Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 8

Results: 14

Polymorphisms in thrombospondin genes and myocardial infarction: a case–control study and a meta-analysis of available evidence.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1120, doi. 10.1093/hmg/ddn001

By:

Koch, Werner;
Hoppmann, Petra;
de Waha, Antoinette;
Schömig, Albert;
Kastrati, Adnan

Publication type:

Article

Polycystin-2 is regulated by endoplasmic reticulum-associated degradation.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1109, doi. 10.1093/hmg/ddm383

By:

Liang, Genqing;
Li, Qiang;
Tang, Yan;
Kokame, Koichi;
Kikuchi, Tadashi;
Wu, Guanqing;
Chen, Xing-Zhen

Publication type:

Article

An Actn3 knockout mouse provides mechanistic insights into the association between α-actinin-3 deficiency and human athletic performance.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1076, doi. 10.1093/hmg/ddm380

By:

MacArthur, Daniel G.;
Seto, Jane T.;
Chan, Stephen;
Quinlan, Kate G.R.;
Raftery, Joanna M.;
Turner, Nigel;
Nicholson, Megan D.;
Kee, Anthony J.;
Hardeman, Edna C.;
Gunning, Peter W.;
Cooney, Gregory J.;
Head, Stewart I.;
Yang, Nan;
North, Kathryn N.

Publication type:

Article

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1169, doi. 10.1093/hmg/ddn006

By:

Bray, Nicholas J.;
Holmans, Peter A.;
van den Bree, Marianne B.;
Jones, Lesley;
Elliston, Lyn A.;
Hughes, Gareth;
Richards, Alexander L.;
Williams, Nigel M.;
Craddock, Nick;
Owen, Michael J.;
O'Donovan, Michael C.

Publication type:

Article

Atypical Mowat–Wilson patient confirms the importance of the novel association between ZFHX1B/SIP1 and NuRD corepressor complex.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1175, doi. 10.1093/hmg/ddn007

By:

Verstappen, Griet;
van Grunsven, Leo A.;
Michiels, Christine;
Van de Putte, Tom;
Souopgui, Jacob;
Van Damme, Jozef;
Bellefroid, Eric;
Vandekerckhove, Joël;
Huylebroeck, Danny

Publication type:

Article

Analysis of copy number variation in the rhesus macaque genome identifies candidate loci for evolutionary and human disease studies.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1127, doi. 10.1093/hmg/ddn002

By:

Lee, Arthur S.;
Gutiérrez-Arcelus, María;
Perry, George H.;
Vallender, Eric J.;
Johnson, Welkin E.;
Miller, Gregory M.;
Korbel, Jan O.;
Lee, Charles

Publication type:

Article

Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1137, doi. 10.1093/hmg/ddn003

By:

Metzger, Silke;
Rong, Juan;
Nguyen, Huu-Phuc;
Cape, Austin;
Tomiuk, Juergen;
Soehn, Anne S.;
Propping, Peter;
Freudenberg-Hua, Yun;
Freudenberg, Jan;
Tong, Liang;
Li, Shi-Hua;
Li, Xiao-Jiang;
Riess, Olaf

Publication type:

Article

MeCP2-dependent repression of an imprinted miR-184 released by depolarization.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1192, doi. 10.1093/hmg/ddn011

By:

Nomura, Tasuku;
Kimura, Mika;
Horii, Takuro;
Morita, Sumiyo;
Soejima, Hidenobu;
Kudo, Shinichi;
Hatada, Izuho

Publication type:

Article

Dysregulation of miRNA 181b in the temporal cortex in schizophrenia.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1156, doi. 10.1093/hmg/ddn005

By:

Beveridge, Natalie J.;
Tooney, Paul A.;
Carroll, Adam P.;
Gardiner, Erin;
Bowden, Nikola;
Scott, Rodney J.;
Tran, Nham;
Dedova, Irina;
Cairns, Murray J.

Publication type:

Article

Two different forms of palindrome resolution in the human genome: deletion or translocation.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1184, doi. 10.1093/hmg/ddn008

By:

Kato, Takema;
Inagaki, Hidehito;
Kogo, Hiroshi;
Ohye, Tamae;
Yamada, Kouji;
Emanuel, Beverly S.;
Kurahashi, Hiroki

Publication type:

Article

Genetic variation in the CRP promoter: association with systemic lupus erythematosus.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1147, doi. 10.1093/hmg/ddn004

By:

Edberg, Jeffrey C.;
Wu, Jianming;
Langefeld, Carl D.;
Brown, Elizabeth E.;
Marion, Miranda C.;
McGwin, Gerald;
Petri, Michelle;
Ramsey-Goldman, Rosalind;
Reveille, John D.;
Frank, Summer G.;
Kaufman, Kenneth M.;
Harley, John B.;
Alarcón, Graciela S.;
Kimberly, Robert P.

Publication type:

Article

Genetic and epigenetic mechanisms combine to control MMP1 expression and its association with preterm premature rupture of membranes.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1087, doi. 10.1093/hmg/ddm381

By:

Wang, Hongyan;
Ogawa, Masaki;
Wood, Jennifer R.;
Bartolomei, Marisa S.;
Sammel, Mary D.;
Kusanovic, Juan Pedro;
Walsh, Scott W.;
Romero, Roberto;
Strauss, Jerome F.

Publication type:

Article

Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the oculopharyngeal muscular dystrophy mutation.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1097, doi. 10.1093/hmg/ddm382

By:

Davies, Janet E.;
Sarkar, Sovan;
Rubinsztein, David C.

Publication type:

Article

Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect.

Published in:

Human Molecular Genetics, 2008, v. 17, n. 8, p. 1063, doi. 10.1093/hmg/ddm379

By:

Gavrilina, Tatiana O.;
McGovern, Vicki L.;
Workman, Eileen;
Crawford, Thomas O.;
Gogliotti, Rocky G.;
DiDonato, Christine J.;
Monani, Umrao R.;
Morris, Glenn E.;
Burghes, Arthur H.M.

Publication type:

Article