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Developmental Dynamics : an Official Publication of the American Association of Anatomists|October 23, 2001
Targeted disruption of Col11a2 produces a mild cartilage phenotype in transgenic mice: comparison with the human disorder otospondylomegaepiphyseal dysplasia (OSMED)S W Li, M Takanosu, M Arita, et al.
Osteoarthritis and Cartilage|July 4, 2012
Intra-articular injection of human mesenchymal stem cells (MSCs) promote rat meniscal regeneration by being activated to express Indian hedgehog that enhances expression of type II collagenM Horie, H Choi, R H Lee, et al.
American Journal of Medical Genetics|November 7, 1998
Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymüller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome)T Pihlajamaa, D J Prockop, J Faber, et al.
Ciba Foundation Symposium|January 1, 1988
Expression of type I procollagen genesD J Prockop, K E Kadler, Y Hojima, et al.
American Journal of Human Genetics|January 1, 1993
A second mutation in the type II procollagen gene (COL2AI) causing stickler syndrome (arthro-ophthalmopathy) is also a premature termination codonN N Ahmad, D M McDonald-McGinn, E H Zackai, et al.
The Journal of Biological Chemistry|June 25, 1985
cDNA clones coding for the pro-alpha1(IV) chain of human type IV procollagen reveal an unusual homology of amino acid sequences in two halves of the carboxyl-terminal domainT Pihlajaniemi, K Tryggvason, J C Myers, et al.
Molecular Medicine (Cambridge, Mass.)|May 1, 1996
Osteopenia in 37 members of seven families: analysis based on a model of dominant inheritanceL D Spotila, J Caminis, M Devoto, et al.
The American Review of Respiratory Disease|January 1, 1982
beta-Aminopropionitrile prevents bleomycin-induced pulmonary fibrosis in the hamsterD J Riley, J S Kerr, R A Berg, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
Human Mutation|August 26, 1998
Five families with arginine 519-cysteine mutation in COL2A1: evidence for three distinct foundersJ F Bleasel, D Holderbaum, V Brancolini, et al.
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