Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23 von Econs, Michael J, Strom, Tim M, White, Kenneth E, Evans, Wayne E, O'Riordan, Jeffery L.H, Speer, Marcy C, Lorenz-Depiereux, Bettina, Grabowski, Monika, Meitinger, Thomas

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Mutations in the vitamin D receptor gene in three kindreds associated with hereditary vitamin D resistant rickets von COCKERILL, F. J, HAWA, N. S, YOUSAF, N, HEWISON, M, O'RIORDAN, J. L. H, FARROW, S. M

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Rickets in the 17th Century von O'Riordan, Jeffrey LH

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Antisense inhibition of vitamin D receptor expression induces apoptosis in monoblastoid U937 cells von Hewison, M, Dabrowski, M, Vadher, S, Faulkner, L, Cockerill, FJ, Brickell, PM, O'Riordan, JL, Katz, DR

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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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Translational regulation of parathyroid hormone gene expression and RNA: Protein interactions von Vadher, Shilpa, Hawa, Nigar S., O'Riordan, Jeffrey L. H., Farrow, Sheelagh M.

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A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets von Poustka, A, Davies, K.E, Lorenz, B, Korn, B, Drezner, M.K, O'Riordan, J.L.H, Pannetier, S, Rowe, P.S.N, Summerfield, T, Nesbitt, T, Meindl, A, Lehrach, H, Strom, T.M, Popowska, E, Mountford, R, Cagnoli, B, Mohnike, K.L, Hanauer, A, Reinhardt, R, Read, A.P, Econs, M.J, Murken, J, de Jong, P, Goulding, J.N, Hennig, S, Meitinger, T, Oudet, C, Francis, F, Pronicka, E

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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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Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP) von Rowe, Peter S. N., Oudet, Claudine L., Francis, Fiona, Sinding, Christiane, Pannetier, Solange, Econs, Mike J., Strom, Tim M., Meitinger, Thomas, Garabedian, Michele, David, Albert, Macher, Marie-Alice, Questiaux, Elisabeth, Popowska, Ewa, Pronicka, Ewa, Read, Andrew P., Mokrzycki, Agnes, Glorieux, Francis H., Drezner, Marc K., Hanauer, Andre, Lehrach, Hans, Goulding, Johnathan N., O'Riordan, Jeffrey L. H.

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Sir John David Nunes Nabarro von O'Riordan, J. L. H.

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The comparative role of 1-25-dihydroxycholecalciferol and phorbol esters in the differentiation of the U937 cell line von HEWISON, M, BRENNAN, A, SINGH-RANGER, R, WALTERS, J. C, KATZ, D. R, O'RIORDAN, J. L. H

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Cytochemical bioassay of parathyroid hormone in maternal and cord blood von Allgrove, J, Adami, S, Manning, R M, O'Riordan, J L

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Autocrine regulation of 1,25-dihydroxycholecalciferol metabolism in myelomonocytic cells von HEWISON, M, BARKER, S, BRENNAN, A, NATHAN, J, KATZ, D. R, O'RIORDAN, J. L. H

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O11. Multiple IGF-I mRNA transcripts are generated in rat bone cells von Farrow, SM, Hawa, NS, O'Riordan, JLH

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P61. Calcium regulates preproparathyroid hormone mRNA translation in the absence of transcription von Farrow, SM, Hawa, NS, O'Riordan, JLH

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Management of hyperparathyroidism in pregnancy von Gelister, J. S. K., Sanderson, J. D., Chapple, C. R., O'Riordan, J. L. H., Cowie, A. G. A., Milroy, E. J. G.

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O2. Regulation of cell adhesion molecules by vitamin D von Hewison, M, Faulkner, L, Vadher, S, Hewson, E, Katz, DR, O'Riordan, JLH

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Regulation of calcium absorption by 1,25,dihydroxy-vitamin D--studies of the effects of a bisphosphonate treatment von Adami, S, Frijlink, W B, Bijvoet, O L, O'Riordan, J L, Clemens, T L, Papapoulos, S E

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P2. Screening of an oncogenic hypophosphataemic osteomalacia (OHO) tumour cDNA library with YAC clones from a contig encompassing the HYP gene von Rowe, PSN, Goulding, J, Francis, F, Econs, M, Read, A, Drezer, M, Lehrach, H, Davies, KE, O'Riordan, JLH

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O8. Vitamin D receptor mutations and their stereochemical consequences von Rut, AR, Hewison, M, Kristjansson, K, Luisi, B, Walker, RE, Hughes, MR, O'Riordan, JLH

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