Pages that link to "Q28277342"

The following pages link to Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasia (Q28277342):

Displaying 16 items.

• Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder (Q24681239) (← links)
• Collagen XI chain misassembly in cartilage of the chondrodysplasia (cho) mouse (Q28586285) (← links)
• Hand and foot abnormalities associated with genetic diseases (Q28972490) (← links)
• Novel insights into the function and dynamics of extracellular matrix in liver fibrosis (Q35622533) (← links)
• New insights into the assembly of extracellular microfibrils from the analysis of the fibrillin 1 mutation in the tight skin mouse (Q36328488) (← links)
• Extracellular matrix remodeling: the common denominator in connective tissue diseases. Possibilities for evaluation and current understanding of the matrix as more than a passive architecture, but a key player in tissue failure (Q36672445) (← links)
• Ophthalmic and molecular genetic findings in Kniest dysplasia. (Q36752264) (← links)
• Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform (Q37691905) (← links)
• The importance of extracellular matrix for cell function and in vivo likeness. (Q38321523) (← links)
• Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies. (Q38600849) (← links)
• Disparate response of articular- and auricular-derived chondrocytes to oxygen tension. (Q42357665) (← links)
• Thyroxine Increases Collagen Type II Expression and Accumulation in Scaffold-Free Tissue-Engineered Articular Cartilage. (Q47574994) (← links)
• Association between Kniest dysplasia and chondrosarcoma in a child. (Q53354589) (← links)
• The development of a mature collagen network in cartilage from human bone marrow stem cells in Transwell culture. (Q55529054) (← links)
• A study of the clinical and radiological features in a cohort of 93 patients with aCOL2A1mutation causing spondyloepiphyseal dysplasia congenita or a related phenotype (Q55738650) (← links)
• Assembly of collagen types II, IX and XI into nascent hetero-fibrils by a rat chondrocyte cell line (Q73686393) (← links)