The von Willebrand factor predicted unpaired cysteines are essential for secretion von Shapiro, S. E., Nowak, A. A., Wooding, C., Birdsey, G., Laffan, M. A., McKinnon, T. A. J.

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The von Willeb teines are essential for secretion von Shapiro, S E, Nowak, A A, Wooding, C, Birdsey, G, Laffan, M A, McKinnon, T A J

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Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism von Pearce, S H, Trump, D, Wooding, C, Besser, G M, Chew, S L, Grant, D B, Heath, D A, Hughes, I A, Paterson, C R, Whyte, M P

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Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1 von Bassett, J.H.D., Forbes, S.A., Pannett, A.A.J., Lloyd, S.E., Christie, P.T., Wooding, C., Harding, B., Besser, G.M., Edwards, C.R., Monson, J.P., Sampson, J., Wass, J.A.H., Wheeler, M.H., Thakker, R.V.

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Clinical studies of multiple endocrine neoplasia type 1 (MEN1) von Trump, D., Farren, B., Wooding, C., Pang, J.T., Besser, G.M., Buchanan, K.D., Edwards, C.R., Heath, D.A., Jackson, C.E., Jansen, S., Lips, K., Monson, J.P., O'Halloran, D., Sampson, J., Shalet, S.M., Wheeler, M.H., Zink, A., Thakker, R.V.

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Membrane phosphatidylserine distribution as a non-apoptotic signalling mechanism in lymphocytes von Elliott, James I, Surprenant, Annmarie, Marelli-Berg, Federica M, Cooper, Joanne C, Cassady-Cain, Robin L, Wooding, Carol, Linton, Kenneth, Alexander, Denis R, Higgins, Christopher F

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Repacking of the transmembrane domains of P-glycoprotein during the transport ATPase cycle von Rosenberg, Mark F., Velarde, Giles, Ford, Robert C., Martin, Catherine, Berridge, Georgina, Kerr, Ian D., Callaghan, Richard, Schmidlin, Andreas, Wooding, Carol, Linton, Kenneth J., Higgins, Christopher F.

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Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations von THAKKER, R. V, POOK, M. A, WOODING, C, BOSCARO, M, SCANARINI, M, CLAYTON, R. N

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KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1 von Borgel, J, Tyl, M, Schiller, K, Pusztai, S, Dooley, CM, Deng, W, Wooding, C, White, RJ, Warnecke, T, Leonhardt, H, Busch-Nentwich, E, Bartke, T

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Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36 von Williamson, C, Pannett, A A, Pang, J T, Wooding, C, McCarthy, M, Sheppard, M N, Monson, J, Clayton, R N, Thakker, R V

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Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies von SCHNEINMAN, S. J, POOK, M. A, WOODING, C, PANG, J. T, FRYMOYER, P. A, THAKKER, R. V

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Localisation of X linked recessive idiopathic hypoparathyroidism to a 1.5 Mb region on Xq26-q27 von Trump, D, Dixon, P H, Mumm, S, Wooding, C, Davies, K E, Schlessinger, D, Whyte, M P, Thakker, R V

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Mapping the gene causing X-linked recessive idiopathic hypoparathyroidism to Xq26-Xq27 by linkage studies von THAKKER, R. V, DAVIES, K. E, WHYTE, M. P, WOODING, C, O'RIORDAN, J. L. H

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Mutational analysis of PHEX gene in X-linked hypophosphatemia von DIXON, P. H, CHRISTIE, P. T, SMITH, C, TAU, C, SCHLESSINGER, D, WHYTE, M. P, THAKKER, R. V, WOODING, C, TRUMP, D, GRIEFF, M, HOLM, I, GERTNER, J. M, SCHMIDTKE, J, SHAH, B, SHAW, N

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Mass and energy analysis of the ions in a plasma flood system von Wooding, A.C., Armour, D.G., van den Berg, J.A., Holmes, A.J.T., Burgess, C., Goldberg, R.D.

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Mapping of the gene encoding the B56β subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrin... von Forbes, S A, Pannett, A A, Bassett, J H, Harding, B, Wooding, C, Thakker, R V, Butler, R, Ogilvie, D, Anand, R, Gaudray, P, Weber, G, Larsson, C, Zhang, C X, Calender, A, Höppener, J W, Lips, C J, Kas, K

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Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families von Thakker, R.V., Davies, K.E., Read, A.P., Tippett, P., Wooding, C., Flint, T., Woob, S., Kruse, T.A., Whyte, M.P., O'Riordan, J.L.H.

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Association of Parathyroid Tumors in Multiple Endocrine Neoplasia Type 1 with Loss of Alleles on Chromosome 11 von Thakker, Rajesh V, Bouloux, Pierre, Wooding, Carol, Chotai, Kokila, Broad, Peter M, Spurr, Nigel K, Besser, Gordon M, O'Riordan, Jeffrey L.H

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Renal Chloride Channel, CLCN5, Mutations in Dent's Disease von Cox, Jeremy P. D., Yamamoto, Katsusuke, Christie, Paul T., Wooding, Carol, Feest, Terry, Flinter, Frances A., Goodyer, Paul R., Leumann, Ernst, Neuhaus, Thomas, Reid, Christopher, Williams, Paul F., Wrong, Oliver, Thakker, Rajesh V.

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Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22 von Pook, Mark A., Wrong, Oliver, Wooding, Carol, Norden, Anthony G.W., Feest, Terry G., Thakker, Rajesh V.

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