Coarse module 36 - Fibroblasts genes - extracellular matrix


Publications with genes in this module (limited to maximum 200 per gene):11449 (10693 unique)
Publications with more than one gene in this module:
Pubmed IDGene symbolsTitle
16445568ABCA8A,ABCA8BAcute digoxin loading reduces ABCA8A mRNA expression in the mouse liver.
12532264ABCA8A,ABCA8BEvolutionary analysis of a cluster of ATP-binding cassette (ABC) genes.
20797428ACTA2,TAGLNResveratrol induces p53 and suppresses myocardin-mediated vascular smooth muscle cell differentiation.
20190033ACTA2,COL1A1,COL1A2,TAGLNAutocrine production of TGF-beta1 promotes myofibroblastic differentiation of neonatal lung mesenchymal stem cells.
20155481ACTA2,COL3A1Spontaneous arterial dissection: phenotype and molecular pathogenesis.
20096952ACTA2,TAGLNProliferation of human primary vascular smooth muscle cells depends on serum response factor.
20089806ACTA2,TAGLN,MMP3Cyclosporine up-regulates Kruppel-like factor-4 (KLF4) in vascular smooth muscle cells and drives phenotypic modulation in vivo.
19956410ACTA2,BMP4Evaluation of differentially expressed genes identified in keratoconus.
19639654ACTA2,COL3A1Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD).
19635739ACTA2,COL3A1,TAGLN,POSTNProgesterone and interferon tau-regulated genes in the ovine uterine endometrium: identification of periostin as a potential mediator of conceptus elongation.
1675193ACTA2,PLATA linkage map of mouse chromosome 8: further definition of homologous linkage relationships between mouse chromosome 8 and human chromosomes 8, 16, and 19.
20889195C1S,C1REnzymatic pathways in the pathogenesis of hereditary angioedema: The role of C1 inhibitor therapy.
20693203C1S,C1RCutaneous manifestations of complement deficiencies.
20682770C1S,C1RIdentification of the Matriptase Second CUB Domain as the Secondary Site for Interaction with Hepatocyte Growth Factor Activator Inhibitor Type-1.
20666732C1S,C1RSelf-association and domain rearrangements between complement C3 and C3u provide insight into the activation mechanism of C3.
20592021C1S,C1RMapping surface accessibility of the C1r/C1s tetramer by chemical modification and mass spectrometry provides new insights into assembly of the human C1 complex.
20580091C1S,C1RThe plasma bradykinin-forming pathways and its interrelationships with complement.
20542571C1S,C1RNew insights into the molecular mechanisms of classical complement activation.
20351192C1S,C1RFunctional characterization of the recombinant human C1 inhibitor serpin domain: insights into heparin binding.
20237569C1S,C1RStructural basis for receptor recognition of vitamin-B(12)-intrinsic factor complexes.
20178990C1S,C1RCalcium-dependent conformational flexibility of a CUB domain controls activation of the complement serine protease C1r.
20153898C1S,C1RMolecular mechanisms involved in the inactivation of the first component of human complement by Trypanosoma cruzi calreticulin.
20118239C1S,C1REngineering novel complement activity into a pulmonary surfactant protein.
20008834C1S,C1RAnalysis 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.
19896716C1S,C1RHuman astrovirus coat protein binds C1q and MBL and inhibits the classical and lectin pathways of complement activation.
19874244C1S,C1RAnti-complementary effect of polysaccharide B3-PS1 in Herba Scutellariae Barbatae (Scutellaria barbata).
19843402C1S,C1RPathogenesis and laboratory diagnosis of hereditary angioedema.
19807696C1S,C1RComplement activation and disease: protective effects of hyperbilirubinaemia.
19806892C1S,C1R[Anti-complement activity of polysaccharide B3-PS2 purified from Herba Scutellariae Barbatae]
19783065C1S,C1RPaths reunited: Initiation of the classical and lectin pathways of complement activation.
19627250C1S,C1RAnti-complementary effect of polysacchride B3-PS1 in Herba Scutellariae Barbatae (Scutellaria barbata).
19564340C1S,C1RMASP-1, a promiscuous complement protease: structure of its catalytic region reveals the basis of its broad specificity.
19522701C1S,SERPING1Modulation of the proteolytic activity of the complement protease C1s by polyanions: implications for polyanion-mediated acceleration of interaction between C1s and SERPING1.
19505678C1S,C1RA protein-bound polysaccharide from the stem bark of Eucommia ulmoides and its anti-complementary effect.
19494305C1S,C1RScabies mite inactivated serine protease paralogs inhibit the human complement system.
19494295C1S,C1RAnalogous interactions in initiating complexes of the classical and lectin pathways of complement.
19477526C1S,C1REarly complement proteases: C1r, C1s and MASPs. A structural insight into activation and functions.
19473974C1S,C1RIdentification of the C1q-binding Sites of Human C1r and C1s: a refined three-dimensional model of the C1 complex of complement.
19357398C1S,C1RMolecular mechanisms of the defective hepcidin inhibition in TMPRSS6 mutations associated with iron-refractory iron deficiency anemia.
19243221C1S,C1RNeto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning.
19150444C1S,C1RUnconjugated bilirubin inhibits C1 esterase activity.
19025126C1S,C1RHuman astrovirus coat protein: a novel C1 inhibitor.
18977695C1S,C1RC1, MBL-MASPs and C1-inhibitor: novel approaches for targeting complement-mediated inflammation.
18760304C1S,C1REvolutionary origin of the vertebrate blood complement and coagulation systems inferred from liver EST analysis of lamprey.
18758157C1S,SERPING1,C1RMutational spectrum of the C1INH (SERPING1) gene in patients with hereditary angioedema.
20476965C1S,C1RComplement deficiency and systemic lupus erythematosus: consensus and dilemma.
18674818C1S,C1RBiological activities of C1 inhibitor.
18664565C1S,C1RMolecular determinants of Xolloid action in vivo.
18602068C1S,C1RIsolation and characterization of an anti-complementary protein-bound polysaccharide from the stem barks of Eucommia ulmoides.
18561091C1S,SERPING1,C1RTranscriptome studies of bovine endometrium reveal molecular profiles characteristic for specific stages of estrous cycle and early pregnancy.
18510966C1S,C1RPlasma concentration of SCUBE1, a novel platelet protein, is elevated in patients with acute coronary syndrome and ischemic stroke.
18369152C1S,C1RRegulation of tumor necrosis factor receptor-1 and the IKK-NF-kappaB pathway by LDL receptor-related protein explains the antiinflammatory activity of this receptor.
18164932C1S,C1RProcollagen C-proteinase enhancer-1 (PCPE-1) interacts with beta2-microglobulin (beta2-m) and may help initiate beta2-m amyloid fibril formation in connective tissues.
18160218C1S,C1RComplement activation in the peripheral nervous system following the spinal nerve ligation model of neuropathic pain.
18062908C1S,C1RGenetic analysis of complement C1s deficiency associated with systemic lupus erythematosus highlights alternative splicing of normal C1s gene.
18054386C1S,C1RStudies on the haemolytic activity of circulating C1q-C3/C4 complexes.
18048067C1S,C1RHuman 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.
17850949C1S,C1RThe initiating proteases of the complement system: controlling the cleavage.
17608619C1S,C1RHuman alpha2-macroglobulin is composed of multiple domains, as predicted by homology with complement component C3.
17544813C1S,C1RAssembly of C1 and the MBL- and ficolin-MASP complexes: structural insights.
17544812C1S,C1RSerine proteases of the classical and lectin pathways: similarities and differences.
17442284C1S,C1RTransgenic overexpression of the secreted, extracellular EGF-CUB domain-containing protein SCUBE3 induces cardiac hypertrophy in mice.
17356516C1S,MGP,TGFB2Microarray reveals complement components are regulated in the serum-deprived rat retinal ganglion cell line.
17244723C1S,C1RAlterations of the classic pathway of complement in adipose tissue of obesity and insulin resistance.
17244159C1S,C1RStudies on the interactions between C-reactive protein and complement proteins.
17178384C1S,C1RIsolation and characterization of an anti-complementary polysaccharide D3-S1 from the roots of Bupleurum smithii.
17143562C1S,C1RConformationally 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.
17137866C1S,C1RFirst case of homozygous C1 inhibitor deficiency.
17071722C1S,C1RComplement levels and activity in the normal and LPS-injured lung.
17051152C1S,C1RThe structure of complement C3b provides insights into complement activation and regulation.
17005253C1S,C1RSynthesis of complement proteins in the human chorion is differentially regulated by cytokines.
16906756C1S,C1RExistence of different but overlapping IgG- and IgM-binding sites on the globular domain of human C1q.
16845603C1S,C1RGene expression profiling in Salmonella Choleraesuis-infected porcine lung using a long oligonucleotide microarray.
16753137C1S,C1RLocalization and characterization of a novel secreted protein SCUBE1 in human platelets.
16716085C1S,C1RThe 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.
16707773C1S,C1RIdentification and characterization of novel and unknown mouse epididymis-specific genes by complementary DNA microarray technology.
16697920C1S,C1RLectin complement system and pattern recognition.
16227207C1S,C1RFunctional 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.
16217168C1S,C1RHereditary angioedema.
16177097C1S,C1RFunctional role of the linker between the complement control protein modules of complement protease C1s.
16167883C1S,C1RImmune function of C1q and its modulators CD91 and CD93.
16003522C1S,C1RCloning of a quail homologue of hatching enzyme: its conserved function and additional function in egg envelope digestion.
15988036C1S,C1RPlatelet-derived growth factor D is activated by urokinase plasminogen activator in prostate carcinoma cells.
15866474C1S,C1RIdentification of an astacin-like metallo-proteinase transcript from the infective larvae of Strongyloides stercoralis.
15774619C1S,C1RCleavage of ultralarge multimers of von Willebrand factor by C-terminal-truncated mutants of ADAMTS-13 under flow.
15705970C1S,C1RHigh throughput substrate specificity profiling of serine and cysteine proteases using solution-phase fluorogenic peptide microarrays.
15670912C1S,C1RInhibition of classical pathway of complement activation with negative charged derivatives of bisphenol A and bisphenol disulphates.
15609759C1S,C1RComplement determinations in human disease.
15596403C1S,C1RThe pathophysiology of hereditary angioedema.
15527420C1S,C1RA novel human complement-related protein, C1r-like protease (C1r-LP), specifically cleaves pro-C1s.
15514703C1S,C1RBiological effects of C1 inhibitor.
15464227C1S,C1RExpression of Btcl2, a novel member of Btcl gene family, during development of the central nervous system.
15385675C1S,C1RProhaptoglobin is proteolytically cleaved in the endoplasmic reticulum by the complement C1r-like protein.
15358180C1S,C1RA novel human dendritic cell-derived C1r-like serine protease analog inhibits complement-mediated cytotoxicity.
15262284C1S,C1RCloning and molecular characterization of a cubilin-related serine proteinase from the hard tick Haemaphysalis longicornis.
15225624C1S,C1RVIGR--a novel inducible adhesion family G-protein coupled receptor in endothelial cells.
15218103C1S,C1ROrigin of the classical complement pathway: Lamprey orthologue of mammalian C1q acts as a lectin.
15159063C1S,C1RcC1q-R (calreticulin) and gC1q-R/p33: ubiquitously expressed multi-ligand binding cellular proteins involved in inflammation and infection.
14996732C1S,C1RA potential oncogenic activity of platelet-derived growth factor d in prostate cancer progression.
14748705C1S,C1RProteases of the complement system.
14674770C1S,C1RImportance of the prime subsites of the C1s protease of the classical complement pathway for recognition of substrates.
14644096C1S,C1RMicroglial activation and increased synthesis of complement component C1q precedes blood-brain barrier dysfunction in rats.
14628103C1S,C1RComplete 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.
14499584C1S,C1RInteraction of fucoidan with the proteins of the complement classical pathway.
12914573C1S,C1RThe human complement component C1R gene: the exon-intron structure and the molecular basis of allelic diversity.
12887296C1S,C1RBiochemistry and genetics of mannan-binding lectin (MBL).
12818633C1S,C1RExpansion of genes encoding complement components in bony fish: biological implications of the complement diversity.
12805391C1S,C1RHigh expression of complement components in omental adipose tissue in obese men.
12788922C1S,C1RX-ray structure of the Ca2+-binding interaction domain of C1s. Insights into the assembly of the C1 complex of complement.
12746311C1S,C1RControl of insulin-like growth factor binding protein-5 protease synthesis and secretion by human fibroblasts and porcine aortic smooth muscle cells.
12744720C1S,C1RMouse matriptase-2: identification, characterization and comparative mRNA expression analysis with mouse hepsin in adult and embryonic tissues.
12730962C1S,C1RExpression of complement messenger RNAs and proteins by human oligodendroglial cells.
12708315C1S,C1R[The mechanism of inhibition of the activation of the complement first component by polyanions and polycations ]
20937261COL1A1,COL3A1Combined use of bFGF and GDF-5 enhances the healing of medial collateral ligament injury.
20922862COL1A1,COL1A2[Osteogenesis imperfecta and achievements in cell and gene therapy]
20869473COL1A1,DCN,LOXSelective isolation and differentiation of a stromal population of human embryonic stem cells with osteogenic potential.
20855225COL1A1,COL1A2Genetics of bone diseases: Paget's disease, fibrous dysplasia, osteopetrosis, and osteogenesis imperfecta.
20842701COL1A1,COL3A1Impact of Smad3 loss of function on scarring and adhesion formation during tendon healing.
20839322COL1A1,COL3A1Cycle-dependent matrix remodeling gene expression response in fatigue-loaded rat patellar tendons.
20839288COL1A1,COL1A2Mutations in FKBP10 cause recessive osteogenesis imperfecta and type 1 bruck syndrome.
20824135COL1A1,COL3A1The effects of aging on the molecular and cellular composition of the prostate microenvironment. LID - e12501 [pii]
20820878COL1A1,HAS2Lactoferrin promotes hyaluronan synthesis in human dermal fibroblasts.
20807599COL1A1,BMP2Deficiency of vitamin A delays bone healing process in association with reduced BMP2 expression after drill-hole injury in mice.
20736093COL1A1,COL1A2Collagen gene polymorphisms influence fracture risk and bone mass acquisition during childhood and adolescent growth.
20724489COL1A1,COL1A2Dietary fluoride restriction does not alter femoral biomechanical strength in col1a2-deficient (oim) mice with type I collagen glomerulopathy.
20721936COL1A1,COL1A2Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants.
20705404COL1A1,COL3A1Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathology.
20698769COL1A1,COL1A2Optimization of genetic engineering and homologous recombination of collagen type I genes in rat bone marrow mesenchymal stem cells (MSC).
20697743COL1A1,COL1A2,COL3A1,MGPAntler development and coupled osteoporosis in the skeleton of red deer Cervus elaphus: expression dynamics for regulatory and effector genes.
20675929COL1A1,COL1A2[The genetic basis for skeletal disease. Osteogenesis imperfecta and genetic abnormalities]
20660018COL1A1,COL1A2A sensitive short-term evaluation of antifibrotic effects using newly established type I collagen reporter transgenic rats.
20646442COL1A1,SFRP1[Microarray analysis of gene expression profiles in pelvic organ prolapse.]
20546554COL1A1,COL3A1Monitoring the healing of combat wounds using Raman spectroscopic mapping.
20543949COL1A1,COL1A2,COL3A1,COL6A3,PRRX1Switch from stress response to homeobox transcription factors in adipose tissue after profound fat loss.
20483354COL1A1,COL3A1Morphological and proteomic analysis of early stage of osteoblast differentiation in osteoblastic progenitor cells.
20479531COL1A1,COL3A1In vivo low-intensity pulsed ultrasound (LIPUS) following tendon injury promotes repair during granulation but suppresses decorin and biglycan expression during remodeling.
20473581COL1A1,IGFBP3Hepatic Gene Networks in Morbidly Obese Patients With Nonalcoholic Fatty Liver Disease.
20456365COL1A1,COL3A1Extracellular matrix in multiple sclerosis lesions: Fibrillar collagens, biglycan and decorin are upregulated and associated with infiltrating immune cells.
20433912COL1A1,COL3A1,GDF10,VEGFC,MGPGene expression profiling of primary human articular chondrocytes in high-density micromasses reveals patterns of recovery, maintenance, re- and dedifferentiation.
20429888COL1A1,COL1A2Transcriptional regulation of matrix metalloproteinase-1 and collagen 1A2 explains the anti-fibrotic effect exerted by proteasome inhibition in human dermal fibroblasts.
20362275COL1A1,COL1A2Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta.
20338150COL1A1,COL1A2Reprogramming of somatic cells induced by fusion of embryonic stem cells using hemagglutinating virus of Japan envelope (HVJ-E).
20301472COL1A1,COL1A2Osteogenesis Imperfecta BTI - GeneReviews
20219212COL1A1,COL1A2,COL3A1,MMP3,LTBP1Cellular phenotype transformation occurs during thoracic aortic aneurysm development.
20194304COL1A1,COL3A1Renal medullary microRNAs in Dahl salt-sensitive rats: miR-29b regulates several collagens and related genes.
20191437COL1A1,COL3A1Analysis 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.
20188343COL1A1,COL1A2Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.
20154713COL1A1,COL3A1Protective action of tetramethylpyrazine phosphate against dilated cardiomyopathy in cTnT(R141W) transgenic mice.
20117381COL1A1,COL3A1Growth differentiation factor 5 regulates cardiac repair after myocardial infarction.
20092892COL1A1,COL1A2,COL6A3,CYP1B1Effect of maternal tobacco smoke exposure on the placental transcriptome.
20083223COL1A1,PLATPeriostin expression distinguishes between light and dark hypertrophic chondrocytes.
20063114COL1A1,COL3A1,COL6A2Vascular gene expression patterns are conserved in primary and metastatic brain tumors.
20051715COL1A1,COL3A1Identification of novel in vitro test systems for the determination of glucocorticoid receptor ligand-induced skin atrophy.
20043993COL1A1,FSTL1,THBS2Downregulated expression of the secreted glycoprotein follistatin-like 1 (Fstl1) is a robust hallmark of preadipocyte to adipocyte conversion.
20034948COL1A1,COL1A2Leg pain in an infant.
19956414COL1A1,COL1A2,COL3A1,ADAM12Role of miR-29b on the regulation of the extracellular matrix in human trabecular meshwork cells under chronic oxidative stress.
19929435COL1A1,COL1A2Relationship between genotype and skeletal phenotype in children and adolescents with osteogenesis imperfecta.
19913322COL1A1,COL1A2Upregulation of hepatoma-derived growth factor is involved in murine hepatic fibrogenesis.
19907330COL1A1,COL1A2Osteogenesis imperfecta: questions and answers.
19875360COL1A1,COL3A1Accelerated healing of the rat Achilles tendon in response to autologous conditioned serum.
19862557COL1A1,COL1A2Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta.
19839042COL1A1,COL1A2Calvarial doughnut lesions and osteoporosis: a new three-generation family and review.
19833228COL1A1,BMP4,BMP2Atlantic salmon (Salmo salar) muscle precursor cells differentiate into osteoblasts in vitro: polyunsaturated fatty acids and hyperthermia influence gene expression and differentiation.
19822105COL1A1,COL1A2Influence of an extract from kudzu symbiosomes containing leghemoglobin on in vitro cutaneous procollagen production.
19790048COL1A1,COL1A2,COL3A1Hypoxia-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.
19772464COL1A1,CXCL1,IGFBP3Induction of cytokine gene expression in human thyroid epithelial cells irradiated with HZE particles (iron ions).
19767743COL1A1,BMP2Signalling mediated by the endoplasmic reticulum stress transducer OASIS is involved in bone formation.
19748963COL1A1,MGPIdentification of phenotypic discriminating markers for intervertebral disc cells and articular chondrocytes.
19723327COL1A1,COL3A1,POSTN,BGNChondrogenic differentiation potential of osteoarthritic chondrocytes and their possible use in matrix-associated autologous chondrocyte transplantation.
19714363COL1A1,COL1A2Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.
19696512COL1A1,MMP3Genetic risk factors for musculoskeletal soft tissue injuries.
19678759COL1A1,BMP2Insight into the molecular pathophysiology of delayed bone healing in a sheep model.
19675075COL1A1,COL1A2,PTNAggressive inherited and sporadic medullary thyroid carcinomas display similar oncogenic pathways.
19649655COL1A1,COL1A2Regulation of bone development and extracellular matrix protein genes by RUNX2.
19629171COL1A1,COL1A2A missense mutation in the SERPINH1 gene in Dachshunds with osteogenesis imperfecta.
19594296COL1A1,COL1A2Variable bone fragility associated with an Amish COL1A2 variant and a knock-in mouse model.
19533842COL1A1,COL1A2Osteogenesis imperfecta: recent findings shed new light on this once well-understood condition.
19491628COL1A1,COL1A2Mutations in COL1A1 of type I collagen genes in Chinese patients with osteogenesis imperfecta.
19404930COL1A1,COL1A2Altered mineralization of human osteoarthritic osteoblasts is attributable to abnormal type I collagen production.
19317096COL1A1,COL1A2[Osteogenesis imperfecta]
19283684COL1A1,COL1A2A novel COL1A1 gene-splicing mutation (c.1875+1G>C) in a Brazilian patient with osteogenesis imperfecta.
19250650COL1A1,COL1A2Reactive nitrogen species switch on early extracellular matrix remodeling via induction of MMP1 and TNFalpha.
19228264COL1A1,MMP3Current evidence for a modulation of low back pain by human genetic variants.
19201335COL1A1,COL3A1Expression of extracellular matrix genes during myocardial recovery from heart failure after left ventricular assist device support.
19170097COL1A1,COL3A1,MMP3Temporal growth factor release from platelet-rich plasma, trehalose lyophilized platelets, and bone marrow aspirate and their effect on tendon and ligament gene expression.
19152976COL1A1,COL1A2,COL3A1,TNXB,ADAMTS2Connective tissue and related disorders and preterm birth: clues to genes contributing to prematurity.
19145252COL1A1,DCN,FBLN1,POSTNDifferential global and extra-cellular matrix focused gene expression patterns between normal and glaucomatous human lamina cribrosa cells.
19082484COL1A1,COL1A2,BGNCombination of microarray profiling and protein-protein interaction databases delineates the minimal discriminators as a metastasis network for esophageal squamous cell carcinoma.
19021896COL1A1,COL1A2Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
19015742COL1A1,COL1A2Allele dependent silencing of COL1A2 using small interfering RNAs.
18996919COL1A1,COL1A2Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships.
20534718COL1A2,COL3A1,LUMEstradiol replacement alters expression of genes related to neurotransmission and immune surveillance in the frontal cortex of middle-aged, ovariectomized rats.
20150539COL1A2,COL3A1,SERPING1Integrative urinary peptidomics in renal transplantation identifies biomarkers for acute rejection.
20048181COL1A2,BGNHypoxia-inducible factor-1 {alpha} expression predicts superior survival in patients with diffuse large B-cell lymphoma treated with R-CHOP.
19949890COL1A2,COL3A1Secreted phosphoprotein 1 upstream invasive network construction and analysis of lung adenocarcinoma compared with human normal adjacent tissues by integrative biocomputation.
19741209COL1A2,COL3A1Reactive oxygen species mediate mitogenic growth factor signaling pathways in human leiomyoma smooth muscle cells.
19531580COL1A2,MGPRetinoic acid cross-talk with calcitriol activity in Atlantic salmon (Salmo salar).
19401702COL1A2,COL6A3,POSTNAnalysis of differential gene expression in colorectal cancer and stroma using fluorescence-activated cell sorting purification.
18816857COL1A2,COL3A1Temporal and spatial expression of collagens during murine atrioventricular heart valve development and maintenance.
18815441COL1A2,COL3A1Expression of collagen types I, II and III in juvenile angiofibromas.
18602130COL1A2,LUMGene expression profiles following exposure to a developmental neurotoxicant, Aroclor 1254: pathway analysis for possible mode(s) of action.
18579462COL1A2,SMOC2Microarray analysis of perichondral and reserve growth plate zones identifies differential gene expressions and signal pathways.
18514395COL1A2,COL6A1Se-methylselenocysteine alters collagen gene and protein expression in human prostate cells.
18499699COL1A2,COL6A3,COL6A2Sulindac treatment alters collagen and matrilysin expression in adenomas of ApcMin/+ mice.
18272325COL1A2,COL3A1Natural variation in four human collagen genes across an ethnically diverse population.
18254958COL1A2,MMP3Transcriptomic dissection of tongue squamous cell carcinoma.
17982090COL1A2,COL3A1,LUMDifferential expression of inflammatory and fibrogenic genes and their regulation by NF-kappaB inhibition in a mouse model of chronic colitis.
17938000COL1A2,COL3A1,LUMCartilage gene expression correlates with radiographic severity of canine elbow osteoarthritis.
17852852COL1A2,COL3A1,TGFB2Multiple inflammatory-, tissue remodelling- and fibrosis genes are differentially transcribed in the livers of Abcb4 (-/ - ) mice harbouring chronic cholangitis.
17822560COL1A2,PTN,MGPThe effect of novel nitrogen-rich plasma polymer coatings on the phenotypic profile of notochordal cells.
17666000COL1A2,COL3A1,COL6A1Downregulation of extracellular matrix-related gene clusters during osteogenic differentiation of human bone marrow- and adipose tissue-derived stromal cells.
17601708COL1A2,COL6A3,THBS2Molecular basis of the differences between normal and tumor tissues of gastric cancer.
17552940COL1A2,MSX1Developmental biology and genetics of dental malformations.
17306970COL1A2,COL3A1Type III collagen is essential for growth acceleration of human osteoblastic cells by ascorbic acid 2-phosphate, a long-acting vitamin C derivative.
17133596COL1A2,COL3A1SPARC, an upstream regulator of connective tissue growth factor in response to transforming growth factor beta stimulation.
17032449COL1A2,COL3A1,LUM,BGNAnalysis of normal and osteoarthritic canine cartilage mRNA expression by quantitative polymerase chain reaction.
17014321COL1A2,COL3A1,COL6A3Assessment of collagen genes involved in fragmented medial coronoid process development in Labrador Retrievers as determined by affected sibling-pair analysis.
16871529COL1A2,COL3A1Attenuation of collagen production with small interfering RNA of SPARC in cultured fibroblasts from the skin of patients with scleroderma.
16583319COL1A2,COL3A1Extracellular matrix containing mutated fibrillin-1 (Fbn1) down regulates Col1a1, Col1a2, Col3a1, Col5a1, and Col5a2 mRNA levels in Tsk/+ and Tsk/Tsk embryonic fibroblasts.
20864640COL3A1,COL6A3Altered Spatiotemporal Expression of Collagen Types I, III, IV, and VI in Lpar3-Deficient Peri-Implantation Mouse Uterus.
19424605COL3A1,MMP3Association of gene polymorphisms with chronic kidney disease in high- or low-risk subjects defined by conventional risk factors.
18467551COL3A1,COL6A3Effects of leptin deficiency on postnatal lung development in mice.
17931229COL3A1,COL6A3,COL6A1Polymorphic microsatellite markers for genetic analysis of collagen genes in suspected collagenopathies in dogs.
17389037COL3A1,ASPNNovel markers for differentiation of lobular and ductal invasive breast carcinomas by laser microdissection and microarray analysis.
17218422COL3A1,COL6A3Variation in senescent-dependent lung changes in inbred mouse strains.
19455257COL3A1,MMEGerminal 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.
16980845COL3A1,PTNDifferential gene expression between juvenile and adult dura mater: a window into what genes play a role in the regeneration of membranous bone.
16856881COL3A1,POSTNExpression profiling analysis of the CD5+ diffuse large B-cell lymphoma subgroup: development of a CD5 signature.
16556917COL3A1,ADAMTS2Regulation of procollagen amino-propeptide processing during mouse embryogenesis by specialization of homologous ADAMTS proteases: insights on collagen biosynthesis and dermatosparaxis.
16251498COL3A1,LUM,POSTNIdentification of endometrial genes regulated by early pregnancy, progesterone, and interferon tau in the ovine uterus.
16035617COL3A1,COL6A3,LOXL1,COL6A1,COL6A2,FBLN1,BGNCaffeine suppresses metastasis in a transgenic mouse model: a prototype molecule for prophylaxis of metastasis.
15716609COL3A1,COL6A1Gene expression analysis of cultured amniotic fluid cell with Down syndrome by DNA microarray.
15054833COL3A1,TNXB,ADAMTS2,COL6A1,COL6A2Exclusion of candidate genes in a family with arterial tortuosity syndrome.
11917104COL3A1,IGFBP5In vitro cartilage formation by human adult stem cells from bone marrow stroma defines the sequence of cellular and molecular events during chondrogenesis.
11283408COL3A1,COL6A1,COL6A2Molecular anatomy of an intracranial aneurysm: coordinated expression of genes involved in wound healing and tissue remodeling.
11279127COL3A1,COL6A3,COL6A1,COL6A2Identification of novel TGF-beta /Smad gene targets in dermal fibroblasts using a combined cDNA microarray/promoter transactivation approach.
20882040COL6A3,COL6A1,COL6A2Expression of the Collagen VI alpha5 and alpha6 Chains in Normal Human Skin and in Skin of Patients with Collagen VI-Related Myopathies.
20576434COL6A3,COL6A1,COL6A2Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern.
20301676COL6A3,COL6A1,COL6A2Collagen Type VI-Related Disorders BTI - GeneReviews
20225280COL6A3,COL6A1,COL6A2Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine.
20106987COL6A3,COL6A1,COL6A2Recessive COL6A2 C-globular missense mutations in Ullrich congenital muscular dystrophy: role of the C2a splice variant.
19884007COL6A3,COL6A1,COL6A2Autosomal recessive inheritance of classic Bethlem myopathy.
19015158COL6A3,COL6A1,COL6A2Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue.
18761340COL6A3,COL6A1,COL6A2An enhancer required for transcription of the Col6a1 gene in muscle connective tissue is induced by signals released from muscle cells.
18378883COL6A3,COL6A1,COL6A2A refined diagnostic algorithm for Bethlem myopathy.
18366090COL6A3,COL6A1,COL6A2Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance.
18219255COL6A3,COL6A1,COL6A2Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem.
18086302COL6A3,POSTNHuman periostin gene expression in normal tissues, tumors and melanoma: evidences for periostin production by both stromal and melanoma cells.
17886299COL6A3,COL6A1,COL6A2Molecular consequences of dominant Bethlem myopathy collagen VI mutations.
17785673COL6A3,COL6A1,COL6A2Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.
17602442COL6A3,COL6A1,COL6A2Quantitative evaluation of collagen type VI and SOD gene expression in the nuchal skin of human fetuses with trisomy 21.
17163796COL6A3,LAMA2,COL6A1,COL6A2The congenital muscular dystrophies: recent advances and molecular insights.
16447767COL6A3,COL6A1,COL6A2[Collagenopathy (Ullrich congenital muscular dystrophy, Bethlem myopathy)]
16142353COL6A3,NDN,GPC4Gene expression profiling of a clonal isolate of oxaliplatin-resistant ovarian carcinoma cell line A2780/C10.
16141002COL6A3,COL6A1,COL6A2Collagen VI related muscle disorders.
16075202COL6A3,COL6A1,COL6A2A homozygous COL6A2 intron mutation causes in-frame triple-helical deletion and nonsense-mediated mRNA decay in a patient with Ullrich congenital muscular dystrophy.
15955946COL6A3,COL6A1,COL6A2Detection of common and private mutations in the COL6A1 gene of patients with Bethlem myopathy.
15882279COL6A3,COL6A1,COL6A2,FBLN1Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: a novel syndrome.
15689448COL6A3,COL6A1,COL6A2Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.
15642389COL6A3,IGFBP5,BGNCharacterization of gene expression in major types of salivary gland carcinomas with epithelial differentiation.
15563506COL6A3,COL6A1,COL6A2Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy.
15127309COL6A3,COL6A1,COL6A2Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci.
12840783COL6A3,COL6A1,COL6A2New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.
12011280COL6A3,COL6A1Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study.
11992252COL6A3,COL6A2Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy.
11707460COL6A3,COL6A1,COL6A2Kinked collagen VI tetramers and reduced microfibril formation as a result of Bethlem myopathy and introduced triple helical glycine mutations.
10419498COL6A3,COL6A1,COL6A2Bethlem myopathy and engineered collagen VI triple helical deletions prevent intracellular multimer assembly and protein secretion.
9536084COL6A3,COL6A1,COL6A2Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathy.
9497154COL6A3,COL6A1Morphological classification of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12-18 weeks and in a trisomy 16 mouse.
9491853COL6A3,COL6A1,COL6A2Collagen type VI gene expression in the skin of trisomy 21 fetuses.
8782832COL6A3,COL6A1,COL6A2Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures.
8817344COL6A3,COL6A1,COL6A2Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.
19438813CRYAB,POSTNDerivation of a novel undifferentiated human foetal phenotype in serum-free cultures with BMP-2.
19401404CRYAB,OGN,PDPNIndividual molecular response to elevated intraocular pressure in perfused postmortem human eyes.
19080366CRYAB,DCN,IGFBP3Identification of differential gene expression profiles of radioresistant lung cancer cell line established by fractionated ionizing radiation in vitro.
20699749CXCL12,LEPRApplication of the chemokine CXCL12 expression plasmid restores wound healing to near normal in a diabetic mouse model.
20602768CXCL12,PCOLCEHind limb unloading of mice modulates gene expression at the protein and mRNA level in mesenchymal bone cells.
20585037CXCL12,CCL11Role of the CXCR4/CXCL12 axis in lymphangioleiomyomatosis and angiomyolipoma.
20538476CXCL12,LIF,CXCL1The expression pattern of inflammatory mediators in cerebrospinal fluid differentiates Guillain-Barre syndrome from chronic inflammatory demyelinating polyneuropathy.
20516641CXCL12,CXCL1CXCR2 and CXCR4 antagonistically regulate neutrophil trafficking from murine bone marrow.
20432237CXCL12,CCL19Epidermis-to-dermis migration of immature Langerhans cells upon topical irritant exposure is dependent on CCL2 and CCL5.
20421491CXCL12,CCL19Requirement of CCL17 for CCR7- and CXCR4-dependent migration of cutaneous dendritic cells.
20376612CXCL12,CXCL1The Chemokine Network in Acute Myelogenous Leukemia: Molecular Mechanisms Involved in Leukemogenesis and Therapeutic Implications.
20369317CXCL12,CCL19Role of Chemokines in the Biology of Natural Killer Cells.
20145264CXCL12,CCL19CXCL12-induced chemotaxis is impaired in T cells from patients with ZAP-70-negative chronic lymphocytic leukemia.
20073989CXCL12,PTNHypoxic/normoxic preconditioning increases endothelial differentiation potential of human bone marrow CD133+ cells.
20042073CXCL12,CCL19The chemokine CXCL13 is a key regulator of B cell recruitment to the cerebrospinal fluid in acute Lyme neuroborreliosis.
20360993DCN,LUM,OGNCandidate gene study to investigate the genetic determinants of normal variation in central corneal thickness.
20357198DCN,LUMLinkage of posterior amorphous corneal dystrophy to chromosome 12q21.33 and exclusion of coding region mutations in KERA, LUM, DCN, and EPYC.
19652764DCN,MFAP5,FBLN1Pathway analysis of differentially expressed genes in patients with acute aortic dissection.
19631729DCN,MGP,BMP2Microarray analysis of senescent vascular smooth muscle cells: A link to atherosclerosis and vascular calcification.
19616852DCN,LUMThe association of haplotype at the lumican gene with high myopia susceptibility in Taiwanese patients.
19571260DCN,NDNCharacterization of conserved and nonconserved imprinted genes in swine.
19379665DCN,BGNGenetic evidence for key roles of decorin and biglycan in dentin mineralization.
19292938DCN,SDC2,MGPEvaluation of differentially expressed genes by shear stress in human osteoarthritic chondrocytes in vitro.
19036156DCN,LUMGenetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies.
18723084DCN,MGPGene expression profile of rabbit cartilage by expressed sequence tag analysis.
18479593DCN,ASPN[Differentially expressed genes between upward and downward progressing types of nasopharyngeal carcinoma]
18245265DCN,BGNEffects of decorin and biglycan on human airway smooth muscle cell proliferation and apoptosis.
18162102DCN,POSTNMapping of the porcine FBN2, YWHAQ, CNN3, DCN, POSTN, SPARC, RBM39 and GNAS genes, expressed in foetal skeletal muscles.
18049164DCN,PTGESDNA methyltransferase 1 knockdown induces silenced CDH1 gene reexpression by demethylation of methylated CpG in hepatocellular carcinoma cell line SMMC-7721.
17977755DCN,LUMUndifferentiated human mesenchymal stem cells (hMSCs) are highly sensitive to mechanical strain: transcriptionally controlled early osteo-chondrogenic response in vitro.
17662275DCN,CCL19,SMOC2,OGNDisease susceptibility of the human macula: differential gene transcription in the retinal pigmented epithelium/choroid.
17558846DCN,LUMAutosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.
17555561DCN,ASPN,LUMMolecular response to aromatase inhibitor treatment in primary breast cancer.
17395685DCN,BGNDifferences in mRNA and protein expression of small proteoglycans in vaginal wall tissue from women with and without stress urinary incontinence.
17188951DCN,BGNImpaired posterior frontal sutural fusion in the biglycan/decorin double deficient mice.
16908595DCN,LUM,BGNMitotic arrest, apoptosis, and sensitization to chemotherapy of melanomas by methionine deprivation stress.
20555348DPT,IGFBP5,MMP3,SFRP1Epigenetically altered wound healing in keloid fibroblasts.
19250647FHL1,ALDH1A1Transcriptional activation by TLX1/HOX11 involves Gro/TLE corepressors.
18073142FHL1,ALDH1A1Transcriptional regulation of FHL1 by TLX1/HOX11 is dosage, cell-type and promoter context-dependent.
17150988FHL1,SFRP1Genetic analysis of anterior posterior expression gradients in the developing mammalian forebrain.
17061120FHL1,MGPIntra- and interindividual variation in gene expression in human adipose tissue.
15910245FHL1,ALDH1A1Differential gene expression profiling of CD34+ CD133+ umbilical cord blood hematopoietic stem progenitor cells.
20739664IGFBP5,IGFBP3,GATA6GATA Depletion Impacts Insulin-like Growth Factor 1 mRNA and Protein Levels in Luteinizing Porcine Granulosa Cells.
20739512IGFBP5,IGFBP3Impact of viral mediated IGF-I gene transfer on skeletal muscle following cast immobilization.
20389077IGFBP5,IGFBP3Differential modulation of Sonic-hedgehog-induced cerebellar granule cell precursor proliferation by the IGF signaling network.
20186495IGFBP5,IGFBP3Inhibitor of differentiation 1 (ID1) promotes cell survival and proliferation of prostate epithelial cells.
19933427IGFBP5,IGFBP3Effect of polymorphisms in candidate genes on reproduction traits in Finnish pig populations.
19665134IGFBP5,IGFBP3Regulatory effects of biomechanical strain on the insulin-like growth factor system in human periodontal cells.
19557575IGFBP5,MGPFOS proliferating network construction in early colorectal cancer (CRC) based on integrative significant function cluster and inferring analysis.
19378418IGFBP5,IGFBP3MRNA expression of members of the IGF system in the organ of Corti, the modiolus and the stria vascularis of newborn rats.
19132093IGFBP5,TGFB2Identification of pax6-dependent gene regulatory networks in the mouse lens.
18997086IGFBP5,IGFBP3Quantification and localization of the IGF/insulin system expression in retinal blood vessels and neurons during oxygen-induced retinopathy in mice.
18936297IGFBP5,IGFBP3The genomic response of a human uterine endometrial adenocarcinoma cell line to 17alpha-ethynyl estradiol.
18608519IGFBP5,IGFBP3mRNA expression of members of the IGF system in the organ of Corti, the modiolus and the stria vascularis of newborn rats.
18276763IGFBP5,IGFBP3Gender-specific changes in bone turnover and skeletal architecture in igfbp-2-null mice.
18222913IGFBP5,MSX1Altered expression of muscle- and cytoskeleton-related genes in a rat strain with inherited cryptorchidism.
18204794IGFBP5,IGFBP3Cancer genes induced by malathion and parathion in the presence of estrogen in breast cells.
17697390IGFBP5,FSTL1Gene expression studies of developing bovine longissimus muscle from two different beef cattle breeds.
17695985IGFBP5,IGFBP3Regulatory effects of biophysical strain on rat TMJ discs.
16249290IGFBP5,FBLN1Endometriosis-specific genes identified by real-time reverse transcription-polymerase chain reaction expression profiling of endometriosis versus autologous uterine endometrium.
15512944IGFBP5,TNFAIP6Microarray analysis identified differentially expressed genes in keratocytes from keratoconus patients.
14755496LAMA2,COL6A2EMG and nerve conduction studies in children with congenital muscular dystrophy.
20809277LIF,BMP4Enhanced effects of secreted soluble factor preserve better pluripotent state of embryonic stem cell culture in a membrane-based compartmentalized micro-bioreactor.
20713452LOX,BMP4,BMP2Involvement of cytoskeleton-associated proteins in the commitment of C3H10T1/2 pluripotent stem cells to adipocyte lineage induced by BMP2/4.
20606470LOX,LOXL1Role of Lysyl Oxidases in Neointima Development in Vascular Allografts.
20569695LOX,PDGFRACNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination.
20559617LOX,LOXL1LOX family enzymes expression in vaginal tissue of premenopausal women with severe pelvic organ prolapse.
20482627LOX,CCL19Aggregatibacter actinomycetemcomitans accelerates atherosclerosis with an increase in atherogenic factors in spontaneously hyperlipidemic mice.
20420713LOX,SFRP1Identifying mRNA targets of microRNA dysregulated in cancer: with application to clear cell Renal Cell Carcinoma.
19565266LOXL1,SFRP1Hypermethylated SFRP1, but none of other nine genes "informative" for western countries, is valuable for bladder cancer detection in Mainland China.
18158636LOXL1,MGPDecreased endopelvic fascia elastin content in uterine prolapse.
20196644MFAP5,MFAP2Parameters in three-dimensional osteospheroids of telomerized human mesenchymal (stromal) stem cells grown on osteoconductive scaffolds that predict in vivo bone-forming potential.
19801232MME,BMP2Stem cell regulatory gene expression in human adult dental pulp and periodontal ligament cells undergoing odontogenic/osteogenic differentiation.
18827820MME,DCBLD2Identification of novel neuroendocrine-specific tumour genes.
16319984MME,TGFB2High-resolution mapping of molecular events associated with immortalization, transformation, and progression to breast cancer in the MCF10 model.
20505979MYL9,COL6A1,HAS2The transcription factor EGR1 regulates metastatic potential of v-src transformed sarcoma cells.
17341888MYL9,TAGLNMethylation status of genes upregulated by demethylating agent 5-aza-2'-deoxycytidine in hepatocellular carcinoma.
20434574NBL1,COL6A2Analysis 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.
16596263NBL1,BMPR1ACER1 is a common target of WNT and NODAL signaling pathways in human embryonic stem cells.
20889717PDGFRA,EGFRPDGFRA gene rearrangements are frequent genetic events in PDGFRA-amplified glioblastomas.
20826533PDGFRA,GATA6A role for PDGF signaling in expansion of the extra-embryonic endoderm lineage of the mouse blastocyst.
20548289PDGFRA,DACT1A molecular portrait of gastrointestinal stromal tumors: an integrative analysis of gene expression profiling and high-resolution genomic copy number.
19968631PDGFRA,CXCL1Gene-gene and gene-environment interactions on IgE production in prenatal stage.
18773962PENK,NDNCarbamazepine protects against neuronal hyperplasia and abnormal gene expression in the megencephaly mouse.
15239838PENK,SFRP4,SAT2,BGNMicroarray profiling of progesterone-regulated endometrial genes during the rhesus monkey secretory phase.
17117407PRELP,LUMNovel mutations in the small leucine-rich repeat protein/proteoglycan (SLRP) genes in high myopia.
12054597PRELP,LUMMolecular analysis of expansion, differentiation, and growth factor treatment of human chondrocytes identifies differentiation markers and growth-related genes.
20840765TAGLN,IGFBP3Transcriptional profiling of ErbB signalling in mammary luminal epithelial cells--interplay of ErbB and IGF1 signalling through IGFBP3 regulation.
20540360TAGLN,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]
18782851TAGLN,RARRES2Putative direct and indirect Wnt targets identified through consistent gene expression changes in APC-mutant intestinal adenomas from humans and mice.
18241852TAGLN,NDNCYP26A1 knockout embryonic stem cells exhibit reduced differentiation and growth arrest in response to retinoic acid.
20702851TNFAIP6,HAS2Does Bone Morphogenetic Protein 6 (BMP6) Affect Female Fertility in the Mouse?
20308529TNFAIP6,HAS2The nuclear receptor cofactor receptor-interacting protein 140 is a positive regulator of amphiregulin expression and cumulus cell-oocyte complex expansion in the mouse ovary.
20168049TNFAIP6,HAS2Progesterone 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.
20034375TNFAIP6,HAS2Activation 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.
19651638TNFAIP6,HAS2Stable expression and characterization of N-terminal tagged recombinant human bone morphogenetic protein 15.
19450457TNFAIP6,MATN2,EFEMP1,LTBP1Gene expression profiling of TGFbeta2- and/or BMP7-treated trabecular meshwork cells: Identification of Smad7 as a critical inhibitor of TGF-beta2 signaling.
18951380TNFAIP6,HAS2Targeted suppression of Has2 mRNA in mouse cumulus cell-oocyte complexes by adenovirus-mediated short-hairpin RNA expression.
18417710TNFAIP6,HAS2Identification of potential markers of oocyte competence expressed in bovine cumulus cells matured with follicle-stimulating hormone and/or phorbol myristate acetate in vitro.
17901238TNFAIP6,HAS2Hormone-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.
16908014TNFAIP6,HAS2The preantral granulosa cell to cumulus cell transition in the mouse ovary: development of competence to undergo expansion.
16707453TNFAIP6,DACT1Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysis.
16650051TNFAIP6,HAS2Towards profiling the gene expression of fibroblasts from atopic dermatitis patients: human 8K complementary DNA microarray.
16453284TNFAIP6,ADAM12Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women.
19184239ADAM12,ALDH1A1Differential gene expression analysis of subcutaneous fat, fascia, and skin overlying a Dupuytren's disease nodule in comparison to control tissue.
19121738ADAM12,POSTN,ALDH1A1Identification of biomarkers in Dupuytren's disease by comparative analysis of fibroblasts versus tissue biopsies in disease-specific phenotypes.
19036616ADAM12,ASPNAttempt to replicate published genetic associations in a large, well-defined osteoarthritis case-control population (the GOAL study).
18790654ADAM12,ADAMTS2Association of a nsSNP in ADAMTS14 to some osteoarthritis phenotypes.
17355265ADAM12,ADAMTS5ADAMs in cancer cell proliferation and progression.
15910695ADAM12,ASPNThe genetic epidemiology of human primary osteoarthritis: current status.
15280379ADAM12,SH3D19ADAM binding protein Eve-1 is required for ectodomain shedding of epidermal growth factor receptor ligands.
14730609ADAMTS12,ADAMTS2,ADAMTS5Expression profiling of metalloproteinases and their inhibitors in cartilage.
20555395ADAMTS2,P4HA2Endoplasmic reticulum stress inhibits collagen synthesis independent of collagen-modifying enzymes in different chondrocyte populations and dermal fibroblasts.
18762113ADAMTS2,ADAMTS5Metalloproteinase gene expression correlates with clinical outcome in Dupuytren's disease.
16470729ADAMTS2,SFRP4Evidence of genetic underexpression in chorionic villi samples of euploid fetuses with increased nuchal translucency at 10-11 weeks' gestation.
12697333ADAMTS2,ADAMTS5Expression of ADAMTS metalloproteinases in the retinal pigment epithelium derived cell line ARPE-19: transcriptional regulation by TNFalpha.
11167130ADAMTS2,ADAMTS5ADAMTS: a novel family of extracellular matrix proteases.
20109188ADAMTS5,PTGESAnalysis of meniscal degeneration and meniscal gene expression.
19922873ADAMTS5,FBLN1,BMP4ADAMTS metalloproteases generate active versican fragments that regulate interdigital web regression.
19840795ADAMTS5,MMP3Matrilin-3 activates the expression of osteoarthritis-associated genes in primary human chondrocytes.
19223608ADAMTS5,POSTNMuscle genome-wide expression profiling during disease evolution in mdx mice.
19040300ADAMTS5,MMP3Telomerase transduced osteoarthritis fibroblast-like synoviocytes display a distinct gene expression profile.
17966030ADAMTS5,MMP3Detection of gene expression in synovium of patients with osteoarthritis using a random sequencing method.
17530714ADAMTS5,PTGESGlobal analyses of gene expression in early experimental osteoarthritis.
16601225ADAMTS5,AOX1Thrombin and NAD(P)H oxidase-mediated regulation of CD44 and BMP4-Id pathway in VSMC, restenosis, and atherosclerosis.
20397748ADAMTSL3,EFEMP1Genome-wide association study of height and body mass index in Australian twin families.
18391952ADAMTSL3,EFEMP1Genome-wide association analysis identifies 20 loci that influence adult height.
18840552AEBP1,ANGPTL4,PRRX1Gene expression profile of the bone microenvironment in human fragility fracture bone.
20230802ANGPTL4,CYGBNeuroglobin, cytoglobin, and transcriptional profiling of hypoxia-related genes in the rat cerebellum after prenatal chronic very mild carbon monoxide exposure (25 ppm).
18505769ANGPTL4,EFEMP1Serial analysis of the vascular endothelial transcriptome under static and shear stress conditions.
18457598ANGPTL4,IGFBP3The role of the small intestine in the development of dietary fat-induced obesity and insulin resistance in C57BL/6J mice.
17033689ANGPTL4,PRRX1Vascular response to hypoxic preconditioning in the immature brain.
16685428ANGPTL4,THBS2Comparative integromics on Angiopoietin family members.
19885562AOX1,FBLN1Microarray gene expression profiling in meningiomas: differential expression according to grade or histopathological subtype.
19781675AOX1,PTNA microarray based identification of osteoporosis-related genes in primary culture of human osteoblasts.
16879361ASPN,OGNPorcine OGN and ASPN: mapping, polymorphisms and use for quantitative trait loci identification for growth and carcass traits in a Meishan x Pietrain intercross.
20680026CCL11,CCL19Expression of chemokine decoy receptors and their ligands at the porcine maternal-fetal interface.
20656925CCL11,CXCL1The migration of T cells in response to influenza virus is altered in neonatal mice.
20625511CCL11,IL33Gene transcription changes in asthmatic chronic rhinosinusitis with nasal polyps and comparison to those in atopic dermatitis.
20502518CCL11,CCL19,CXCL1Co-ordinated gene expression in the liver and spleen during Schistosoma japonicum infection regulates cell migration.
20335622CCL11,CCL19Chemokine levels in subretinal fluid obtained during scleral buckling surgery after rhegmatogenous retinal detachment.
20187767CCL11,CXCL1Associations of four circulating chemokines with multiple atherosclerosis phenotypes in a large population-based sample: results from the dallas heart study.
20161726CCL11,CXCL1Temporal expression of chemokines dictates the hepatic inflammatory infiltrate in a murine model of schistosomiasis.
19893035CCL11,CXCL1Treatment with a novel chemokine-binding protein or eosinophil lineage-ablation protects mice from experimental colitis.
19845793CCL11,CXCL1Eosinophils infiltrate thyroids, but have no apparent role in induction or resolution of experimental autoimmune thyroiditis in interferon-gamma(-/-) mice.
19473542CCL11,IL7Potential plasma markers of Type 1 and Type 2 leprosy reactions: a preliminary report.
19428942CCL11,CXCL1Cytokine and chemokine expression patterns in lung epithelial cells exposed to components characteristic of particulate air pollution.
18286574CCL11,CCL19Immunomodulation by herpesvirus U51A chemokine receptor via CCL5 and FOG-2 down-regulation plus XCR1 and CCR7 mimicry in human leukocytes.
17982926CCL11,CCL19Complementary DNA microarray analysis of chemokines and their receptors in allergic rhinitis.
20139367CCL19,CXCL1Mouse aorta smooth muscle cells differentiate into lymphoid tissue organizer-like cells on combined tumor necrosis factor receptor-1/lymphotoxin beta-receptor NF-kappaB signaling.
19800444CCL19,CXCL1Local cytokine and inflammatory responses to candidate vaginal adjuvants in mice.
19737877CCL19,PDPNExpression of podoplanin and other lymphatic markers in the human anterior eye segment.
19164539CCL19,IL7Characterization of the thymic IL-7 niche in vivo.
20060954CLEC3B,MSX1Genome-wide expression profiling reveals new candidate genes associated with osteoarthritis.
20302629COL6A1,COL6A2Identification 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.
19777066COL6A1,SLIT3Regulation of adipose tissue stromal cells behaviors by endogenic Oct4 expression control.
19309692COL6A1,COL6A2Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophy.
16317594COL6A1,COL6A2[Myopathy with trabecular fibers associated with familiar autoimmune polyglandular syndrome type 1]
15372526COL6A1,COL6A2Dilated ascending aorta in a child with ring chromosome 21 syndrome.
19078680COL6A1,COL6A2Bethlem myopathy in a black creole pedigree.
11865138COL6A1,COL6A2Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype.
11331940COL6A1,COL6A2Physical mapping of mouse collagen genes on chromosome 10 by high-resolution FISH.
9107679COL6A1,COL6A2Human COL6A1: genomic characterization of the globular domains, structural and evolutionary comparison with COL6A2.
8812475COL6A1,COL6A2Fine genetic map of mouse chromosome 10 around the polycystic kidney disease gene, jcpk, and ankyrin 3.
8575781COL6A1,COL6A2Head to tail organization of the human COL6A1 and COL6A2 genes by fiber-FISH.
7486833COL6A1,COL6A2Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome).
7782083COL6A1,COL6A2Structure of the terminal 300 kb of DNA from human chromosome 21q.
8188291COL6A1,COL6A2Cloning 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.
8094066COL6A1,COL6A2Polymorphisms 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.
1837533COL6A1,COL6A2Fine structure physical mapping of the region of mouse chromosome 10 homologous to human chromosome 21.
1676701COL6A1,COL6A2The COL6A1 and COL6A2 genes exist as a gene cluster and detect highly informative DNA polymorphisms in the telomeric region of human chromosome 21q.
1979060COL6A1,COL6A2Physical mapping by PFGE localizes the COL3A1 and COL5A2 genes to a 35-kb region on human chromosome 2.
19073771DACT1,SFRP1Dact1, a nutritionally regulated preadipocyte gene, controls adipogenesis by coordinating the Wnt/beta-catenin signaling network.
17943183DACT1,SFRP4Increased expression of Wnt2 and SFRP4 in Tsk mouse skin: role of Wnt signaling in altered dermal fibrillin deposition and systemic sclerosis.
17873379DACT1,SFRP1Networking of WNT, FGF, Notch, BMP, and Hedgehog signaling pathways during carcinogenesis.
19955106DKK2,SFRP4Excessive ovarian stimulation up-regulates the Wnt-signaling molecule DKK1 in human endometrium and may affect implantation: an in vitro co-culture study.
19815336DKK2,MSX1,SFRP1MSX1 induces the Wnt pathway antagonist genes DKK1, DKK2, DKK3, and SFRP1 in neuroblastoma cells, but does not block Wnt3 and Wnt5A signalling to DVL3.
19562778DKK2,SFRP4Wnt antagonist gene polymorphisms and renal cancer.
19185060DKK2,SFRP1Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation.
18021006DKK2,SFRP1Genetic analyses in a sample of individuals with high or low BMD shows association with multiple Wnt pathway genes.
17392486DKK2,SFRP1Gene expression change in the Mullerian duct of the mouse fetus exposed to diethylstilbestrol in utero.
17143565DKK2,SFRP4,SFRP1WNT 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.
16328026DKK2,SFRP4,SFRP1WNT antagonist, SFRP1, is Hedgehog signaling target.
16077992DKK2,SFRP4Comparative genomics on SFRP2 orthologs.
16077939DKK2,SFRP4Comparative genomics on SFRP1 orthologs.
16778180EFEMP2,UNC5C,TGFB2Silencing of Peroxiredoxin 2 and aberrant methylation of 33 CpG islands in putative promoter regions in human malignant melanomas.
10982184EFEMP2,EFEMP1Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13.
19347865EPHA3,ROBO2Characterization 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.
17185612EPHA3,TMEM45ATranscriptional profiling of human cord blood CD133+ and cultured bone marrow mesenchymal stem cells in response to hypoxia.
20722018FBLN1,GDF10Characterisation of the human nucleus pulposus cell phenotype and evaluation of novel marker gene expression to define adult stem cell differentiation.
19924294FSTL1,BMP4Correlating global gene regulation to angiogenesis in the developing chick extra-embryonic vascular system.
19017814GDF10,MMP3Identification of uterine leiomyoma genes developmentally reprogrammed by neonatal exposure to diethylstilbestrol.
18703560GDF10,MGPRetinoic acid receptor gamma-induced misregulation of chondrogenesis in the murine limb bud in vitro.
19941983GPC6,GPC4An interstitial duplication of chromosome 13q31.3q32.1 further delineates the critical region for postaxial polydactyly type A2.
19259985GPC6,SDC2The osteogenic transcription factor Runx2 regulates components of the fibroblast growth factor/proteoglycan signaling axis in osteoblasts.
11566272GPC6,GPC4A 4-Mb BAC/PAC contig and complete genomic structure of the GPC5/GPC6 gene cluster on chromosome 13q32.
10480909GPC6,GPC4Glypican-6, a new member of the glypican family of cell surface heparan sulfate proteoglycans.
10329016GPC6,GPC4GPC6, a novel member of the glypican gene family, encodes a product structurally related to GPC4 and is colocalized with GPC5 on human chromosome 13.
19265796LEPR,LUMHepatic gene expression in morbidly obese women: implications for disease susceptibility.
17069581LUM,PHLDA1Identification of transcripts modulated by ETV6 expression.
11092399LUM,BGNA comparison of the expression pattern of five genes of the family of small leucine-rich proteoglycans during mouse development.
18407260MEIS2,SFRP1Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways for early limb and skeletal patterning.
15735049MRC2,P4HA2Gene expression profile of papillary thyroid cancer: sources of variability and diagnostic implications.
20845426MSX1,BMP4Regulation of Tbx22 during facial and palatal development.
20702560MSX1,BMP4BMP-mediated inhibition of FGF signaling promotes cardiomyocyte differentiation of anterior heart field progenitors.
20672350MSX1,BMP2Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
20505756MSX1,BMP4A data integration approach to mapping OCT4 gene regulatory networks operative in embryonic stem cells and embryonal carcinoma cells.
20493240MSX1,BMP4,BMP2The expression of twisted gastrulation in postnatal mouse brain and functional implications.
20392740MSX1,BMPR1AOpposing Fgf and Bmp activities regulate the specification of olfactory sensory and respiratory epithelial cell fates.
20339300MSX1,BMP4Nicotine promotes cardiomyocyte apoptosis via oxidative stress and altered apoptosis-related gene expression.
20123092MSX1,BMP4,BMP2Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis.
19913004MSX1,BMP4Requirement for Lmo4 in the vestibular morphogenesis of mouse inner ear.
19766620MSX1,BMP2Essential mesenchymal role of small GTPase Rac1 in interdigital programmed cell death during limb development.
19622795MSX1,SCARA5,PTNGene expression profiles of bovine caruncular and intercaruncular endometrium at implantation.
19117070MSX1,SFRP1Sfrp1, Sfrp2, and Sfrp5 regulate the Wnt/beta-catenin and the planar cell polarity pathways during early trunk formation in mouse.
18836915MSX1,POSTNThe effect of type I collagen on osteochondrogenic differentiation in adipose-derived stromal cells in vivo.
18667074MSX1,HAS2Msx1 and Msx2 are required for endothelial-mesenchymal transformation of the atrioventricular cushions and patterning of the atrioventricular myocardium.
18990770NPAS2,IGFBP3Correlation between circadian gene variants and serum levels of sex steroids and insulin-like growth factor-I.
19864897PDZRN3,ROBO2Characterization of a 5.8-Mb interstitial deletion of chromosome 3p in a girl with 46,XX,inv(7)dn karyotype and phenotypic abnormalities.
20634963PLA2R1,ROBO2,PDPNSystematic analysis of a novel human renal glomerulus-enriched gene expression dataset.
19204725PLAT,SFRP1Chromosome 8p as a potential hub for developmental neuropsychiatric disorders: implications for schizophrenia, autism and cancer.
18492260PLAT,POSTN,PDPNAnaplastic oligodendrogliomas with 1p19q codeletion have a proneural gene expression profile.
19723774POSTN,PTNLack of periostin leads to suppression of Notch1 signaling and calcific aortic valve disease.
18490578POSTN,MMP3Examination of oral cancer biomarkers by tissue microarray analysis.
18076769POSTN,PTNUnravelling the molecular control of calvarial suture fusion in children with craniosynostosis.
16360395RARRES2,ALDH1A1Expression profiling of adrenocortical neoplasms suggests a molecular signature of malignancy.
20651036ROBO2,SLIT3Expression of the repulsive SLIT/ROBO pathway in the human endometrium and Fallopian tube.
20631173ROBO2,SLIT3Collaborative and specialized functions of Robo1 and Robo2 in spinal commissural axon guidance.
20123755ROBO2,SLIT3Prefrontal-enriched SLIT1 expression in Old World monkey cortex established during the postnatal development.
19900988ROBO2,SLIT3Involvement of the SLIT/ROBO pathway in follicle development in the fetal ovary.
19114000ROBO2,SLIT3Quantification of SLIT-ROBO transcripts in hepatocellular carcinoma reveals two groups of genes with coordinate expression.
18566128ROBO2,SLIT3Novel regulated expression of the SLIT/ROBO pathway in the ovary: possible role during luteolysis in women.
17581972ROBO2,SLIT3Dual branch-promoting and branch-repelling actions of Slit/Robo signaling on peripheral and central branches of developing sensory axons.
12471613ROBO2,SLIT3,UNC5C,NEO1Quantification of expression of netrins, slits and their receptors in human prostate tumors.
11804569ROBO2,SLIT3Pathfinding and error correction by retinal axons: the role of astray/robo2.
11755787ROBO2,SLIT3Role of Slit proteins in the vertebrate brain.
11754167ROBO2,SLIT3Spatiotemporal expression patterns of slit and robo genes in the rat brain.
11472852ROBO2,SLIT3Expression patterns of Slit and Robo family members during vertebrate limb development.
10864956ROBO2,SLIT3Slit inhibition of retinal axon growth and its role in retinal axon pathfinding and innervation patterns in the diencephalon.
10842075ROBO2,SLIT3Expression of the vertebrate Slit gene family and their putative receptors, the Robo genes, in the developing murine kidney.
20863401SDC2,SNAI2Runx2 transcriptome of prostate cancer cells: insights into invasiveness and bone metastasis.
20824703SFRP4,SFRP1Integrated genetic and epigenetic analysis of bladder cancer reveals an additive diagnostic value of FGFR3 mutations and hypermethylation events.
20795789SFRP4,SFRP1Acute myeloid leukemia is characterized by Wnt pathway inhibitor promoter hypermethylation.
20364027SFRP4,SFRP1Methylation of cyclin-dependent kinase inhibitors, XAF1, JUNB, CDH13 and soluble Wnt inhibitors in essential thrombocythaemia.
20145299SFRP4,SMOC2Transcriptomic signature of cell lines isolated from canine mammary adenocarcinoma metastases to lungs.
20097210SFRP4,SFRP1Isorhamnetin-induced anti-adipogenesis is mediated by stabilization of beta-catenin protein.
20030932SFRP4,SFRP1[Methylation status of CpG islands in secreted frizzled-related protein gene promoter region of malignant hematopoietic cell lines]
19874621SFRP4,SFRP1Wnt pathway reprogramming during human embryonal carcinoma differentiation and potential for therapeutic targeting.
19847810SFRP4,SFRP1Frequent promoter hypermethylation of Wnt pathway inhibitor genes in malignant astrocytic gliomas.
19730886SFRP4,SFRP1SFRP4 was overexpressed in colorectal carcinoma.
19513747SFRP4,SFRP1Methylation analysis of SFRP genes family in cervical adenocarcinoma.
19387464SFRP4,SFRP1Wnt signaling pathway is epigenetically regulated by methylation of Wnt antagonists in acute myeloid leukemia.
19299079SFRP4,SFRP1Epigenetic dysregulation of secreted Frizzled-related proteins in multiple myeloma.
19038436SFRP4,SFRP1Promoter methylation of SFRPs gene family in cervical cancer.
18765431SFRP4,SFRP1Epigenetic dysregulation of the Wnt signalling pathway in chronic lymphocytic leukaemia.
18716850SFRP4,SFRP1Epigenetic regulation of WNT signaling pathway genes in inflammatory bowel disease (IBD) associated neoplasia.
18592156SFRP4,SFRP1Frequent epigenetic inactivation of SFRP genes in hepatocellular carcinoma.
18549404SFRP4,SFRP1Methylation status of Wnt signaling pathway genes affects the clinical outcome of Philadelphia-positive acute lymphoblastic leukemia.
18542073SFRP4,SFRP1Profiling CpG island field methylation in both morphologically normal and neoplastic human colonic mucosa.
18537968SFRP4,SFRP1Epigenetic inactivation of secreted Frizzled-related proteins in acute myeloid leukaemia.
18519763SFRP4,SFRP1Aneuploidy predicts outcome in patients with endometrial carcinoma and is related to lack of CDH13 hypermethylation.
17882284SFRP4,SFRP1Epigenetic dysregulation of Wnt signaling pathway in multiple myeloma.
17462603SFRP4,SFRP1Wnt3a binds to several sFRPs in the nanomolar range.
17443492SFRP4,SFRP1SFRP1 suppressed hepatoma cells growth through Wnt canonical signaling pathway.
17314492SFRP4,SFRP1Wnt signaling pathway in mammary gland development and carcinogenesis.
17148581SFRP4,SFRP1Epigenetic regulation of Wnt-signaling pathway in acute lymphoblastic leukemia.
16708382SFRP4,SFRP1Epigenetic inactivation of the SFRP genes is associated with drinking, smoking and HPV in head and neck squamous cell carcinoma.
16423993SFRP4,SFRP1CpG island methylation and expression of the secreted frizzled-related protein gene family in chronic lymphocytic leukemia.
16093361SFRP4,VEGFCMice null for Frizzled4 (Fzd4-/-) are infertile and exhibit impaired corpora lutea formation and function.
15579438SFRP4,TGFB2CTNNB1 mutations and overexpression of Wnt/beta-catenin target genes in WT1-mutant Wilms' tumors.
20298552SLIT3,MMP3Slit3 inhibits Robo3-induced invasion of synovial fibroblasts in rheumatoid arthritis.
17942002SRPX,SRPX2Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.
20236627SRPX2,SVEP1Characterization of SVEP1, KIAA, and SRPX2 in an in vitro cell culture model of endotoxemia.
17616930UNC5C,NEO1Analysis of Netrin 1 receptors during inner ear development.
20215856VEGFC,IGFBP3Genetic association of angiogenesis- and hypoxia-related gene polymorphisms with osteonecrosis of the femoral head.
19827050VEGFC,CXCL1Microarray analysis reveals potential target genes of NF-kappaB2/p52 in LNCaP prostate cancer cells.
19778204VEGFC,FIGFExistence of the lymphatic system in the primate corpus luteum.
19279691VEGFC,MMP3Alterations in gene expression induced by cyclic mechanical stress in trabecular meshwork cells.
16685460VEGFC,FIGFComparative integromics on VEGF family members.
15614775VEGFC,FIGFVascular gene expression and phenotypic correlation during differentiation of human embryonic stem cells.
20949628BMP4,BMP2Evaluation of germline BMP4 mutation as a cause of colorectal cancer.
20926645BMP4,BMP2Severe polyposis in Apc1322T mice is associated with submaximal Wnt signalling and increased expression of the stem cell marker Lgr5.
20886619BMP4,BMP2BMP2 expression in the adult rat brain.
20861306BMP4,BMP2Heparan Sulfate Acts as a BMP Co-receptor by Facilitating Ligand-induced Receptor Hetero-oligomerization.
20830741BMP4,BMP2Low-level laser irradiation enhances BMP-induced osteoblast differentiation by stimulating the BMP/Smad signaling pathway.
20739376BMP4,BMP2,BMPR1AChanges 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.
20727875BMP4,BMP2Modulation of BMP signaling by Noggin is required for the maintenance of palatal epithelial integrity during palatogenesis.
20691278BMP4,BMP2Highly efficient osteogenic differentiation of human mesenchymal stem cells by eradication of STAT3 signaling.
20679827BMP4,BMP2Divergent modulation of adipose-derived stromal cell differentiation by TGF-beta1 based on species of derivation.
20665672BMP4,TGFB2Chondro/osteoblastic and cardiovascular gene modulation in human artery smooth muscle cells that calcify in the presence of phosphate and calcitriol or paricalcitol.
20660069BMP4,IGFBP3Identification of early response genes and pathway activated by androgens in the initial segment and caput regions of the regressed rat epididymis.
20546278BMP4,BMP2Investigation of the association of BMP gene variants with nephropathy in Type 1 diabetes mellitus.
20506112BMP4,BMP2BMP signaling in the human fetal ovary is developmentally regulated and promotes primordial germ cell apoptosis.
20505824BMP4,BMP2Agrin binds BMP2, BMP4 and TGFbeta1.
20376510BMP4,BMP2Identification of oxytetracycline as a chondrogenic compound using a cell-based screening system.
20303683BMP4,BMP2Differential expression of mRNAs encoding BMP/Smad pathway molecules in antral follicles of high- and low-fecundity Hu sheep.
20230640BMP4,BMP2Nuclear variants of bone morphogenetic proteins.
20175188BMP4,BMP2Expression patterns of hormones, signaling molecules, and transcription factors during adenohypophysis development in the chick embryo.
20155803BMP4,BMP2Tieg1/Klf10 is upregulated by NGF and attenuates cell cycle progression in the pheochromocytoma cell line PC12.
20130285BMP4,BMP2Regulation of retinal progenitor cell differentiation by bone morphogenetic protein 4 is mediated by the smad/id cascade.
20124834BMP4,BMP2Human adipose-derived stromal cells respond to and elaborate bone morphogenetic protein-2 during in vitro osteogenic differentiation.
20063299BMP4,BMP2Role of bone morphogenetic proteins on cochlear hair cell formation: analyses of Noggin and Bmp2 mutant mice.
20042692BMP4,BMP2Bmp2 and Bmp4 exert opposing effects in hypoxic pulmonary hypertension.
20034106BMP4,BMP2Retinoic acid controls expression of tissue remodeling genes Hmgn1 and Fgf18 at the digit-interdigit junction.
20019778BMP4,BMP2[Effect of icariin on the mRNA expressions of Cbfalpha1, BMP2, BMP4 in rat osteoblasts]
20001953BMP4,BMP2Regulation of oligodendrocyte progenitor cell maturation by PPARdelta: effects on bone morphogenetic proteins.
19937756BMP4,GATA6Heparan sulfation-dependent fibroblast growth factor signaling maintains embryonic stem cells primed for differentiation in a heterogeneous state.
19923894BMP4,BMP2Interplay between BMP4 and IL-7 in human intrathymic precursor cells.
19900834BMP4,BMP2Control of BMP gene expression by long-range regulatory elements.
19879168BMP4,BMP2A common SNP near BMP2 is associated with severity of the iron burden in HFE p.C282Y homozygous patients: a follow-up study.
19861972BMP4,BMP2Iba1(+)/NG2(+) macrophage-like cells expressing a variety of neuroprotective factors ameliorate ischemic damage of the brain.
19860666BMP4,SNAI2Hedgehog target genes: mechanisms of carcinogenesis induced by aberrant hedgehog signaling activation.
19846762BMP4,HAS2,BMP2T-box 2, a mediator of Bmp-Smad signaling, induced hyaluronan synthase 2 and Tgfbeta2 expression and endocardial cushion formation.
19846600BMP4,BMP2Defining the window of germline genesis in vitro from murine embryonic stem cells.
19786120BMP4,BMP2Interaction between bone morphogenetic proteins and endothelin-1 in human pulmonary artery smooth muscle.
19786029BMP4,BMP2Iron-induced expression of bone morphogenic protein 6 in intestinal cells is the main regulator of hepatic hepcidin expression in vivo.
19763374BMP4,BMP2Marrow 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.
19737815BMP4,BMP2Axin2 controls bone remodeling through the beta-catenin-BMP signaling pathway in adult mice.
19733655BMP4,BMP2Spemann's organizer and the self-regulation of embryonic fields.
19729534BMP4,BMP2Bone morphogenetic proteins.
20688128HAS2,MMP3Chondrotoxicity and toxicokinetics of novel quinolone antibacterial agents DC-159a and DX-619 in juvenile rats.
18572299HAS2,MMP3Gene expression profiles in the articular cartilage of juvenile rats receiving the quinolone antibacterial agent ofloxacin.
17980161HAS2,TGFB2Regulation of hyaluronan and versican deposition by growth factors in fibrosarcoma cell lines.
16314491HAS2,BMPR1ABmp2 is essential for cardiac cushion epithelial-mesenchymal transition and myocardial patterning.
20617365IGFBP3,BMP2Identification of diagnostic serum protein profiles of glioblastoma patients.
20553613IGFBP3,GATA6Establishment and characterization of a new human pancreatic adenocarcinoma cell line with high metastatic potential to the lung.
20180422IGFBP3,TGFB2[Literature-mining and bioinformatic analysis of androgen-independent prostate cancer-specific genes]
20042640IGFBP3,PTGESHypoxia activates the cyclooxygenase-2-prostaglandin E synthase axis.
19551141IGFBP3,MMP3Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in familial and sporadic renal cell carcinoma.
17912462IGFBP3,PTGESGenes regulated by interferon-gamma in human uterine microvascular endothelial cells.
19953602MMP3,TGFB2Estrogen modulates iodoacetate-induced gene expression in bovine cartilage explants.
18023983MMP3,C1RProteomic analysis of the LPS-induced stress response in rat chondrocytes reveals induction of innate immune response components in articular cartilage.
20457798PTN,PDPNLymphatic capillary hypoplasia in the skin of fetuses with increased nuchal translucency and Turner's syndrome: comparison with trisomies and controls.
19478889PTN,MGPThe Potential of N-Rich Plasma-Polymerized Ethylene (PPE:N) Films for Regulating the Phenotype of the Nucleus Pulposus.
17786487PTN,MGPA phenotypic comparison of intervertebral disc and articular cartilage cells in the rat.
16079240PTN,ALDH1A1Expression quantitative trait loci analysis of 13 genes in the rat prostate.
19424592SFRP1,SNAI2Integrative genomic analyses of ZEB2: Transcriptional regulation of ZEB2 based on SMADs, ETS1, HIF1alpha, POU/OCT, and NF-kappaB.
18698484SFRP1,SNAI2Hedgehog signaling, epithelial-to-mesenchymal transition and miRNA (review).
18398573SNAI2,PDPNGene expression profile analysis of primary glioblastomas and non-neoplastic brain tissue: identification of potential target genes by oligonucleotide microarray and real-time quantitative PCR.
20396349MGP,BMP2[Effect of age on vascular calcification induced by vitamin D3 and nicotine]
15629771SERPING1,PTGESGene 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.
20523179BMP2,TGFB2Growth factors and gene expression of stem cells: bone marrow compared with peripheral blood.
20499346BMP2,TGFB2NVP-BEZ235, a dual pan class I PI3 kinase and mTOR inhibitor, promotes osteogenic differentiation in human mesenchymal stromal cells.
20304956BMP2,BMPR1AEpithelial to mesenchymal transition in human skin wound healing is induced by tumor necrosis factor-alpha through bone morphogenic protein-2.
19874086BMP2,BMPR1AWnt inhibitors Dkk1 and Sost are downstream targets of BMP signaling through the type IA receptor (BMPRIA) in osteoblasts.
19760469BMP2,BMPR1AAre endogenous BMPs necessary for bone healing during distraction osteogenesis?
19318548BMPR1A,PTGESInduction of prostaglandin E2 pathway promotes gastric hamartoma development with suppression of bone morphogenetic protein signaling.