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Showing results 1 to 4 of 4

	Title	Author(s)	Issue Date
	Abnormal compartmentalization of cartilage matrix components in mice lacking collagen X: Implications for function Journal:Journal of Cell Biology	Kwan, KM Pang, MKM Zhou, S Cowan, SK Kong, RYC Pfordte, T Olsen, BR Sillence, DO Tam, PPL Cheah, KSE	1997
	COL10A1 nonsense and frame-shift mutations have a gain-of-function effect on the growth plate in human and mouse metaphyseal chondrodysplasia type Schmid Journal:Human Molecular Genetics	Ho, MSP Tsang, KY Lo, RLK Susic, M Mäkitie, O Chan, TWY Ng, VCW Sillence, DO BootHandford, RP Gibson, G Cheung, KMC Cole, WG Cheah, KSE Chan, D	2007
	Endoplasmic reticulum-mediated quality control of type I collagen production by cells from osteogenesis imperfecta patients with mutations in the proα1(I) chain carboxyl-terminal propeptide which impair subunit assembly Journal:Journal of Biological Chemistry	Lamande, SR Chessler, SD Golub, SB Byers, PH Chan, D Cole, WG Sillence, DO Bateman, JF	1995
	Multiexon deletions in the type I collagen COL1A2 gene in osteogenesis imperfecta type IB. Molecules containing the shortened α2(I) chains show differential incorporation into the bone and skin extracellular matrix Journal:Journal of Biological Chemistry	Mundlos, S Chan, D Weng, YM Sillence, DO Cole, WG Bateman, JF	1996

Showing results 1 to 4 of 4