Works matching IS 1061-4036 AND VI 30 AND IP 4 AND DT 2002


Results: 28
    1

    Wag the dogma.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 343, doi. 10.1038/ng0402-343
    Publication type:
    Article
    2

    Ten years on.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 344, doi. 10.1038/ng0402-344
    Publication type:
    Article
    3

    A roundabout route to gene therapy.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 345, doi. 10.1038/ng0402-345
    By:
    • Turnbull, Douglass M.;
    • Lightowlers, Robert N.
    Publication type:
    Article
    4

    Putting tubby on the MAP.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 347, doi. 10.1038/ng0402-347
    By:
    • Grant, Seth G.N.
    Publication type:
    Article
    5
    6

    Evaluating adaptive evolution.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 350, doi. 10.1038/ng0402-350
    By:
    • Yokoyama, Shozo
    Publication type:
    Article
    7
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    Genetic analysis of the mouse brain proteome.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 385, doi. 10.1038/ng861
    By:
    • Klose, Joachim;
    • Nock, Christina;
    • Herrmann, Marion;
    • Stühler, Kai;
    • Marcus, Katrin;
    • Blüggel, Martin;
    • Krause, Eberhard;
    • Schalkwyk, Leonard C.;
    • Rastan, Sohaila;
    • Brown, Steve D.M.;
    • Büssow, Konrad;
    • Himmelbauer, Heinz;
    • Lehrach, Hans
    Publication type:
    Article
    10
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    TOUCHINGbase.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 355
    Publication type:
    Article
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    16

    Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 406
    By:
    • Tomlinson, Ian P.M.;
    • Alam, N. Afrina;
    • Rowan, Andrew J.;
    • Barclay, Ella;
    • Jaeger, Emma E. M.;
    • Kelsell, David;
    • Leigh, Irene;
    • Gorman, Patricia;
    • Lamlum, Hanan;
    • Rahman, Shamima;
    • Roylance, Rebecca R.;
    • Olpin, Simon;
    • Bevan, Stephen;
    • Barker, Karen;
    • Hearle, Nicholas;
    • Houlston, Richard S.;
    • Kiuru, Maija;
    • Lehtonen, Rainer;
    • Karhu, Auli
    Publication type:
    Article
    17
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    21

    Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 441
    By:
    • Strømme, Petter;
    • Mangelsdorf, Marie E.;
    • Shaw, Marie A.;
    • Lower, Karen M.;
    • Lewis, Suzanne M.E.;
    • Bruyere, Helene;
    • Lütcherath, Viggo;
    • Gedeon, Ági K.;
    • Wallace, Robyn H.;
    • Scheffer, Ingrid E.;
    • Turner, Gillian;
    • Partington, Michael;
    • Frints, Suzanna G.M.;
    • Fryns, Jean-Pierre;
    • Sutherland, Grant R.;
    • Mulley, John C.;
    • Gécz, Jozef
    Publication type:
    Article
    22

    Haploinsufficiency of NSD1 causes Sotos syndrome.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 365, doi. 10.1038/ng863
    By:
    • Kurotaki, Naohiro;
    • Imaizumi, Kiyoshi;
    • Harada, Naoki;
    • Masuno, Mitsuo;
    • Kondoh, Tatsuro;
    • Nagai, Toshiro;
    • Ohashi, Hirofumi;
    • Naritomi, Kenji;
    • Tsukahara, Masato;
    • Makita, Yoshio;
    • Sugimoto, Tateo;
    • Sonoda, Tohru;
    • Hasegawa, Tomoko;
    • Chinen, Yasuaki;
    • Tomita, Hiro-aki;
    • Kinoshita, Akira;
    • Mizuguchi, Tsuyoshi;
    • Yoshiura, Koh-ichiro;
    • Ohta, Tohru
    Publication type:
    Article
    23
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    FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation.

    Published in:
    Nature Genetics, 2002, v. 30, n. 4, p. 436, doi. 10.1038/ng857
    By:
    • Meloni, Ilaria;
    • Muscettola, Maddalena;
    • Raynaud, Martine;
    • Longo, Ilaria;
    • Bruttini, Mirella;
    • Moizard, Marie-Pierre;
    • Gomot, Marie;
    • Chelly, Jamel;
    • des Portes, Vincent;
    • Fryns, Jean-Pierre;
    • Ropers, Hans-Hilger;
    • Magi, Barbara;
    • Bellan, Cristina;
    • Volpi, Nila;
    • Yntema, Helger G.;
    • Lewis, Sarah E.;
    • Schaffer, Jean E.;
    • Renieri, Alessandra
    Publication type:
    Article
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