Mutations in the gene for the E1β subunit: a novel cause of pyruvate dehydrogenase deficiency by Brown, R, Head, R, Boubriak, I, Leonard, J, Thomas, N, Brown, G

Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia. by Nesbit, M, Hannan, F, Howles, SA, Babinsky, V, Head, R, Cranston, T, Rust, N, Hobbs, MR, Heath, H, Thakker, R

GATA3 mutations found in breast cancers may be associated with aberrant nuclear localization, reduced transactivation and cell invasiveness. by Gaynor, K, Grigorieva, I, Allen, MD, Esapa, C, Head, R, Gopinath, P, Christie, P, Nesbit, M, Jones, J, Thakker, R

GATA3 Mutations Found in Breast Cancers May Be Associated with Aberrant Nuclear Localization, Reduced Transactivation and Cell Invasiveness by Gaynor, K, Grigorieva, I, Allen, MD, Esapa, C, Head, R, Gopinath, P, Christie, P, Nesbit, M, Jones, J, Thakker, R

A Mouse with a Ser1386Pro Mutation in the C-propeptide Domain of col2aI Provides a Model for Spondyloepiphyseal Dysplasia Congenita by Esapa, C, Hough, T, Testori, S, Head, R, Crane, E, Chan, C, Brown, M, Brown, S, Croucher, P, Cox, R, Cheeseman, M, Thakker, R

A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation. by Piret, S, Esapa, C, Gorvin, C, Head, R, Loh, N, Devuyst, O, Thomas, G, Brown, s, Brown, M, Croucher, P, Cox, R, Thakker, R

Genetic models of bone disease using ENU mutagenesis by Brown, S, Esapa, C, Barbaric, I, Hough, T, Brown, M, Croucher, P, Head, R, Chan, C, Crane, E, Cox, R, Cheeseman, M, Thakker, R

A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis by Esapa, C, Head, R, Jeyabalan, J, Evans, H, Hough, T, Cheeseman, M, McNally, E, Carr, A, Thomas, G, Brown, M, Croucher, P, Brown, S, Cox, R, 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

Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas. by Newey, P, Nesbit, M, Rimmer, A, Attar, M, Head, R, Christie, P, Gorvin, C, Stechman, M, Gregory, L, Mihai, R, Sadler, G, McVean, G, Buck, D, Thakker, R

Whole-exome sequencing studies of nonfunctioning pituitary adenomas. by Newey, P, Nesbit, M, Rimmer, A, Head, R, Gorvin, C, Attar, M, Gregory, L, Wass, J, Buck, D, Karavitaki, N, Grossman, A, McVean, G, Ansorge, O, 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

An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess. by Bentley, L, Esapa, C, Nesbit, M, Head, R, Evans, H, Lath, D, Scudamore, C, Hough, T, Podrini, C, Hannan, F, Fraser, W, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

An N-ethyl-n-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess by Bentley, L, Esapa, C, Nesbit, M, Head, R, Evans, H, Lath, D, Scudamore, C, Hough, T, Podrini, C, Hannan, F, Fraser, W, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

Glass-coated beryllium mirrors for the LHCb RICH1 detector by Barber, G, Brook, N, Cameron, W, D'Ambrosio, C, Frei, C, Harnew, N, Head, R, Khimitch, Y, Khmelnikov, V, Loveridge, P, Metlica, F, Obraztsov, V, Piedigrossi, D, Sizenev, V, Szczypka, P, Ullaland, O, Vygosky, E, Websdale, D

First radiation hardness results of the TeraPixel Active Calorimeter (TPAC) sensor by Price, T, Watson, N, Wilson, J, Rajovic, V, Cussans, D, Goldstein, J, Head, R, Nash, S, Page, R, Velthuis, J, Strube, J, Stanitzki, M, Dauncey, P, Gao, R, Nomerotski, A, Coath, R, Crooks, J, Turchetta, R, Tyndel, M, Wormh, S, Zhangh, Z

Beam test results of FORTIS, a 4T MAPS sensor with a signal-to-noise ratio exceeding 100 by Velthuis, J, Cussans, D, Goldstein, J, Page, R, Wilson, J, Worm, S, Coath, R, Crooks, J, Dauncey, P, Gao, R, Head, R, Miller, O, Nash, S, Nomerotski, A, Price, T, Rajovic, V, Stanitzki, M, Strube, J, Turchetta, R, Tyndel, M, Watson, N, Zhang, Z

Beam test results of FORTIS, a 4T MAPS sensor with a signal-to-noise ratio exceeding 100 by Velthuis, J, Cussans, D, Goldstein, J, Page, R, Wilson, J, Worm, S, Coath, R, Crooks, J, Dauncey, P, Gao, R, Head, R, Miller, O, Nash, S, Nomerotski, A, Price, T, Rajovic, V, Stanitzki, M, Strube, J, Turchetta, R, Tyndel, M, Watson, N, Zhang, Z

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