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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

  • Wilson, R, Norris, EL, Brachvogel, B, Angelucci, C, Zivkovic, S, Gordon, L, Bernardo, BC, Stermann, J, Sekiguchi, K, Gorman, JJ, et al. Changes in the chondrocyte and extracellular matrix proteome during post-natal mouse cartilage development.. Mol Cell Proteomics 11(1) : M111.014159 2012
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  • Hansen, U, Allen, JM, White, R, Moscibrocki, C, Bruckner, P, Bateman, JF, Fitzgerald, J. WARP interacts with collagen VI-containing microfibrils in the pericellular matrix of human chondrocytes.. PLoS One 7(12) : e52793 2012
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  • Boyden, ED, Campos-Xavier, AB, Kalamajski, S, Cameron, TL, Suarez, P, Tanackovic, G, Andria, G, Ballhausen, D, Briggs, MD, Hartley, C, et al. Recurrent Dominant Mutations Affecting Two Adjacent Residues in the Motor Domain of the Monomeric Kinesin KIF22 Result in Skeletal Dysplasia and Joint Laxity. American Journal of Human Genetics 90(1) : 170 2012
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  • Boyden, ED, Campos-Xavier, AB, Kalamajski, S, Cameron, TL, Suarez, P, Tanackovic, G, Andria, G, Ballhausen, D, Briggs, MD, Hartley, C, et al. Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.. Am J Hum Genet 89(6) : 767 -772 2011
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  • Bernardo, BC, Belluoccio, D, Rowley, L, Little, CB, Hansen, U, Bateman, JF. Cartilage intermediate layer protein 2 (CILP-2) is expressed in articular and meniscal cartilage and down-regulated in experimental osteoarthritis.. J Biol Chem 286(43) : 37758 -37767 2011
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