Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas von Newey, Paul J, Nesbit, M. Andrew, Rimmer, Andrew J, Attar, Moustafa, Head, Rosie T, Christie, Paul T, Gorvin, Caroline M, Stechman, Michael, Gregory, Lorna, Mihai, Radu, Sadler, Greg, McVean, Gil, Buck, David, Thakker, Rajesh V

Volltext

Mutations Affecting G-Protein Subunit α11 in Hypercalcemia and Hypocalcemia von Nesbit, M. Andrew, Hannan, Fadil M, Howles, Sarah A, Babinsky, Valerie N, Head, Rosie A, Cranston, Treena, Rust, Nigel, Hobbs, Maurine R, Heath, Hunter, Thakker, Rajesh V

Volltext

A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis von Esapa, Christopher T, Head, Rosie A, Jeyabalan, Jeshmi, Evans, Holly, Hough, Tertius A, Cheeseman, Michael T, McNally, Eugene G, Carr, Andrew J, Thomas, Gethin P, Brown, Matthew A, Croucher, Peter I, Brown, Steve D M, Cox, Roger D, Thakker, Rajesh V

Volltext

An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess von Bentley, Liz, Esapa, Christopher T, Nesbit, M. Andrew, Head, Rosie A, Evans, Holly, Lath, Darren, Scudamore, Cheryl L, Hough, Tertius A, Podrini, Christine, Hannan, Fadil M, Fraser, William D, Croucher, Peter I, Brown, Matthew A, Brown, Steve D. M, Cox, Roger D, Thakker, Rajesh V

Volltext

Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas von Newey, Paul J, Nesbit, M. Andrew, Rimmer, Andrew J, Head, Rosie A, Gorvin, Caroline M, Attar, Moustafa, Gregory, Lorna, Wass, John A. H, Buck, David, Karavitaki, Niki, Grossman, Ashley B, McVean, Gilean, Ansorge, Olaf, Thakker, Rajesh V

Volltext

Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and... von Karunaratne, Angelo, Esapa, Christopher R, Hiller, Jennifer, Boyde, Alan, Head, Rosie, Bassett, JH Duncan, Terrill, Nicholas J, Williams, Graham R, Brown, Matthew A, Croucher, Peter I, Brown, Steve DM, Cox, Roger D, Barber, Asa H, Thakker, Rajesh V, Gupta, Himadri S

Volltext

Assessing and further developing age‐appropriate information for young people about reporting suspected adverse drug reactions von Bioletti, Louis, Khan, Hannah, Greene, Gemma, Nagra, Prem, Rerri‐Bekibele, Jess, Saunders, Evie, Maher, Julie, Perry, Jack, Connell, Simon, Henderson, Daisy, Adams, Dan, Lynch, Jess, Halton, Belinda, Kharabish, Jomana, Clift, Richard, Alam, Zayan, Kelly, Victoria, Head, Amy, Bioletti, David, Lazenby‐Tracey, Scarlett, Sandhu, Shaktee, Reay, Sian Edney, Ventre, Cath, McCabe, Vincent, Wheadon, Richard, Bratherton, Lara, Shaw, A., Gouldbourne, Molly, Mathison, Helen, Woods, Anna, Mueller, Annett, Ferenczy, Theo, Butler, John, Taylor, Olivia, Marchant, Katie, MacDonald, Rosie, Griffiths, Louise, Jones, Lewis, Jones, Carmel, Robertswood, Lucas, Webb, David, Smith, Sophie, Ogunmyiwa, Jenny, Woodward, Charlotte, Jadeja, Mitul, Hawcutt, Daniel B.

Volltext

A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation von Esapa, Christopher T, Hough, Tertius A, Testori, Sarah, Head, Rosie A, Crane, Elizabeth A, Chan, Carol PS, Evans, Holly, Bassett, JH Duncan, Tylzanowski, Przemko, McNally, Eugene G, Carr, Andrew J, Boyde, Alan, Howell, Peter GT, Clark, Anne, Williams, Graham R, Brown, Matthew A, Croucher, Peter I, Nesbit, M Andrew, Brown, Steve DM, Cox, Roger D, Cheeseman, Michael T, Thakker, Rajesh V

Volltext

A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation von Piret, Sian E, Esapa, Christopher T, Gorvin, Caroline M, Head, Rosie, Loh, Nellie Y, Devuyst, Olivier, Thomas, Gethin, Brown, Steve D M, Brown, Matthew, Croucher, Peter, Cox, Roger, Thakker, Rajesh V

Volltext

Mutations Affecting G-Protein Subunit α 11 in Hypercalcemia and Hypocalcemia von Nesbit, M. Andrew, Hannan, Fadil M., Howles, Sarah A., Babinsky, Valerie N., Head, Rosie A., Cranston, Treena, Rust, Nigel, Hobbs, Maurine R., Heath, Hunter, Thakker, Rajesh V.

Volltext

A Mouse with an N-Ethyl-N-Nitrosourea von Esapa, Christopher T, Head, Rosie A, Jeyabalan, Jeshmi, Evans, Holly, Hough, Tertius A, Cheeseman, Michael T, McNally, Eugene G, Carr, Andrew J, Thomas, Gethin P, Brown, Matthew A, Croucher, Peter I, Brown, Steve D. M, Cox, Roger D, Thakker, Rajesh V

Volltext

A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation von Piret, Sian E, Esapa, Christopher T, Gorvin, Caroline M, Head, Rosie, Loh, Nellie Y, Devuyst, Olivier, Thomas, Gethin, Brown, Steve D M, Brown, Matthew, Croucher, Peter, Cox, Roger, Thakker, Rajesh V

Volltext

Pyruvate dehydrogenase E3 binding protein deficiency von BROWN, Ruth M, HEAD, Rosie A, BROWN, Garry K

Volltext