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Details

Role Esteemed Honorary Fellow
Research area Stem Cell Medicine
Group Blood Development

Contact

Available for student supervision
Formation of the human skeleton and proper bone, cartilage, joint and muscle function are determined by complex interactions between developmental signalling pathways. Genetic and acquired disorders affecting these tissues are common. The group’s research is aimed at understanding the molecular basis of these disorders to improve diagnosis and counselling, identify new therapeutic targets and test the effectiveness of new treatments to ultimately improve the quality of life for children with these debilitating conditions
Formation of the human skeleton and proper bone, cartilage, joint and muscle function are determined by complex interactions between developmental signalling pathways. Genetic and acquired disorders affecting these tissues are common. The group’s...
Formation of the human skeleton and proper bone, cartilage, joint and muscle function are determined by complex interactions between developmental signalling pathways. Genetic and acquired disorders affecting these tissues are common. The group’s research is aimed at understanding the molecular basis of these disorders to improve diagnosis and counselling, identify new therapeutic targets and test the effectiveness of new treatments to ultimately improve the quality of life for children with these debilitating conditions

Top Publications

  • Cole, WG, Campbell, PE, Rogers, JG, Bateman, JF. The clinical features of osteogenesis imperfecta resulting from a non-functional carboxy terminal pro alpha 1(I) propeptide of type I procollagen and a severe deficiency of normal type I collagen in tissues.. J Med Genet 27(9) : 545 -551 1990
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  • Chan, D, Lamande, SR, Cole, WG, Bateman, JF. Regulation of procollagen synthesis and processing during ascorbate-induced extracellular matrix accumulation in vitro.. Biochem J 269(1) : 175 -181 1990
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  • Bateman, JF, Golub, SB. Assessment of procollagen processing defects by fibroblasts cultured in the presence of dextran sulphate.. Biochem J 267(3) : 573 -577 1990
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  • Wu, H, Bateman, JF, Schnieke, A, Sharpe, A, Barker, D, Mascara, T, Eyre, D, Bruns, R, Krimpenfort, P, Berns, A. Human-mouse interspecies collagen I heterotrimer is functional during embryonic development of Mov13 mutant mouse embryos.. Mol Cell Biol 10(4) : 1452 -1460 1990
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  • Cole, WG, Chow, CW, Rogers, JG, Bateman, JF. The clinical features of three babies with osteogenesis imperfecta resulting from the substitution of glycine by arginine in the pro alpha 1(I) chain of type I procollagen.. J Med Genet 27(4) : 228 -235 1990
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