Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 10

Results: 18

New susceptibility locus for hypertension on chromosome 8q by efficient pedigree-breaking in an Italian isolate.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1735, doi. 10.1093/hmg/ddl097

By:

Ciullo, Marina;
Bellenguez, Céline;
Colonna, Vincenza;
Nutile, Teresa;
Calabria, Antonietta;
Pacente, Rosalinda;
Iovino, Gianluigi;
Trimarco, Bruno;
Bourgain, Catherine;
Persico, M. Graziella

Publication type:

Article

A haplotype spanning two genes, ELN and LIMK1, decreases their transcripts and confers susceptibility to intracranial aneurysms.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1722, doi. 10.1093/hmg/ddl096

By:

Akagawa, Hiroyuki;
Tajima, Atsushi;
Sakamoto, Yoshiko;
Krischek, Boris;
Yoneyama, Taku;
Kasuya, Hidetoshi;
Onda, Hideaki;
Hori, Tomokatsu;
Kubota, Motoo;
Machida, Toshio;
Saeki, Naokatsu;
Hata, Akira;
Hashiguchi, Kazunari;
Kimura, Eizou;
Kim, Chul-Jin;
Yang, Tae-Ki;
Lee, Jong-Young;
Kimm, Kuchan;
Inoue, Ituro

Publication type:

Article

Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1713

By:

Björkqvist, Maria;
Petersén, Åsa;
Bacos, Karl;
Isaacs, Jeremy;
Norlén, Per;
Gil, Joana;
Popovic, Natalija;
Sundler, Frank;
Bates, Gillian P.;
Tabrizi, Sarah J.;
Brundin, Patrik;
Mulder, Hindrik

Publication type:

Article

E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1704, doi. 10.1093/hmg/ddl093

By:

Pereira, Paulo S.;
Teixeira, Alexandra;
Pinho, Sofia;
Ferreira, Paulo;
Fernandes, Joana;
Oliveira, Carla;
Seruca, Raquel;
Suriano, Gianpaolo;
Casares, Fernando

Publication type:

Article

Early development of aberrant synaptic plasticity in a mouse model of Huntington's disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1690, doi. 10.1093/hmg/ddl092

By:

Milnerwood, Austen J.;
Cummings, Damian M.;
Dallérac, Glenn M.;
Brown, Jacki Y.;
Vatsavayai, Sarat C.;
Hirst, Mark C.;
Rezaie, Payam;
Murphy, Kerry P.S.J.

Publication type:

Article

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1680, doi. 10.1093/hmg/ddl091

By:

Shu, Xinhua;
Tulloch, Brian;
Lennon, Alan;
Vlachantoni, Dafni;
Zhou, Xinzhi;
Hayward, Caroline;
Wright, Alan F.

Publication type:

Article

Neuropeptide S and G protein-coupled receptor 154 modulate macrophage immune responses.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1667, doi. 10.1093/hmg/ddl090

By:

Pulkkinen, Ville;
Majuri, Marja-Leena;
Wang, Guoying;
Holopainen, Päivi;
Obase, Yasushi;
Vendelin, Johanna;
Wolff, Henrik;
Rytilä, Paula;
Laitinen, Lauri A.;
Haahtela, Tari;
Laitinen, Tarja;
Alenius, Harri;
Kere, Juha;
Rehn, Marko

Publication type:

Article

The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1659, doi. 10.1093/hmg/ddl089

By:

Paracchini, Silvia;
Thomas, Ankur;
Castro, Sandra;
Lai, Cecilia;
Paramasivam, Murugan;
Wang, Yu;
Keating, Brendan J.;
Taylor, Jennifer M.;
Hacking, Douglas F.;
Scerri, Thomas;
Francks, Clyde;
Richardson, Alex J.;
Wade-Martins, Richard;
Stein, John F.;
Knight, Julian C.;
Copp, Andrew J.;
LoTurco, Joseph;
Monaco, Anthony P.

Publication type:

Article

Genetic linkage of hyperglycemia, body weight and serum amyloid-P in an intercross between C57BL/6 and C3H apolipoprotein E-deficient mice.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1650, doi. 10.1093/hmg/ddl088

By:

Su, Zhiguang;
Li, Yuhua;
James, Jessica C.;
Matsumoto, Alan H.;
Helm, Gregory A.;
Lusis, Aldons J.;
Shi, Weibin

Publication type:

Article

Genetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) study.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1640, doi. 10.1093/hmg/ddl085

By:

Lee, Craig R.;
North, Kari E.;
Bray, Molly S.;
Fornage, Myriam;
Seubert, John M.;
Newman, John W.;
Hammock, Bruce D.;
Couper, David J.;
Heiss, Gerardo;
Zeldin, Darryl C.

Publication type:

Article

Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1629, doi. 10.1093/hmg/ddl084

By:

Arnold, Jelena S.;
Braunstein, Evan M.;
Ohyama, Takahiro;
Groves, Andrew K.;
Adams, Joe C.;
Brown, M. Christian;
Morrow, Bernice E.

Publication type:

Article

Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1623, doi. 10.1093/hmg/ddl083

By:

Kleopa, Kleopas A.;
Drousiotou, Anthi;
Mavrikiou, Eleni;
Ormiston, Annita;
Kyriakides, Theodoros

Publication type:

Article

A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1610, doi. 10.1093/hmg/ddl082

By:

Li, Sheng;
Kimura, En;
Ng, Rainer;
Fall, Brent M.;
Meuse, Leonard;
Reyes, Morayma;
Faulkner, John A.;
Chamberlain, Jeffrey S.

Publication type:

Article

WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic β-cells.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1600, doi. 10.1093/hmg/ddl081

By:

Yamada, Takahiro;
Ishihara, Hisamitsu;
Tamura, Akira;
Takahashi, Rui;
Yamaguchi, Suguru;
Takei, Daisuke;
Tokita, Ai;
Satake, Chihiro;
Tashiro, Fumi;
Katagiri, Hideki;
Aburatani, Hiroyuki;
Miyazaki, Jun-ichi;
Oka, Yoshitomo

Publication type:

Article

C-termini of P/Q-type Ca2+ channel α1A subunits translocate to nuclei and promote polyglutamine-mediated toxicity.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1587, doi. 10.1093/hmg/ddl080

By:

Kordasiewicz, Holly B.;
Thompson, Randall M.;
Clark, H. Brent;
Gomez, Christopher M.

Publication type:

Article

Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1580, doi. 10.1093/hmg/ddl078

By:

Kim, Sung-Jo;
Zhang, Zhongjian;
Lee, Yi-Ching;
Mukherjee, Anil B.

Publication type:

Article

A quantitative trait locus (QTL) on chromosome 6q influences birth weight in two independent family studies.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1569, doi. 10.1093/hmg/ddl076

By:

Arya, Rector;
Demerath, Ellen;
Jenkinson, Christopher P.;
Göring, Harald H.H.;
Puppala, Sobha;
Farook, Vidya;
Fowler, Sharon;
Schneider, Jennifer;
Granato, Richard;
Resendez, Roy G.;
Dyer, Thomas D.;
Cole, Shelley A.;
Almasy, Laura;
Comuzzie, Anthony G.;
Siervogel, Roger M.;
Bradshaw, Benjamin;
DeFronzo, Ralph A.;
MacCluer, Jean;
Stern, Michael P.;
Towne, Bradford

Publication type:

Article

Genetic variation in DTNBP1 influences general cognitive ability.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 10, p. 1563, doi. 10.1093/hmg/ddi481

By:

Burdick, Katherine E.;
Lencz, Todd;
Funke, Birgit;
Finn, Christine T.;
Szeszko, Philip R.;
Kane, John M.;
Kucherlapati, Raju;
Malhotra, Anil K.

Publication type:

Article