Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and CAST[original query] |
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| Testing genetic susceptibility loci for alcoholic heart muscle disease. Alcoholism, clinical and experimental research 2001 Oct 25 (10): 1409-13. Kajander O A, Kupari M, Perola M, Pajarinen J, Savolainen V, Penttilä A, Karhunen P |
| Mutation analysis of the calpastatin gene (CAST) in patients with Alzheimer's disease. Neuroscience letters 2002 Mar 320 (1-2): 77-80. Nakayama Junko, Yoshizawa Toshihiro, Yamamoto Nao, Arinami Tad |
| GSTM1 and CYP1A1 polymorphisms, tobacco, air pollution, and lung cancer: a study in rural Thailand. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006 Apr 15 (4): 667-74. Pisani Paola, Srivatanakul Petcharin, Randerson-Moor Juliette, Vipasrinimit Sutee, Lalitwongsa Somkiat, Unpunyo Piyapong, Bashir Saghir, Bishop D Timot |
| A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease. Genetic epidemiology 2009 Dec 33 (8): 657-67. Allen Andrew S, Satten Glen |
| Venous thromboembolism in young female while on oral contraceptives: high frequency of inherited thrombophilia and analysis of thrombotic events in 400 czech women. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009 Oct 15 (5): 567-73. Dulícek Petr, Malý Jaroslav, Pecka Miroslav, Beránek Martin, Cermáková Eva, Malý Radov |
| SNPs in CAST are associated with Parkinson disease: a confirmation study. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Jun 153B (4): 973-9. Allen Andrew S, Satten Glen |
Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels.
Journal of human genetics 2011 Nov 56 (11): 801-5. Shen Haiqing, Damcott Coleen, Shuldiner Scott R, Chai Sumbul, Yang Rongze, Hu Hong, Gibson Quince, Ryan Kathleen A, Mitchell Braxton D, Gong Da-W |
| No shorter telomeres in subjects with a family history of cardiovascular disease in the Asklepios study. Arteriosclerosis, thrombosis, and vascular biology 2012 Oct . De Meyer T, Van Daele CM, De Buyzere ML, Denil SL, De Bacquer D, Segers P, Cooman L, De Backer GG, Gillebert TC, Bekaert S, Rietzschel ER |
| Calpastatin gene (CAST) is not associated with late onset sporadic Parkinson's disease in the Han Chinese population. PloS one 2013 8 (8): e70935. Zhang Lan, Ding Hui, Wang Dan-Hui, Zhang Yan-Li, Baskys Andrius, Chan Piu, Zhong Yu, Cai Yan-Ni |
| Susceptibility to DNA damage in workers occupationally exposed to pesticides, to tannery chemicals and to coal dust during mining. Genetics and molecular biology 2012 Dec 35 (4 (suppl)): 1060-8. Kvitko Katia, Bandinelli Eliane, Henriques João A P, Heuser Vanina D, Rohr Paula, da Silva Fernanda R, Schneider Naye Balzan, Fernandes Simone, Ancines Camile, da Silva Julia |
| JOINT ANALYSIS OF SNP AND GENE EXPRESSION DATA IN GENETIC ASSOCIATION STUDIES OF COMPLEX DISEASES. The annals of applied statistics 2014 Mar 8 (1): 352-376. Huang Yen-Tsung, Vanderweele Tyler J, Lin Xiho |
| Association of mitochondrial DNA variants with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) symptoms. Journal of translational medicine 2016 Dec 14 (1): 342. Hanson Maureen R, Gu Zhenglong, Keinan Alon, Ye Kaixiong, Germain Arnaud, Billing-Ross Pa |
| Association of Single Nucleotide Polymorphisms in XRCC1 (194) and XPD (751) with Age-related cataract. International ophthalmology 2017 May . Khosa Tafheem, Aslam Sana, Mustafa Saima, Akbar Atif, Shaikh Rehan Sadiq, Iqbal Furh |
| Overexpression of FGFR3 in HPV-positive Tonsillar and Base of Tongue Cancer Is Correlated to Outcome. Anticancer research 2018 Aug 38 (8): 4683-4690. Bersani Cinzia, Haeggblom Linnea, Ursu Ramona G, Giusca Simona E, Marklund Linda, Ramqvist Torbjörn, Näsman Anders, Dalianis Ti |
| GATA3 rs3824662 gene polymorphism as possible risk factor for systemic lupus erythematosus. Lupus 2018 Oct 961203318804894. Mosaad Y M, Hammad A, Elghzaly A A, Tawhid Z M E, Hammad E M, Showma A, Abdelsalam R, Elmoughy A, Fawzy I M, Anber |
| The Genetic Architecture of Chronic Mountain Sickness in Peru.
Frontiers in genetics 2019 10 690. Gazal Steven, Espinoza Jose R, Austerlitz Frédéric, Marchant Dominique, Macarlupu Jose Luis, Rodriguez Jorge, Ju-Preciado Hugo, Rivera-Chira Maria, Hermine Olivier, Leon-Velarde Fabiola, Villafuerte Francisco C, Richalet Jean-Paul, Gouya Laure |
| Clinical relevance of genome-wide polygenic score may be less than claimed. Annals of human genetics 2019 3 83 (4): 274-277. Curtis Dav |
| Variants in Genes of Calpain System as Modifiers of Spinocerebellar Ataxia Type 3 Phenotype. Journal of molecular neuroscience : MN 2021 6 71 (9): 1906-1913. Martins Ana Carolina, Rieck Mariana, Leotti Vanessa Bielefeldt, Saraiva-Pereira Maria Luiza, Jardim Laura Banna |
| Combining single-cell and transcriptomic analysis revealed the immunomodulatory effect of GOT2 on a glutamine-dependent manner in cutaneous melanoma. Frontiers in pharmacology 2023 9 14 1241454. Lebin Song, Xiyi Wei, Xi Zhang, Yan |
| Gene?Environment Interaction Between CAST Gene and Eye-Rubbing in the Chinese Keratoconus Cohort Study: A Case-Only Study. Investigative ophthalmology & visual science 2024 8 65 (10): 36. Shanshan Yin, Liyan Xu, Kaili Yang, Qi Fan, Yuwei Gu, Chenchen Yin, Yonghao Zang, Yifan Wang, Yi Yuan, Anqi Chang, Chenjiu Pang, Shengwei R |
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