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The Journal of Clinical Investigation|February 1, 1993
Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineralR Pereira, J S Khillan, H J Helminen, et al.
The Journal of Biological Chemistry|June 21, 1996
Assembly in vitro of thin and thick fibrils of collagen II from recombinant procollagen II. The monomers in the tips of thick fibrils have the opposite orientation from monomers in the growing tips of collagen I fibrilsA Fertala, D F Holmes, K E Kadler, et al.
Genomics|July 1, 1993
A fourth example suggests that premature termination codons in the COL2A1 gene are a common cause of the Stickler syndrome: analysis of the COL2A1 gene by denaturing gradient gel electrophoresisP Ritvaniemi, J Hyland, J Ignatius, et al.
European Journal of Biochemistry|August 1, 1981
Comparison of the NH2-Terminal sequences of chick Type I preprocollagen chains synthesized in an nRNA-dependent reticulocyte lysateP N Graves, B R Olsen, P P Fietzek, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|August 26, 1998
Human COL9A1 and COL9A2 genes. Two genes of 90 and 15 kb code for similar polypeptides of the same collagen moleculeT Pihlajamaa, M M Vuoristo, S Annunen, et al.
The Journal of Biological Chemistry|December 15, 1988
A substitution of cysteine for glycine 748 of the alpha 1 chain produces a kink at this site in the procollagen I molecule and an altered N-proteinase cleavage site over 225 nm awayB E Vogel, R Doelz, K E Kadler, et al.
British Journal of Haematology|December 3, 1999
Propagation and senescence of human marrow stromal cells in culture: a simple colony-forming assay identifies samples with the greatest potential to propagate and differentiateC M Digirolamo, D Stokes, D Colter, et al.
The Journal of Biological Chemistry|September 25, 1980
Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VIIB Steinmann, L Tuderman, L Peltonen, et al.
American Journal of Human Genetics|November 1, 1984
Molecular heterogeneity in the mild autosomal dominant forms of osteogenesis imperfectaP Tsipouras, A L Børresen, L A Dickson, et al.
Biochemical Society Transactions|August 30, 2000
Potential use of stem cells from bone marrow to repair the extracellular matrix and the central nervous systemD J Prockop, S A Azizi, D Colter, et al.
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