Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function
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Normal proliferation and differentiation of Hoxc-8 transgenic chondrocytes in vitroCartilage-specific deletion of ephrin-B2 in mice results in early developmental defects and an osteoarthritis-like phenotype during aging in vivo.A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic miceA Novel Synthesized Sulfonamido-Based Gallate-JEZ-C as Potential Therapeutic Agents for OsteoarthritisGrowth defect in Grg5 null mice is associated with reduced Ihh signaling in growth platesThe extracellular matrix in development and morphogenesis: a dynamic view.Partial characterization of cell-type X collagen interactions.Surviving endoplasmic reticulum stress is coupled to altered chondrocyte differentiation and functionIdentification of mechanosensitive genes during embryonic bone formation.Targeted induction of endoplasmic reticulum stress induces cartilage pathology.Matrix recruitment and calcium sequestration for spatial specific otoconia developmentSOX9 governs differentiation stage-specific gene expression in growth plate chondrocytes via direct concomitant transactivation and repression.Hypertrophic chondrocytes can become osteoblasts and osteocytes in endochondral bone formation.Effect of JJYMD-C, a novel synthetic derivative of gallic acid, on proliferation and phenotype maintenance in rabbit articular chondrocytes in vitro.Effect of epigallocatechin-3-gallate on proliferation and phenotype maintenance in rabbit articular chondrocytes in vitro.COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid.Chaperoning osteogenesis: new protein-folding disease paradigms.Andrographolide enhances proliferation and prevents dedifferentiation of rabbit articular chondrocytes: an in vitro study.Runx2 contributes to murine Col10a1 gene regulation through direct interaction with its cis-enhancerRenal fibrosis: collagen composition and assembly regulates epithelial-mesenchymal transdifferentiationLinking hematopoiesis to endochondral skeletogenesis through analysis of mice transgenic for collagen X.Altered trabecular bone structure and delayed cartilage degeneration in the knees of collagen VI null miceThe role of type X collagen in facilitating and regulating endochondral ossification of articular cartilage.Association of cartilage-specific deletion of peroxisome proliferator-activated receptor γ with abnormal endochondral ossification and impaired cartilage growth and development in a murine modelIdentification and characterization of the novel Col10a1 regulatory mechanism during chondrocyte hypertrophic differentiation.Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.Growth plate compressions and altered hematopoiesis in collagen X null mice.Effect of intradiscal monopolar pulsed radiofrequency on chronic discogenic back pain diagnosed by pressure-controlled provocative discography: a one year prospective study.Molecular basis for skeletal variation: insights from developmental genetic studies in mice.Altered endochondral ossification in collagen X mouse models leads to impaired immune responsesHeparan sulfate proteoglycans: a GAGgle of skeletal-hematopoietic regulators.Defective endochondral ossification-derived matrix and bone cells alter the lymphopoietic niche in collagen X mouse modelsLocalization of the cis-enhancer element for mouse type X collagen expression in hypertrophic chondrocytes in vivo.Smurf2 induces degradation of GSK-3beta and upregulates beta-catenin in chondrocytes: a potential mechanism for Smurf2-induced degeneration of articular cartilage.A nonsense mutation in the carboxyl-terminal domain of type X collagen causes haploinsufficiency in schmid metaphyseal chondrodysplasiaDose-dependent effects of Runx2 on bone development.Bigenic Cre/loxP, puDeltatk conditional genetic ablation.Beta-catenin, cartilage, and osteoarthritis.Altered matrix at the chondro-osseous junction leads to defects in lymphopoiesis.Coming together is a beginning: the making of an intervertebral disc.
P2860
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P2860
Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: implications for function
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh
1997年學術文章
@zh-hant
name
Abnormal compartmentalization ...... n X: implications for function
@ast
Abnormal compartmentalization ...... n X: implications for function
@en
type
label
Abnormal compartmentalization ...... n X: implications for function
@ast
Abnormal compartmentalization ...... n X: implications for function
@en
prefLabel
Abnormal compartmentalization ...... n X: implications for function
@ast
Abnormal compartmentalization ...... n X: implications for function
@en
P2093
P2860
P356
P1476
Abnormal compartmentalization ...... n X: implications for function
@en
P2093
D O Sillence
P2860
P304
P356
10.1083/JCB.136.2.459
P407
P577
1997-01-01T00:00:00Z