Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 2


Results: 29
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    Expressing physiology.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 140, doi. 10.1038/ng0206-140
    By:
    • Hubner, Norbert
    Publication type:
    Article
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    Touching base.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 145, doi. 10.1038/ng0206-145
    Publication type:
    Article
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    Research Highlights.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 147, doi. 10.1038/ng0206-147
    Publication type:
    Article
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    Corrigendum: Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome).

    Published in:
    2006
    By:
    • Zenker, Martin;
    • Mayerle, Julia;
    • Lerch, Markus M;
    • Tagariello, Andreas;
    • Zerres, Klaus;
    • Durie, Peter R;
    • Beier, Matthias;
    • Hülskamp, Georg;
    • Guzman, Celina;
    • Rehder, Helga;
    • Beemer, Frits A;
    • Hamel, Ben;
    • Vanlieferinghen, Philippe;
    • Gershoni-Baruch, Ruth;
    • Vieira, Marta W;
    • Dumic, Miroslav;
    • Auslender, Ron;
    • Gil-da-Silva-Lopes, Vera L;
    • Steinlicht, Simone;
    • Rauh, Manfred
    Publication type:
    Correction Notice
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    Physiogenomic resources for rat models of heart, lung and blood disorders.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 234, doi. 10.1038/ng1693
    By:
    • Malek, Renae L.;
    • Hong-ying Wang;
    • Kwitek, Anne E.;
    • Greene, Andrew S.;
    • Bhagabati, Nirmal;
    • Borchardt, Gretta;
    • Cahill, Lisa;
    • Currier, Tracey;
    • Frank, Bryan;
    • Xianping Fu;
    • Hasinoff, Michael;
    • Howe, Eleanor;
    • Letwin, Noah;
    • Luu, Truong V.;
    • Saeed, Alexander;
    • Sajadi, Hedieh;
    • Salzberg, Steven L.;
    • Sultana, Razvan;
    • Thiagarajan, Mathangi;
    • Tsai, Jennifer
    Publication type:
    Article
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    The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 191, doi. 10.1038/ng1713
    By:
    • Smith, Ursula M.;
    • Consugar, Mark;
    • Tee, Louise J.;
    • McKee, Brandy M.;
    • Esther N.Maina;
    • Whelan, Shelly;
    • Neil V.Morgan;
    • Goranson, Erin;
    • Gissen, Paul;
    • Lilliquist, Stacie;
    • Aligianis, Irene A.;
    • Ward, Christopher J.;
    • Pasha, Shanaz;
    • Punyashthiti, Rachaneekorn;
    • Sharif, Saghira Malik;
    • Batman, Philip A.;
    • Bennett, Christopher P.;
    • Woods, C. Geoffrey;
    • McKeown, Carole;
    • Bucourt, Martine
    Publication type:
    Article
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    Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 197, doi. 10.1038/ng1727
    By:
    • Jordanova, Albena;
    • Irobi, Joy;
    • Thomas, Florian P.;
    • Van Dijck, Patrick;
    • Meerschaert, Kris;
    • Dewil, Maarten;
    • Dierick, Ines;
    • Jacobs, An;
    • De Vriendt, Els;
    • Guergueltcheva, Velina;
    • Rao, Chitharanjan V.;
    • Tournev, Ivailo;
    • Gondim, Francisco A. A.;
    • D'Hooghe, Marc;
    • Van Gerwen, Veerle;
    • Callaerts, Patrick;
    • Van Den Bosch, Ludo;
    • Timmermans, Jean-Pièrre;
    • Robberecht, Wim;
    • Gettemans, Jan
    Publication type:
    Article
    27

    Spectrin mutations cause spinocerebellar ataxia type 5.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 184, doi. 10.1038/ng1728
    By:
    • Ikeda, Yoshio;
    • Dick, Katherine A.;
    • Weatherspoon, Marcy R.;
    • Gincel, Dan;
    • Armbrust, Karen R.;
    • Dalton, Joline C.;
    • Stevanin, Giovanni;
    • Dürr, Alexandra;
    • Zühlke, Christine;
    • Bürk, Katrin;
    • Clark, H. Brent;
    • Brice, Alexis;
    • Rothstein, Jeffrey D.;
    • Schut, Lawrence J.;
    • Day, John W.;
    • Ranum, Laura P. W.
    Publication type:
    Article
    28

    Comparative analysis of chimpanzee and human Y chromosomes unveils complex evolutionary pathway.

    Published in:
    Nature Genetics, 2006, v. 38, n. 2, p. 1, doi. 10.1038/ng1729
    By:
    • Kuroki, Yoko;
    • Toyoda, Atsushi;
    • Noguchi, Hideki;
    • Taylor, Todd D.;
    • Itoh, Takehiko;
    • Dae-Soo Kim;
    • Dae-Won Kim;
    • Sang-Haeng Choi;
    • Il-Chul Kim;
    • Han Ho Choi;
    • Yong Sung Kim;
    • Satta, Yoko;
    • Saitou, Naruya;
    • Yamada, Tomoyuki;
    • Morishita, Shinichi;
    • Hattori, Masahira;
    • Sakaki, Yoshiyuki;
    • Hong-Seog Park;
    • Fujiyama, Asao
    Publication type:
    Article
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