Works matching IS 09646906 AND DT 2008 AND VI 17 AND IP 5

Results: 13

Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 759, doi. 10.1093/hmg/ddm348
By:
- Li, Yonghong;
- Grupe, Andrew;
- Rowland, Charles;
- Holmans, Peter;
- Segurado, Ricardo;
- Abraham, Richard;
- Jones, Lesley;
- Catanese, Joseph;
- Ross, David;
- Mayo, Kevin;
- Martinez, Maribel;
- Hollingworth, Paul;
- Goate, Alison;
- Cairns, Nigel J.;
- Racette, Brad A.;
- Perlmutter, Joel S.;
- O'Donovan, Michael C.;
- Morris, John C.;
- Brayne, Carol;
- Rubinsztein, David C.
Publication type:
Article
A network of dopaminergic gene variations implicated as risk factors for schizophrenia.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 747, doi. 10.1093/hmg/ddm347
By:
- Talkowski, Michael E.;
- Kirov, George;
- Bamne, Mikhil;
- Georgieva, Lyudmila;
- Torres, Gonzalo;
- Mansour, Hader;
- Chowdari, Kodavali V.;
- Milanova, Vihra;
- Wood, Joel;
- McClain, Lora;
- Prasad, Konasale;
- Shirts, Brian;
- Zhang, Jianping;
- O’Donovan, Michael C.;
- Owen, Michael J.;
- Devlin, Bernie;
- Nimgaonkar, Vishwajit L.
Publication type:
Article
The neuronal nicotinic receptor subunit genes (CHRNA6 and CHRNB3) are associated with subjective responses to tobacco.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 724
By:
- Zeiger, Joanna S.;
- Haberstick, Brett C.;
- Schlaepfer, Isabel;
- Collins, Allan C.;
- Corley, Robin P.;
- Crowley, Thomas J.;
- Hewitt, John K.;
- Hopfer, Christian J.;
- Lessem, Jeffrey;
- McQueen, Matthew B.;
- Rhee, Soo Hyun;
- Ehringer, Marissa A.
Publication type:
Article
The Friedreich ataxia GAA repeat expansion mutation induces comparable epigenetic changes in human and transgenic mouse brain and heart tissues.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 735
By:
- Al-Mahdawi, Sahar;
- Pinto, Ricardo Mouro;
- Ismail, Ozama;
- Varshney, Dhaval;
- Lymperi, Stefania;
- Sandi, Chiranjeevi;
- Trabzuni, Daniah;
- Pook, Mark
Publication type:
Article
Long, abundantly expressed non-coding transcripts are altered in cancer.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 642, doi. 10.1093/hmg/ddm336
By:
- Perez, Damon S.;
- Hoage, Tiffany R.;
- Pritchett, Jay R.;
- Ducharme-Smith, Allison L.;
- Halling, Meredith L.;
- Ganapathiraju, Sree C.;
- Streng, Paul S.;
- Smith, David I.
Publication type:
Article
SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 656, doi. 10.1093/hmg/ddm337
By:
- Vithana, Eranga N.;
- Morgan, Patricio E.;
- Ramprasad, Vedam;
- Tan, Donald T.H.;
- Yong, Victor H.K;
- Venkataraman, Divya;
- Venkatraman, Anandalakshmi;
- Yam, Gary H.F.;
- Nagasamy, Soumittra;
- Law, Ricky W.K.;
- Rajagopal, Rama;
- Pang, Chi P.;
- Kumaramanickevel, Govindsamy;
- Casey, Joseph R.;
- Aung, Tin
Publication type:
Article
Loss of CHK1 function impedes DNA damage-induced FANCD2 monoubiquitination but normalizes the abnormal G2 arrest in Fanconi anemia.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 679, doi. 10.1093/hmg/ddm340
By:
- Guervilly, Jean-Hugues;
- Macé-Aimé, Gaëtane;
- Rosselli, Filippo
Publication type:
Article
Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 631
By:
- Farrington-Rock, Claire;
- Kirilova, Veneta;
- Dillard-Telm, Lisa;
- Borowsky, Alexander D.;
- Chalk, Sara;
- Rock, Matthew J.;
- Cohn, Daniel H.;
- Krakow, Deborah
Publication type:
Article
Ancestral LOXL1 variants are associated with pseudoexfoliation in Caucasian Australians but with markedly lower penetrance than in Nordic people.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 710
By:
- Hewitt, Alex W.;
- Sharma, Shiwani;
- Burdon, Kathryn P.;
- Wang, Jie Jin;
- Baird, Paul N.;
- Dimasi, David P.;
- Mackey, David A.;
- Mitchell, Paul;
- Craig, Jamie E.
Publication type:
Article
Regulation of glycogen synthesis by the laforin–malin complex is modulated by the AMP-activated protein kinase pathway.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 667, doi. 10.1093/hmg/ddm339
By:
- Solaz-Fuster, Maria Carmen;
- Gimeno-Alcañiz, José Vicente;
- Ros, Susana;
- Fernandez-Sanchez, Maria Elena;
- Garcia-Fojeda, Belen;
- Garcia, Olga Criado;
- Vilchez, David;
- Dominguez, Jorge;
- Garcia-Rocha, Mar;
- Sanchez-Piris, Maribel;
- Aguado, Carmen;
- Knecht, Erwin;
- Serratosa, Jose;
- Guinovart, Joan Josep;
- Sanz, Pascual;
- de Córdoba, Santiago Rodriguez
Publication type:
Article
DNA methyltransferase 3B (DNMT3B) mutations in ICF syndrome lead to altered epigenetic modifications and aberrant expression of genes regulating development, neurogenesis and immune function.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 690, doi. 10.1093/hmg/ddm341
By:
- Jin, Bilian;
- Tao, Qian;
- Peng, Jinrong;
- Soo, Hui Meng;
- Wu, Wei;
- Ying, Jianming;
- Fields, C. Robert;
- Delmas, Amber L.;
- Liu, Xuefeng;
- Qiu, Jingxin;
- Robertson, Keith D.
Publication type:
Article
A genome-wide association study of sporadic ALS in a homogenous Irish population.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 768
By:
- Cronin, Simon;
- Berger, Stephen;
- Ding, Jinhui;
- Schymick, Jennifer C;
- Washecka, Nicole;
- Hernandez, Dena G.;
- Greenway, Matthew J.;
- Bradley, Daniel G.;
- Traynor, Bryan J.;
- Hardiman, Orla
Publication type:
Article
A novel, putative gain-of-function haplotype at SLC6A4 associates with obsessive-compulsive disorder.
Published in:
Human Molecular Genetics, 2008, v. 17, n. 5, p. 717
By:
- Wendland, Jens R.;
- Moya, Pablo R.;
- Kruse, Matthew R.;
- Ren-Patterson, Renee F.;
- Jensen, Catherine L.;
- Timpano, Kiara R.;
- Murphy, Dennis L.
Publication type:
Article