Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: TRPM6[original query] |
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Genetic determinants of extracellular magnesium concentration: analysis of multiple candidate genes, and evidence for association with the estrogen receptor alpha (ESR1) locus. Clinica chimica acta; international journal of clinical chemistry 2009 Nov 409 (1-2): 28-32. Shuen Andrew Y, Wong Betty Y L, Wei Cuihong, Liu Zhanqin, Li Mei, Cole David E |
Common genetic variants of the ion channel transient receptor potential membrane melastatin 6 and 7 (TRPM6 and TRPM7), magnesium intake, and risk of type 2 diabetes in women. BMC medical genetics 2009 10 (1): 4. Song Yiqing, Hsu Yi-Hsiang, Niu Tianhua, Manson Joann E, Buring Julie E, Liu Sim |
Gene variation of the transient receptor potential cation channel, subfamily M, members 6 (TRPM6) and 7 (TRPM7), and type 2 diabetes mellitus: a case-control study. Translational research : the journal of laboratory and clinical medicine 2010 Oct 156 (4): 235-41. Romero José R, Castonguay Amy J, Barton Nathaniel S, Germer Soren, Martin Mitchell, Zee Robert Y |
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.
PLoS genetics 2010 Aug 6 (8): 8. Meyer Tamra E, Verwoert Germaine C, Hwang Shih-Jen, Glazer Nicole L, Smith Albert V, van Rooij Frank J A, Ehret Georg B, Boerwinkle Eric, Felix Janine F, Leak Tennille S, Harris Tamara B, Yang Qiong, Dehghan Abbas, Aspelund Thor, Katz Ronit, Homuth Georg, Kocher Thomas, Rettig Rainer, Ried Janina S, Gieger Christian, Prucha Hanna, Pfeufer Arne, Meitinger Thomas, Coresh Josef, Hofman Albert, Sarnak Mark J, Chen Yii-Der Ida, Uitterlinden André G, Chakravarti Aravinda, Psaty Bruce M, van Duijn Cornelia M, Kao W H Linda, Witteman Jacqueline C M, Gudnason Vilmundur, Siscovick David S, Fox Caroline S, Köttgen Anna, , |
Loss of insulin-induced activation of TRPM6 magnesium channels results in impaired glucose tolerance during pregnancy. Proceedings of the National Academy of Sciences of the United States of America 2012 Jul 109 (28): 11324-9. Nair Anil V, Hocher Berthold, Verkaart Sjoerd, van Zeeland Femke, Pfab Thiemo, Slowinski Torsten, Chen You-Peng, Schlingmann Karl Peter, Schaller André, Gallati Sabina, Bindels René J, Konrad Martin, Hoenderop Joost |
Higher magnesium intake is associated with lower fasting glucose and insulin, with no evidence of interaction with select genetic loci, in a meta-analysis of 15 CHARGE Consortium Studies. The Journal of nutrition 2013 Jan . Hruby A, Ngwa JS, Renström F, Wojczynski MK, Ganna A, Hallmans G, Houston DK, Jacques PF, Kanoni S, Lehtimäki T, Lemaitre RN, Manichaikul A, North KE, Ntalla I, Sonestedt E, Tanaka T, van Rooij FJ, Bandinelli S, Djoussé L, Grigoriou E, Johansson I, Lohman KK, Pankow JS, Raitakari OT, Riserus U, Yannakoulia M, Zillikens MC, Hassanali N, Liu Y, Mozaffarian D, Papoutsakis C, Syvänen AC, Uitterlinden AG, Viikari J, Groves CJ, Hofman A, Lind L, McCarthy MI, Mikkilä V, Mukamal K, Franco OH, Borecki IB, Cupples LA, Dedoussis GV, Ferrucci L, Hu FB, Ingelsson E, Kähönen M, Kao WH, Kritchevsky SB, Orho-Melander M, Prokopenko I, Rotter JI, Siscovick DS, Witteman JC, Franks PW, Meigs JB, McKeown NM, Nettleton JA |
Comprehensive next-generation sequencing analyses of hypoparathyroidism: identification of novel GCM2 mutations. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2421-8. Mitsui Toshikatsu, Narumi Satoshi, Inokuchi Mikako, Nagasaki Keisuke, Nakazawa Mie, Sasaki Goro, Hasegawa Tomono |
A meta-analysis of somatic mutations from next generation sequencing of 241 melanomas: a road map for the study of genes with potential clinical relevance. Molecular cancer therapeutics 2014 Jul 13 (7): 1918-28. Xia Junfeng, Jia Peilin, Hutchinson Katherine E, Dahlman Kimberly B, Johnson Douglas, Sosman Jeffrey, Pao William, Zhao Zhongmi |
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study.
BMC genetics 2015 May 16 56. Tin Adrienne, Köttgen Anna, Folsom Aaron R, Maruthur Nisa M, Tajuddin Salman M, Nalls Mike A, Evans Michele K, Zonderman Alan B, Friedrich Christopher A, Boerwinkle Eric, Coresh Josef, Kao Wen Hong Lin |
[A genomic study of adult-onset idiopathic hypoparathyroidism in Chinese by targeted next-generation sequencing]. Zhonghua nei ke za zhi 2016 Aug 55 (8): 604-8. Li Y P, Wang O, Quan T T, Xia W B, Jiang Y, Li M, Meng X W, Xing X |
Whole-Exome Sequencing Identifies Novel Somatic Mutations in Chinese Breast Cancer Patients. Journal of molecular and genetic medicine : an international journal of biomedical research 2015 Dec 9 (4): . Zhang Yanfeng, Cai Qiuyin, Shu Xiao-Ou, Gao Yu-Tang, Li Chun, Zheng Wei, Long Jiro |
Common single nucleotide polymorphisms in transient receptor potential melastatin type 6 increase the risk for proton pump inhibitor-induced hypomagnesemia: a case-control study. Pharmacogenetics and genomics 2016 Dec . Hess Mark W, de Baaij Jeroen H F, Broekman Mark M T J, Bisseling Tanya M, Haarhuis Bertram J T, Tan Adriaan C I T L, Te Morsche René H M, Hoenderop Joost G J, Bindels René J M, Drenth Joost P |
Magnesium-permeable TRPM6 polymorphisms in patients with meningomyelocele. SpringerPlus 2016 5 (1): 1703. Saraç Mehmet, Önalan Ebru, Bakal Ünal, Tartar Tugay, Ayd?n Mustafa, Orman Ay?en, Tektemur Ahmet, Ta?k?n Erdal, Erol Fatih Serhat, Kazez Ahm |
Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.
Journal of the American Society of Nephrology : JASN 2018 Jan 29 (1): 335-348. Corre Tanguy, Arjona Francisco J, Hayward Caroline, Youhanna Sonia, de Baaij Jeroen H F, Belge Hendrica, Nägele Nadine, Debaix Huguette, Blanchard Maxime G, Traglia Michela, Harris Sarah E, Ulivi Sheila, Rueedi Rico, Lamparter David, Macé Aurélien, Sala Cinzia, Lenarduzzi Stefania, Ponte Belen, Pruijm Menno, Ackermann Daniel, Ehret Georg, Baptista Daniela, Polasek Ozren, Rudan Igor, Hurd Toby W, Hastie Nicholas D, Vitart Veronique, Waeber Geràrd, Kutalik Zoltán, Bergmann Sven, Vargas-Poussou Rosa, Konrad Martin, Gasparini Paolo, Deary Ian J, Starr John M, Toniolo Daniela, Vollenweider Peter, Hoenderop Joost G J, Bindels René J M, Bochud Murielle, Devuyst Olivi |
[Analysis of TRPM6 gene variant in a pedigree affected with hypocalcemia secondary to hypomagnesemia]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2019 8 36 (8): 805-808. Tan Jianqiang, Yan Tizhen, Li Zhetao, Huang Jun, Cai R |
Increased risk of post-stroke epilepsy in Chinese patients with a TRPM6 polymorphism. Neurological research 2019 Feb 1-6. Fu Chuan-Yi, Chen Shui-Jie, Cai Nan-Hua, Liu Zhao-Hui, Zhang Mao, Wang Peng-Cheng, Zhao Jian-No |
Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid.
Mayo Clinic proceedings. Innovations, quality & outcomes 2019 Dec 3 (4): 448-460. Ware Erin B, Smith Jennifer A, Zhao Wei, Ganesvoort Ron T, Curhan Gary C, Pollak Martin, Mount David B, Turner Stephen T, Chen Guotao, Shah Ronak Jagdeep, Kardia Sharon L R, Lieske John |
Cyclin M2 (CNNM2) knockout mice show mild hypomagnesaemia and developmental defects. Scientific reports 2021 4 11 (1): 8217. Franken Gijs A C, Seker Murat, Bos Caro, Siemons Laura A H, van der Eerden Bram C J, Christ Annabel, Hoenderop Joost G J, Bindels René J M, Müller Dominik, Breiderhoff Tilman, de Baaij Jeroen H |
Magnesium Status, Genetic Variants of Magnesium-Related Ion Channel Transient Receptor Potential Membrane Melastatin 6 (TRPM6) and the Risk of Gestational Diabetes Mellitus in Chinese Pregnant Women: A Nested Case-Control Study. Molecular nutrition & food research 2023 9 e2200835. Shanshan Huang, Yanyan Ge, Yan Li, Ningning Cui, Le Tan, Shu Guo, Shanshan Wang, Liping Hao, Gang Lei, Xuefeng Ya |
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- Page last updated:Apr 22, 2024
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