Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 8

Results: 25

Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 977, doi. 10.1038/ng2062

By:

Gudmundsson, Julius;
Sulem, Patrick;
Steinthorsdottir, Valgerdur;
Bergthorsson, Jon T.;
Thorleifsson, Gudmar;
Manolescu, Andrei;
Rafnar, Thorunn;
Gudbjartsson, Daniel;
Agnarsson, Bjarni A.;
Baker, Adam;
Sigurdsson, Asgeir;
Benediktsdottir, Kristrun R.;
Jakobsdottir, Margret;
Thorarinn Blondal1,;
Stacey, Simon N.;
Helgason, Agnar;
Gunnarsdottir, Steinunn;
Olafsdottir, Adalheidur;
Kristinsson, Kari T.;
Birgisdottir, Birgitta

Publication type:

Article

Compete, collaborate, compel.

Published in:: 2007
Publication type:: Editorial

Splinkerette PCR for more efficient characterization of gene trap events.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 933, doi. 10.1038/ng0807-933

By:

Horn, Carsten;
Hansen, Jens;
Schnütgen, Frank;
Seisenberger, Claudia;
Floss, Thomas;
Irgang, Markus;
De-Zolt, Silke;
Wurst, Wolfgang;
von Melchner, Harald;
Noppinger, Patricia Ruiz

Publication type:

Article

Target mimics modulate miRNAs.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 935, doi. 10.1038/ng0807-935

By:

Chitwood, Daniel H.;
Timmermans, Marja C. P.

Publication type:

Article

Axons need glial peroxisomes.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 936, doi. 10.1038/ng0807-936

By:

Aubourg, Patrick

Publication type:

Article

A step forward for restless legs syndrome.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 938, doi. 10.1038/ng0807-938

By:

Mignot, Emmanuel

Publication type:

Article

Touching base.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 941, doi. 10.1038/ng0807-941

By:

Bahcall, Orli;
Niemitz, Emily;
Vogan, Kyle

Publication type:

Article

Research Highlights.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 943, doi. 10.1038/ng0807-943

By:

Bahcall, Orli;
Niemitz, Emily;
Vogan, Kyle

Publication type:

Article

Loss of GLIS2 causes nephronophthisis in humans and mice by increased apoptosis and fibrosis.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1018, doi. 10.1038/ng2072

By:

Attanasio, Massimo;
Uhlenhaut, N. Henriette;
Sousa, Vitor H.;
O'Toole, John F.;
Otto, Edgar;
Anlag, Katrin;
Klugmann, Claudia;
Treier, Anna-Corina;
Helou, Juliana;
Sayer, John A.;
Seelow, Dominik;
Nürnberg, Gudrun;
Becker, Christian;
Chudley, Albert E.;
Nürnberg, Peter;
Hildebrandt, Friedhelm;
Treier, Mathias

Publication type:

Article

Genetic variation in Mon1a affects protein trafficking and modifies macrophage iron loading in mice.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1025, doi. 10.1038/ng2059

By:

Wang, Fudi;
Paradkar, Prasad N.;
Custodio, Angel O.;
Ward, Diane McVey;
Fleming, Mark D.;
Campagna, Dean;
Roberts, Kristina A.;
Boyartchuk, Victor;
Dietrich, William F.;
Kaplan, Jerry;
Andrews, Nancy C.

Publication type:

Article

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 957, doi. 10.1038/ng2063

By:

Kantarci, Sibel;
Al-Gazali, Lihadh;
Hill, R. Sean;
Donnai, Dian;
Black, Graeme C. M.;
Bieth, Eric;
Chassaing, Nicolas;
Lacombe, Didier;
Devriendt, Koen;
Teebi, Ahmad;
Loscertales, Maria;
Robson, Caroline;
Tianming Liu;
MacLaughlin, David T.;
Noonan, Kristin M.;
Russell, Meaghan K.;
Walsh, Christopher A.;
Donahoe, Patricia K.;
Pober, Barbara R.

Publication type:

Article

Bi-orientation of achiasmatic chromosomes in meiosis I oocytes contributes to aneuploidy in mice.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 966, doi. 10.1038/ng2065

By:

Kouznetsova, Anna;
Lister, Lisa;
Nordenskjöld, Magnus;
Herbert, Mary;
Höög, Christer

Publication type:

Article

Common variants in WFS1 confer risk of type 2 diabetes.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 951, doi. 10.1038/ng2067

By:

Sandhu, Manjinder S.;
Weedon, Michael N.;
Fawcett, Katherine A.;
Wasson, Jon;
Debenham, Sally L.;
Daly, Allan;
Lango, Hana;
Frayling, Timothy M.;
Neumann, Rosalind J.;
Sherva, Richard;
Blech, Ilana;
Pharoah, Paul D.;
Palmer, Colin N. A.;
Kimber, Charlotte;
Tavendale, Roger;
Morris, Andrew D.;
McCarthy, Mark I.;
Walker, Mark;
Hitman, Graham;
Glaser, Benjamin

Publication type:

Article

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1007, doi. 10.1038/ng2073

By:

Pandit, Bhaswati;
Sarkozy, Anna;
Pennacchio, Len A.;
Carta, Claudio;
Oishi, Kimihiko;
Martinelli, Simone;
Pogna, Edgar A.;
Schackwitz, Wendy;
Ustaszewska, Anna;
Landstrom, Andrew;
Bos, J. Martijn;
Ommen, Steve R.;
Esposito, Giorgia;
Lepri, Francesca;
Faul, Christian;
Mundel, Peter;
Siguero, Juan P. López;
Tenconi, Romano;
Selicorni, Angelo;
Rossi, Cesare

Publication type:

Article

Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 969, doi. 10.1038/ng2070

By:

Kassmann, Celia M.;
Lappe-Siefke, Corinna;
Baes, Myriam;
Brügger, Britta;
Mildner, Alexander;
Werner, Hauke B.;
Natt, Oliver;
Michaelis, Thomas;
Prinz, Marco;
Frahm, Jens;
Nave, Klaus-Armin

Publication type:

Article

Evolution of chromosome organization driven by selection for reduced gene expression noise.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 945, doi. 10.1038/ng2071

By:

Batada, Nizar N.;
Hurst, Laurence D.

Publication type:

Article

Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 960, doi. 10.1038/ng2076

By:

Sobacchi, Cristina;
Frattini, Annalisa;
Guerrini, Matteo M.;
Abinun, Mario;
Pangrazio, Alessandra;
Susani, Lucia;
Bredius, Robbert;
Mancini, Grazia;
Cant, Andrew;
Bishop, Nick;
Grabowski, Peter;
del Fattore, Andrea;
Messina, Chiara;
Errigo, Gabriella;
Coxon, Fraser P.;
Scott, Debbie I.;
Teti, Anna;
Rogers, Michael J.;
Vezzoni, Paolo;
Villa, Anna

Publication type:

Article

Germline gain-of-function mutations in RAF1 cause Noonan syndrome.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1013, doi. 10.1038/ng2078

By:

Razzaque, M. Abdur;
Nishizawa, Tsutomu;
Komoike, Yuta;
Yagi, Hisato;
Furutani, Michiko;
Amo, Ryunosuke;
Kamisago, Mitsuhiro;
Momma, Kazuo;
Katayama, Hiroshi;
Nakagawa, Masao;
Fujiwara, Yuko;
Matsushima, Masaki;
Mizuno, Katsumi;
Tokuyama, Mika;
Hirota, Hamao;
Muneuchi, Jun;
Higashinakagawa, Toru;
Matsuoka, Rumiko

Publication type:

Article

Target mimicry provides a new mechanism for regulation of microRNA activity.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1033, doi. 10.1038/ng2079

By:

Franco-Zorrilla, José Manuel;
Valli, Adrián;
Todesco, Marco;
Mateos, Isabel;
Puga, María Isabel;
Rubio-Somoza, Ignacio;
Leyva, Antonio;
Weigel, Detlef;
García, Juan Antonio;
Paz-Ares, Javier

Publication type:

Article

Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 963, doi. 10.1038/ng2083

By:

Douglas, Jenny;
Cilliers, Deirdre;
Coleman, Kim;
Tatton-Brown, Katrina;
Barker, Karen;
Bernhard, Brigitte;
Burn, John;
Huson, Susan;
Josifova, Dragana;
Lacombe, Didier;
Malik, Mohsin;
Mansour, Sahar;
Reid, Evan;
Cormier-Daire, Valerie;
Cole, Trevor;
Rahman, Nazneen

Publication type:

Article

A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 984, doi. 10.1038/ng2085

By:

Tomlinson, Ian;
Webb, Emily;
Carvajal-Carmona, Luis;
Broderick, Peter;
Kemp, Zoe;
Spain, Sarah;
Penegar, Steven;
Chandler, Ian;
Gorman, Maggie;
Wood, Wendy;
Barclay, Ella;
Lubbe, Steven;
Martin, Lynn;
Sellick, Gabrielle;
Jaeger, Emma;
Hubner, Richard;
Wild, Ruth;
Rowan, Andrew;
Fielding, Sarah;
Howarth, Kimberley

Publication type:

Article

Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 989, doi. 10.1038/ng2089

By:

Zanke, Brent W.;
Greenwood, Celia M. T.;
Rangrej, Jagadish;
Kustra, Rafal;
Tenesa, Albert;
Farrington, Susan M.;
Prendergast, James;
Olschwang, Sylviane;
Chiang, Theodore;
Crowdy, Edgar;
Ferretti, Vincent;
Laflamme, Philippe;
Sundararajan, Saravanan;
Roumy, Stéphanie;
Olivier, Jean-François;
Robidoux, Frédérick;
Sladek, Robert;
Montpetit, Alexandre;
Campbell, Peter;
Bezieau, Stephane

Publication type:

Article

A common genetic risk factor for colorectal and prostate cancer.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 954, doi. 10.1038/ng2098

By:

Haiman, Christopher A.;
Le Marchand, Loïc;
Yamamato, Jennifer;
Stram, Daniel O.;
Xin Sheng;
Kolonel, Laurence N.;
Wu, Anna H.;
Reich, David;
Henderson, Brian E.

Publication type:

Article

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 1000, doi. 10.1038/ng2099

By:

Winkelmann, Juliane;
Schormair, Barbara;
Lichtner, Peter;
Ripke, Stephan;
Lan Xiong;
Jalilzadeh, Shapour;
Fulda, Stephany;
Pütz, Benno;
Eckstein, Gertrud;
Hauk, Stephanie;
Trenkwalder, Claudia;
Zimprich, Alexander;
Stiasny-Kolster, Karin;
Oertel, Wolfgang;
Bachmann, Cornelius G.;
Paulus, Walter;
Peglau, Ines;
Eisensehr, Ilonka;
Montplaisir, Jacques;
Turecki, Gustavo

Publication type:

Article

A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.

Published in:

Nature Genetics, 2007, v. 39, n. 8, p. 995, doi. 10.1038/ng2101

By:

Buch, Stephan;
Schafmayer, Clemens;
Völzke, Henry;
Becker, Christian;
Franke, Andre;
von Eller-Eberstein, Huberta;
Kluck, Christian;
Bässmann, Ingelore;
Brosch, Mario;
Lammert, Frank;
Miquel, Juan Francisco;
Nervi, Flavio;
Wittig, Michael;
Rosskopf, Dieter;
Timm, Birgit;
Höll, Christine;
Seeger, Marcus;
ElSharawy, Abdou;
Tim Lu;
Egberts, Jan

Publication type:

Article