Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 40 Records) |
Query Trace: TRPM8[original query] |
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Selectivity in genetic association with sub-classified migraine in women. PLoS genetics 2014 May 10 (5): e1004366. Chasman Daniel I, Anttila Verneri, Buring Julie E, Ridker Paul M, Schürks Markus, Kurth Tobias, |
Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura. Cephalalgia : an international journal of headache 2015 Aug 35 (9): 776-82. Sintas Cèlia, Fernández-Morales Jèssica, Vila-Pueyo Marta, Narberhaus Bernat, Arenas Concepció, Pozo-Rosich Patricia, Macaya Alfons, Cormand B |
[Respiratory system response to cooling in subjects with single nucleotide polymorphism rs11562975 in gene of thermosensitive TRPM8 ion channel]. Fiziologiia cheloveka 0 40 (2): 94-8. Kozyreva T V, Tkachenko E Ia, Potapova T A, Voevoda M |
Associations of cold receptor TRPM8 gene single nucleotide polymorphism with blood lipids and anthropometric parameters in Russian population. Bulletin of experimental biology and medicine 2014 Oct 157 (6): 757-61. Potapova T A, Babenko V N, Kobzev V F, Romashchenko A G, Maksimov V N, Voevoda M |
Transient receptor potential melastatin 8 gene polymorphism is associated with cold-induced airway hyperresponsiveness in bronchial asthma. Respirology (Carlton, Vic.) 2015 Aug . Naumov Denis E, Perelman Juliy M, Kolosov Victor P, Potapova Tatyana A, Maksimov Vladimir N, Zhou Xiangdo |
Role of the transient receptor potential (TRP) channel gene expressions and TRP melastatin (TRPM) channel gene polymorphisms in obesity-related metabolic syndrome. European review for medical and pharmacological sciences 2015 Apr 19 (8): 1388-97. Tabur S, Oztuzcu S, Duzen I V, Eraydin A, Eroglu S, Ozkaya M, Demiryürek A |
Exome sequencing in Thai patients with familial obesity. Genetics and molecular research : GMR 2016 15 (2): . Kaewsutthi S, Santiprabhob J, Phonrat B, Tungtrongchitr A, Lertrit P, Tungtrongchitr |
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 |
TRPM8 polymorphisms associated with increased risk of IBS-C and IBS-M. Gut 2016 Dec . Henström Maria, Hadizadeh Fatemeh, Beyder Arthur, Bonfiglio Ferdinando, Zheng Tenghao, Assadi Ghazaleh, Rafter Joseph, Bujanda Luis, Agreus Lars, Andreasson Anna, Dlugosz Aldona, Lindberg Greger, Schmidt Peter T, Karling Pontus, Ohlsson Bodil, Talley Nicholas J, Simren Magnus, Walter Susanna, Wouters Mira, Farrugia Gianrico, D'Amato Mau |
TRPM8 genetic variations associated with COPD risk in the Chinese Han population. International journal of chronic obstructive pulmonary disease 2016 11 2563-2571. Xiong Mingmei, Wang Jian, Guo Meihua, Zhou Qipeng, Lu Wen |
Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan.
Cephalalgia : an international journal of headache 2017 Jan 333102417695105. Chen Shih-Pin, Fuh Jong-Ling, Chung Ming-Yi, Lin Ying-Chao, Liao Yi-Chu, Wang Yen-Feng, Hsu Chia-Lin, Yang Ueng-Cheng, Lin Ming-Wei, Chiou Jen-Jie, Wang Po-Jen, Chen Ping-Kun, Fan Pi-Chuan, Wu Jer-Yuan, Chen Yuan-Tsong, Kao Lung-Sen, Shen-Jang Fann Cathy, Wang Shuu-Ji |
Using a Genetic Risk Score Approach to Predict Headache Response to Triptans in Migraine Without Aura. Journal of clinical pharmacology 2018 Sep . Cargnin Sarah, Viana Michele, Sances Grazia, Cantello Roberto, Tassorelli Cristina, Terrazzino Salvato |
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 |
Association of Raynaud's phenomenon with a polymorphism in the NOS1 gene. PloS one 2018 13 (4): e0196279. Munir Sabrina, Freidin Maxim B, Brain Susan, Williams Frances M |
Overexpression of certain transient receptor potential and Orai channels in prostate cancer is associated with decreased risk of systemic recurrence after radical prostatectomy. The Prostate 2019 9 79 (16): 1793-1804. Perrouin-Verbe M A, Schoentgen N, Talagas M, Garlantezec R, Uguen A, Doucet L, Rosec S, Marcorelles P, Potier-Cartereau M, Vandier C, Ferec C, Fromont G, Fournier G, Valeri A, Mignen |
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 |
Association between PRDM16, MEF2D, TRPM8, LRP1 gene polymorphisms and migraine susceptibility in the She ethnic population in China. Clinical and investigative medicine. Medecine clinique et experimentale 2019 Mar 42 (1): E21-E30. Fu Xianguo, Yang Jing, Wu Xiaoyang, Lin Qifang, Zeng Yuli, Xia Qiaoqing, Cao Luoyuan, Huang Baoying, Huang Genb |
Reduced TRPM8 expression underpins reduced migraine risk and attenuated cold pain sensation in humans. Scientific reports 2019 12 9 (1): 19655. Gavva Narender R, Sandrock Robert, Arnold Gregory E, Davis Michael, Lamas Edwin, Lindvay Chris, Li Chi-Ming, Smith Brian, Backonja Miroslav, Gabriel Kristin, Vargas Gabri |
TRPM8 genetic variant is associated with chronic migraine and allodynia. The journal of headache and pain 2019 Dec 20 (1): 115. Ling Yu-Hsiang, Chen Shih-Pin, Fann Cathy Shen-Jang, Wang Shuu-Jiun, Wang Yen-Fe |
rs2651899 variant is associated with risk for migraine without aura from North Indian population. Molecular biology reports 2019 Jan . Kaur Sukhvinder, Ali Arif, Ahmad Uzair, Pandey A K, Singh Balkir |
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, |
PRDM16, LRP1 and TRPM8 genetic polymorphisms are risk factor for Pakistani migraine patients. Saudi journal of biological sciences 2021 Oct 28 (10): 5793-5799. Zafar R, Saleem T, Sheikh N, Maqbool H, Mukhtar M, Abbasi M |
Cold pain sensitivity is associated with single-nucleotide polymorphisms of PAR2/F2RL1 and TRPM8. Molecular pain 0 17 17448069211002009. Soeda Moe, Ohka Seii, Nishizawa Daisuke, Hasegawa Junko, Nakayama Kyoko, Ebata Yuko, Ichinohe Tatsuya, Fukuda Ken-Ichi, Ikeda Kazuta |
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 |
A Comprehensive Review on the Role of Genetic Factors in the Pathogenesis of Migraine. Journal of molecular neuroscience : MN 2021 1 71 (10): 1987-2006. Ebahimzadeh Kaveh, Gholipour Mahdi, Samadian Mohammad, Taheri Mohammad, Ghafouri-Fard Soud |
Comprehensive Pan-Cancer Analysis of TRPM8 in Tumor Metabolism and Immune Escape. Frontiers in oncology 2022 7 12 914060. Zhang Wei, Qiao Xin-Yu, Li Qian, Cui Chun, Qiao Chen-Meng, Shen Yan-Qin, Zhao Wei-Jia |
Deciphering the Role of the rs2651899, rs10166942, and rs11172113 Polymorphisms in Migraine: A Meta-Analysis. Medicina (Kaunas, Lithuania) 2022 4 58 (4): . Siokas Vasileios, Liampas Ioannis, Aloizou Athina-Maria, Papasavva Maria, Bakirtzis Christos, Lavdas Eleftherios, Liakos Panagiotis, Drakoulis Nikolaos, Bogdanos Dimitrios P, Dardiotis Efthimi |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
Association between TRP channels and glutamatergic synapse gene polymorphisms and migraine and the comorbidities anxiety and depression in a Chinese population. Frontiers in genetics 2023 6 14 1158028. Mingxue Wang, Yujia Gu, Shuhan Meng, Lixin Kang, Jing Yang, Degang Sun, Yuxing Liu, Ze Wan, Yi Shan, Dongjie Xue, Chang Su, Shufen Li, Ran Yan, Yu Liu, Yashuang Zhao, Yonghui P |
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohort. Brain communications 2023 3 5 (2): fcad037. Themistocleous Andreas C, Baskozos Georgios, Blesneac Iulia, Comini Maddalena, Megy Karyn, Chong Sam, Deevi Sri V V, Ginsberg Lionel, Gosal David, Hadden Robert D M, Horvath Rita, Mahdi-Rogers Mohamed, Manzur Adnan, Mapeta Rutendo, Marshall Andrew, Matthews Emma, McCarthy Mark I, Reilly Mary M, Renton Tara, Rice Andrew S C, Vale Tom A, van Zuydam Natalie, Walker Suellen M, Woods Christopher Geoffrey, Bennett David L |
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- Page last updated:Apr 22, 2024
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