Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 22

Results: 11

The N-terminal domain of the Aurora-A Phe-31 variant encodes an E3 ubiquitin ligase and mediates ubiquitination of IκBα.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3343, doi. 10.1093/hmg/ddl410

By:

Briassouli, Paraskevi;
Chan, Florence;
Linardopoulos, Spiros

Publication type:

Article

Sesn1 is a novel gene for left–right asymmetry and mediating nodal signaling.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3369, doi. 10.1093/hmg/ddl413

By:

Peeters, Hilde;
Voz, Marianne L.;
Verschueren, Kristin;
De Cat, Bart;
Pendeville, Hélène;
Thienpont, Bernard;
Schellens, Ann;
Belmont, John W.;
David, Guido;
Van De Ven, Wim J.M.;
Fryns, Jean-Pierre;
Gewillig, Marc;
Huylebroeck, Danny;
Peers, Bernard;
Devriendt, Koen

Publication type:

Article

Evidence in favor of the contribution of genes involved in the maintenance of the extracellular matrix of the arterial wall to the development of intracranial aneurysms.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3361, doi. 10.1093/hmg/ddl412

By:

Ruigrok, Ynte M.;
Rinkel, Gabriël J.E.;
van't Slot, Ruben;
Wolfs, Marcel;
Tang, Song;
Wijmenga, Cisca

Publication type:

Article

Identification of susceptibility loci for cervical carcinoma by genome scan of affected sib-pairs.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3351, doi. 10.1093/hmg/ddl411

By:

Engelmark, Malin T.;
Ivansson, Emma L.;
Magnusson, Jessica J.;
Gustavsson, Inger M.;
Beskow, Anna H.;
Magnusson, Patrik K.E.;
Gyllensten, Ulf B.

Publication type:

Article

Haplotypes spanning SPEC2, PDZ-GEF2 and ACSL6 genes are associated with schizophrenia.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3329, doi. 10.1093/hmg/ddl409

By:

Chen, Xiangning;
Wang, Xu;
Hossain, Shaon;
O'Neill, F. Anthony;
Walsh, Dermot;
Pless, Lora;
Chowdari, Kodavali V.;
Nimgaonkar, Vishwajit L.;
Schwab, Sibylle G.;
Wildenauer, Dieter B.;
Sullivan, Patrick F.;
van den Oord, Edwin;
Kendler, Kenneth S.

Publication type:

Article

Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3324, doi. 10.1093/hmg/ddl408

By:

Keen-Kim, Dianne;
Mathews, Carol A.;
Reus, Victor I.;
Lowe, Thomas L.;
Herrera, Luis Diego;
Budman, Cathy L.;
Gross-Tsur, Varda;
Pulver, Ann E.;
Bruun, Ruth D.;
Erenberg, Gerald;
Naarden, Allan;
Sabatti, Chiara;
Freimer, Nelson B.

Publication type:

Article

A major susceptibility locus for HTLV-1 infection in childhood maps to chromosome 6q27.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3306, doi. 10.1093/hmg/ddl406

By:

Plancoulaine, Sabine;
Gessain, Antoine;
Tortevoye, Patricia;
Boland-Auge, Anne;
Vasilescu, Alexandre;
Matsuda, Fumihiko;
Abel, Laurent

Publication type:

Article

Analysis of Nsdhl-deficient embryos reveals a role for Hedgehog signaling in early placental development.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3293, doi. 10.1093/hmg/ddl405

By:

Jiang, Fenglei;
Herman, Gail E.

Publication type:

Article

Kinesin-2 mediates physical and functional interactions between polycystin-2 and fibrocystin.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3280, doi. 10.1093/hmg/ddl404

By:

Wu, Yuliang;
Dai, Xiao-Qing;
Li, Qiang;
Chen, Carl X.;
Mai, Weiyi;
Hussain, Zahir;
Long, Wentong;
Montalbetti, Nicolás;
Li, Guochun;
Glynne, Richard;
Wang, Shaohua;
Cantiello, Horacio F.;
Wu, Guanqing;
Chen, Xing-Zhen

Publication type:

Article

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3273, doi. 10.1093/hmg/ddl403

By:

Hardisty-Hughes, Rachel E.;
Tateossian, Hilda;
Morse, Susan A.;
Romero, M. Rosario;
Middleton, Alice;
Tymowska-Lalanne, Zuzanna;
Hunter, A. Jackie;
Cheeseman, Michael;
Brown, Steve D.M.

Publication type:

Article

DISC1–NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 22, p. 3313, doi. 10.1093/hmg/ddl407

By:

Kamiya, Atsushi;
Tomoda, Toshifumi;
Chang, Jennifer;
Takaki, Manabu;
Zhan, Caixin;
Morita, Masahiko;
Cascio, Matthew B.;
Elashvili, Sarah;
Koizumi, Hiroyuki;
Takanezawa, Yasukazu;
Dickerson, Faith;
Yolken, Robert;
Arai, Hiroyuki;
Sawa, Akira

Publication type:

Article