Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 5

Results: 13

ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 797, doi. 10.1093/hmg/ddi494

By:

Ho, G.-T.;
Soranzo, N.;
Nimmo, E.R.;
Tenesa, A.;
Goldstein, D.B.;
Satsangi, J.

Publication type:

Article

Extended tracts of homozygosity in outbred human populations.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 789, doi. 10.1093/hmg/ddi493

By:

Gibson, Jane;
Morton, Newton E.;
Collins, Andrew

Publication type:

Article

Differential expression of novel naturally occurring splice variants of PTEN and their functional consequences in Cowden syndrome and sporadic breast cancer.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 777, doi. 10.1093/hmg/ddi492

By:

Agrawal, Shipra;
Eng, Charis

Publication type:

Article

Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 767

By:

Lefèvre, Caroline;
Bouadjar, Bakar;
Ferrand, Véronique;
Tadini, Gianluca;
Mégarbané, André;
Lathrop, Mark;
Prud'homme, Jean-François;
Fischer, Judith

Publication type:

Article

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 751, doi. 10.1093/hmg/ddi490

By:

van Wijk, Erwin;
van der Zwaag, Bert;
Peters, Theo;
Zimmermann, Ulrike;
te Brinke, Heleen;
Kersten, Ferry F.J.;
Märker, Tina;
Aller, Elena;
Hoefsloot, Lies H.;
Cremers, Cor W.R.J.;
Cremers, Frans P.M.;
Wolfrum, Uwe;
Knipper, Marlies;
Roepman, Ronald;
Kremer, Hannie

Publication type:

Article

DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signaling.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 743, doi. 10.1093/hmg/ddi489

By:

Wilson, Gary M.;
Flibotte, Stephane;
Chopra, Vikramjit;
Melnyk, Brianna L.;
Honer, William G.;
Holt, Robert A.

Publication type:

Article

Podocalyxin variants and risk of prostate cancer and tumor aggressiveness.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 735, doi. 10.1093/hmg/ddi487

By:

Casey, Graham;
Neville, Phillippa J.;
Liu, Xin;
Plummer, Sarah J.;
Cicek, Mine S.;
Krumroy, Lisa M.;
Curran, Anthony P.;
McGreevy, Michelle R.;
Catalona, William J.;
Klein, Eric A.;
Witte, John S.

Publication type:

Article

Structural stability and chromosome-specific telomere length is governed by cis-acting determinants in humans.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 725, doi. 10.1093/hmg/ddi486

By:

Britt-Compton, Bethan;
Rowson, Jan;
Locke, Matthew;
Mackenzie, Ian;
Kipling, David;
Baird, Duncan M.

Publication type:

Article

Allele-specific deposition of macroH2A1 in imprinting control regions.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 717, doi. 10.1093/hmg/ddi485

By:

Choo, Jung Ha;
Kim, Jeong Do;
Chung, Jae Hoon;
Stubbs, Lisa;
Kim, Joomyeong

Publication type:

Article

Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 705, doi. 10.1093/hmg/ddi484

By:

Waterland, Robert A.;
Lin, Juan-Ru;
Smith, Charlotte A.;
Jirtle, Randy L.

Publication type:

Article

Polyglutamine expansion causes neurodegeneration by altering the neuronal differentiation program.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 691, doi. 10.1093/hmg/ddi483

By:

Abou-Sleymane, Gretta;
Chalmel, Frédéric;
Helmlinger, Dominique;
Lardenois, Aurélie;
Thibault, Christelle;
Weber, Chantal;
Mérienne, Karine;
Mandel, Jean-Louis;
Poch, Olivier;
Devys, Didier;
Trottier, Yvon

Publication type:

Article

Bardet–Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia function.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 667, doi. 10.1093/hmg/ddi468

By:

Yen, Hsan-Jan;
Tayeh, Marwan K.;
Mullins, Robert F.;
Stone, Edwin M.;
Sheffield, Val C.;
Slusarski, Diane C.

Publication type:

Article

Mild Nijmegen breakage syndrome phenotype due to alternative splicing.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 679, doi. 10.1093/hmg/ddi482

By:

Varon, Raymonda;
Dutrannoy, Véronique;
Weikert, Georg;
Tanzarella, Caterina;
Antoccia, Antonio;
Stöckl, Lars;
Spadoni, Emanuela;
Krüger, Lars-Arne;
Masi, Alessandra di;
Sperling, Karl;
Digweed, Martin;
Maraschio, Paola

Publication type:

Article