Molecular genetics of disorders of calcium homeostasis. by Bassett, J, Thakker, R

Novel DAX1 mutations in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism. by Bassett, J, O'Halloran, D, Williams, G, Beardwell, C, Shalet, S, Thakker, R

Temporal regulation of CFTR expression during ovine lung development: implications for CF gene therapy. by Broackes-Carter, F, Mouchel, N, Gill, D, Hyde, S, Bassett, J, Harris, A

Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1. by Bassett, J, Rashbass, P, Harding, B, Forbes, SA, Pannett, A, Thakker, R

Ovine male genital duct epithelial cells differentiate in vitro and express functional CFTR and ENaC by Bertog, M, Smith, D, Bielfeld-Ackermann, A, Bassett, J, Ferguson, D, Korbmacher, C, Harris, A

Ovine male genital duct epithelial cells differentiate in vitro and express functional CFTR and ENaC. by Bertog, M, Smith, D, Bielfeld-Ackermann, A, Bassett, J, Ferguson, D, Korbmacher, C, Harris, A

Linear order of new and established DNA markers around the fragile site at Xq27.3. by Hirst, M, Roche, A, Flint, T, MacKinnon, R, Bassett, J, Nakahori, Y, Watson, J, Bell, M, Patterson, M, Boyd, Y

Intrauterine transplantation of human fetal mesenchymal stem cells from first-trimester blood repairs bone and reduces fractures in osteogenesis imperfecta mice. by Guillot, P, Abass, O, Bassett, J, Shefelbine, S, Bou-Gharios, G, Chan, J, Kurata, H, Williams, G, Polak, J, Fisk, N

Transplantation of human fetal blood stem cells in the osteogenesis imperfecta mouse leads to improvement in multiscale tissue properties. by Vanleene, M, Saldanha, Z, Cloyd, K, Jell, G, Bou-Gharios, G, Bassett, J, Williams, G, Fisk, N, Oyen, M, Stevens, M, Guillot, P, Shefelbine, S

Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism. by Pannett, A, Kennedy, A, Turner, J, Forbes, SA, Cavaco, B, Bassett, J, Cianferotti, L, Harding, B, Shine, B, Flinter, F, Maidment, C, Trembath, R, Thakker, R

Potential of human fetal chorionic stem cells for the treatment of osteogenesis imperfecta. by Jones, G, Moschidou, D, Abdulrazzak, H, Kalirai, B, Vanleene, M, Osatis, S, Shefelbine, S, Horwood, N, Marenzana, M, De Coppi, P, Bassett, J, Williams, G, Fisk, N, Guillot, P

Characterization of mutations in patients with multiple endocrine neoplasia type 1. by Bassett, J, Forbes, SA, Pannett, A, Lloyd, SE, Christie, P, Wooding, C, Harding, B, Besser, G, Edwards, C, Monson, J, Sampson, J, Wass, J, Wheeler, M, Thakker, R

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and... by Karunaratne, A, Esapa, C, Hiller, J, Boyde, A, Head, R, Bassett, J, Terrill, N, Williams, G, Brown, M, Croucher, P, Brown, S, Cox, R, Barber, A, Thakker, R, Gupta, H

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and... by Karunaratne, A, Esapa, C, Hiller, J, Boyde, A, Head, R, Bassett, J, Terrill, N, Williams, G, Brown, M, Croucher, P, Brown, S, Cox, R, Barber, A, Thakker, R, Gupta, H

Frequent occurrence of an intron 4 mutation in multiple endocrine neoplasia type 1. by Turner, J, Leotlela, P, Pannett, A, Forbes, SA, Bassett, J, Harding, B, Christie, P, Bowen-Jones, D, Ellard, S, Hattersley, A, Jackson, C, Pope, R, Quarrell, O, Trembath, R, Thakker, R

The European Consortium on MEN1. 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 can... by Forbes, SA, Pannett, A, Bassett, J, Harding, B, Wooding, C, Thakker, R, Butler, R, Ogilvie, D, Anand, R, Gaudray, P, Weber, G, Larsson, C, Zhang, C, Calender, A, Höppener, J, Lips, C, Kas, K

Mapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endo... by Forbes, SA, Pannett, A, Bassett, J, Harding, B, Wooding, C, Thakker, R, Butler, R, Ogilvie, D, Anand, R, Gaudray, P, Weber, G, Larsson, C, Zhang, C, Calender, A, Höppener, J, Lips, C, Kas, K

The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1) by Bassett, J, Pannett, A, Forbes, SA, Thakker, R, McCarthy, M, Read, A, Teh, B, Larsson, C, Kytola, S, Leisti, J, Salmela, P, Weber, G, Giraud, S, Zhang, C, Calender, A, Hoppener, J, vanAmstel, H, Lips, C, Kas, K, VandeVen, W, Gaudray, P

A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation by Esapa, C, Hough, T, Testori, S, Head, R, Crane, E, Chan, C, Evans, H, Bassett, J, Tylzanowski, P, McNally, E, Carr, A, Boyde, A, Howell, P, Clark, A, Williams, G, Brown, M, Croucher, P, Nesbit, M, Brown, S, Cox, R, Cheeseman, M, Thakker, R

A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation. by Esapa, C, Hough, T, Testori, S, Head, R, Crane, E, Chan, C, Evans, H, Bassett, J, Tylzanowski, P, McNally, E, Carr, A, Boyde, A, Howell, P, Clark, A, Williams, G, Brown, M, Croucher, P, Nesbit, M, Brown, S, Cox, R, Cheeseman, M, Thakker, R