Works matching IS 10614036 AND DT 2001 AND VI 29 AND IP 2

Results: 32
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    The promoter connection.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 105, doi. 10.1038/ng1001-105
    By:
    • Werner, Thomas
    Publication type:
    Article
    4

    The adaptable lin-39.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 106, doi. 10.1038/ng1001-106
    By:
    • Chamberlin, Helen M.
    Publication type:
    Article
    5

    Time for T.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 107, doi. 10.1038/ng1001-107
    By:
    • Murray, Jeffrey C.
    Publication type:
    Article
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    TOUCHINGbase.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 113
    Publication type:
    Article
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    A role for MLH3 in hereditary nonpolyposis colorectal cancer.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 137, doi. 10.1038/ng1001-137
    By:
    • Wu, Ying;
    • Berends, Maran J.W.;
    • Sijmons, Rolf H.;
    • Mensink, Rob G.J.;
    • Verlind, Edwin;
    • Kooi, Krista A.;
    • van der Sluis, Tineke;
    • Kempinga, Claudia;
    • van der Zee, Ate G.J.;
    • Hollema, Harry;
    • Buys, Charles H.C.M.;
    • Kleibeuker, Jan H.;
    • Hofstra, Robert M.W.
    Publication type:
    Article
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    The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 160, doi. 10.1038/ng1001-160
    By:
    • Yang, Yi;
    • Hentati, Afif;
    • Deng, Han-Xiang;
    • Dabbagh, Omar;
    • Sasaki, Toru;
    • Hirano, Makito;
    • Hung, Wu-Yen;
    • Ouahchi, Karim;
    • Yan, Jianhua;
    • Azim, Anser C.;
    • Cole, Natalie;
    • Gascon, Generoso;
    • Yagmour, Ayesha;
    • Ben-Hamida, Mongi;
    • Pericak-Vance, Margaret;
    • Hentati, Fayçal;
    • Siddique, Teepu
    Publication type:
    Article
    16

    A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 166, doi. 10.1038/ng1001-166
    By:
    • Hadano, Shinji;
    • Hand, Collette K.;
    • Osuga, Hitoshi;
    • Yanagisawa, Yoshiko;
    • Otomo, Asako;
    • Devon, Rebecca S.;
    • Miyamoto, Natsuki;
    • Showguchi-Miyata, Junko;
    • Okada, Yoshinori;
    • Singaraja, Roshni;
    • Figlewicz, Denise A.;
    • Kwiatkowski, Thomas;
    • Hosler, Betsy A.;
    • Sagie, Tally;
    • Skaug, Jennifer;
    • Nasir, Jamal;
    • Brown, Robert H.;
    • Scherer, Stephen W.;
    • Rouleau, Guy A.
    Publication type:
    Article
    17

    Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 184, doi. 10.1038/ng1001-184
    By:
    • Date, Hidetoshi;
    • Onodera, Osamu;
    • Tanaka, Hajime;
    • Iwabuchi, Kiyoshi;
    • Uekawa, Kazutoshi;
    • Igarashi, Shuichi;
    • Koike, Ryoko;
    • Hiroi, Tadashi;
    • Yuasa, Tatsuhiko;
    • Awaya, Yutaka;
    • Sakai, Tetsuo;
    • Takahashi, Tatsuya;
    • Nagatomo, Hideki;
    • Sekijima, Yoshiki;
    • Kawachi, Izumi;
    • Takiyama, Yoshihisa;
    • Nishizawa, Masatoyo;
    • Fukuhara, Nobuyoshi;
    • Saito, Kayoko
    Publication type:
    Article
    18

    The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 189, doi. 10.1038/ng1001-189
    By:
    • Moreira, Maria-Céu;
    • Barbot, Clara;
    • Tachi, Nobutada;
    • Kozuka, Naoki;
    • Uchida, Eiji;
    • Gibson, Toby;
    • Mendonça, Pedro;
    • Costa, Manuela;
    • Barros, José;
    • Yanagisawa, Takayuki;
    • Watanabe, Mitsunori;
    • Ikeda, Yoshio;
    • Aoki, Masashi;
    • Nagata, Tetsuya;
    • Coutinho, Paula;
    • Sequeiros, Jorge;
    • Koenig, Michel
    Publication type:
    Article
    19

    A radiation hybrid transcript map of the mouse genome.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 194, doi. 10.1038/ng1001-194
    By:
    • Avner, Philip;
    • Bruls, Thomas;
    • Poras, Isabelle;
    • Eley, Lorraine;
    • Gas, Shahinaz;
    • Ruiz, Patricia;
    • Wiles, Michael V.;
    • Sousa-Nunes, Rita;
    • Kettleborough, Ross;
    • Rana, Amer;
    • Morissette, Jean;
    • Bentley, Liz;
    • Goldsworthy, Michelle;
    • Haynes, Alison;
    • Herbert, Eifion;
    • Southam, Lorraine;
    • Lehrach, Hans;
    • Weissenbach, Jean;
    • Manenti, Giacomo
    Publication type:
    Article
    20

    A radiation hybrid map of mouse genes.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 201, doi. 10.1038/ng1001-201
    By:
    • Hudson, Thomas J.;
    • Church, Deanna M.;
    • Greenaway, Simon;
    • Nguyen, Huy;
    • Cook, April;
    • Steen, Robert G.;
    • Van Etten, William J.;
    • Castle, Andrew B.;
    • Strivens, Mark A.;
    • Trickett, Pamela;
    • Heuston, Christine;
    • Davison, Claire;
    • Southwell, Anne;
    • Hardisty, Rachel;
    • Varela-Carver, Anabel;
    • Haynes, Andrew R.;
    • Rodriguez-Tome, Patricia;
    • Doi, Hirofumi;
    • Ko, Minoru S.H.
    Publication type:
    Article
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    Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 223, doi. 10.1038/ng1001-223
    By:
    • Rioux, John D.;
    • Daly, Mark J.;
    • Silverberg, Mark S.;
    • Lindblad, Kerstin;
    • Steinhart, Hillary;
    • Cohen, Zane;
    • Delmonte, Terrye;
    • Kocher, Kerry;
    • Miller, Katie;
    • Guschwan, Sheila;
    • Kulbokas, Edward J.;
    • O'Leary, Sinead;
    • Winchester, Ellen;
    • Dewar, Ken;
    • Green, Todd;
    • Stone, Valerie;
    • Chow, Christine;
    • Cohen, Albert;
    • Langelier, Diane
    Publication type:
    Article
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    Haplotype tagging for the identification of common disease genes.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 233, doi. 10.1038/ng1001-233
    By:
    • Johnson, Gillian C.L.;
    • Esposito, Laura;
    • Barratt, Bryan J.;
    • Smith, Annabel N.;
    • Heward, Joanne;
    • Di Genova, Gianfranco;
    • Ueda, Hironori;
    • Cordell, Heather J.;
    • Eaves, Iain A.;
    • Dudbridge, Frank;
    • Twells, Rebecca C.J.;
    • Payne, Felicity;
    • Hughes, Wil;
    • Nutland, Sarah;
    • Stevens, Helen;
    • Carr, Phillipa;
    • Tuomilehto-Wolf, Eva;
    • Tuomilehto, Jaakko;
    • Gough, Stephen C.L.
    Publication type:
    Article
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    Gene polymorphism in Netherton and common atopic disease.

    Published in:
    Nature Genetics, 2001, v. 29, n. 2, p. 175, doi. 10.1038/ng728
    By:
    • Walley, Andrew J.;
    • Chavanas, Stéphane;
    • Moffatt, Miriam F.;
    • Esnouf, Robert M.;
    • Ubhi, Baljinder;
    • Lawrence, Robert;
    • Wong, Kenny;
    • Abecasis, Gonçalo R;
    • Jones, E. Yvonne;
    • Harper, John I.;
    • Hovnanian, Alain;
    • Cookson, William O.C.M.
    Publication type:
    Article
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