Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 1

Results: 26

Embracing risk.

Published in:: 2006
Publication type:: Editorial

Amyloid double trouble.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 11, doi. 10.1038/ng0106-11

By:

Hardy, John

Publication type:

Article

Beyond the beta cell in diabetes.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 12, doi. 10.1038/ng0106-12

By:

Hattersley, Andrew T

Publication type:

Article

Confronting ethnicity-specific disease risk.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 13, doi. 10.1038/ng0106-13

By:

Hua Tang

Publication type:

Article

Touching base.

Published in:: Nature Genetics, 2006, v. 38, n. 1, p. 17, doi. 10.1038/ng0106-17
Publication type:: Article

Research Highlights.

Published in:: Nature Genetics, 2006, v. 38, n. 1, p. 19, doi. 10.1038/ng0106-19
Publication type:: Article

A road map for efficient and reliable human genome epidemiology.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 3, doi. 10.1038/ng0106-3

By:

Ioannidis, John P. A.;
Gwinn, Marta;
Little, Julian;
Higgins, Julian P. T.;
Bernstein, Jonine L.;
Boffetta, Paolo;
Bondy, Melissa;
Bray, Molly S.;
Brenchley, Paul E.;
Buffler, Patricia A.;
Casas, Juan Pablo;
Chokkalingam, Anand;
Danesh, John;
Smith, George Davey;
Dolan, Siobhan;
Duncan, Ross;
Gruis, Nelleke A.;
Hartge, Patricia;
Hashibe, Mia;
Hunter, David J.

Publication type:

Article

Evolution's secret.

Published in:

2006

By:

Goldman, Michael A

Publication type:

Book Review

Widening the spectrum of human genetic variation.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 9, doi. 10.1038/ng0106-9

By:

Eichler, Evan E.

Publication type:

Article

Lymphoid cell growth and transformation are suppressed by a key regulatory element of the gene encoding PU.1.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 27, doi. 10.1038/ng1679

By:

Rosenbauer, Frank;
Owens, Bronwyn M.;
Li Yu;
Tumang, Joseph R.;
Steidl, Ulrich;
Kutok, Jeffery L.;
Clayton, Linda K.;
Wagner, Katharina;
Scheller, Marina;
Iwasaki, Hiromi;
Liu, Chunhui;
Hackanson, Björn;
Akashi, Koichi;
Leutz, Achim;
Rothstein, Thomas L.;
Plass, Christoph;
Tenen, Daniel G.

Publication type:

Article

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 93, doi. 10.1038/ng1683

By:

Lerner-Ellis, Jordan P;
Tirone, Jamie C;
Pawelek, Peter D;
Doré, Carole;
Atkinson, Janet L;
Watkins, David;
Morel, Chantal F;
Fujiwara, T Mary;
Moras, Emily;
Hosack, Angela R;
Dunbar, Gail V;
Antonicka, Hana;
Forgetta, Vince;
Dobson, C Melissa;
Leclerc, Daniel;
Gravel, Roy A;
Shoubridge, Eric A;
Coulton, James W;
Lepage, Pierre;
Rommens, Johanna M

Publication type:

Article

Dosage compensation of the active X chromosome in mammals.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 47, doi. 10.1038/ng1705

By:

Nguyen, Di Kim;
Disteche, Christine M

Publication type:

Article

Oral-facial-digital type I protein is required for primary cilia formation and left-right axis specification.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 112, doi. 10.1038/ng1684

By:

Ferrante, Maria Immacolata;
Zullo, Alessandro;
Barra, Adriano;
Bimonte, Sabrina;
Messaddeq, Nadia;
Studer, Michèle;
Dollé, Pascal;
Franco, Brunella

Publication type:

Article

A positive signal from the fertilization of the egg cell sets off endosperm proliferation in angiosperm embryogenesis.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 63, doi. 10.1038/ng1694

By:

Nowack, Moritz K.;
Grini, Paul E.;
Jakoby, Marc J.;
Lafos, Marcel;
Koncz, Csaba;
Schnittger, Arp

Publication type:

Article

Common deletions and SNPs are in linkage disequilibrium in the human genome.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 82, doi. 10.1038/ng1695

By:

Hinds, David A;
Kloek, Andrew P;
Jen, Michael;
Chen, Xiyin;
Frazer, Kelly A

Publication type:

Article

Common deletion polymorphisms in the human genome.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 86, doi. 10.1038/ng1696

By:

McCarroll, Steven A.;
Hadnott, Tracy N.;
Perry, George H.;
Sabeti, Pardis C.;
Zody, Michael C.;
Barrett, Jeffrey C.;
Dallaire, Stephanie;
Gabriel, Stacey B.;
Lee, Charles;
Daly, Mark J.;
Altshuler, David M.

Publication type:

Article

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 68, doi. 10.1038/ng1692

By:

Helgadottir, Anna;
Manolescu, Andrei;
Helgason, Agnar;
Thorleifsson, Gudmar;
Thorsteinsdottir, Unnur;
Gudbjartsson, Daniel F;
Gretarsdottir, Solveig;
Magnusson, Kristinn P;
Gudmundsson, Gudmundur;
Hicks, Andrew;
Jonsson, Thorlakur;
Grant, Struan F A;
Sainz, Jesus;
O'Brien, Stephen J;
Sveinbjornsdottir, Sigurlaug;
Valdimarsson, Einar M;
Matthiasson, Stefan E;
Levey, Allan I;
Abramson, Jerome L;
Reilly, Murdach P

Publication type:

Article

Homozygous L-SIGN (CLEC4M) plays a protective role in SARS coronavirus infection.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 38, doi. 10.1038/ng1698

By:

Chan, Vera S. F.;
Chan, Kelvin Y. K.;
Chen, Yongxiong;
Poon, Leo L. M;
Cheung, Annie N. Y.;
Bojian Zheng;
Kwok-Hung Chan;
Mak, William;
Ngan, Hextan Y. S.;
Xiaoning Xu;
Screaton, Gavin;
Tam, Paul K. H.;
Austyn, Jonathan M.;
Li-Chong Chan;
Shea-Ping Yip;
Peiris, Malik;
Ui-Soon Khoo;
Lin, Chen-Lung S.

Publication type:

Article

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 54, doi. 10.1038/ng1708

By:

Ræder, Helge;
Johansson, Stefan;
Holm, Pål I;
Haldorsen, Ingfrid S;
Mas, Eric;
Sbarra, Véronique;
Nermoen, Ingrid;
Eide, Stig Å;
Grevle, Louise;
Bjørkhaug, Lise;
Sagen, Jørn V;
Aksnes, Lage;
Søvik, Oddmund;
Lombardo, Dominique;
Molven, Anders;
Njølstad, Pål Rasmus

Publication type:

Article

A high-resolution survey of deletion polymorphism in the human genome.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 75, doi. 10.1038/ng1697

By:

Conrad, Donald F.;
Andrews, T. Daniel;
Carter, Nigel P.;
Hurles, Matthew E.;
Pritchard, Jonathan K.

Publication type:

Article

Deletion of Peg10, an imprinted gene acquired from a retrotransposon, causes early embryonic lethality.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 101, doi. 10.1038/ng1699

By:

Ryuichi Ono;
Kenji Nakamura;
Kimiko Inoue;
Mie Naruse;
Takako Usami;
Noriko Wakisaka-Saito;
Toshiaki Hino;
Suzuki-Migishima, Rika;
Narumi Ogonuki;
Hiromi Miki;
Takashi Kohda;
Atsuo Ogura;
Minesuke Yokoyama;
Tomoko Kaneko-Ishino;
Fumitoshi Ishino

Publication type:

Article

Genetic analysis of cavefish reveals molecular convergence in the evolution of albinism.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 107, doi. 10.1038/ng1700

By:

Protas, Meredith E.;
Hersey, Candace;
Kochanek, Dawn;
Yi Zhou;
Wilkens, Horst;
Jeffery, William R.;
Zon, Leonard I.;
Borowsky, Richard;
Tabin, Clifford J.

Publication type:

Article

Defective planar cell polarity in polycystic kidney disease.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 21, doi. 10.1038/ng1701

By:

Fischer, Evelyne;
Legue, Emilie;
Doyen, Antonia;
Nato, Faridabano;
Nicolas, Jean-François;
Torres, Vicente;
Yaniv, Moshe;
Pontoglio, Marco

Publication type:

Article

Nras loss induces metastatic conversion of Rb1-deficient neuroendocrine thyroid tumor.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 118, doi. 10.1038/ng1703

By:

Takahashi, Chiaki;
Contreras, Bernardo;
Iwanaga, Tsuyoshi;
Takegami, Yujiro;
Bakker, Anke;
Bronson, Roderick T.;
Noda, Makoto;
Loda, Massimo;
Hunt, Jennifer L.;
Ewen, Mark E.

Publication type:

Article

Genome-wide transcription analyses in rice using tiling microarrays.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 124, doi. 10.1038/ng1704

By:

Lei Li;
Xiangfeng Wang;
Stolc, Viktor;
Xueyong Li;
Dongfen Zhang;
Ning Su;
Tongprasit, Waraporn;
Songgang Li;
Zhukuan Cheng;
Jun Wang;
Xing Wang Deng

Publication type:

Article

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

Published in:

Nature Genetics, 2006, v. 38, n. 1, p. 24, doi. 10.1038/ng1718

By:

Rovelet-Lecrux, Anne;
Hannequin, Didier;
Raux, Gregory;
Meur, Nathalie Le;
Laquerrière, Annie;
Vital, Anne;
Dumanchin, Cécile;
Feuillette, Sébastien;
Brice, Alexis;
Vercelletto, Martine;
Dubas, Frédéric;
Frebourg, Thierry;
Campion, Dominique

Publication type:

Article