Works matching IS 10614036 AND DT 2013 AND VI 45 AND IP 9

Results: 29
    1
    2

    Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1097, doi. 10.1038/ng.2725
    By:
    • Uga, Yusaku;
    • Sugimoto, Kazuhiko;
    • Ogawa, Satoshi;
    • Rane, Jagadish;
    • Ishitani, Manabu;
    • Hara, Naho;
    • Kitomi, Yuka;
    • Inukai, Yoshiaki;
    • Ono, Kazuko;
    • Kanno, Noriko;
    • Inoue, Haruhiko;
    • Takehisa, Hinako;
    • Motoyama, Ritsuko;
    • Nagamura, Yoshiaki;
    • Wu, Jianzhong;
    • Matsumoto, Takashi;
    • Takai, Toshiyuki;
    • Okuno, Kazutoshi;
    • Yano, Masahiro
    Publication type:
    Article
    3
    4

    Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1044, doi. 10.1038/ng.2712
    By:
    • Bezzina, Connie R;
    • Barc, Julien;
    • Mizusawa, Yuka;
    • Remme, Carol Ann;
    • Gourraud, Jean-Baptiste;
    • Simonet, Floriane;
    • Verkerk, Arie O;
    • Schwartz, Peter J;
    • Crotti, Lia;
    • Dagradi, Federica;
    • Guicheney, Pascale;
    • Fressart, Véronique;
    • Leenhardt, Antoine;
    • Antzelevitch, Charles;
    • Bartkowiak, Susan;
    • Schulze-Bahr, Eric;
    • Zumhagen, Sven;
    • Behr, Elijah R;
    • Bastiaenen, Rachel;
    • Tfelt-Hansen, Jacob
    Publication type:
    Article
    5

    The wheat powdery mildew genome shows the unique evolution of an obligate biotroph.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1092, doi. 10.1038/ng.2704
    By:
    • Wicker, Thomas;
    • Oberhaensli, Simone;
    • Parlange, Francis;
    • Buchmann, Jan P;
    • Shatalina, Margarita;
    • Roffler, Stefan;
    • Ben-David, Roi;
    • Doležel, Jaroslav;
    • Šimková, Hana;
    • Schulze-Lefert, Paul;
    • Spanu, Pietro D;
    • Bruggmann, Rémy;
    • Amselem, Joelle;
    • Quesneville, Hadi;
    • Ver Loren van Themaat, Emiel;
    • Paape, Timothy;
    • Shimizu, Kentaro K;
    • Keller, Beat
    Publication type:
    Article
    6

    GRIN2A mutations cause epilepsy-aphasia spectrum disorders.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1073, doi. 10.1038/ng.2727
    By:
    • Carvill, Gemma L;
    • Regan, Brigid M;
    • Yendle, Simone C;
    • O'Roak, Brian J;
    • Lozovaya, Natalia;
    • Bruneau, Nadine;
    • Burnashev, Nail;
    • Khan, Adiba;
    • Cook, Joseph;
    • Geraghty, Eileen;
    • Sadleir, Lynette G;
    • Turner, Samantha J;
    • Tsai, Meng-Han;
    • Webster, Richard;
    • Ouvrier, Robert;
    • Damiano, John A;
    • Berkovic, Samuel F;
    • Shendure, Jay;
    • Hildebrand, Michael S;
    • Szepetowski, Pierre
    Publication type:
    Article
    7
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    10

    Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1067, doi. 10.1038/ng.2728
    By:
    • Lemke, Johannes R;
    • Lal, Dennis;
    • Reinthaler, Eva M;
    • Steiner, Isabelle;
    • Nothnagel, Michael;
    • Alber, Michael;
    • Geider, Kirsten;
    • Laube, Bodo;
    • Schwake, Michael;
    • Finsterwalder, Katrin;
    • Franke, Andre;
    • Schilhabel, Markus;
    • Jähn, Johanna A;
    • Muhle, Hiltrud;
    • Boor, Rainer;
    • Van Paesschen, Wim;
    • Caraballo, Roberto;
    • Fejerman, Natalio;
    • Weckhuysen, Sarah;
    • De Jonghe, Peter
    Publication type:
    Article
    11
    12

    Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1050, doi. 10.1038/ng.2695
    By:
    • Scholl, Ute I;
    • Goh, Gerald;
    • Stölting, Gabriel;
    • de Oliveira, Regina Campos;
    • Choi, Murim;
    • Overton, John D;
    • Fonseca, Annabelle L;
    • Korah, Reju;
    • Starker, Lee F;
    • Kunstman, John W;
    • Prasad, Manju L;
    • Hartung, Erum A;
    • Mauras, Nelly;
    • Benson, Matthew R;
    • Brady, Tammy;
    • Shapiro, Jay R;
    • Loring, Erin;
    • Nelson-Williams, Carol;
    • Libutti, Steven K;
    • Mane, Shrikant
    Publication type:
    Article
    13

    An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 970, doi. 10.1038/ng.2702
    By:
    • Roberts, Steven A;
    • Lawrence, Michael S;
    • Klimczak, Leszek J;
    • Grimm, Sara A;
    • Fargo, David;
    • Stojanov, Petar;
    • Kiezun, Adam;
    • Kryukov, Gregory V;
    • Carter, Scott L;
    • Saksena, Gordon;
    • Harris, Shawn;
    • Shah, Ruchir R;
    • Resnick, Michael A;
    • Getz, Gad;
    • Gordenin, Dmitry A
    Publication type:
    Article
    14
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    16

    DYX1C1 is required for axonemal dynein assembly and ciliary motility.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 995, doi. 10.1038/ng.2707
    By:
    • Tarkar, Aarti;
    • Loges, Niki T;
    • Slagle, Christopher E;
    • Francis, Richard;
    • Dougherty, Gerard W;
    • Tamayo, Joel V;
    • Shook, Brett;
    • Cantino, Marie;
    • Schwartz, Daniel;
    • Jahnke, Charlotte;
    • Olbrich, Heike;
    • Werner, Claudius;
    • Raidt, Johanna;
    • Pennekamp, Petra;
    • Abouhamed, Marouan;
    • Hjeij, Rim;
    • Köhler, Gabriele;
    • Griese, Matthias;
    • Li, You;
    • Lemke, Kristi
    Publication type:
    Article
    17

    Schizophrenia exomes.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2750
    By:
    • Feliciano, Pamela
    Publication type:
    Article
    18

    Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1077, doi. 10.1038/ng.2723
    By:
    • Keller, Annika;
    • Westenberger, Ana;
    • Sobrido, Maria J;
    • García-Murias, Maria;
    • Domingo, Aloysius;
    • Sears, Renee L;
    • Lemos, Roberta R;
    • Ordoñez-Ugalde, Andres;
    • Nicolas, Gael;
    • da Cunha, José E Gomes;
    • Rushing, Elisabeth J;
    • Hugelshofer, Michael;
    • Wurnig, Moritz C;
    • Kaech, Andres;
    • Reimann, Regina;
    • Lohmann, Katja;
    • Dobričić, Valerija;
    • Carracedo, Angel;
    • Petrović, Igor;
    • Miyasaki, Janis M
    Publication type:
    Article
    19
    20

    APOBEC3B mutagenesis in cancer.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 964, doi. 10.1038/ng.2736
    By:
    • Kuong, Kawai J;
    • Loeb, Lawrence A
    Publication type:
    Article
    21
    22

    A deeper look back at Y.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 969, doi. 10.1038/ng.2753
    By:
    • Bahcall, Orli
    Publication type:
    Article
    23
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    Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1055, doi. 10.1038/ng.2716
    By:
    • Azizan, Elena A B;
    • Poulsen, Hanne;
    • Tuluc, Petronel;
    • Zhou, Junhua;
    • Clausen, Michael V;
    • Lieb, Andreas;
    • Maniero, Carmela;
    • Garg, Sumedha;
    • Bochukova, Elena G;
    • Zhao, Wanfeng;
    • Shaikh, Lalarukh Haris;
    • Brighton, Cheryl A;
    • Teo, Ada E D;
    • Davenport, Anthony P;
    • Dekkers, Tanja;
    • Tops, Bas;
    • Küsters, Benno;
    • Ceral, Jiri;
    • Yeo, Giles S H;
    • Neogi, Sudeshna Guha
    Publication type:
    Article
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    28

    GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 1061, doi. 10.1038/ng.2726
    By:
    • Lesca, Gaetan;
    • Rudolf, Gabrielle;
    • Bruneau, Nadine;
    • Lozovaya, Natalia;
    • Labalme, Audrey;
    • Boutry-Kryza, Nadia;
    • Salmi, Manal;
    • Tsintsadze, Timur;
    • Addis, Laura;
    • Motte, Jacques;
    • Wright, Sukhvir;
    • Tsintsadze, Vera;
    • Michel, Anne;
    • Doummar, Diane;
    • Lascelles, Karine;
    • Strug, Lisa;
    • Waters, Patrick;
    • de Bellescize, Julitta;
    • Vrielynck, Pascal;
    • de Saint Martin, Anne
    Publication type:
    Article
    29

    Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

    Published in:
    Nature Genetics, 2013, v. 45, n. 9, p. 984, doi. 10.1038/ng.2711
    By:
    • Lee, S Hong;
    • Ripke, Stephan;
    • Neale, Benjamin M;
    • Faraone, Stephen V;
    • Purcell, Shaun M;
    • Perlis, Roy H;
    • Mowry, Bryan J;
    • Thapar, Anita;
    • Goddard, Michael E;
    • Witte, John S;
    • Absher, Devin;
    • Agartz, Ingrid;
    • Akil, Huda;
    • Amin, Farooq;
    • Andreassen, Ole A;
    • Anjorin, Adebayo;
    • Anney, Richard;
    • Anttila, Verneri;
    • Arking, Dan E;
    • Asherson, Philip
    Publication type:
    Article