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

Results: 22

Subscription Page.
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
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
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
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 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
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
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
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
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
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