| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | L Xu | |
| Y Li | |||
| B R Olsen | |||
| P2860 | cites work | The discoidin domain receptor tyrosine kinases are activated by collagen | Q24313329 |
| Autosomal dominant and recessive osteochondrodysplasias associated with the COL11A2 locus | Q24313449 | ||
| A family with Stickler syndrome type 2 has a mutation in the COL11A1 gene resulting in the substitution of glycine 97 by valine in alpha 1 (XI) collagen | Q24314597 | ||
| A mutation in COL9A1 causes multiple epiphyseal dysplasia: further evidence for locus heterogeneity | Q24536139 | ||
| Cloning, expression, and type II collagenolytic activity of matrix metalloproteinase-13 from human osteoarthritic cartilage | Q24562729 | ||
| A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy | Q24671376 | ||
| Spondylo-epi-metaphyseal dysplasia (SEMD) matrilin 3 type: homozygote matrilin 3 mutation in a novel form of SEMD | Q24675483 | ||
| Clinical and Molecular genetics of Stickler syndrome | Q24681792 | ||
| The role of structural genes in the pathogenesis of osteoarthritic disorders | Q24793861 | ||
| Transcriptional regulation of collagenase (MMP-1, MMP-13) genes in arthritis: integration of complex signaling pathways for the recruitment of gene-specific transcription factors | Q24806147 | ||
| Molecular cloning and expression of collagenase-3, a novel human matrix metalloproteinase produced by breast carcinomas | Q28116247 | ||
| AP-1 and Cbfa/runt physically interact and regulate parathyroid hormone-dependent MMP13 expression in osteoblasts through a new osteoblast-specific element 2/AP-1 composite element | Q28207292 | ||
| Structural analysis and promoter characterization of the human collagenase-3 gene (MMP13) | Q28236176 | ||
| Molecular cloning of trkE, a novel trk-related putative tyrosine kinase receptor isolated from normal human keratinocytes and widely expressed by normal human tissues | Q28255837 | ||
| Structure, expression and chromosomal mapping of TKT from man and mouse: a new subclass of receptor tyrosine kinases with a factor VIII-like domain | Q28256857 | ||
| Stickler syndrome without eye involvement is caused by mutations in COL11A2, the gene encoding the alpha2(XI) chain of type XI collagen | Q28264950 | ||
| A mutation in the gene encoding the alpha 2 chain of the fibril-associated collagen IX, COL9A2, causes multiple epiphyseal dysplasia (EDM2) | Q28270822 | ||
| An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors | Q28276070 | ||
| Ultrastructural localization of collagen types II, IX, and XI in the growth plate of human rib and fetal bovine epiphyseal cartilage: type XI collagen is restricted to thin fibrils | Q28289636 | ||
| The D2 period of collagen II contains a specific binding site for the human discoidin domain receptor, DDR2 | Q28293395 | ||
| Mutations in exon 17B of cartilage oligomeric matrix protein (COMP) cause pseudoachondroplasia | Q28297153 | ||
| The collagen receptor DDR2 regulates proliferation and its elimination leads to dwarfism | Q28365928 | ||
| A new chondrodystrophic mutant in mice. Electron microscopy of normal and abnormal chondrogenesis | Q28505144 | ||
| Mice lacking alpha 1 (IX) collagen develop noninflammatory degenerative joint disease | Q28509200 | ||
| A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis | Q28586684 | ||
| Fibronectin fragment activation of proline-rich tyrosine kinase PYK2 mediates integrin signals regulating collagenase-3 expression by human chondrocytes through a protein kinase C-dependent pathway | Q30433820 | ||
| Osteoarthritis: new insights. Part 1: the disease and its risk factors. | Q33921631 | ||
| Age-dependent increase of discoidin domain receptor 2 and matrix metalloproteinase 13 expression in temporomandibular joint cartilage of type IX and type XI collagen-deficient mice | Q37301301 | ||
| The new collagenase, collagenase-3, is expressed and synthesized by human chondrocytes but not by synoviocytes. A role in osteoarthritis | Q37354475 | ||
| The biology of osteoarthritis | Q38627467 | ||
| IL-1 induces collagenase-3 (MMP-13) promoter activity in stably transfected chondrocytic cells: requirement for Runx-2 and activation by p38 MAPK and JNK pathways | Q39227819 | ||
| Postnatal expression in hyaline cartilage of constitutively active human collagenase-3 (MMP-13) induces osteoarthritis in mice | Q39904130 | ||
| The AP-1 site and MMP gene regulation: what is all the fuss about? | Q41460650 | ||
| Ultrastructure of adult human articular cartilage matrix after cryotechnical processing | Q41499360 | ||
| Both AP-1 and Cbfa1-like factors are required for the induction of interstitial collagenase by parathyroid hormone | Q42467906 | ||
| Matrix metalloproteinase and proinflammatory cytokine production by chondrocytes of human osteoarthritic cartilage: associations with degenerative changes | Q43550723 | ||
| Inhibition of interleukin-1-stimulated MAP kinases, activating protein-1 (AP-1) and nuclear factor kappa B (NF-kappa B) transcription factors down-regulates matrix metalloproteinase gene expression in articular chondrocytes | Q43992050 | ||
| Fibronectin fragments and blocking antibodies to alpha2beta1 and alpha5beta1 integrins stimulate mitogen-activated protein kinase signaling and increase collagenase 3 (matrix metalloproteinase 13) production by human articular chondrocytes | Q44159758 | ||
| Relative messenger RNA expression profiling of collagenases and aggrecanases in human articular chondrocytes in vivo and in vitro | Q44183277 | ||
| Structure, expression, and activity of Tyro 3, a neural adhesion-related receptor tyrosine kinase. | Q46943661 | ||
| The type XI collagenopathies. | Q50503590 | ||
| Identification of col2a1 gene mutations in patients with chondrodysplasias and familial osteoarthritis | Q57137534 | ||
| Genetic linkage of a polymorphism in the type II procollagen gene (COL2A1) to primary osteoarthritis associated with mild chondrodysplasia | Q68702209 | ||
| NEP: a novel receptor-like tyrosine kinase expressed in proliferating neuroepithelia | Q70476499 | ||
| Early-onset osteoarthritis linked to the type II procollagen gene. Detailed clinical phenotype and further analyses of the gene | Q70607971 | ||
| Osteoarthritis-like changes and decreased mechanical function of articular cartilage in the joints of mice with the chondrodysplasia gene (cho) | Q73401298 | ||
| Absence of the alpha1(IX) chain leads to a functional knock-out of the entire collagen IX protein in mice | Q73575439 | ||
| Interleukin-1 induction of collagenase 3 (matrix metalloproteinase 13) gene expression in chondrocytes requires p38, c-Jun N-terminal kinase, and nuclear factor kappaB: differential regulation of collagenase 1 and collagenase 3 | Q73678522 | ||
| Linkage analysis of candidate genes as susceptibility loci for osteoarthritis-suggestive linkage of COL9A1 to female hip osteoarthritis | Q73731506 | ||
| Osteoarthritic lesions: involvement of three different collagenases | Q73867207 | ||
| Effect of collagen turnover on the accumulation of advanced glycation end products | Q74281392 | ||
| Pathogenesis of osteoarthritis-like changes in the joints of mice deficient in type IX collagen | Q80201579 | ||
| Increased expression of the collagen receptor discoidin domain receptor 2 in articular cartilage as a key event in the pathogenesis of osteoarthritis | Q80707124 | ||
| Activation of the discoidin domain receptor 2 induces expression of matrix metalloproteinase 13 associated with osteoarthritis in mice | Q80918755 | ||
| P433 | issue | 10 | |
| P921 | main subject | osteoarthritis | Q62736 |
| P304 | page(s) | 1101-1105 | |
| P577 | publication date | 2007-06-14 | |
| P1433 | published in | Osteoarthritis and Cartilage | Q7107605 |
| P1476 | title | Lessons from genetic forms of osteoarthritis for the pathogenesis of the disease | |
| P478 | volume | 15 |
| Q33645936 | A missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans |
| Q85178335 | A secreted variant of cartilage oligomeric matrix protein carrying a chondrodysplasia‐causing mutation (p.H587R) disrupts collagen fibrillogenesis |
| Q37730947 | Beta-catenin, cartilage, and osteoarthritis |
| Q37270714 | Cartilage homeostasis in health and rheumatic diseases |
| Q37331102 | Defining the roles of inflammatory and anabolic cytokines in cartilage metabolism |
| Q37310621 | Immunomodulatory and anti-inflammatory effects of chondroitin sulphate |
| Q35167937 | Intact pericellular matrix of articular cartilage is required for unactivated discoidin domain receptor 2 in the mouse model |
| Q34955182 | Interaction between extracellular matrix molecules and microbial pathogens: evidence for the missing link in autoimmunity with rheumatoid arthritis as a disease model. |
| Q26750960 | Matrilin-3 Role in Cartilage Development and Osteoarthritis |
| Q38317248 | Matrix-embedded cytokines to simulate osteoarthritis-like cartilage microenvironments |
| Q36960089 | Notch Signaling and the Skeleton |
| Q26865318 | Osteoarthritis pathogenesis: a review of molecular mechanisms |
| Q37980346 | Participation in athletic activities may be associated with later development of hip and knee osteoarthritis |
| Q37816952 | The bone-cartilage unit in osteoarthritis |
| Q42561581 | The link between structural damage and pain in a genetic model of osteoarthritis and intervertebral disc degeneration: a joint misadventure |
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