Works matching IS 10614036 AND DT 2008 AND VI 40 AND IP 8

Results: 24
    1

    Identification of renal Cd36 as a determinant of blood pressure and risk for hypertension.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 952, doi. 10.1038/ng.164
    By:
    • Pravenec, Michal;
    • Churchill, Paul C.;
    • Churchill, Monique C.;
    • Viklicky, Ondrej;
    • Kazdova, Ludmila;
    • Aitman, Timothy J.;
    • Petretto, Enrico;
    • Hubner, Norbert;
    • AWallace, Caroline;
    • Zimdahl, Heike;
    • Zidek, Vaclav;
    • Landa, Vladimir;
    • Dunbar, Joseph;
    • Bidani, Anil;
    • Griffin, Karen;
    • Qi, Nathan;
    • Maxova, Martina;
    • Kren, Vladimir;
    • Mlejnek, Petr;
    • Jiaming Wang
    Publication type:
    Article
    2

    Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 999, doi. 10.1038/ng.166
    By:
    • Rock, Matthew J.;
    • Prenen, Jean;
    • Funari, Vincent A.;
    • Funari, Tara L.;
    • Merriman, Barry;
    • Nelson, Stanley F.;
    • Lachman, Ralph S.;
    • Wilcox, William R.;
    • Reyno, Soraya;
    • Quadrelli, Roberto;
    • Vaglio, Alicia;
    • Owsianik, Grzegorz;
    • Janssens, Annelies;
    • Voets, Thomas;
    • Ikegawa, Shiro;
    • Nagai, Toshiro;
    • Rimoin, David L.;
    • Nilius, Bernd;
    • Cohn, Daniel H.
    Publication type:
    Article
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    Common nonsynonymous variants in PCSK1 confer risk of obesity.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 943, doi. 10.1038/ng.177
    By:
    • Benzinou, Michael;
    • Creemers, John W. M.;
    • Choquet, Helene;
    • Lobbens, Stephane;
    • Dina, Christian;
    • Durand, Emmanuelle;
    • Guerardel, Audrey;
    • Boutin, Philippe;
    • Jouret, Beatrice;
    • Heude, Barbara;
    • Balkau, Beverley;
    • Tichet, Jean;
    • Marre, Michel;
    • Potoczna, Natascha;
    • Horber, Fritz;
    • Le Stunff, Catherine;
    • Czernichow, Sebastien;
    • Sandbaek, Annelli;
    • Lauritzen, Torsten;
    • Borch-Johnsen, Knut
    Publication type:
    Article
    8
    9

    A cis-acting regulatory mutation causes premature hair graying and susceptibility to melanoma in the horse.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 1004, doi. 10.1038/ng.185
    By:
    • Pielberg, Gerli Rosengren;
    • Golovko, Anna;
    • Sundström, Elisabeth;
    • Curik, Ino;
    • Lennartsson, Johan;
    • Seltenhammer, Monika H.;
    • Druml, Thomas;
    • Binns, Matthew;
    • Fitzsimmons, Carolyn;
    • Lindgren, Gabriella;
    • Sandberg, Kaj;
    • Baumung, Roswitha;
    • Vetterlein, Monika;
    • Strömberg, Sara;
    • Grabherr, Manfred;
    • Wade, Claire;
    • Lindblad-Toh, Kerstin;
    • Pontén, Fredrik;
    • Heldin, Carl-Henrik;
    • Sölkner, Johann
    Publication type:
    Article
    10

    Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 955, doi. 10.1038/ng.175
    By:
    • Barrett, Jeffrey C.;
    • Hansoul, Sarah;
    • Nicolae, Dan L.;
    • Cho, Judy H.;
    • Duerr, Richard H.;
    • Rioux, John D.;
    • Brant, Steven R.;
    • Silverberg, Mark S.;
    • Taylor, Kent D.;
    • Barmada, M. Michael;
    • Bitton, Alain;
    • Dassopoulos, Themistocles;
    • Datta, Lisa Wu;
    • Green, Todd;
    • Griffiths, Anne M.;
    • Kistner, Emily O.;
    • Murtha, Michael T.;
    • Regueiro, Miguel D.;
    • Rotter, Jerome I.;
    • Schumm, L. Philip
    Publication type:
    Article
    11

    Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 949, doi. 10.1038/ng.187
    By:
    • Mackay, Deborah J. G.;
    • Callaway, Jonathan L. A.;
    • Marks, Sophie M.;
    • White, Helen E.;
    • Acerini, Carlo L.;
    • Boonen, Susanne E.;
    • Dayanikli, Pinar;
    • Firth, Helen V.;
    • Goodship, Judith A.;
    • Haemers, Andreas P.;
    • Hahnemann, Johanne M. D.;
    • Kordonouri, Olga;
    • Masoud, Ahmed F.;
    • Oestergaard, Elsebet;
    • Storr, John;
    • Ellard, Sian;
    • Hattersley, Andrew T.;
    • Robinson, David O.;
    • Temple, I. Karen
    Publication type:
    Article
    12

    Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 963, doi. 10.1038/ng.188
    By:
    • McGowan, Kelly A.;
    • Li, Jun Z.;
    • Park, Christopher Y.;
    • Beaudry, Veronica;
    • Tabor, Holly K.;
    • Sabnis, Amit J.;
    • Weibin Zhang;
    • Fuchs, Helmut;
    • Angelis, Martin Hrabé de;
    • Myers, Richard M.;
    • Attardi, Laura D.;
    • Barsh, Gregory S.
    Publication type:
    Article
    13

    PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 946, doi. 10.1038/ng.190
    By:
    • Schormair, Barbara;
    • Kemlink, David;
    • Roeske, Darina;
    • Eckstein, Gertrud;
    • Lan Xiong;
    • Lichtner, Peter;
    • Ripke, Stephan;
    • Trenkwalder, Claudia;
    • Zimprich, Alexander;
    • Stiasny-Kolster, Karin;
    • Oertel, Wolfgang;
    • Bachmann, Cornelius G.;
    • Paulus, Walter;
    • Högl, Birgit;
    • Frauscher, Birgit;
    • Gschliesser, Viola;
    • Poewe, Werner;
    • Peglau, Ines;
    • Vodicka, Pavel;
    • Vávrová, Jana
    Publication type:
    Article
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    Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.

    Published in:
    2008
    By:
    • Gudbjartsson, Daniel F;
    • Sulem, Patrick;
    • Stacey, Simon N;
    • Goldstein, Alisa M;
    • Rafnar, Thorunn;
    • Sigurgeirsson, Bardur;
    • Benediktsdottir, Kristrun R;
    • Thorisdottir, Kristin;
    • Ragnarsson, Rafn;
    • Sveinsdottir, Steinunn G;
    • Magnusson, Veronica;
    • Lindblom, Annika;
    • Kostulas, Konstantinos;
    • Botella-Estrada, Rafael;
    • Soriano, Virtudes;
    • Juberías, Pablo;
    • Grasa, Matilde;
    • Saez, Berta;
    • Andres, Raquel;
    • Scherer, Dominique
    Publication type:
    Correction Notice
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    H19 in the pouch.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 932, doi. 10.1038/ng0808-932
    By:
    • Bartolomei, Marisa S.;
    • Vigneau, Sebastien;
    • O'Neill, Michael J.
    Publication type:
    Article
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    Research highlights.

    Published in:
    Nature Genetics, 2008, v. 40, n. 8, p. 937, doi. 10.1038/ng0808-937
    By:
    • Niemitz, Emily;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
    24