Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and TRPM8[original query] |
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| Natural killer cells and single nucleotide polymorphisms of specific ion channels and receptor genes in myalgic encephalomyelitis/chronic fatigue syndrome. The application of clinical genetics 2016 9 39-47. Marshall-Gradisnik Sonya, Huth Teilah, Chacko Anu, Johnston Samantha, Smith Pete, Staines Dona |
| 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 |
Bilirubin and risk of ischemic heart disease in Korea: a two-sample Mendelian randomization study.
Epidemiology and health 2019 41 e2019034. Jeon Christina, Lee Ji-Young, Lee Sun Ju, Jung Keum Ji, Kimm Heejin, Jee Sun |
| Genome-Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor. Movement disorders : official journal of the Movement Disorder Society 2020 2 35 (4): 705-707. Williams Nigel M, Hubbard Leon, Sandor Cynthia, Webber Caleb, Hendry Hannah, Lawton Michael, Carroll Camille, Chaudhuri K Ray, Morris Huw, Hu Michele T, Grosset Donald G, Kobylecki Christopher, Silverdale Monty, |
| 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 |
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