Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 3


Results: 30
    1
    2
    3
    4

    Upending the hair follicle.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 273, doi. 10.1038/ng0306-273
    By:
    • Morgan, Bruce A.
    Publication type:
    Article
    5
    6

    Marking time.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 276, doi. 10.1038/ng0306-276
    By:
    • Eissenberg, Joel C.;
    • Elgin, Sarah C. R.
    Publication type:
    Article
    7
    8

    Touching base.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 281, doi. 10.1038/ng0306-281
    By:
    • Bahcall, Orli;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
    9

    Research Highlights.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 283, doi. 10.1038/ng0306-283
    By:
    • Bahcall, Orli;
    • Packer, Alan;
    • Vogan, Kyle
    Publication type:
    Article
    10
    11
    12
    13
    14
    15
    16

    Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 320, doi. 10.1038/ng1732
    By:
    • Grant, Struan F. A.;
    • Thorleifsson, Gudmar;
    • Reynisdottir, Inga;
    • Benediktsson, Rafn;
    • Manolescu, Andrei;
    • Sainz, Jesus;
    • Helgason, Agnar;
    • Stefansson, Hreinn;
    • Emilsson, Valur;
    • Helgadottir, Anna;
    • Styrkarsdottir, Unnur;
    • Magnusson, Kristinn P.;
    • Walters, G. Bragi;
    • Palsdottir, Ebba;
    • Jonsdottir, Thorbjorg;
    • Gudmundsdottir, Thorunn;
    • Gylfason, Arnaldur;
    • Saemundsdottir, Jona;
    • Wilensky, Robert L.;
    • Reilly, Muredach P.
    Publication type:
    Article
    17

    A SNP in the ABCC11 gene is the determinant of human earwax type.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 324, doi. 10.1038/ng1733
    By:
    • Yoshiura, Koh-Ichiro;
    • Kinoshita, Akira;
    • Ishida, Takafumi;
    • Ninokata, Aya;
    • Ishikawa, Toshihisa;
    • Kaname, Tadashi;
    • Bannai, Makoto;
    • Tokunaga, Katsushi;
    • Sonoda, Shunro;
    • Komaki, Ryoichi;
    • Ihara, Makoto;
    • Saenko, Vladimir A.;
    • Alipov, Gabit K.;
    • Sekine, Ichiro;
    • Komatsu, Kazuki;
    • Takahashi, Haruo;
    • Nakashima, Mitsuko;
    • Sosonkina, Nadiya;
    • Mapendano, Christophe K.;
    • Ghadami, Mohsen
    Publication type:
    Article
    18
    19
    20
    21
    22
    23

    Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 337, doi. 10.1038/ng1743
    By:
    • Smith, Frances J. D.;
    • Irvine, Alan D.;
    • Terron-Kwiatkowski, Ana;
    • Sandilands, Aileen;
    • Campbell, Linda E.;
    • Yiwei Zhao;
    • Haihui Liao;
    • Evans, Alan T.;
    • Goudie, David R.;
    • Lewis-Jones, Sue;
    • Arseculeratne, Gehan;
    • Munro, Colin S.;
    • Sergeant, Ann;
    • O'Regan, Gráinne;
    • Bale, Sherri J.;
    • Compton, John G.;
    • DiGiovanna, John J.;
    • Presland, Richard B.;
    • Fleckman, Philip;
    • McLean, W. H. Irwin
    Publication type:
    Article
    24

    Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 294, doi. 10.1038/ng1749
    By:
    • Niihori, Tetsuya;
    • Aoki, Yoko;
    • Narumi, Yoko;
    • Neri, Giovanni;
    • Cavé, Hélène;
    • Verloes, Alain;
    • Okamoto, Nobuhiko;
    • Hennekam, Raoul C. M.;
    • Gillessen-Kaesbach, Gabriele;
    • Wieczorek, Dagmar;
    • Kavamura, Maria Ines;
    • Kurosawa, Kenji;
    • Ohashi, Hirofumi;
    • Wilson, Louise;
    • Heron, Delphine;
    • Bonneau, Dominique;
    • Corona, Giuseppina;
    • Kaname, Tadashi;
    • Naritomi, Kenji;
    • Baumann, Clarisse
    Publication type:
    Article
    25
    26
    27
    28
    29

    Analysis of the human protein interactome and comparison with yeast, worm and fly interaction datasets.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 285, doi. 10.1038/ng1747
    By:
    • Gandhi, T. K. B.;
    • Zhong, Jun;
    • Mathivanan, Suresh;
    • Karthick, L.;
    • Chandrika, K. N.;
    • Mohan, S. Sujatha;
    • Sharma, Salil;
    • Pinkert, Stefan;
    • Nagaraju, Shilpa;
    • Periaswamy, Balamurugan;
    • Mishra, Goparani;
    • Nandakumar, Kannabiran;
    • Beiyi Shen;
    • Deshpande, Nandan;
    • Nayak, Rashmi;
    • Sarker, Malabika;
    • Boeke, Jef D.;
    • Parmigiani, Giovanni;
    • Schultz, Jörg;
    • Bader, Joel S.
    Publication type:
    Article
    30

    Germline KRAS mutations cause Noonan syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 3, p. 331, doi. 10.1038/ng1748
    By:
    • Schubbert, Suzanne;
    • Zenker, Martin;
    • Rowe, Sara L.;
    • Böll, Silke;
    • Klein, Cornelia;
    • Bollag, Gideon;
    • van der Burgt, Ineke;
    • Musante, Luciana;
    • Kalscheuer, Vera;
    • Wehner, Lars-Erik;
    • Nguyen, Hoa;
    • West, Brian;
    • Zhang, Kam Y. J.;
    • Sistermans, Erik;
    • Rauch, Anita;
    • Niemeyer, Charlotte M.;
    • Shannon, Kevin;
    • Kratz, Christian P.
    Publication type:
    Article