Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 4


Results: 37
    1

    The human promoter methylome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 442, doi. 10.1038/ng0407-442
    By:
    • Zilberman, Daniel
    Publication type:
    Article
    2
    3
    4

    Analysis of published PKD1 gene sequence variants.

    Published in:
    2007
    By:
    • Gout, Alexander M.;
    • Ravine, David;
    • Harris, Peter C.;
    • Rossetti, Sandro;
    • Peters, Dorien;
    • Breuning, Martijn;
    • Henske, Elizabeth Petri;
    • Koizumi, Akio;
    • Inoue, Sumiko;
    • Shimizu, Yoshiko;
    • Thongnoppakhun, Wanna;
    • Yenchitsomanus, Pa-thai;
    • Deltas, Constantinos;
    • Sandford, Richard;
    • Torra, Roser;
    • Turco, Alberto E.;
    • Jeffery, Steve;
    • Fontes, Michel;
    • Somlo, Stefan;
    • Furu, Laszlo M.
    Publication type:
    Letter
    5
    6

    The way we were?

    Published in:
    2007
    By:
    • Mountain, Joanna
    Publication type:
    Book Review
    7
    8

    The resequencing imperative.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 439, doi. 10.1038/ng0407-439
    By:
    • Topol, Eric J.;
    • Frazer, Kelly A.
    Publication type:
    Article
    9

    How missing genes interact.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 440, doi. 10.1038/ng0407-440
    By:
    • Zeyl, Clifford
    Publication type:
    Article
    10
    11
    12
    13
    14

    Touching base.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 447, doi. 10.1038/ng0407-447
    By:
    • Bahcall, Orli;
    • Niemitz, Emily;
    • Packer, Alan
    Publication type:
    Article
    15

    A Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosis.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 523, doi. 10.1038/ng1976
    By:
    • Khor, Chiea C.;
    • Chapman, Stephen J.;
    • Vannberg, Fredrik O.;
    • Dunne, Aisling;
    • Murphy, Caroline;
    • Ling, Edmund Y.;
    • Frodsham, Angela J.;
    • Walley, Andrew J.;
    • Kyrieleis, Otto;
    • Khan, Amir;
    • Aucan, Christophe;
    • Segal, Shelley;
    • Moore, Catrin E.;
    • Knox, Kyle;
    • Campbell, Sarah J.;
    • Lienhardt, Christian;
    • Scott, Anthony;
    • Aaby, Peter;
    • Sow, Oumou Y.;
    • Grignani, Robert T.
    Publication type:
    Article
    16

    A module of negative feedback regulators defines growth factor signaling.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 503, doi. 10.1038/ng1987
    By:
    • Amit, Ido;
    • Citri, Ami;
    • Shay, Tal;
    • Lu, Yiling;
    • Katz, Menachem;
    • Zhang, Fan;
    • Tarcic, Gabi;
    • Siwak, Doris;
    • Lahad, John;
    • Jacob-Hirsch, Jasmine;
    • Amariglio, Ninette;
    • Vaisman, Nora;
    • Segal, Eran;
    • Rechavi, Gideon;
    • Alon, Uri;
    • Mills, Gordon B;
    • Domany, Eytan;
    • Yarden, Yosef
    Publication type:
    Article
    17
    18

    Research highlights.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 449, doi. 10.1038/ng0407-449
    By:
    • Bahcall, Orli;
    • Niemitz, Emily;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
    19

    Corrigendum: High-throughput oncogene mutation profiling in human cancer.

    Published in:
    2007
    By:
    • Thomas, Roman K.;
    • Baker, Alissa C.;
    • DeBiasi, Ralph M.;
    • Winckler, Wendy;
    • LaFramboise, Thomas;
    • Lin, William M.;
    • Wang, Meng;
    • Feng, Whei;
    • Zander, Thomas;
    • MacConnaill, Laura E.;
    • Lee, Jeffrey C.;
    • Nicoletti, Rick;
    • Hatton, Charlie;
    • Goyette, Mary;
    • Girard, Luc;
    • Majmudar, Kuntal;
    • Ziaugra, Liuda;
    • Wong, Kwok-Kin;
    • Gabriel, Stacey;
    • Beroukhim, Rameen
    Publication type:
    Correction Notice
    20
    21
    22
    23
    24
    25
    26

    A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 451, doi. 10.1038/ng1992
    By:
    • Risheg, Hiba;
    • Graham Jr., John M.;
    • Clark, Robin D.;
    • Rogers, R. Curtis;
    • Opitz, John M.;
    • Moeschler, John B.;
    • Peiffer, Andreas P.;
    • May, Melanie;
    • Joseph, Sumy M.;
    • Jones, Julie R.;
    • Stevenson, Roger E.;
    • Schwartz, Charles E.;
    • Friez, Michael J.
    Publication type:
    Article
    27

    Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 454, doi. 10.1038/ng1993
    By:
    • Baala, Lekbir;
    • Briault, Sylvain;
    • Etchevers, Heather C;
    • Laumonnier, Frédéric;
    • Natiq, Abdelhafid;
    • Amiel, Jeanne;
    • Boddaert, Nathalie;
    • Picard, Capucine;
    • Sbiti, Aziza;
    • Asermouh, Abdellah;
    • Attié-Bitach, Tania;
    • Encha-Razavi, Féréchté;
    • Munnich, Arnold;
    • Sefiani, Abdelaziz;
    • Lyonnet, Stanislas
    Publication type:
    Article
    28
    29
    30
    31
    32
    33

    Genome-wide functional analysis of pathogenicity genes in the rice blast fungus.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 561, doi. 10.1038/ng2002
    By:
    • Jeon, Junhyun;
    • Park, Sook-Young;
    • Chi, Myoung-Hwan;
    • Choi, Jaehyuk;
    • Park, Jongsun;
    • Rho, Hee-Sool;
    • Kim, Soonok;
    • Goh, Jaeduk;
    • Yoo, Sungyong;
    • Choi, Jinhee;
    • Park, Ju-Young;
    • Yi, Mihwa;
    • Yang, Seonyoung;
    • Kwon, Min-Jung;
    • Han, Seong-Sook;
    • Kim, Byeong Ryun;
    • Khang, Chang Hyun;
    • Park, Bongsoo;
    • Lim, Se-Eun;
    • Jung, Kyongyong
    Publication type:
    Article
    34

    Recommendations of the 2006 Human Variome Project meeting.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 433, doi. 10.1038/ng2024
    By:
    • Appelbe, William;
    • Auerbach, Arleen D.;
    • Becker, Kevin;
    • Bodmer, Walter;
    • Boone, D. Joe;
    • Boulyjenkov, Victor;
    • Brahmachari, Samir;
    • Brody, Lawrence;
    • Brookes, Anthony;
    • Brown, Alastair F.;
    • Byers, Peter;
    • Maria Cantu, Jose;
    • Cassiman, Jean-Jacques;
    • Claustres, Mireille;
    • Concannon, Patrick;
    • Cotton, Richard G. H.;
    • den Dunnen, Johan T.;
    • Flicek, Paul;
    • Gibbs, Richard;
    • Hall, Judith
    Publication type:
    Article
    35

    Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation.

    Published in:
    Nature Genetics, 2007, v. 39, n. 4, p. 534, doi. 10.1038/ng2013
    By:
    • Scheper, Gert C.;
    • van der Klok, Thom;
    • van Andel, Rob J.;
    • van Berkel, Carola G. M.;
    • Sissler, Marie;
    • Smet, Joél;
    • Muravina, Tatjana I.;
    • Serkov, Sergey V.;
    • Uziel, Graziella;
    • Bugiani, Marianna;
    • Schiffmann, Raphael;
    • Krägeloh-Mann, Ingeborg;
    • Smeitink, Jan A. M.;
    • Florentz, Catherine;
    • Van Coster, Rudy;
    • Pronk, Jan C.;
    • van der Knaap, Marjo S.
    Publication type:
    Article
    36
    37