Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: TRPV4[original query] |
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A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia. Proceedings of the National Academy of Sciences of the United States of America 2009 Aug 106 (33): 14034-9. Tian Wei, Fu Yi, Garcia-Elias Anna, Fernández-Fernández José M, Vicente Rubén, Kramer Patricia L, Klein Robert F, Hitzemann Robert, Orwoll Eric S, Wilmot Beth, McWeeney Shannon, Valverde Miguel A, Cohen David |
Association of TRPV4 gene polymorphisms with chronic obstructive pulmonary disease. Human molecular genetics 2009 Jun 18 (11): 2053-62. Zhu Guohua, , Gulsvik Amund, Bakke Per, Ghatta Srinivas, Anderson Wayne, Lomas David A, Silverman Edwin K, Pillai Sreekumar |
Loss of function of transient receptor potential vanilloid 1 (TRPV1) genetic variant is associated with lower risk of active childhood asthma. The Journal of biological chemistry 2010 Sep 285 (36): 27532-5. Cantero-Recasens Gerard, Gonzalez Juan R, Fandos César, Duran-Tauleria Enric, Smit Lidwien A M, Kauffmann Francine, Antó Josep M, Valverde Miguel |
A comprehensive evaluation of potential lung function associated genes in the SpiroMeta general population sample. PloS one 2011 6 (5): e19382. Obeidat Ma'en, Wain Louise V, Shrine Nick, Kalsheker Noor, Soler Artigas Maria, Repapi Emmanouela, Burton Paul R, Johnson Toby, Ramasamy Adaikalavan, Zhao Jing Hua, Zhai Guangju, Huffman Jennifer E, Vitart Veronique, Albrecht Eva, Igl Wilmar, Hartikainen Anna-Liisa, Pouta Anneli, Cadby Gemma, Hui Jennie, Palmer Lyle J, Hadley David, McArdle Wendy L, Rudnicka Alicja R, Barroso Inês, Loos Ruth J F, Wareham Nicholas J, Mangino Massimo, Soranzo Nicole, Spector Tim D, Gläser Sven, Homuth Georg, Völzke Henry, Deloukas Panos, Granell Raquel, Henderson John, Grkovic Ivica, Jankovic Stipan, Zgaga Lina, Polašek Ozren, Rudan Igor, Wright Alan F, Campbell Harry, Wild Sarah H, Wilson James F, Heinrich Joachim, Imboden Medea, Probst-Hensch Nicole M, Gyllensten Ulf, Johansson Åsa, Zaboli Ghazal, Mustelin Linda, Rantanen Taina, Surakka Ida, Kaprio Jaakko, Jarvelin Marjo-Riitta, Hayward Caroline, Evans David M, Koch Beate, Musk Arthur William, Elliott Paul, Strachan David P, Tobin Martin D, Sayers Ian, Hall Ian P, |
Transient receptor potential genes, smoking, occupational exposures and cough in adults. Respiratory research 2012 13 (1): 26. Smit Lidwien A M, Kogevinas Manolis, Antó Josep M, Bouzigon Emmanuelle, González Juan Ramón, Le Moual Nicole, Kromhout Hans, Carsin Anne-Elie, Pin Isabelle, Jarvis Deborah, Vermeulen Roel, Janson Christer, Heinrich Joachim, Gut Ivo, Lathrop Mark, Valverde Miguel A, Demenais Florence, Kauffmann Franci |
A pilot study of gene testing of genetic bone dysplasia using targeted next-generation sequencing. Journal of human genetics 2015 Sep . Zhang Huiwen, Yang Rui, Wang Yu, Ye Jun, Han Lianshu, Qiu Wenjuan, Gu Xuef |
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 |
Associations between TRPV4 genotypes and body mass index in Taiwanese subjects. Molecular genetics and genomics : MGG 2015 Aug 290 (4): 1357-65. Duan De-Min, Wu Semon, Hsu Lung-An, Teng Ming-Sheng, Lin Jeng-Feng, Sun Yu-Chen, Cheng Ching-Feng, Ko Yu-L |
Influence of TRPV4 gene polymorphisms on the development of osmotic airway hyperresponsiveness in patients with bronchial asthma. Doklady. Biochemistry and biophysics 2016 Jul 469 (1): 260-3. Naumov D E, Kolosov V P, Perelman J M, Prikhodko A |
Incidence and Clinical Features of TRPV4-Linked Axonal Neuropathies in a USA Cohort of Charcot-Marie-Tooth Disease Type 2. Neuromolecular medicine 2019 8 22 (1): 68-72. Deng Sheng, Feely Shawna M E, Shi Yong, Zhai Hong, Zhan Luna, Siddique Teepu, Deng Han-Xiang, Shy Michael |
Gene testing for osteonecrosis of the femoral head in systemic lupus erythematosus using targeted next-generation sequencing: A pilot study. World journal of clinical cases 2020 7 8 (12): 2530-2541. Sun Hong-Sheng, Yang Qing-Rui, Bai Yan-Yan, Hu Nai-Wen, Liu Dong-Xia, Qin Cheng-Yo |
TRPV4 is a Prognostic Biomarker that Correlates with the Immunosuppressive Microenvironment and Chemoresistance of Anti-Cancer Drugs. Frontiers in molecular biosciences 2021 7 8 690500. Wang Kai, Feng Xingjun, Zheng Lingzhi, Chai Zeying, Yu Junhui, You Xinxin, Li Xiaodan, Cheng Xiaodo |
Novel TRPV4 Pathogenic Variant in Severe Metatropic Skeletal Dysplasia: A Case Report. Malaysian orthopaedic journal 2022 8 16 (2): 145-149. James D, Subramanian L, Selina A, Palocaren T, Madhuri |
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 |
Significant association between FGFR1 mutation frequency and age in central giant cell granuloma. Pathology 2022 11 . Niada Stefania, Varazzani Andrea, Giannasi Chiara, Fusco Nicola, Armiraglio Elisabetta, Di Bernardo Andrea, Cherchi Alessandro, Baj Alessandro, Corradi Domenico, Tafuni Alessandro, Parafioriti Antonina, Ferrero Stefano, Bianchi Andrea Edoardo, Giannì Aldo Bruno, Poli Tito, Latif Farida, Brini Anna Tere |
AQP5 pathogenic variants induce palmoplantar keratoderma Bothnia type in two Chinese families. The Journal of dermatology 2022 1 49 (4): 463-468. Wang Yumeng, Wang Jianbo, Li Yue, Pan Chaolan, Zhou Wange, Cao Qiaoyu, Yao Zhirong, Han Jianwen, Li Mi |
Erratum. Association of novel mutation in TRPV4 with familial nonsyndromic craniosynostosis with complete penetrance and variable expressivity. Journal of neurosurgery. Pediatrics 2023 8 1. Roy W R Dudl |
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 |
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- Page last updated:Apr 29, 2024
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