Sox9 is required for cartilage formation
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Summary
The results identify Sox9 as the first transcription factor that is essential for chondrocyte differentiation and cartilage formation and Sox9 is identified as a regulator of the chondROcyte lineage.
- Type
- article
- Published
- 1999-04-29
- Cited by
- 1,795
- References
- 30
- OpenAlex
- https://openalex.org/W1574722884
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:20279868
Keywords
SOX9, Chondrocyte, Chondrogenesis, Biology, Mesenchyme
References
- Cartilage Molecular Aspects
- Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.
- Manipulating the mouse embryo: A laboratory manual
- Parallel expression of Sox9 and Col2a1 in cells undergoing chondrogenesis
- Detection of messenger RNA by in situ hybridization to tissue sections and whole mounts.
- Teratocarcinomas and embryonic stem cells : a practical approach
- Biology of cartilage cells
- Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development‐matrix components and their homeostasis
- Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
- Specific hybridization probes for mouse type I, II, III and IX collagen mRNAs.
- Toward a molecular understanding of skeletal development.
- Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds
- Analysis of aggrecan and tenascin gene expression in mouse skeletal tissues by northern and in situ hybridization using species specific cDNA probes.
- Chondrocyte-specific Enhancer Elements in the Col11a2Gene Resemble the Col2a1 Tissue-specific Enhancer*
- SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse.
- Dicistronic targeting constructs: reporters and modifiers of mammalian gene expression.
- The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos
- SOX9 directly regulates the type-ll collagen gene
- Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversal.
- Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development‐transcription factors and signaling pathways 1
Cited by
- The Molecular Genetics of Bone Formation
- Skeletal development--Wnts are in control.
- Requisite roles of Runx2 and Cbfb in skeletal development
- Secondary chondrocyte-derived Ihh stimulates proliferation of periosteal cells during chick development
- Differentiation of Mesenchymal Stem Cells Towards a Nucleus Pulposus-like Phenotype In Vitro: Implications for Cell-Based Transplantation Therapy
- Highly conserved proximal promoter element harbouring paired Sox9-binding sites contributes to the tissue- and developmental stage-specific activity of the matrilin-1 gene.
- A predominantly articular cartilage-associated gene, SCRG1, is induced by glucocorticoid and stimulates chondrogenesis in vitro.
- Human immortalized chondrocytes carrying heterozygous FGFR3 mutations: An in vitro model to study chondrodysplasias
- Chordoma and chondrosarcoma gene profile: implications for immunotherapy
- Bone morphogenetic proteins are involved in the pathobiology of synovial chondromatosis.
- Expression of master regulatory genes controlling skeletal development in benign cartilage and bone forming tumors
- Gluococorticoid could influence extracellular matrix synthesis through Sox9 via p38 MAPK pathway
- The effect of ultrasound stimulation on the gene and protein expression of chondrocytes seeded in chitosan scaffolds
- The protein kinase MLTK regulates chondrogenesis by inducing the transcription factor Sox6
- Cartilage defects in Sox9 heterozygotes
- Contribution of the Interleukin‐6/STAT‐3 Signaling Pathway to Chondrogenic Differentiation of Human Mesenchymal Stem Cells
- A pathway to bone: signaling molecules and transcription factors involved in chondrocyte development and maturation
- Signaling Pathways Regulating Cartilage Growth Plate Formation and Activity
- BMP-2-enhanced chondrogenesis involves p38 MAPK-mediated down-regulation of Wnt-7a pathway.
- Overview of skeletal development.
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