Works matching IS 10614036 AND DT 1999 AND VI 21 AND IP 1

Results: 24
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    Fgf10 is essential for limb and lung formation.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 138, doi. 10.1038/5096
    By:
    • Sekine, Keisuke;
    • Ohuchi, Hideyo;
    • Fujiwara, Masanori;
    • Yamasaki, Masahiro;
    • Yoshizawa, Tatsuya;
    • Sato, Takashi;
    • Yagishita, Naoko;
    • Matsui, Daisuke;
    • Koga, Yoshihiko;
    • Itoh, Nobuyuki;
    • Kato, Shigeaki
    Publication type:
    Article
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    TOUCHINGbase.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 69
    Publication type:
    Article
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    Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 71, doi. 10.1038/5009
    By:
    • Kehoe, Patrick G.;
    • Russ, Carsten;
    • McIlroy, Stephen;
    • Williams, Hywel;
    • Holmans, Peter;
    • Holmes, Clive;
    • Liolitsa, Danae;
    • Vahidassr, Djamil;
    • Powell, John;
    • McGleenon, Bronagh;
    • Liddell, Malcolm;
    • Plomin, Robert;
    • Dynan, Kevin;
    • Williams, Nigel;
    • Neal, Jim;
    • Cairns, Nigel J.;
    • Wilcock, Gordon;
    • Passmore, Peter;
    • Lovestone, Simon
    Publication type:
    Article
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    An action plan for mouse genomics.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 73, doi. 10.1038/5012
    By:
    • Battey, James;
    • Jordan, Elke;
    • Cox, David;
    • Dove, William
    Publication type:
    Article
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    Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 76, doi. 10.1038/5013
    By:
    • Aitman, Timothy J.;
    • Glazier, Anne M.;
    • Wallace, Caroline A.;
    • Cooper, Lisa D.;
    • Norsworthy, Penny J.;
    • Wahid, Faisal N.;
    • Al-Majali, Khulood M.;
    • Trembling, Paul M.;
    • Mann, Christopher J.;
    • Shoulders, Carol C.;
    • Graf, Daniel;
    • Lezin, Elizabeth St.;
    • Kurtz, Theodore W.;
    • Kren, Vladimir;
    • Pravenec, Michal;
    • Ibrahimi, Azeddine;
    • Abumrad, Nada A.;
    • Stanton, Lawrence W.;
    • Scott, James
    Publication type:
    Article
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    Mutations in the gene encoding B1 subunit of H<sup>+</sup>-ATPase cause renal tubular acidosis with sensorineural deafness.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 84, doi. 10.1038/5022
    By:
    • Karet, Fiona E.;
    • Finberg, Karin E.;
    • Nelson, Raoul D.;
    • Nayir, Ahmet;
    • Mocan, Hilal;
    • Sanjad, Sami A.;
    • Rodriguez-Soriano, Juan;
    • Santos, Fernando;
    • Cremers, Cor W.R.J.;
    • Pietro, Antonio Di;
    • Hoffbrand, Barry I.;
    • Winiarski, Jacek;
    • Bakkaloglu, Aysin;
    • Ozen, Seza;
    • Dusunsel, Ruhan;
    • Goodyer, Paul;
    • Hulton, Sally A.;
    • Wu, Doris K.;
    • Skvorak, Anne B.
    Publication type:
    Article
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    Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 91, doi. 10.1038/5030
    By:
    • Nezu, Jun-ichi;
    • Tamai, Ikumi;
    • Oku, Asuka;
    • Ohashi, Rikiya;
    • Yabuuchi, Hikaru;
    • Hashimoto, Noriyoshi;
    • Nikaido, Hiroko;
    • Sai, Yoshimichi;
    • Koizumi, Akio;
    • Shoji, Yutaka;
    • Takada, Goro;
    • Matsuishi, Toyojiro;
    • Yoshino, Makoto;
    • Kato, Hirohisa;
    • Ohura, Toshihiro;
    • Tsujimoto, Gozoh;
    • Hayakawa, Jun-ichiro;
    • Shimane, Miyuki;
    • Tsuji, Akira
    Publication type:
    Article
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    PIK3CA is implicated as an oncogene in ovarian cancer.

    Published in:
    Nature Genetics, 1999, v. 21, n. 1, p. 99, doi. 10.1038/5042
    By:
    • Shayesteh, Laleh;
    • Lu, Yiling;
    • Kuo, Wen-Lin;
    • Baldocchi, Russell;
    • Godfrey, Tony;
    • Collins, Colin;
    • Pinkel, Daniel;
    • Powell, Bethan;
    • Mills, Gordon B.;
    • Gray, Joe W.
    Publication type:
    Article