Works matching IS 10614036 AND DT 2002 AND VI 32


Results: 160
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    Chipping away at genomic medicine.

    Published in:
    Nature Genetics, 2002, v. 32, p. 462, doi. 10.1038/ng1025
    By:
    • Trent, Jeffrey M.;
    • Baxevanis, Andreas D.
    Publication type:
    Article
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    Post-analysis follow-up and validation of microarray experiments.

    Published in:
    Nature Genetics, 2002, v. 32, p. 509, doi. 10.1038/ng1034
    By:
    • Chuaqui, Rodrigo F.;
    • Bonner, Robert F.;
    • Best, Carolyn J.M.;
    • Gillespie, John W.;
    • Flaig, Michael J.;
    • Hewitt, Stephen M.;
    • Phillips, John L.;
    • Krizman, David B.;
    • Tangrea, Michael A.;
    • Ahram, Mamoun;
    • Linehan, W. Marston;
    • Knezevic, Vladimir;
    • Emmert-Buck, Michael R.
    Publication type:
    Article
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    Disruption of oxygen homeostasis underlies congenital Chuvash polycythemia.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 614, doi. 10.1038/ng1019
    By:
    • Ang, Sonny O.;
    • Chen, Hua;
    • Hirota, Kiichi;
    • Gordeuk, Victor R.;
    • Jelinek, Jaroslav;
    • Guan, Yongli;
    • Liu, Enli;
    • Sergueeva, Adelina I.;
    • Miasnikova, Galina Y.;
    • Mole, David;
    • Maxwell, Patrick H.;
    • Stockton, David W.;
    • Semenza, Gregg L.;
    • Prchal, Josef T.
    Publication type:
    Article
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    A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 666, doi. 10.1038/ng1020
    By:
    • Prokunina, Ludmila;
    • Castillejo-López, Casimiro;
    • Öberg, Fredrik;
    • Gunnarsson, Iva;
    • Berg, Louise;
    • Magnusson, Veronica;
    • Brookes, Anthony J.;
    • Tentler, Dmitry;
    • Kristjansdóttir, Helga;
    • Gröndal, Gerdur;
    • Bolstad, Anne Isine;
    • Svenungsson, Elisabet;
    • Lundberg, Ingrid;
    • Sturfelt, Gunnar;
    • Jönssen, Andreas;
    • Truedsson, Lennart;
    • Lima, Guadalupe;
    • Alcocer-Varela, Jorge;
    • Jonsson, Roland;
    • Gyllensten, Ulf B.
    Publication type:
    Article
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    A mouse model of human L1 retrotransposition.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 655, doi. 10.1038/ng1022
    By:
    • Ostertag, Eric M.;
    • DeBerardinis, Ralph J.;
    • Goodier, John L.;
    • Zhang, Yue;
    • Yang, Nuo;
    • Gerton, George L.;
    • Kazazian, Haig H.
    Publication type:
    Article
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    Mutations in PHF6 are associated with Börjeson–Forssman–Lehmann syndrome.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 661, doi. 10.1038/ng1040
    By:
    • Lower, Karen M.;
    • Turner, Gillian;
    • Kerr, Bronwyn A.;
    • Mathews, Katherine D.;
    • Shaw, Marie A.;
    • Gedeon, Ági K.;
    • Schelley, Susan;
    • Hoyme, H. Eugene;
    • White, Susan M.;
    • Delatycki, Martin B.;
    • Lampe, Anne K.;
    • Clayton-Smith, Jill;
    • Stewart, Helen;
    • van Ravenswaay, Conny M. A.;
    • de Vries, Bert B. A.;
    • Cox, Barbara;
    • Grompe, Markus;
    • Ross, Shelley;
    • Thomas, Paul;
    • Mulley, John C.
    Publication type:
    Article
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    Of man in mice.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 562, doi. 10.1038/ng1043
    By:
    • Athanikar, Jyoti N.;
    • Morrish, Tammy A.;
    • Moran, John V.
    Publication type:
    Article
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    HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 676, doi. 10.1038/ng1048
    By:
    • Carpten, J.D.;
    • Robbins, C.M.;
    • Villablanca, A.;
    • Forsberg, L.;
    • Presciuttini, S.;
    • Bailey-Wilson, J.;
    • Simonds, W.F.;
    • Gillanders, E.M.;
    • Kennedy, A.M.;
    • Chen, J.D.;
    • Agarwal, S.K.;
    • Sood, R.;
    • Jones, M.P.;
    • Moses, T.Y.;
    • Haven, C.;
    • Petillo, D.;
    • Leotlela, P.D.;
    • Harding, B.;
    • Cameron, D.;
    • Pannett, A.A.
    Publication type:
    Article
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    TRAPping enhancer function.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 555, doi. 10.1038/ng1202-555
    By:
    • Bulger, Michael;
    • Groudine, Mark
    Publication type:
    Article
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    Pluripotency and tumorigenicity.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 557, doi. 10.1038/ng1202-557
    By:
    • Brickman, Joshua M.;
    • Burdon, Thomas G.
    Publication type:
    Article
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    Cellular clockwork.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 559, doi. 10.1038/ng1202-559
    By:
    • Nitabach, Michael N.;
    • Blau, Justin
    Publication type:
    Article
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    TOUCHINGbase.

    Published in:
    Nature Genetics, 2002, v. 32, n. 4, p. 565
    Publication type:
    Article
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    The K–Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.

    Published in:
    Nature Genetics, 2002, v. 32, n. 3, p. 384, doi. 10.1038/ng1002
    By:
    • Howard, Heidi C.;
    • Mount, David B.;
    • Rochefort, Daniel;
    • Byun, Nellie;
    • Dupré, Nicolas;
    • Lu, Jianming;
    • Fan, Xuemo;
    • Song, Luyan;
    • Rivière, Jean-Baptiste;
    • Prévost, Claude;
    • Horst, Jürgen;
    • Simonati, Alessandro;
    • Lemcke, Beate;
    • Welch, Rick;
    • England, Roger;
    • Zhan, Frank Q.;
    • Mercado, Adriana;
    • Siesser, William B.;
    • George, Alfred L.;
    • McDonald, Michael P.
    Publication type:
    Article
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    Chromosomal instability in ulcerative colitis is related to telomere shortening.

    Published in:
    Nature Genetics, 2002, v. 32, n. 2, p. 280, doi. 10.1038/ng989
    By:
    • O'Sullivan, Jacintha N.;
    • Bronner, Mary P.;
    • Brentnall, Teresa A.;
    • Finley, Jennifer C.;
    • Shen, Wen-Tang;
    • Emerson, Scott;
    • Emond, Mary J.;
    • Gollahon, Katherine A.;
    • Moskovitz, Alexander H.;
    • Crispin, David A.;
    • Potter, John D.;
    • Rabinovitch, Peter S.
    Publication type:
    Article