Works matching IS 09646906 AND DT 2009 AND VI 18 AND IP 11

Results: 22

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Published in:: Human Molecular Genetics, 2009, v. 18, n. 11, p. NP, doi. 10.1093/hmg/ddp175
Publication type:: Article

Cover Page.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 11, p. NP, doi. 10.1093/hmg/ddp173
Publication type:: Article

Short 42°C heat shock induces phosphorylation and degradation of Cdc25A which depends on p38MAPK, Chk2 and 14.3.3.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1990, doi. 10.1093/hmg/ddp123

By:

Madlener, Sibylle;
Rosner, Margit;
Krieger, Sigurd;
Giessrigl, Benedikt;
Gridling, Manuela;
Vo, Thanh Phuong Nha;
Leisser, Christina;
Lackner, Andreas;
Raab, Ingrid;
Grusch, Michael;
Hengstschläger, Markus;
Dolznig, Helmut;
Krupitza, Georg

Publication type:

Article

Attenuated muscle regeneration is a key factor in dysferlin-deficient muscular dystrophy.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1976, doi. 10.1093/hmg/ddp121

By:

Chiu, Yen-Hui;
Hornsey, Mark A.;
Klinge, Lars;
Jørgensen, Louise H.;
Laval, Steven H.;
Charlton, Richard;
Barresi, Rita;
Straub, Volker;
Lochmüller, Hanns;
Bushby, Kate

Publication type:

Article

Genetic interaction between the m-AAA protease isoenzymes reveals novel roles in cerebellar degeneration.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2001, doi. 10.1093/hmg/ddp124

By:

Martinelli, Paola;
La Mattina, Veronica;
Bernacchia, Andrea;
Magnoni, Raffaella;
Cerri, Federica;
Cox, Gregory;
Quattrini, Angelo;
Casari, Giorgio;
Rugarli, Elena I.

Publication type:

Article

Reproductive and epigenetic outcomes associated with aging mouse oocytes.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2032, doi. 10.1093/hmg/ddp127

By:

Lopes, Flavia L.;
Fortier, Amanda L.;
Darricarrère, Nicole;
Chan, Donovan;
Arnold, Daniel R.;
Trasler, Jacquetta M.

Publication type:

Article

The STAT4 gene influences the genetic predisposition to systemic sclerosis phenotype.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2071, doi. 10.1093/hmg/ddp119

By:

Rueda, B.;
Broen, J.;
Simeon, C.;
Hesselstrand, R.;
Diaz, B.;
Suárez, H.;
Ortego-Centeno, N.;
Riemekasten, G.;
Fonollosa, V.;
Vonk, M.C.;
van den Hoogen, F.H.J.;
Sanchez-Román, J.;
Aguirre-Zamorano, M.A.;
García-Portales, R.;
Pros, A.;
Camps, M.T.;
Gonzalez-Gay, M.A.;
Coenen, M.J.H.;
Airo, P.;
Beretta, L.

Publication type:

Article

A novel interaction between fibroblast growth factor receptor 3 and the p85 subunit of phosphoinositide 3-kinase: activation-dependent regulation of ERK by p85 in multiple myeloma cells.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1951, doi. 10.1093/hmg/ddp116

By:

Salazar, Lisa;
Kashiwada, Tamara;
Krejci, Pavel;
Muchowski, Paul;
Donoghue, Daniel;
Wilcox, William R.;
Thompson, Leslie Michels

Publication type:

Article

Distinct mutations in the glycogen debranching enzyme found in glycogen storage disease type III lead to impairment in diverse cellular functions.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2045, doi. 10.1093/hmg/ddp128

By:

Cheng, Alan;
Zhang, Mei;
Okubo, Minoru;
Omichi, Kaoru;
Saltiel, Alan R.

Publication type:

Article

Cytoplasmic retention of polyglutamine-expanded androgen receptor ameliorates disease via autophagy in a mouse model of spinal and bulbar muscular atrophy.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1937, doi. 10.1093/hmg/ddp115

By:

Montie, Heather L.;
Cho, Maria S.;
Holder, Latia;
Liu, Yuhong;
Tsvetkov, Andrey S.;
Finkbeiner, Steven;
Merry, Diane E.

Publication type:

Article

Molecular mechanisms for subtelomeric rearrangements associated with the 9q34.3 microdeletion syndrome.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1924, doi. 10.1093/hmg/ddp114

By:

Yatsenko, Svetlana A.;
Brundage, Ellen K.;
Roney, Erin K.;
Cheung, Sau Wai;
Chinault, A. Craig;
Lupski, James R.

Publication type:

Article

Pathway and network-based analysis of genome-wide association studies in multiple sclerosis.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2078

By:

Baranzini, Sergio E.;
Galwey, Nicholas W.;
Wang, Joanne;
Khankhanian, Pouya;
Lindberg, Raija;
Pelletier, Daniel;
Wu, Wen;
Uitdehaag, Bernard M.J.;
Kappos, Ludwig;
Polman, Chris H.;
Matthews, Paul M.;
Hauser, Stephen L.;
Gibson, Rachel A.;
Oksenberg, Jorge R.;
Barnes, Michael R.

Publication type:

Article

ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2063, doi. 10.1093/hmg/ddp118

By:

Yang, Wanling;
Zhao, Minghui;
Hirankarn, Nattiya;
Lau, Chak Sing;
Mok, Chi Chiu;
Chan, Tak Mao;
Wong, Raymond W.S.;
Lee, Ka Wing;
Mok, Mo Yin;
Wong, Sik Nin;
Avihingsanon, Yingyos;
N.G., Irene Oi Lin;
Lee, Tsz Leung;
Ho, Marco Hok Kung;
Lee, Pamela Pui Wah;
Wong, Wilfred Hing Sang;
Sham, Pak Chung;
Lau, Yu Lung

Publication type:

Article

Association of TRPV4 gene polymorphisms with chronic obstructive pulmonary disease.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2053

By:

Zhu, Guohua;
Gulsvik, Amund;
Bakke, Per;
Ghatta, Srinivas;
Anderson, Wayne;
Lomas, David A.;
Silverman, Edwin K.;
Pillai, Sreekumar G.

Publication type:

Article

Admixture mapping of quantitative trait loci for blood lipids in African-Americans.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2091, doi. 10.1093/hmg/ddp122

By:

Basu, Analabha;
Tang, Hua;
Lewis, Cora E.;
North, Kari;
Curb, J. David;
Quertermous, Thomas;
Mosley, Thomas H.;
Boerwinkle, Eric;
Zhu, Xiaofeng;
Risch, Neil J.

Publication type:

Article

Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1909, doi. 10.1093/hmg/ddp112

By:

Layman, W.S.;
McEwen, D.P.;
Beyer, L.A.;
Lalani, S.R.;
Fernbach, S.D.;
Oh, E.;
Swaroop, A.;
Hegg, C.C.;
Raphael, Y.;
Martens, J.R.;
Martin, D.M.

Publication type:

Article

Defects in myelination, paranode organization and Purkinje cell innervation in the ether lipid-deficient mouse cerebellum.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1897, doi. 10.1093/hmg/ddp110

By:

Teigler, Andre;
Komljenovic, Dorde;
Draguhn, Andreas;
Gorgas, Karin;
Just, Wilhelm W.

Publication type:

Article

Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2024, doi. 10.1093/hmg/ddp126

By:

Palma, Elena;
Tiepolo, Tania;
Angelin, Alessia;
Sabatelli, Patrizia;
Maraldi, Nadir M.;
Basso, Emy;
Forte, Michael A.;
Bernardi, Paolo;
Bonaldo, Paolo

Publication type:

Article

Identification of interactive networks of gene expression associated with osteosarcoma oncogenesis by integrated molecular profiling.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 1962, doi. 10.1093/hmg/ddp117

By:

Sadikovic, Bekim;
Yoshimoto, Maisa;
Chilton-MacNeill, Susan;
Thorner, Paul;
Squire, Jeremy A.;
Zielenska, Maria

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 11, p. NP, doi. 10.1093/hmg/ddp172
Publication type:: Article

A mutation linked to retinitis pigmentosa in HPRP31 causes protein instability and impairs its interactions with spliceosomal snRNPs.

Published in:

Human Molecular Genetics, 2009, v. 18, n. 11, p. 2014, doi. 10.1093/hmg/ddp125

By:

Huranová, Martina;
Hnilicová, Jarmila;
Fleischer, Branislav;
Cvačková, Zuzana;
Staněk, David

Publication type:

Article

Editorial Board.

Published in:: Human Molecular Genetics, 2009, v. 18, n. 11, p. NP, doi. 10.1093/hmg/ddp174
Publication type:: Article