Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and TRPA1[original query] |
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A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.
Atherosclerosis 2015 Nov 245 62-70. Wakil Salma M, Ram Ramesh, Muiya Nzioka P, Mehta Munish, Andres Editha, Mazhar Nejat, Baz Batoul, Hagos Samya, Alshahid Maie, Meyer Brian F, Morahan Grant, Dzimiri Ndu |
| Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia. Scandinavian journal of pain 2018 6 5 (4): 217-225. Zhang Zhiping, Schmelz Martin, Segerdahl Märta, Quiding Hans, Centerholt Carina, Juréus Anna, Carr Thomas Hedley, Whiteley Jessica, Salter Hugh, Kvernebo Mari Skylstad, Ørstavik Kristin, Helås Tormod, Kleggetveit Inge-Petter, Lunden Lars Kristian, Jørum Ell |
| Transient receptor potential polymorphism and haplotype associate with crisis pain in sickle cell disease. Pharmacogenomics 2018 4 19 (5): 401-411. Jhun Ellie H, Hu Xiaoyu, Sadhu Nilanjana, Yao Yingwei, He Ying, Wilkie Diana J, Molokie Robert E, Wang Zaijie |
| Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine. Current genomics 2020 Apr 21 (3): 224-236. Kowalska Marta, Prendecki Micha?, Kapelusiak-Pielok Magdalena, Grzelak Teresa, ?agan-J?drzejczyk Urszula, Wiszniewska Ma?gorzata, Kozubski Wojciech, Dorszewska Jolan |
| Effect of TRPM8 and TRPA1 Polymorphisms on COPD Predisposition and Lung Function in COPD Patients. Journal of personalized medicine 2021 2 11 (2): . Naumov Denis E, Kotova Olesya O, Gassan Dina A, Sugaylo Ivana Y, Afanas'eva Evgeniya Y, Sheludko Elizaveta G, Perelman Juliy |
| Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
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