NKX2-1 homeobox gene, brain-lung-thyroid syndrome: a case study von Cox, RD, Mehdi, N

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500 - NKX2-1 homeobox gene, brain-lung-thyroid syndrome: a case study von Cox, RD, Mehdi, N

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Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition von Small, Kerrin S., Todorčević, Marijana, Civelek, Mete, El-Sayed Moustafa, Julia S., Wang, Xiao, Simon, Michelle M., Fernandez-Tajes, Juan, Mahajan, Anubha, Horikoshi, Momoko, Hugill, Alison, Glastonbury, Craig A., Quaye, Lydia, Neville, Matt J., Sethi, Siddharth, Yon, Marianne, Pan, Calvin, Che, Nam, Viñuela, Ana, Tsai, Pei-Chien, Nag, Abhishek, Buil, Alfonso, Thorleifsson, Gudmar, Raghavan, Avanthi, Ding, Qiurong, Morris, Andrew P., Bell, Jordana T., Thorsteinsdottir, Unnur, Stefansson, Kari, Laakso, Markku, Dahlman, Ingrid, Arner, Peter, Gloyn, Anna L., Musunuru, Kiran, Lusis, Aldons J., Cox, Roger D., Karpe, Fredrik, McCarthy, Mark I.

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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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A genetic and physiological study of impaired glucose homeostasis control in C57BL/6J mice von TOYE, A. A, LIPPIAT, J. D, QUARTERMAN, J, FREEMAN, H. C, ASHCROFT, F. M, COX, R. D, PROKS, P, SHIMOMURA, K, BENTLEY, L, HUGILL, A, MIJAT, V, GOLDSWORTHY, M, MOIR, L, HAYNES, A

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The Collaborative Cross, a community resource for the genetic analysis of complex traits von Churchill, Gary A, Airey, David C, Allayee, Hooman, Angel, Joe M, Attie, Alan D, Beatty, Jackson, Beavis, William D, Belknap, John K, Bennett, Beth, Berrettini, Wade, Bleich, Andre, Bogue, Molly, Broman, Karl W, Buck, Kari J, Buckler, Ed, Burmeister, Margit, Chesler, Elissa J, Cheverud, James M, Clapcote, Steven, Cook, Melloni N, Cox, Roger D, Crabbe, John C, Crusio, Wim E, Darvasi, Ariel, Deschepper, Christian F, Doerge, R W, Farber, Charles R, Forejt, Jiri, Gaile, Daniel, Garlow, Steven J, Geiger, Hartmut, Gershenfeld, Howard, Gordon, Terry, Gu, Jing, Gu, Weikuan, de Haan, Gerald, Hayes, Nancy L, Heller, Craig, Himmelbauer, Heinz, Hitzemann, Robert, Hunter, Kent, Hsu, Hui-Chen, Iraqi, Fuad A, Ivandic, Boris, Jacob, Howard J, Jansen, Ritsert C, Jepsen, Karl J, Johnson, Dabney K, Johnson, Thomas E, Kempermann, Gerd, Kendziorski, Christina, Kotb, Malak, Kooy, R Frank, Llamas, Bastien, Lammert, Frank, Lassalle, Jean-Michel, Lowenstein, Pedro R, Lu, Lu, Lusis, Aldons, Manly, Kenneth F, Marcucio, Ralph, Matthews, Doug, Medrano, Juan F, Miller, Darla R, Mittleman, Guy, Mock, Beverly A, Mogil, Jeffrey S, Montagutelli, Xavier, Morahan, Grant, Morris, David G, Mott, Richard, Nadeau, Joseph H, Nagase, Hiroki, Nowakowski, Richard S, O'Hara, Bruce F, Osadchuk, Alexander V, Page, Grier P, Paigen, Beverly, Paigen, Kenneth, Palmer, Abraham A, Pan, Huei-Ju, Peltonen-Palotie, Leena, Peirce, Jeremy, Pomp, Daniel, Pravenec, Michal, Prows, Daniel R, Qi, Zhonghua, Reeves, Roger H, Roder, John, Rosen, Glenn D, Schadt, Eric E, Schalkwyk, Leonard C, Seltzer, Ze'ev, Shimomura, Kazuhiro, Shou, Siming, Sillanpää, Mikko J, Siracusa, Linda D, Snoeck, Hans-Willem, Spearow, Jimmy L, Svenson, Karen

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Nicotinamide nucleotide transhydrogenase: a key role in insulin secretion von Freeman, Helen, Shimomura, Kenju, Horner, Emma, Cox, Roger D, Ashcroft, Frances M

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Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) von Yamagata, Kazuya, Oda, Naohisa, Kaisaki, Pamela J, Menzel, Stephan, Furuta, Hiroto, Vaxillaire, Martine, Southam, Lorraine, Cox, Roger D, Lathrop, G. Mark, Boriraj, V. Vicky, Chen, Xiangna, Cox, Nancy J, Oda, Yukie, Yano, Hideki, Le Beau, Michelle M, Yamada, Shirou, Nishigori, Hidekazu, Takeda, Jun, Fajans, Stefan S, Hattersley, Andrew T, Iwasaki, Naoko, Hansen, Torben, Pedersen, Oluf, Polonsky, Kenneth S, Turner, Robert C, Velho, Gilberto, Chèvre, Jean-Claude, Froguel, Philippe, Bell, Graeme I

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Author Correction: Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition von Small, Kerrin S., Todorčević, Marijana, Civelek, Mete, El-Sayed Moustafa, Julia S., Wang, Xiao, Simon, Michelle M., Fernandez-Tajes, Juan, Mahajan, Anubha, Horikoshi, Momoko, Hugill, Alison, Glastonbury, Craig A., Quaye, Lydia, Neville, Matt J., Sethi, Siddharth, Yon, Marianne, Pan, Calvin, Che, Nam, Vinuela, Ana, Tsai, Pei-Chien, Nag, Abhishek, Buil, Alfonso, Thorleifsson, Gudmar, Raghavan, Avanthi, Ding, Qiurong, Morris, Andrew P., Bell, Jordana T., Thorsteinsdottir, Unnur, Stefansson, Kari, Laakso, Markku, Dahlman, Ingrid, Arner, Peter, Gloyn, Anna L., Musunuru, Kiran, Lusis, Aldons J., Cox, Roger D., Karpe, Fredrik, McCarthy, Mark I.

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A gene-driven approach to the identification of ENU mutants in the mouse von Brown, Steve D.M, Coghill, Emma L, Hugill, Alison, Parkinson, Nick, Davison, Claire, Glenister, Peter, Clements, Sian, Hunter, Jackie, Cox, Roger D

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A mouse model with a frameshift mutation in the nuclear factor I/X (NFIX) gene has phenotypic features of Marshall-Smith syndrome von Kooblall, KG, Stevenson, M, Stewart, M, Harris, L, Zalucki, O, Dewhurst, H, Butterfield, N, Leng, H, Hough, TA, Ma, D, Siow, B, Potter, P, Cox, RD, Brown, SDM, Horwood, N, Wright, B, Lockstone, H, Buck, D, Vincent, TL, Hannan, FM, Bassett, JHD, Williams, GR, Lines, KE, Piper, M, Wells, S, Teboul, L, Hennekam, RC, Thakker, RV

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Online Education as Institutional Myth: Rituals and Realities at Community Colleges von Cox, Rebecca D

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The role of intestinal microbiota in murine models of acetaminophen-induced hepatotoxicity von Possamai, LA, McPhail, MJW, Khamri, W, Wu, B, Concas, D, Harrison, M, Williams, R, Cox, RD, Cox, IJ, Anstee, QM, Thursz, MR

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A gene-driven ENU-based approach to generating an allelic series in any gene von Quwailid, Mohamed Mohideen, Hugill, Alison, Dear, Neil, Vizor, Lucie, Wells, Sara, Horner, Emma, Fuller, Shelly, Weedon, Jessica, McMath, Hamish, Woodman, Paul, Edwards, David, Campbell, David, Rodger, Susan, Carey, Joanne, Roberts, Ann, Glenister, Pete, Lalanne, Zuzanna, Parkinson, Nick, Coghill, Emma L, McKeone, Richard, Cox, Sam, Willan, John, Greenfield, Andy, Keays, David, Brady, Saffron, Spurr, Nigel, Gray, Ian, Hunter, Jackie, Brown, Steve D M, Cox, Roger D

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In Vitro Photodynamic Activity of a Series of Methylene Blue Analogues von Mellish, Kirste J., Cox, Russell D., Vernon, David I., Griffiths, John, Brown, Stanley B.

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Polygenic Control of Idiopathic Generalized Epilepsy Phenotypes in the Genetic Absence Rats from Strasbourg (GAERS) von Rudolf, Gabrielle, Thérèse Bihoreau, Marie, F. Godfrey, Richard, P. Wilder, Steven, D. Cox, Roger, Lathrop, Mark, Marescaux, Christian, Gauguier, Dominique

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Chromosomal Mapping of Genetic Loci Controlling Absence Epilepsy Phenotypes in the WAG/Rij Rat von Gauguier, Dominique, Luijtelaar, Gilles van, Bihoreau, Marie Thérèse, Wilder, Steven P., Godfrey, Richard F., Vossen, Jo, Coenen, Anton, Cox, Roger D.

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Isolation and characterization of LRP6, a novel member of the low density lipoprotein receptor gene family von Brown, S D, Twells, R C, Hey, P J, Cox, R D, Levy, E R, Soderman, A R, Metzker, M L, Caskey, C T, Todd, J A, Hess, J F

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A New Mouse Model of Type 2 Diabetes, Produced by N-Ethyl-Nitrosourea Mutagenesis, Is the Result of a Missense Mutation in the Glucokinase Gene von TOYE, Ayo A, MOIR, Lee, BROWNE, Mick, SPURR, Nigel, COX, Roger D, HUGILL, Alison, BENTLEY, Liz, QUARTERMAN, Julie, MIJAT, Vesna, HONGH, Tertius, GOLDSWORTHY, Michelle, HAYNES, Alison, HUNTER, A. Jacqueline

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Rodent models of genetic disease von Cox, Roger D, Brown, Steve DM

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