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Title	Author(s)	Issue Date	Views
A 5' splice site mutation affecting the pre-mRNA splicing of two upstream exons in the collagen COL1A1 gene. Exon 8 skipping and altered definition of exon 7 generates truncated proα1(I) chains with a non-collagenous insertion destabilizing the triple helix Journal:Biochemical Journal	Bateman, JF Chan, D Moeller, I Hannagan, M Cole, WG	1994	188
Abnormal cell cycle regulation and chondrocyte differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia mutation in COL10A1. Proceeding/Conference:CSHL 2002 Mouse Molecular Genetics Meeting	Cheah, KSE Tsang, KY Chan, D Cheslett, D Kwan, KM Cheung, KMC Hunziker, E Sillence, D Bateman, JF	2002	118
Abnormal chondroctye differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia Col10al mutation Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2002	Tsang, KY Chan, D Kwan, KM Cheung, KMC Hunziker, E Sillence, D Bateman, JF Cheah, KSE	2002	133
Abnormal chondrocyte differentiation in transgenic mice expressing a schmid metaphyseal chondrodysplasia col10a1 mutation Proceeding/Conference:Research Postgraduate Symposium, RPS 2002	Tsang, KY Chan, D Cheslett, D Kwan, KM Cheung, KMC Hunziker, E Sillence, D Boot-Handford, R Bateman, JF Cheah, KSE	2002	111
Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta Journal:Biochemical Journal	Bateman, JF Mascara, T Chan, D Cole, WG	1984	169
A base substitution at a splice site in the COL3A1 gene causes exon skipping and generates abnormal type III procollagen in a patient with Ehlers-Danlos syndrome type IV Journal:Journal of Biological Chemistry	Cole, WG Chiodo, AA Lamande, SR Janeczko, R Ramirez, F Dahl, HHM Chan, D Bateman, JF	1990	171
A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos Syndrome Type VII Journal:EMBO Journal	Weil, D D'alessio, M Ramirez, F De Wet, W Cole, WG Chan, D Bateman, JF	1989	207
Biochemical heterogeneity of type I collagen mutations in osteogenesis imperfecta. Journal:Annals of the New York Academy of Sciences	Bateman, JF Chan, D Lamande, S Mascara, T Cole, WG	1988	109
Changes in collagen stability and folding in lethal perinatal osteogenesis imperfecta. The effect of α1(I)-chain glycine-to-arginine substitutions Journal:Biochemical Journal	Baker, AT Ramshaw, RAM Chan, D Cole, WG Bateman, JF	1989	243
Characterization of a type I collagen α2(I) glycine-586 to valine substitution in osteogenesis imperfecta type IV. Detection of the mutation and prenatal diagnosis by a chemical cleavage method Journal:Biochemical Journal	Bateman, JF Hannagan, M Chan, D Cole, WG	1991	116
Characterization of three osteogenesis imperfecta collagen α1(I) glycine to serine mutations demonstrating a position-dependent gradient of phenotypic severity Journal:Biochemical Journal	Bateman, JF Moeller, I Hannagan, M Chan, D Cole, WG	1992	136
Chondrocytes survive ER stress caused by unfolded proteins via re-programming Proceeding/Conference:HUGO Annual Human Genome Meeting, HGM 2005	Cheah, KSE Tsang, KY Cheslett, D Chan, WCW So, CL Kwan, KM Hunziker, EB Yamada, Y Bateman, JF Cheung, KMC Chan, D	2005	122
A COL2A1 mutation in achondrogenesis type II results in the replacement of type II collagen by type I and III collagens in cartilage Journal:Journal of Biological Chemistry	Chan, D Cole, WG Chow, CW Mundlos, S Bateman, JF	1995	131
Collagen defects in lethal perinatal osteogenesis imperfecta Journal:Biochemical Journal	Bateman, JF Chan, D Mascara, T	1986	158
Collagen II is essential for the removal of the notochord and the formation of intervertebral discs Journal:Journal of Cell Biology	Aszódi, A Chan, D Hunziker, E Bateman, JF Fässler, R	1998	192
Comprehensive analysis of collagen metabolism in vitro using [43H]/[14C]proline dual-labeling and polyacrylamide gel electrophoresis Journal:Analytical Biochemistry	Bateman, JF Harley, V Chan, D Cole, WG	1988	156
Depletion of annexin A5, annexin A6 and collagen X causes no gross changes in matrix vesicle-mediated mineralization, but lack of collagen X affects hematopoiesis and the Th1/Th2 response Journal:Journal of Bone and Mineral Research	Grskovic, I Kutsch, A Frie, C Groma, G Stermann, J,Schlötzer-Schrehardt, U Niehoff, A,Moss, SE Rosenbaum, S Pöschl, E Chmielewski, M Rappl, G Abken, H Bateman, JF Cheah, KSE Paulsson, M Brachvogel, B	2012	211
Disrupted growth plates and progressive deformities in osteogenesis imperfecta as a result of the substitution of glycine 585 by valine in the α2(I) chain of type I collagen Journal:Journal of Medical Genetics	Cole, WG Chan, D Chow, CW Rogers, JG Bateman, JF	1996	144
A dominant interference collagen X mutation disrupts hypertrophic chondrocyte pericellular matrix and glycosaminoglycan and proteoglycan distribution in transgenic mice Journal:American Journal of Pathology	Jacenko, O Chan, D Franklin, A Ito, S Underhill, CB Bateman, JF Campbell, MR	2001	169
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	172

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