Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 6

Results: 14

The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 859, doi. 10.1093/hmg/ddm358

By:

Velayos-Baeza, Antonio;
Toma, Claudio;
Paracchini, Silvia;
Monaco, Anthony P.

Publication type:

Article

AKT-sensitive or insensitive pathways of toxicity in glial cells and neurons in Drosophila models of Huntington's disease.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 882

By:

Liévens, Jean-Charles;
Iché, Magali;
Laval, Monique;
Faivre-Sarrailh, Catherine;
Birman, Serge

Publication type:

Article

Ubiquitination of α-synuclein by Siah-1 promotes α-synuclein aggregation and apoptotic cell death.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 906

By:

Lee, James T.;
Wheeler, Tiffany C.;
Li, Lian;
Chin, Lih-Shen

Publication type:

Article

A scan for genetic determinants of human hair morphology: EDAR is associated with Asian hair thickness.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 835, doi. 10.1093/hmg/ddm355

By:

Fujimoto, Akihiro;
Kimura, Ryosuke;
Ohashi, Jun;
Omi, Kazuya;
Yuliwulandari, Rika;
Batubara, Lilian;
Mustofa, Mohammad Syamsul;
Samakkarn, Urai;
Settheetham-Ishida, Wannapa;
Ishida, Takafumi;
Morishita, Yasuyuki;
Furusawa, Takuro;
Nakazawa, Minato;
Ohtsuka, Ryutaro;
Tokunaga, Katsushi

Publication type:

Article

Haemoglobin S and haemoglobin C: ‘quick but costly’ versus ‘slow but gratis’ genetic adaptations to Plasmodium falciparum malaria.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 789

By:

Modiano, David;
Bancone, Germana;
Ciminelli, Bianca Maria;
Pompei, Fiorenza;
Blot, Isa;
Simporé, Jacques;
Modiano, Guido

Publication type:

Article

Comprehensive association testing of common genetic variation in DNA repair pathway genes in relationship with breast cancer risk in multiple populations.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 825, doi. 10.1093/hmg/ddm354

By:

Haiman, Christopher A.;
Hsu, Chris;
de Bakker, Paul I.W.;
Frasco, Melissa;
Sheng, Xin;
Van Den Berg, David;
Casagrande, John T.;
Kolonel, Laurence N.;
Le Marchand, Loic;
Hankinson, Susan E.;
Han, Jiali;
Dunning, Alison M.;
Pooley, Karen A.;
Freedman, Matthew L.;
Hunter, David J.;
Wu, Anna H.;
Stram, Daniel O.;
Henderson, Brian E.

Publication type:

Article

Major genetic components underlying alcoholism in Korean population.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 854, doi. 10.1093/hmg/ddm357

By:

Kim, Dai-Jin;
Choi, Ihn-Geun;
Park, Byung Lae;
Lee, Boung-Chul;
Ham, Byung-Joo;
Yoon, Sujung;
Bae, Joon Seol;
Cheong, Hyun Sub;
Shin, Hyoung Doo

Publication type:

Article

Comprehensive evaluation of the genetic variants of interferon regulatory factor 5 (IRF5) reveals a novel 5 bp length polymorphism as strong risk factor for systemic lupus erythematosus.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 872, doi. 10.1093/hmg/ddm359

By:

Sigurdsson, Snaevar;
Göring, Harald H.H.;
Kristjansdottir, Gudlaug;
Milani, Lili;
Nordmark, Gunnel;
Sandling, Johanna K.;
Eloranta, Maija-Leena;
Feng, Di;
Sangster-Guity, Niquiche;
Gunnarsson, Iva;
Svenungsson, Elisabet;
Sturfelt, Gunnar;
Jönsen, Andreas;
Truedsson, Lennart;
Barnes, Betsy J.;
Alm, Gunnar;
Rönnblom, Lars;
Syvänen, Ann-Christine

Publication type:

Article

Transcriptional activators HAP/NF-Y rescue a cytochrome c oxidase defect in yeast and human cells.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 775, doi. 10.1093/hmg/ddm349

By:

Fontanesi, Flavia;
Jin, Can;
Tzagoloff, Alexander;
Barrientos, Antoni

Publication type:

Article

Comprehensive analysis of the role of DNA repair gene polymorphisms on risk of glioma.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 800, doi. 10.1093/hmg/ddm351

By:

Bethke, Lara;
Webb, Emily;
Murray, Anne;
Schoemaker, Minouk;
Johansen, Christoffer;
Christensen, Helle Collatz;
Muir, Kenneth;
McKinney, Patricia;
Hepworth, Sarah;
Dimitropoulou, Polyxeni;
Lophatananon, Artitaya;
Feychting, Maria;
Lönn, Stefan;
Ahlbom, Anders;
Malmer, Beatrice;
Henriksson, Roger;
Auvinen, Anssi;
Kiuru, Anne;
Salminen, Tiina;
Swerdlow, Anthony

Publication type:

Article

Noggin heterozygous mice: an animal model for congenital conductive hearing loss in humans.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 844, doi. 10.1093/hmg/ddm356

By:

Hwang, Chan-Ho;
Wu, Doris K.

Publication type:

Article

p21-activated kinase 1 promotes soluble mutant huntingtin self-interaction and enhances toxicity.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 895, doi. 10.1093/hmg/ddm362

By:

Luo, Shouqing;
Mizuta, Haruo;
Rubinsztein, David C.

Publication type:

Article

Enzyme replacement therapy in a murine model of Morquio A syndrome.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 815

By:

Tomatsu, Shunji;
Montaño, Adriana M.;
Ohashi, Amiko;
Gutierrez, Monica A.;
Oikawa, Hirotaka;
Oguma, Toshihiro;
Dung, Vu Chi;
Nishioka, Tatsuo;
Orii, Tadao;
Sly, William S.

Publication type:

Article

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 6, p. 806, doi. 10.1093/hmg/ddm352

By:

Broadbent, Helen M.;
Peden, John F.;
Lorkowski, Stefan;
Goel, Anuj;
Ongen, Halit;
Green, Fiona;
Clarke, Robert;
Collins, Rory;
Franzosi, Maria Grazia;
Tognoni, Gianni;
Seedorf, Udo;
Rust, Stephan;
Eriksson, Per;
Hamsten, Anders;
Farrall, Martin;
Watkins, Hugh

Publication type:

Article