | HAS2,TGFB2 | Regulation of hyaluronan and versican deposition by growth factors in
fibrosarcoma cell lines.
|
16314491 | HAS2,BMPR1A | Bmp2 is essential for cardiac cushion epithelial-mesenchymal transition and
myocardial patterning.
|
20617365 | IGFBP3,BMP2 | Identification of diagnostic serum protein profiles of glioblastoma patients.
|
20553613 | IGFBP3,GATA6 | Establishment and characterization of a new human pancreatic adenocarcinoma cell
line with high metastatic potential to the lung.
|
20180422 | IGFBP3,TGFB2 | [Literature-mining and bioinformatic analysis of androgen-independent prostate
cancer-specific genes]
|
20042640 | IGFBP3,PTGES | Hypoxia activates the cyclooxygenase-2-prostaglandin E synthase axis.
|
19551141 | IGFBP3,MMP3 | Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in
familial and sporadic renal cell carcinoma.
|
17912462 | IGFBP3,PTGES | Genes regulated by interferon-gamma in human uterine microvascular endothelial
cells.
|
19953602 | MMP3,TGFB2 | Estrogen modulates iodoacetate-induced gene expression in bovine cartilage
explants.
|
18023983 | MMP3,C1R | Proteomic analysis of the LPS-induced stress response in rat chondrocytes reveals
induction of innate immune response components in articular cartilage.
|
20457798 | PTN,PDPN | Lymphatic capillary hypoplasia in the skin of fetuses with increased nuchal
translucency and Turner's syndrome: comparison with trisomies and controls.
|
19478889 | PTN,MGP | The Potential of N-Rich Plasma-Polymerized Ethylene (PPE:N) Films for Regulating
the Phenotype of the Nucleus Pulposus.
|
17786487 | PTN,MGP | A phenotypic comparison of intervertebral disc and articular cartilage cells in
the rat.
|
16079240 | PTN,ALDH1A1 | Expression quantitative trait loci analysis of 13 genes in the rat prostate.
|
19424592 | SFRP1,SNAI2 | Integrative genomic analyses of ZEB2: Transcriptional regulation of ZEB2 based on
SMADs, ETS1, HIF1alpha, POU/OCT, and NF-kappaB.
|
18698484 | SFRP1,SNAI2 | Hedgehog signaling, epithelial-to-mesenchymal transition and miRNA (review).
|
18398573 | SNAI2,PDPN | Gene expression profile analysis of primary glioblastomas and non-neoplastic
brain tissue: identification of potential target genes by oligonucleotide
microarray and real-time quantitative PCR.
|
20396349 | MGP,BMP2 | [Effect of age on vascular calcification induced by vitamin D3 and nicotine]
|
15629771 | SERPING1,PTGES | Gene expression profiles of primary HPV16- and HPV18-infected early stage
cervical cancers and normal cervical epithelium: identification of novel
candidate molecular markers for cervical cancer diagnosis and therapy.
|
20523179 | BMP2,TGFB2 | Growth factors and gene expression of stem cells: bone marrow compared with
peripheral blood.
|
20499346 | BMP2,TGFB2 | NVP-BEZ235, a dual pan class I PI3 kinase and mTOR inhibitor, promotes osteogenic
differentiation in human mesenchymal stromal cells.
|
20304956 | BMP2,BMPR1A | Epithelial to mesenchymal transition in human skin wound healing is induced by
tumor necrosis factor-alpha through bone morphogenic protein-2.
|
19874086 | BMP2,BMPR1A | Wnt inhibitors Dkk1 and Sost are downstream targets of BMP signaling through the
type IA receptor (BMPRIA) in osteoblasts.
|
19760469 | BMP2,BMPR1A | Are endogenous BMPs necessary for bone healing during distraction osteogenesis?
|
19318548 | BMPR1A,PTGES | Induction of prostaglandin E2 pathway promotes gastric hamartoma development with
suppression of bone morphogenetic protein signaling.
|