Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs) von Ramage, John K, Ahmed, A, Ardill, J, Bax, N, Breen, D J, Caplin, M E, Corrie, P, Davar, J, Davies, A H, Lewington, V, Meyer, T, Newell-Price, J, Poston, G, Reed, N, Rockall, A, Steward, W, Thakker, R V, Toubanakis, C, Valle, J, Verbeke, C, Grossman, A B

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Genetics of parathyroid tumours von Thakker, R. V.

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Parafibromin – functional insights von Newey, P. J., Bowl, M. R., Thakker, R. V.

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Bone matrix development in steroid-induced osteoporosis is associated with a consistently reduced fibrillar stiffness linked to altered bone mineral quality von Xi, L., De Falco, P., Barbieri, E., Karunaratne, A., Bentley, L., Esapa, C.T., Terrill, N.J., Brown, S.D.M., Cox, R.D., Davis, G.R., Pugno, N.M., Thakker, R.V., Gupta, H.S.

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Genetic Contribution to Bone Metabolism, Calcium Excretion, and Vitamin D and Parathyroid Hormone Regulation von Hunter, D., De Lange, M., Snieder, H., MacGregor, A. J., Swaminathan, R., Thakker, R. V., Spector, T. D.

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Genetics of neuroendocrine and carcinoid tumours von Leotlela, P D, Jauch, A, Holtgreve-Grez, H, Thakker, R V

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Guidelines for diagnosis and therapy of MEN type 1 and type 2 von Brandi, M L, Gagel, R F, Angeli, A, Bilezikian, J P, Beck-Peccoz, P, Bordi, C, Conte-Devolx, B, Falchetti, A, Gheri, R G, Libroia, A, Lips, C J, Lombardi, G, Mannelli, M, Pacini, F, Ponder, B A, Raue, F, Skogseid, B, Tamburrano, G, Thakker, R V, Thompson, N W, Tomassetti, P, Tonelli, F, Wells, Jr, S A, Marx, S J

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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome von BRADLEY, K. J., HOBBS, M. R., BULEY, I. D., CARPTEN, J. D., CAVACO, B. M., FARES, J. E., LAIDLER, P., MANEK, S., ROBBINS, C. M., SALTI, I. S., THOMPSON, N. W., JACKSON, C. E., THAKKER, R. V.

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Symmetrically reduced stiffness and increased extensibility in compression and tension at the mineralized fibrillar level in rachitic bone von Karunaratne, A, Boyde, A, Esapa, C.T, Hiller, J, Terrill, N.J, Brown, S.D.M, Cox, R.D, Thakker, R.V, Gupta, H.S

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Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours von Bradley, K. J., Cavaco, B. M., Bowl, M. R., Harding, B., Cranston, T., Fratter, C., Besser, G. M., da Conceição Pereira, M., Davie, M. W. J., Dudley, N., Leite, V., Sadler, G. P., Seller, A., Thakker, R. V.

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UROMODULIN Mutations Cause Familial Juvenile Hyperuricemic Nephropathy von Turner, J. J. O., Stacey, J. M., Harding, B., Kotanko, P., Lhotta, K., Puig, J. G., Roberts, I., Torres, R. J., Thakker, R. V.

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Phase II study of single agent capecitabine in the treatment of metastatic non-pancreatic neuroendocrine tumours von Medley, L, Morel, A N, Farrugia, D, Reed, N, Hayward, N, Davies, J M, Kirichek, O, Thakker, R V, Talbot, D C

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GATA3 haplo-insufficiency causes human HDR syndrome von Thakker, Rajesh V, Devriendt, Koenraad, Van Esch, Hilde, Groenen, Peter, Nesbit, M. Andrew, Schuffenhauer, Simone, Lichtner, Peter, Vanderlinden, Gert, Harding, Brian, Beetz, Rolf, Bilous, Rudolf W, Holdaway, Ian, Shaw, Nicholas J, Fryns, Jean-Pierre, Van de Ven, Wim

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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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Parafibromin is a nuclear protein with a functional monopartite nuclear localization signal von BRADLEY, K. J, BOWL, M. R, WILLIAMS, S. E, AHMAD, B. N, PARTRIDGE, C. J, PATMANIDI, A. L, KENNEDY, A. M, LOH, N. Y, THAKKER, R. V

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Hypophosphatemic rickets is associated with disruption of mineral orientation at the nanoscale in the flat scapula bones of rachitic mice with development von Karunaratne, A, Davis, G.R, Hiller, J, Esapa, C.T, Terrill, N.J, Brown, S.D.M, Cox, R.D, Thakker, R.V, Gupta, H.S

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A MEN1 pancreatic neuroendocrine tumour mouse model under temporal control von Lines, K E, Vas Nunes, R P, Frost, M, Yates, C J, Stevenson, M, Thakker, R V

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Multiple endocrine neoplasia type 1 von Pannett, A A, Thakker, R V

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Intra-Renal and Subcellular Distribution of the Human Chloride Channel, CLC-5, Reveals a Pathophysiological Basis for Dent's Disease von Devuyst, Olivier, Christie, Paul T., Courtoy, Pierre J., Beauwens, Renaud, Thakker, Rajesh V.

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Developments for funding clinical research in the UK von Walley, T, Thakker, RV

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