Works matching IS 09646906 AND DT 2006 AND VI 15 AND IP 14

Results: 10

Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD).

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2276, doi. 10.1093/hmg/ddl152

By:

Li, Dawei;
Sham, Pak C.;
Owen, Michael J.;
He, Lin

Publication type:

Article

Smooth muscle-specific dystrophin expression improves aberrant vasoregulation in mdx mice.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2266, doi. 10.1093/hmg/ddl151

By:

Ito, Kaori;
Kimura, Shigemi;
Ozasa, Shiro;
Matsukura, Makoto;
Ikezawa, Makoto;
Yoshioka, Kowashi;
Ueno, Hiroe;
Suzuki, Misao;
Araki, Kimi;
Yamamura, Ken-ichi;
Miwa, Takeshi;
Dickson, George;
Thomas, Gail D.;
Miike, Teruhisa

Publication type:

Article

Role of genomic architecture in PLP1 duplication causing Pelizaeus-Merzbacher disease.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2250, doi. 10.1093/hmg/ddl150

By:

Lee, Jennifer A.;
Inoue, Ken;
Cheung, Sau W.;
Shaw, Chad A.;
Stankiewicz, Pawel;
Lupski, James R.

Publication type:

Article

Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2239, doi. 10.1093/hmg/ddl149

By:

Becherel, Olivier J.;
Gueven, Nuri;
Birrell, Geoff W.;
Schreiber, Valérie;
Suraweera, Amila;
Jakob, Burkhard;
Taucher-Scholz, Gisela;
Lavin, Martin F.

Publication type:

Article

Loss of endogenous androgen receptor protein accelerates motor neuron degeneration and accentuates androgen insensitivity in a mouse model of X-linked spinal and bulbar muscular atrophy.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2225, doi. 10.1093/hmg/ddl148

By:

Thomas, Patrick S.;
Fraley, Gregory S.;
Damien, Vincent;
Woodke, Lillie B.;
Zapata, Francisco;
Sopher, Bryce L.;
Plymate, Stephen R.;
La Spada, Albert R.

Publication type:

Article

Isomers of the TCF1 gene encoding hepatocyte nuclear factor-1 alpha show differential expression in the pancreas and define the relationship between mutation position and clinical phenotype in monogenic diabetes.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2216, doi. 10.1093/hmg/ddl147

By:

Harries, Lorna W.;
Ellard, Sian;
Stride, Amanda

Publication type:

Article

Ube3a expression is not altered in Mecp2 mutant mice.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2210, doi. 10.1093/hmg/ddl146

By:

Jordan, ChaRandle;
Francke, Uta

Publication type:

Article

Calcium-sensing receptor dimerizes in the endoplasmic reticulum: biochemical and biophysical characterization of CASR mutants retained intracellularly.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2200, doi. 10.1093/hmg/ddl145

By:

Pidasheva, Svetlana;
Grant, Michael;
Canaff, Lucie;
Ercan, Oya;
Kumar, Ujendra;
Hendy, Geoffrey N.

Publication type:

Article

Intronic variants in the dopa decarboxylase (DDC) gene are associated with smoking behavior in European-Americans and African-Americans.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2192, doi. 10.1093/hmg/ddl144

By:

Yu, Yi;
Panhuysen, Carolien;
Kranzler, Henry R.;
Hesselbrock, Victor;
Rounsaville, Bruce;
Weiss, Roger;
Brady, Kathleen;
Farrer, Lindsay A.;
Gelernter, Joel

Publication type:

Article

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 14, p. 2185, doi. 10.1093/hmg/ddl143

By:

Olson, Timothy M.;
Alekseev, Alexey E.;
Liu, Xiaoke K.;
Park, Sungjo;
Zingman, Leonid V.;
Bienengraeber, Martin;
Sattiraju, Srinivasan;
Ballew, Jeffrey D.;
Jahangir, Arshad;
Terzic, Andre

Publication type:

Article