Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 1

Results: 27
    1
    2
    3
    4

    Touching base.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 13, doi. 10.1038/ng0107-13
    Publication type:
    Article
    5

    Corrigendum: Cxorf6 is a causative gene for hypospadias.

    Published in:
    2007
    By:
    • Fukami, Maki;
    • Wada, Yuka;
    • Miyabayashi, Kanako;
    • Nishino, Ichizo;
    • Hasegawa, Tomonobu;
    • Camerino, Giovanna;
    • Kretz, Christine;
    • Buj-Bello, Anna;
    • Laporte, Jocelyn;
    • Yamada, Gen;
    • Morohashi, Ken-ichirou;
    • Ogata, Tsutomu
    Publication type:
    Correction Notice
    6

    Research highlights.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 15, doi. 10.1038/ng0107-15
    Publication type:
    Article
    7

    HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease).

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 86, doi. 10.1038/ng1940
    By:
    • Klein, Christoph;
    • Grudzien, Magda;
    • Appaswamy, Giridharan;
    • Germeshausen, Manuela;
    • Sandrock, Inga;
    • Schäffer, Alejandro A.;
    • Rathinam, Chozhavendan;
    • Boztug, Kaan;
    • Schwinzer, Beate;
    • Rezaei, Nima;
    • Bohn, Georg;
    • Melin, Malin;
    • Carlsson, Göran;
    • Fadeel, Bengt;
    • Dahl, Niklas;
    • Palmblad, Jan;
    • Henter, Jan-Inge;
    • Zeidler, Cornelia;
    • Grimbacher, Bodo;
    • Welte, Karl
    Publication type:
    Article
    8

    Sending out an SOS.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 8, doi. 10.1038/ng0107-8
    By:
    • Shannon, Kevin;
    • Bollag, Gideon
    Publication type:
    Article
    9

    Germline gain-of-function mutations in SOS1 cause Noonan syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 70, doi. 10.1038/ng1926
    By:
    • Roberts, Amy E.;
    • Araki, Toshiyuki;
    • Swanson, Kenneth D.;
    • Montgomery, Kate T.;
    • Schiripo, Taryn A.;
    • Joshi, Victoria A.;
    • Li, Li;
    • Yassin, Yosuf;
    • Tamburino, Alex M.;
    • Neel, Benjamin G.;
    • Kucherlapati, Raju S.
    Publication type:
    Article
    10

    Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 75, doi. 10.1038/ng1939
    By:
    • Tartaglia, Marco;
    • Pennacchio, Len A.;
    • Zhao, Chen;
    • Yadav, Kamlesh K.;
    • Fodale, Valentina;
    • Sarkozy, Anna;
    • Pandit, Bhaswati;
    • Oishi, Kimihiko;
    • Martinelli, Simone;
    • Schackwitz, Wendy;
    • Ustaszewska, Anna;
    • Martin, Joel;
    • Bristow, James;
    • Carta, Claudio;
    • Lepri, Francesca;
    • Neri, Cinzia;
    • Vasta, Isabella;
    • Gibson, Kate;
    • Curry, Cynthia J.;
    • Siguero, Juan Pedro López
    Publication type:
    Article
    11
    12
    13
    14

    Following the herd.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 7, doi. 10.1038/ng0107-7
    By:
    • Wooding, Stephen P.
    Publication type:
    Article
    15
    16

    Convergent adaptation of human lactase persistence in Africa and Europe.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 31, doi. 10.1038/ng1946
    By:
    • Tishkoff, Sarah A.;
    • Reed, Floyd A.;
    • Ranciaro, Alessia;
    • Voight, Benjamin F.;
    • Babbitt, Courtney C.;
    • Silverman, Jesse S.;
    • Powell, Kweli;
    • Mortensen, Holly M.;
    • Hirbo, Jibril B.;
    • Osman, Maha;
    • Ibrahim, Muntaser;
    • Omar, Sabah A.;
    • Lema, Godfrey;
    • Nyambo, Thomas B.;
    • Ghori, Jilur;
    • Bumpstead, Suzannah;
    • Pritchard, Jonathan K.;
    • Wray, Gregory A.;
    • Deloukas, Panos
    Publication type:
    Article
    17
    18

    Integrative molecular concept modeling of prostate cancer progression.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 41, doi. 10.1038/ng1935
    By:
    • Tomlins, Scott A.;
    • Mehra, Rohit;
    • Rhodes, Daniel R.;
    • Cao, Xuhong;
    • Wang, Lei;
    • Dhanasekaran, Saravana M.;
    • Kalyana-Sundaram, Shanker;
    • Wei, John T.;
    • Rubin, Mark A.;
    • Pienta, Kenneth J.;
    • Shah, Rajal B.;
    • Chinnaiyan, Arul M.
    Publication type:
    Article
    19

    Cdkn1a deletion improves stem cell function and lifespan of mice with dysfunctional telomeres without accelerating cancer formation.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 99, doi. 10.1038/ng1937
    By:
    • Choudhury, Aaheli Roy;
    • Ju, Zhenyu;
    • Djojosubroto, Meta W.;
    • Schienke, Andrea;
    • Lechel, Andre;
    • Schaetzlein, Sonja;
    • Jiang, Hong;
    • Stepczynska, Anna;
    • Wang, Chunfang;
    • Buer, Jan;
    • Lee, Han-Woong;
    • von Zglinicki, Thomas;
    • Ganser, Arnold;
    • Schirmacher, Peter;
    • Nakauchi, Hiromitsu;
    • Rudolph, K. Lenhard
    Publication type:
    Article
    20
    21

    A genome-wide map of diversity in Plasmodium falciparum.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 113, doi. 10.1038/ng1930
    By:
    • Volkman, Sarah K.;
    • Sabeti, Pardis C.;
    • DeCaprio, David;
    • Neafsey, Daniel E.;
    • Schaffner, Stephen F.;
    • Milner Jr., Danny A.;
    • Daily, Johanna P.;
    • Sarr, Ousmane;
    • Ndiaye, Daouda;
    • Ndir, Omar;
    • Mboup, Soulyemane;
    • Duraisingh, Manoj T.;
    • Lukens, Amanda;
    • Derr, Alan;
    • Stange-Thomann, Nicole;
    • Waggoner, Skye;
    • Onofrio, Robert;
    • Ziaugra, Liuda;
    • Mauceli, Evan;
    • Gnerre, Sante
    Publication type:
    Article
    22

    Genome variation and evolution of the malaria parasite Plasmodium falciparum.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 120, doi. 10.1038/ng1931
    By:
    • Jeffares, Daniel C.;
    • Pain, Arnab;
    • Berry, Andrew;
    • Cox, Anthony V.;
    • Stalker, James;
    • Ingle, Catherine E.;
    • Thomas, Alan;
    • Quail, Michael A.;
    • Siebenthall, Kyle;
    • Uhlemann, Anne-Catrin;
    • Kyes, Sue;
    • Krishna, Sanjeev;
    • Newbold, Chris;
    • Dermitzakis, Emmanouil T.;
    • Berriman, Matthew
    Publication type:
    Article
    23

    Wnt-β-catenin signaling initiates taste papilla development.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 106, doi. 10.1038/ng1932
    By:
    • Liu, Fei;
    • Thirumangalathu, Shoba;
    • Gallant, Natalie M.;
    • Yang, Steven H.;
    • Stoick-Cooper, Cristi L.;
    • Reddy, Seshamma T.;
    • Andl, Thomas;
    • Taketo, Makoto M.;
    • Dlugosz, Andrzej A.;
    • Moon, Randall T.;
    • Barlow, Linda A.;
    • Millar, Sarah E.
    Publication type:
    Article
    24

    Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.

    Published in:
    Nature Genetics, 2007, v. 39, n. 1, p. 25, doi. 10.1038/ng1933
    By:
    • Durand, Christelle M;
    • Betancur, Catalina;
    • Boeckers, Tobias M;
    • Bockmann, Juergen;
    • Chaste, Pauline;
    • Fauchereau, Fabien;
    • Nygren, Gudrun;
    • Rastam, Maria;
    • Gillberg, I Carina;
    • Anckarsäter, Henrik;
    • Sponheim, Eili;
    • Goubran-Botros, Hany;
    • Delorme, Richard;
    • Chabane, Nadia;
    • Mouren-Simeoni, Marie-Christine;
    • de Mas, Philippe;
    • Bieth, Eric;
    • Rogé, Bernadette;
    • Héron, Delphine;
    • Burglen, Lydie
    Publication type:
    Article
    25
    26
    27