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Matrix Biology : Journal of the International Society for Matrix Biology|April 26, 2003
Identification, characterization and expression analysis of a new fibrillar collagen gene, COL27A1James M Pace, Marcella Corrado, Caterina Missero, et al.Matrix Biology : Journal of the International Society for Matrix Biology|June 1, 2005
The new collagen gene COL27A1 contains SOX9-responsive enhancer elementsElizabeth Jenkins, Jennie B Moss, James M Pace, et al.Plos One|December 31, 2009
Critical early roles for col27a1a and col27a1b in zebrafish notochord morphogenesis, vertebral mineralization and post-embryonic axial growthHelena E Christiansen, Michael R Lang, James M Pace, et al.Human Mutation|March 19, 2005
Bovine model of Marfan syndrome results from an amino acid change (c.3598G > A, p.E1200K) in a calcium-binding epidermal growth factor-like domain of fibrillin-1Annie C Singleton, Anna L Mitchell, Peter H Byers, et al.The Journal of Biological Chemistry|October 5, 2006
The NH2-terminal propeptide of type I procollagen acts intracellularly to modulate cell functionAnush Oganesian, Sandra Au, Jeremy A Horst, et al.The Journal of Biological Chemistry|April 1, 2008
Defective C-propeptides of the proalpha2(I) chain of type I procollagen impede molecular assembly and result in osteogenesis imperfectaJames M Pace, Mary Wiese, Andrea S Drenguis, et al.Science (New York, N.Y.)|February 21, 2004
Gene targeting in stem cells from individuals with osteogenesis imperfectaJoel R Chamberlain, Ulrike Schwarze, Pei-Rong Wang, et al.Bone|August 19, 2007
Type XXVII collagen at the transition of cartilage to bone during skeletogenesisRebecca Hjorten, Uwe Hansen, Robert A Underwood, et al.Cell|October 24, 2006
CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfectaRoy Morello, Terry K Bertin, Yuqing Chen, et al.Human Mutation|June 21, 2008
CRTAP and LEPRE1 mutations in recessive osteogenesis imperfectaDustin Baldridge, Ulrike Schwarze, Roy Morello, et al.Pageof 1