Whole-Exome Sequencing Studies of Nonhereditary (Sporadic) Parathyroid Adenomas by 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

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Rosie Head oral history interview conducted by John Dittmer in Tchula, Mississippi, 2013 March 13

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A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis by 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

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An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess by 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

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Whole-Exome Sequencing Studies of Nonfunctioning Pituitary Adenomas by 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

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Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and... by 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

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Assessing and further developing age‐appropriate information for young people about reporting suspected adverse drug reactions by 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.

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A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation by 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

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A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation by 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

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A Mouse with an N-Ethyl-N-Nitrosourea by 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

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

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