Works matching IS 10614036 AND DT 2007 AND VI 39 AND IP 9

Results: 30

A haplotype map for the laboratory mouse.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1054, doi. 10.1038/ng0907-1054

By:

Mott, Richard

Publication type:

Article

An Arabidopsis haplotype map takes root.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1056, doi. 10.1038/ng0907-1056

By:

Buckler, Edward;
Gore, Michael

Publication type:

Article

Patchwork women.

Published in:

2007

By:

Brown, Carolyn

Publication type:

Book Review

IL-7Rα and multiple sclerosis risk.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1053, doi. 10.1038/ng0907-1053

By:

Harley, John B.

Publication type:

Article

Cancer drugs to treat birth defects.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1057, doi. 10.1038/ng0907-1057

By:

Wilkie, Andrew O. M.

Publication type:

Article

America competes—for now.

Published in:: 2007
Publication type:: Editorial

Anne McLaren 1927–2007.

Published in:

2007

By:

Burgoyne, Paul

Publication type:

Obituary

Touching base.

Published in:: Nature Genetics, 2007, v. 39, n. 9, p. 1061, doi. 10.1038/ng0907-1061
Publication type:: Article

Research Highlights.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1063, doi. 10.1038/ng0907-1063

By:

E. N.;
K. V.;
A. P.

Publication type:

Article

Corrigendum: Spontaneous DNA breakage in single living Escherichia coli cells.

Published in:

2007

By:

Pennington, Jeanine M.;
Rosenberg, Susan M.

Publication type:

Correction Notice

Corrigendum: Genome-wide analysis of mammalian promoter architecture and evolution.

Published in:

2007

By:

Carninci, Piero;
Sandelin, Albin;
Lenhard, Boris;
Katayama, Shintaro;
Shimokawa, Kazuro;
Ponjavic, Jasmina;
Semple, Colin A. M.;
Taylor, Martin S.;
Engström G, Pär G.;
Frith, Martin C.;
Forrest, Alistair R. R.;
Alkema, Wynand B.;
Tan, Sin Lam;
Plessy, Charles;
Kodzius, Rimantas;
Ravasi, Timothy;
Kasukawa, Takeya;
Fukuda, Shiro;
Kanamori-Katayama, Mutsumi;
Kitazume, Yayoi

Publication type:

Correction Notice

Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1083, doi. 10.1038/ng2103

By:

Gregory, Simon G.;
Schmidt, Silke;
Seth, Puneet;
Oksenberg, Jorge R.;
Hart, John;
Prokop, Angela;
Caillier, Stacy J.;
Ban, Maria;
Goris, An;
Barcellos, Lisa F.;
Lincoln, Robin;
McCauley, Jacob L.;
Sawcer, Stephen J.;
Compston, D. A. S.;
Dubois, Benedicte;
Hauser, Stephen L.;
Garcia-Blanco, Mariano A.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

Mutations in amphiphysin 2 (BIN1) disrupt interaction with dynamin 2 and cause autosomal recessive centronuclear myopathy.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1134, doi. 10.1038/ng2086

By:

Nicot, Anne-Sophie;
Toussaint, Anne;
Tosch, Valérie;
Kretz, Christine;
Wallgren-Pettersson, Carina;
Iwarsson, Erik;
Kingston, Helen;
Garnier, Jean-Marie;
Biancalana, Valérie;
Oldfors, Anders;
Mandel, Jean-Louis;
Laporte, Jocelyn

Publication type:

Article

A gene in the multidrug and toxic compound extrusion (MATE) family confers aluminum tolerance in sorghum.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1156, doi. 10.1038/ng2074

By:

Magalhaes, Jurandir V.;
Jiping Liu;
Guimarães, Claudia T.;
Lana, Ubiraci G. P.;
Alves, Vera M. C.;
Yi-Hong Wang;
Schaffert, Robert E.;
Hoekenga, Owen A.;
Piñeros, Miguel A.;
Shaff, Jon E.;
Klein, Patricia E.;
Carneiro, Newton P.;
Coelho, Cintia M.;
Trick, Harold N.;
Kochian, Leon V.

Publication type:

Article

Large-scale genetic fine mapping and genotype-phenotype associations implicate polymorphism in the IL2RA region in type 1 diabetes.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1074, doi. 10.1038/ng2102

By:

Lowe, Christopher E.;
Cooper, Jason D.;
Brusko, Todd;
Walker, Neil M.;
Smyth, Deborah J.;
Bailey, Rebecca;
Bourget, Kirsi;
Plagnol, Vincent;
Field, Sarah;
Atkinson, Mark;
Clayton, David G.;
Wicker, Linda S.;
Todd, John A.

Publication type:

Article

Global diversity and evidence for coevolution of KIR and HLA.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1114, doi. 10.1038/ng2077

By:

Single, Richard M.;
Martin, Maureen P.;
Xiaojiang Gao;
Meyer, Diogo;
Yeager, Meredith;
Kidd, Judith R.;
Kidd, Kenneth K.;
Carrington, Mary

Publication type:

Article

A single positively selected West Nile viral mutation confers increased virogenesis in American crows.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1162, doi. 10.1038/ng2097

By:

Brault, Aaron C.;
Huang, Claire Y.-H.;
Langevin, Stanley A.;
Kinney, Richard M.;
Bowen, Richard A.;
Ramey, Wanichaya N.;
Panella, Nicholas A.;
Holmes, Edward C.;
Powers, Ann M.;
Miller, Barry R.

Publication type:

Article

C-terminal truncations in human 3′-5′ DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1068, doi. 10.1038/ng2082

By:

Richards, Anna;
van den Maagdenberg, Arn M. J. M.;
Jen, Joanna C.;
Kavanagh, David;
Bertram, Paula;
Spitzer, Dirk;
Liszewski, M. Kathryn;
Barilla-LaBarca, Maria-Louise;
Terwindt, Gisela M.;
Kasai, Yumi;
McLellan, Mike;
Grand, Mark Gilbert;
Vanmolkot, Kaate R. J.;
de Vries, Boukje;
Jijun Wan;
Kane, Michael J.;
Mamsa, Hafsa;
Schäfer, Ruth;
Stam, Anine H.;
Haan, Joost

Publication type:

Article

Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1065, doi. 10.1038/ng2091

By:

Min Ae Lee-Kirsch;
Gong, Maolian;
Chowdhury, Dipanjan;
Senenko, Lydia;
Engel, Kerstin;
Lee, Young-Ae;
de Silva, Udesh;
Bailey, Suzanna L.;
Witte, Torsten;
Vyse, Timothy J.;
Kere, Juha;
Pfeiffer, Christiane;
Harvey, Scott;
Wong, Andrew;
Koskenmies, Sari;
Hummel, Oliver;
Rohde, Klaus;
Schmidt, Reinhold E.;
Anna F.Dominiczak;
Gahr, Manfred

Publication type:

Article

RNA interference and inhibition of MEK-ERK signaling prevent abnormal skeletal phenotypes in a mouse model of craniosynostosis.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1145, doi. 10.1038/ng2096

By:

Shukla, Vivek;
Coumoul, Xavier;
Rui-Hong Wang;
Hyun-Seok Kim;
Chu-Xia Deng

Publication type:

Article

On the subspecific origin of the laboratory mouse.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1100, doi. 10.1038/ng2087

By:

Hyuna Yang;
Bell, Timothy A.;
Churchill, Gary A.;
Pardo-Manuel de Villena, Fernando

Publication type:

Article

Promoter regions of many neural- and nutrition-related genes have experienced positive selection during human evolution.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1140, doi. 10.1038/ng2104

By:

Haygood, Ralph;
Fedrigo, Olivier;
Hanson, Brian;
Yokoyama, Ken-Daigoro;
Wray, Gregory A.

Publication type:

Article

Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1108, doi. 10.1038/ng2106

By:

Lundmark, Frida;
Duvefelt, Kristina;
Iacobaeus, Ellen;
Kockum, Ingrid;
Wallström, Erik;
Khademi, Mohsen;
Oturai, Annette;
Ryder, Lars P.;
Saarela, Janna;
Harbo, Hanne F.;
Celius, Elisabeth G.;
Salter, Hugh;
Olsson, Tomas;
Hillert, Jan

Publication type:

Article

New models of collaboration in genome-wide association studies: the Genetic Association Information Network.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1045, doi. 10.1038/ng2127

By:

Manolio, Teri A.;
Rodriguez, Laura Lyman;
Brooks, Lisa;
Abecasis, Gonçalo;
Ballinger, Dennis;
Daly, Mark;
Donnelly, Peter;
Faraone, Stephen V.;
Frazer, Kelly;
Gabriel, Stacey;
Gejman, Pablo;
Guttmacher, Alan;
Harris, Emily L.;
Insel, Thomas;
Kelsoe, John R.;
Lander, Eric;
McCowin, Norma;
Mailman, Matthew D.;
Nabel, Elizabeth;
Ostell, James

Publication type:

Article

Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1127, doi. 10.1038/ng2100

By:

Tarpey, Patrick S.;
Lucy Raymond, F.;
Nguyen, Lam S.;
Rodriguez, Jayson;
Hackett, Anna;
Vandeleur, Lucianne;
Smith, Raffaella;
Shoubridge, Cheryl;
Edkins, Sarah;
Stevens, Claire;
O'Meara, Sarah;
Tofts, Calli;
Barthorpe, Syd;
Buck, Gemma;
Cole, Jennifer;
Halliday, Kelly;
Hills, Katy;
Jones, David;
Mironenko, Tatiana;
Perry, Janet

Publication type:

Article

Bayesian inference of epistatic interactions in case-control studies.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1167, doi. 10.1038/ng2110

By:

Yu Zhang;
Liu, Jun S.

Publication type:

Article

Unusual selection on the KIR3DL1/S1 natural killer cell receptor in Africans.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1092, doi. 10.1038/ng2111

By:

Norman, Paul J.;
Abi-Rached, Laurent;
Gendzekhadze, Ketevan;
Korbel, Daniel;
Gleimer, Michael;
Rowley, Don;
Bruno, Dan;
Carrington, Christine V. F.;
Chandanayingyong, Dasdayanee;
Yih-Hsin Chang;
Crespí, Catalina;
Saruhan-Direskeneli, Güher;
Fraser, Patricia A.;
Hameed, Kamran;
Kamkamidze, Giorgi;
Koram, Kwadwo A;
Layrisse, Zulay;
Matamoros, Nuria;
Milà, Joan;
Park, Myoung Hee

Publication type:

Article

Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1–like phenotype.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1120, doi. 10.1038/ng2113

By:

Brems, Hilde;
Chmara, Magdalena;
Sahbatou, Mourad;
Denayer, Ellen;
Taniguchi, Koji;
Kato, Reiko;
Somers, Riet;
Messiaen, Ludwine;
De Schepper, Sofie;
Fryns, Jean-Pierre;
Cools, Jan;
Marynen, Peter;
Thomas, Gilles;
Yoshimura, Akihiko;
Legius, Eric

Publication type:

Article

Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1071, doi. 10.1038/ng2107

By:

Ballif, Blake C.;
Hornor, Sara A.;
Jenkins, Elizabeth;
Madan-Khetarpal, Suneeta;
Surti, Urvashi;
Jackson, Kelly E.;
Asamoah, Alexander;
Brock, Pamela L.;
Gowans, Gordon C.;
Conway, Robert L.;
Graham Jr., John M.;
Medne, Livija;
Zackai, Elaine H.;
Shaikh, Tamim H.;
Geoghegan, Joel;
Selzer, Rebecca R.;
Eis, Peggy S.;
Bejjani, Bassem A.;
Shaffer, Lisa G.

Publication type:

Article

Recombination and linkage disequilibrium in Arabidopsis thaliana.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1151, doi. 10.1038/ng2115

By:

Kim, Sung;
Plagnol, Vincent;
Hu, Tina T.;
Toomajian, Christopher;
Clark, Richard M.;
Ossowski, Stephan;
Ecker, Joseph R.;
Weigel, Detlef;
Nordborg, Magnus

Publication type:

Article