Works matching IS 10614036 AND DT 2008 AND VI 40 AND IP 3

Results: 28
    1

    Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 281, doi. 10.1038/ng.89
    By:
    • Gudmundsson, Julius;
    • Sulem, Patrick;
    • Rafnar, Thorunn;
    • Bergthorsson, Jon T;
    • Manolescu, Andrei;
    • Gudbjartsson, Daniel;
    • Agnarsson, Bjarni A;
    • Sigurdsson, Asgeir;
    • Benediktsdottir, Kristrun R;
    • Blondal, Thorarinn;
    • Jakobsdottir, Margret;
    • Stacey, Simon N;
    • Kostic, Jelena;
    • Kristinsson, Kari T;
    • Birgisdottir, Birgitta;
    • Ghosh, Shyamali;
    • Magnusdottir, Droplaug N;
    • Thorlacius, Steinunn;
    • Thorleifsson, Gudmar;
    • S Lilly Zheng
    Publication type:
    Article
    2

    Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome).

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 284, doi. 10.1038/ng.2007.66
    By:
    • Geneviève, David;
    • Proulle, Valérie;
    • Isidor, Bertrand;
    • Bellais, Samuel;
    • Serre, Valérie;
    • Djouadi, Fatima;
    • Picard, Capucine;
    • Vignon-Savoye, Capucine;
    • Bader-Meunier, Brigitte;
    • Blanche, Stéphane;
    • de Vernejoul, Marie-Christine;
    • Legeai-Mallet, Laurence;
    • Fischer, Anne-Marie;
    • Le Merrer, Martine;
    • Dreyfus, Marie;
    • Gaussem, Pascale;
    • Munnich, Arnold;
    • Cormier-Daire, Valérie
    Publication type:
    Article
    3

    A phenylalanine in DGAT is a key determinant of oil content and composition in maize.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 367, doi. 10.1038/ng.85
    By:
    • Peizhong Zheng;
    • Allen, William B;
    • Roesler, Keith;
    • Williams, Mark E;
    • Shirong Zhang;
    • Jiming Li;
    • Glassman, Kimberly;
    • Ranch, Jerry;
    • Nubel, Douglas;
    • Solawetz, William;
    • Bhattramakki, Dinakar;
    • Llaca, Victor;
    • Deschamps, Stéphane;
    • Gan-Yuan Zhong;
    • Tarczynski, Mitchell C;
    • Bo Shen
    Publication type:
    Article
    4
    5

    What causes mitochondrial DNA deletions in human cells?

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 275, doi. 10.1038/ng.f.94
    By:
    • Krishnan, Kim J.;
    • Reeve, Amy K.;
    • Samuels, David C.;
    • Chinnery, Patrick F.;
    • Blackwood, John K.;
    • Taylor, Robert W.;
    • Wanrooij, Sjoerd;
    • Spelbrink, Johannes N.;
    • Lightowlers, Robert N.;
    • Turnbull, Doug M.
    Publication type:
    Article
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    MicroRNA Mirn140 modulates Pdgf signaling during palatogenesis.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 290, doi. 10.1038/ng.82
    By:
    • Eberhart, Johann K;
    • Xinjun He;
    • Swartz, Mary E;
    • Yi-Lin Yan;
    • Hao Song;
    • Boling, Taylor C;
    • Kunerth, Allison K;
    • Walker, Macie B;
    • Kimmel, Charles B;
    • Postlethwait, John H
    Publication type:
    Article
    13
    14

    Multiple loci identified in a genome-wide association study of prostate cancer.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 310, doi. 10.1038/ng.91
    By:
    • Thomas, Gilles;
    • Jacobs, Kevin B;
    • Yeager, Meredith;
    • Kraft, Peter;
    • Wacholder, Sholom;
    • Orr, Nick;
    • Kai Yu;
    • Chatterjee, Nilanjan;
    • Welch, Robert;
    • Hutchinson, Amy;
    • Crenshaw, Andrew;
    • Cancel-Tassin, Geraldine;
    • Staats, Brian J;
    • Zhaoming Wang;
    • Gonzalez-Bosquet, Jesus;
    • Jun Fang;
    • Xiang Deng;
    • Berndt, Sonja I;
    • Calle, Eugenia E;
    • Feigelson, Heather Spencer
    Publication type:
    Article
    15
    16

    A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 322, doi. 10.1038/ng.93
    By:
    • Sharp, Andrew J.;
    • Mefford, Heather C.;
    • Kelly Li;
    • Baker, Carl;
    • Skinner, Cindy;
    • Stevenson, Roger E.;
    • Schroer, Richard J.;
    • Novara, Francesca;
    • De Gregori, Manuela;
    • Ciccone, Roberto;
    • Broomer, Adam;
    • Casuga, Iris;
    • Yu Wang;
    • Chunlin Xiao;
    • Barbacioru, Catalin;
    • Gimelli, Giorgio;
    • Bernardina, Bernardo Dalla;
    • Torniero, Claudia;
    • Giorda, Roberto;
    • Regan, Regina
    Publication type:
    Article
    17

    Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 287, doi. 10.1038/ng.86
    By:
    • Unger, Sheila;
    • Böhm, Detlef;
    • Kaiser, Frank J;
    • Kaulfuß, Silke;
    • Borozdin, Wiktor;
    • Buiting, Karin;
    • Burfeind, Peter;
    • Böhm, Johann;
    • Barrionuevo, Francisco;
    • Craig, Alexander;
    • Borowski, Kristi;
    • Keppler-Noreuil, Kim;
    • Schmitt-Mechelke, Thomas;
    • Steiner, Bernhard;
    • Bartholdi, Deborah;
    • Lemke, Johannes;
    • Mortier, Geert;
    • Sandford, Richard;
    • Zabel, Bernhard;
    • Superti-Furga, Andrea
    Publication type:
    Article
    18
    19

    Multiple newly identified loci associated with prostate cancer susceptibility.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 316, doi. 10.1038/ng.90
    By:
    • Eeles, Rosalind A;
    • Kote-Jarai, Zsofia;
    • Giles, Graham G;
    • Olama, Ali Amin Al;
    • Guy, Michelle;
    • Jugurnauth, Sarah K;
    • Mulholland, Shani;
    • Leongamornlert, Daniel A;
    • Edwards, Stephen M;
    • Morrison, Jonathan;
    • Field, Helen I;
    • Southey, Melissa C;
    • Severi, Gianluca;
    • Donovan, Jenny L;
    • Hamdy, Freddie C;
    • Dearnaley, David P;
    • Muir, Kenneth R;
    • Smith, Charmaine;
    • Bagnato, Melisa;
    • Ardern-Jones, Audrey T
    Publication type:
    Article
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    Research highlights.

    Published in:
    Nature Genetics, 2008, v. 40, n. 3, p. 273, doi. 10.1038/ng0308-273
    By:
    • A. P.;
    • O. B.;
    • K. V.;
    • E. N.
    Publication type:
    Article
    28

    Corrigendum: Regional copy number–independent deregulation of transcription in cancer.

    Published in:
    2008
    By:
    • Stransky, Nicolas;
    • Vallot, Céline;
    • Reyal, Fabien;
    • Bernard-Pierrot, Isabelle;
    • de Medina, Sixtina Gil Diez;
    • Segraves, Rick;
    • de Rycke, Yann;
    • Elvin, Paul;
    • Cassidy, Andrew;
    • Spraggon, Carolyn;
    • Graham, Alexander;
    • Southgate, Jennifer;
    • Asselain, Bernard;
    • Allory, Yves;
    • Abbou, Claude C;
    • Albertson, Donna G;
    • Thiery, Jean Paul;
    • Chopin, Dominique K;
    • Pinkel, Daniel;
    • Radvanyi, François
    Publication type:
    Correction Notice