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