Works matching IS 10614036 AND DT 2005 AND VI 37 AND IP 5

Results: 29

All about alleles.

Published in:

2005

By:

Bucan, Maja

Publication type:

Book Review

Poster child.

Published in:: Nature Genetics, 2005, v. 37, n. 5, p. 447, doi. 10.1038/ng0505-447
Publication type:: Article

Getting the science and the ethics right in forensic genetics.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 449, doi. 10.1038/ng0505-449

By:

Shriver, Mark;
Frudakis, Tony;
Budowle, Bruce

Publication type:

Article

Reply to "Getting the science and the ethics right in forensic genetics".

Published in:

2005

By:

Cho, Mildred K;
Sankar, Pamela

Publication type:

Letter

Linking cilia to Wnts.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 455, doi. 10.1038/ng0505-455

By:

Germino, Gregory G.

Publication type:

Article

Universal epistasis analysis.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 457, doi. 10.1038/ng0505-457

By:

Hughes, Timothy R.

Publication type:

Article

Mutation accumulation of the transcriptome.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 458, doi. 10.1038/ng0505-458

By:

Gibson, Greg

Publication type:

Article

Epigenetics of hypertension in pregnancy.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 460, doi. 10.1038/ng0505-460

By:

Arngrímsson, Reynir

Publication type:

Article

Touching base.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 463, doi. 10.1038/ng0505-463

By:

Axton, Myles;
Bahcall, Orli;
Vogan, Kyle

Publication type:

Article

Research Highlights.

Published in:: Nature Genetics, 2005, v. 37, n. 5, p. 464, doi. 10.1038/ng0505-464
Publication type:: Article

Corrigendum: The gene encoding phosphodiesterase 4D confers risk of ischemic stroke.

Published in:

2005

By:

Gretarsdottir, S.;
Thorleifsson, G.;
Reynisdottir, S. Th.;
Manolescu, A.;
Jonsdottir, S.;
Jonsdottir, T.;
Gudmundsdottir, T.;
Bjarnadottir, S. M.;
Einarsson, O. B.;
Gudjonsdottir, H. M.;
Hawkins, M.;
Gudmundsson, G.;
Gudmundsdottir, H.;
Andrason, H.;
Gudmundsdottir, A. S.;
Sigurdardottir, M.;
Chou, T. T.;
Nahmias, J.;
Goss, S.;
Sveinbjörnsdottir, S.

Publication type:

Correction Notice

Corrigendum: Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons.

Published in:

2005

By:

Parker, J. A.;
Arango, M.;
Abderrahmane, S.;
Lambert, E.;
Tourette, C.;
Catoire, H.;
Néri, C.

Publication type:

Correction Notice

Corrigendum: Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse.

Published in:

2005

By:

Bomar, J. M.;
Benke, P. J.;
Slattery, E. L.;
Puttagunta, R.;
Taylor, L. P.;
Seong, E.;
Nystuen, A.;
Chen, W.;
Albin, R. L.;
Patel, P. D.;
Kittles, R. A.;
Sheffield, V. C.;
Burmeister, M.

Publication type:

Correction Notice

Corrigendum: A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size.

Published in:

2005

By:

Bond, J.;
Roberts, E.;
Springel, K.;
Lizarraga, S.;
Scott, S.;
Higgins, J.;
Hampshire, D. J.;
Morrison, E. E.;
Leal, G. F.;
Silva, E. O.;
Costa, S. M. R.;
Baralle,, D.;
Raponi, M.;
Karbani, G.;
Rashid, Y.;
Jafri, H.;
Bennett, C.;
Corry, P.;
Walsh, C. A.;
Woods, C. G.

Publication type:

Correction Notice

Combinatorial microRNA target predictions.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 495, doi. 10.1038/ng1536

By:

Krek, Azra;
Grün, Dominic;
Poy, Matthew N;
Wolf, Rachel;
Rosenberg, Lauren;
Epstein, Eric J;
MacMenamin, Philip;
da Piedade, Isabelle;
Gunsalus, Kristin C;
Stoffel, Markus;
Rajewsky, Nikolaus

Publication type:

Article

A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 478, doi. 10.1038/ng1540

By:

Kochi, Yuta;
Yamada, Ryo;
Suzuki, Akari;
Harley, John B;
Shirasawa, Senji;
Sawada, Tetsuji;
Bae, Sang-Cheol;
Tokuhiro, Shinya;
Chang, Xiaotian;
Sekine, Akihiro;
Takahashi, Atsushi;
Tsunoda, Tatsuhiko;
Ohnishi, Yozo;
Kaufman, Kenneth M;
Kang, Changsoo Paul;
Kang, Changwon;
Otsubo, Shigeru;
Yumura, Wako;
Mimori, Akio;
Koike, Takao

Publication type:

Article

Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 514, doi. 10.1038/ng1541

By:

van Dijk, Marie;
Mulders, Joyce;
Poutsma, Ankie;
Könst, Andrea A M;
Lachmeijer, Augusta M A;
Dekker, Gustaaf A;
Blankenstein, Marinus A;
Oudejans, Cees B M

Publication type:

Article

A genomic screen in yeast implicates kynurenine 3-monooxygenase as a therapeutic target for Huntington disease.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 526, doi. 10.1038/ng1542

By:

Giorgini, Flaviano;
Guidetti, Paolo;
Nguyen, QuangVu;
Bennett, Simone C;
Muchowski, Paul J

Publication type:

Article

A gene expression map of Arabidopsis thaliana development.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 501, doi. 10.1038/ng1543

By:

Schmid, Markus;
Davison, Timothy S;
Henz, Stefan R;
Pape, Utz J;
Demar, Monika;
Vingron, Martin;
Schölkopf, Bernhard;
Weigel, Detlef;
Lohmann, Jan U

Publication type:

Article

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 486, doi. 10.1038/ng1544

By:

Swanberg, Maria;
Lidman, Olle;
Padyukov, Leonid;
Eriksson, Per;
Åkesson, Eva;
Jagodic, Maja;
Lobell, Anna;
Khademi, Mohsen;
Börjesson, Ola;
Lindgren, Cecilia M;
Lundman, Pia;
Brookes, Anthony J;
Kere, Juha;
Luthman, Holger;
Alfredsson, Lars;
Hillert, Jan;
Klareskog, Lars;
Hamsten, Anders;
Piehl, Fredrik;
Olsson, Tomas

Publication type:

Article

Epistasis analysis with global transcriptional phenotypes.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 471, doi. 10.1038/ng1545

By:

Van Driessche, Nancy;
Demsar, Janez;
Booth, Ezgi O;
Hill, Paul;
Juvan, Peter;
Zupan, Blaz;
Kuspa, Adam;
Shaulsky, Gad

Publication type:

Article

A genome-wide scalable SNP genotyping assay using microarray technology.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 549, doi. 10.1038/ng1547

By:

Gunderson, Kevin L;
Steemers, Frank J;
Lee, Grace;
Mendoza, Leo G;
Chee, Mark S

Publication type:

Article

Roberts syndrome is caused by mutations in ESCO2, a human homolog of yeast ECO1 that is essential for the establishment of sister chromatid cohesion.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 468, doi. 10.1038/ng1548

By:

Vega, Hugo;
Waisfisz, Quinten;
Gordillo, Miriam;
Sakai, Norio;
Yanagihara, Itaru;
Yamada, Minoru;
Gosliga, Djoke van;
Kayserili, Hülya;
Xu, Chengzhe;
Ozono, Keiichi;
Jabs, Ethylin Wang;
Inui, Koji;
Joenje, Hans

Publication type:

Article

Inversin, the gene product mutated in nephronophthisis type II, functions as a molecular switch between Wnt signaling pathways.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 537, doi. 10.1038/ng1552

By:

Simons, Matias;
Gloy, Joachim;
Ganner, Athina;
Bullerkotte, Axel;
Bashkurov, Mikhail;
Krönig, Corinna;
Schermer, Bernhard;
Benzing, Thomas;
Cabello, Olga A;
Jenny, Andreas;
Mlodzik, Marek;
Polok, Bozena;
Driever, Wolfgang;
Obara, Tomoko;
Walz, Gerd

Publication type:

Article

MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 465, doi. 10.1038/ng1546

By:

van Bokhoven, Hans;
Celli, Jacopo;
van Reeuwijk, Jeroen;
Rinne, Tuula;
Glaudemans, Bob;
van Beusekom, Ellen;
Rieu, Paul;
Newbury-Ecob, Ruth A;
Chiang, Chin;
Brunner, Han G

Publication type:

Article

Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 520, doi. 10.1038/ng1549

By:

Jadeja, Shalini;
Smyth, Ian;
Pitera, Jolanta E;
Taylor, Martin S;
van Haelst, Mieke;
Bentley, Elizabeth;
McGregor, Lesley;
Hopkins, Jason;
Chalepakis, Georges;
Philip, Nicole;
Perez Aytes, Antonio;
Watt, Fiona M;
Darling, Susan M;
Jackson, Ian;
Woolf, Adrian S;
Scambler, Peter J

Publication type:

Article

A variant in the CD209 promoter is associated with severity of dengue disease.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 507, doi. 10.1038/ng1550

By:

Sakuntabhai, Anavaj;
Turbpaiboon, Chairat;
Casadémont, Isabelle;
Chuansumrit, Ampaiwan;
Lowhnoo, Tassanee;
Kajaste-Rudnitski, Anna;
Kalayanarooj, Sita Mint;
Tangnararatchakit, Kanchana;
Tangthawornchaikul, Nattaya;
Vasanawathana, Sirijit;
Chaiyaratana, Wathanee;
Yenchitsomanus, Pa-thai;
Suriyaphol, Prapat;
Avirutnan, Panisadee;
Chokephaibulkit, Kulkanya;
Matsuda, Fumihiko;
Yoksan, Sutee;
Jacob, Yves;
Lathrop, G Mark;
Malasit, Prida

Publication type:

Article

Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 532, doi. 10.1038/ng1551

By:

Adams, David J;
Dermitzakis, Emmanouil T;
Cox, Tony;
Smith, James;
Davies, Rob;
Banerjee, Ruby;
Bonfield, James;
Mullikin, James C;
Chung, Yeun Jun;
Rogers, Jane;
Bradley, Allan

Publication type:

Article

The transcriptional consequences of mutation and natural selection in Caenorhabditis elegans.

Published in:

Nature Genetics, 2005, v. 37, n. 5, p. 544, doi. 10.1038/ng1554

By:

Denver, Dee R;
Morris, Krystalynne;
Streelman, J Todd;
Kim, Stuart K;
Lynch, Michael;
Thomas, W Kelley

Publication type:

Article