Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Disease and CA2[original query] |
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| Vitamin D receptor gene polymorphism detected by digestion with Apa I influences the parathyroid response to extracellular calcium in Japanese chronic dialysis patients. Nephron 2001 Nov 89 (3): 315-20. Yokoyama K, Shigematsu T, Kagami S, Tsukada T, Arai T, Hara S, Yamada A, Kawaguchi Y, Hosoya |
| Evaluation of genetic variation and association in the matrix metalloproteinase 9 (MMP9) gene in ESRD patients. American journal of kidney diseases : the official journal of the National Kidney Foundation 2003 Jul 42 (1): 133-42. Hirakawa Shohei, Lange Ethan M, Colicigno Carla J, Freedman Barry I, Rich Stephen S, Bowden Donald |
| Phospholamban gene mutations are not associated with hypertrophic cardiomyopathy in a Northern Greek population. Biochemical genetics 2005 Dec 43 (11-12): 637-42. Kalemi Theodora, Efthimiadis Georgios, Zioutas Dimitrios, Lambropoulos Alexandros, Mitakidou Anastasia, Giannakoulas Georgios, Vassilikos Vassilios, Karvounis Haralambos, Kotsis Alexandros, Parharidis Georgios, Louridas Georgi |
| Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk. Circulation research 2005 Dec 97 (12): 1360-5. Sentí Mariano, Fernández-Fernández José M, Tomás Marta, Vázquez Esther, Elosua Roberto, Marrugat Jaume, Valverde Miguel |
| P2Y2 receptor polymorphisms and haplotypes in cystic fibrosis and their impact on Ca2+ influx. Pharmacogenetics and genomics 2006 Mar 16 (3): 199-205. Büscher Rainer, Hoerning André, Patel Hemal H, Zhang Shen, Arthur David B, Grasemann Hartmut, Ratjen Felix, Insel Paul |
| The 77C->G mutation in the human CD45 (PTPRC) gene leads to increased intensity of TCR signaling in T cell lines from healthy individuals and patients with multiple sclerosis. Journal of immunology (Baltimore, Md. : 1950) 2006 Jan 176 (2): 931-8. Do Hue-Tran, Baars Wiebke, Borns Katja, Windhagen Anja, Schwinzer Reinha |
| A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk. Cell 2008 Jun 133 (7): 1149-61. Dreses-Werringloer Ute, Lambert Jean-Charles, Vingtdeux Valérie, Zhao Haitian, Vais Horia, Siebert Adam, Jain Ankit, Koppel Jeremy, Rovelet-Lecrux Anne, Hannequin Didier, Pasquier Florence, Galimberti Daniela, Scarpini Elio, Mann David, Lendon Corinne, Campion Dominique, Amouyel Philippe, Davies Peter, Foskett J Kevin, Campagne Fabien, Marambaud Philip |
| Genetic variation in the KCNMA1 potassium channel alpha subunit as risk factor for severe essential hypertension and myocardial infarction. Journal of hypertension 2008 Nov 26 (11): 2147-53. Tomás Marta, Vázquez Esther, Fernández-Fernández José M, Subirana Isaac, Plata Cristina, Heras Magda, Vila Joan, Marrugat Jaume, Valverde Miguel A, Sentí Maria |
| The clinical significance of parathyroid tissue calcium sensing receptor gene polymorphisms and expression levels in end-stage renal disease patients. Clinical nephrology 2009 Aug 72 (2): 114-21. Eren P A, Turan K, Berber I, Canbakan M, Kara M, Tellioglu G, Bugan U, Sevinç C, Turkmen F, Titiz M |
| The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis. Bone 2009 Aug 45 (2): 289-94. Huang Qing-Yang, Li Gloria H Y, Kung Annie W |
| Impact of vitamin D receptor VDR rs2228570 polymorphism in oldest old. Kidney & blood pressure research 2013 37 (4-5): 311-22. Glocke Melanie, Lang Florian, Schaeffeler Elke, Lang Thomas, Schwab Matthias, Lang Undine |
| The roles of Ca2+/NFAT signaling genes in Kawasaki disease: single- and multiple-risk genetic variants. Scientific reports 2014 4 5208. Wang Wei, Lou Jiao, Zhong Rong, Qi Yan-qi, Shen Na, Lu Xu-zai, Wang Yu-jia, Zhang Qing, Zou Li, Duan Jia-yu, Ke Jun-tao, Miao Xiao-ping, Gong Fang- |
| Neuronal Na+ channel blockade suppresses arrhythmogenic diastolic Ca2+ release. Cardiovascular research 2015 Apr 106 (1): 143-52. Radwa?ski Przemys?aw B, Brunello Lucia, Veeraraghavan Rengasayee, Ho Hsiang-Ting, Lou Qing, Makara Michael A, Belevych Andriy E, Anghelescu Mircea, Priori Silvia G, Volpe Pompeo, Hund Thomas J, Janssen Paul M L, Mohler Peter J, Bridge John H B, Poelzing Steven, Györke Sánd |
| High prevalence of rare ryanodine receptor type 1 variants in patients suffering from aneurysmatic subarachnoid hemorrhage: A pilot study. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2017 Jul . Coburger Jan, Kapapa Thomas, Wirtz Cristian Rainer, Jurkat-Rott Karin, Klingler Wern |
| Association of Cardiomyopathy With MYBPC3 D389V and MYBPC3?25bpIntronic Deletion in South Asian Descendants. JAMA cardiology 2018 Apr . Viswanathan Shiv Kumar, Puckelwartz Megan J, Mehta Ashish, Ramachandra Chrishan J A, Jagadeesan Aravindakshan, Fritsche-Danielson Regina, Bhat Ratan V, Wong Philip, Kandoi Sangeetha, Schwanekamp Jennifer A, Kuffel Gina, Pesce Lorenzo L, Zilliox Michael J, Durai U Nalla B, Verma Rama Shanker, Molokie Robert E, Suresh Domodhar P, Khoury Philip R, Thomas Annie, Sanagala Thriveni, Tang Hak Chiaw, Becker Richard C, Knöll Ralph, Shim Winston, McNally Elizabeth M, Sadayappan Sakthiv |
| Polymorphisms Within RYR3 Gene Are Associated With Risk and Age at Onset of Hypertension, Diabetes, and Alzheimer's Disease. American journal of hypertension 2018 Mar . Gong Shaoqing, Su Brenda Bin, Tovar Hugo, Mao ChunXiang, Gonzalez Valeria, Liu Ying, Lu Yongke, Wang Ke-Sheng, Xu Ch |
| Increased prevalence of granulovacuolar degeneration in C9orf72 mutation. Acta neuropathologica 2019 5 138 (5): 783-793. Riku Yuichi, Duyckaerts Charles, Boluda Susana, Plu Isabelle, Le Ber Isabelle, Millecamps Stéphanie, Salachas François, , Yoshida Mari, Ando Takashi, Katsuno Masahisa, Sobue Gen, Seilhean Daniel |
| Mitochondrial Energetics and Ca2-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy. Journal of clinical medicine 2020 6 9 (6): . Lombardi Maria, Lazzeroni Davide, Pisano Annalinda, Girolami Francesca, Alfieri Ottavio, La Canna Giovanni, d'Amati Giulia, Olivotto Iacopo, Rimoldi Ornella E, Foglieni Chiara, Camici Paolo |
| A TREML2 missense variant influences specific hippocampal subfield volumes in cognitively normal elderly subjects. Brain and behavior 2020 Feb e01573. Wang Si-Yu, Xue Xiao, Duan Rui, Gong Peng-Yu, E Yan, Jiang Teng, Zhang Ying-Dong, |
| Genetic Polymorphisms of RGS14 and Renal Stone Disease. Archives of medical research 2020 Dec . Guan Fanglin, Han Wei, Ni Tong, Zhao Longrui, Li Xiaoming, Zhang Bo, Zhang Tianxi |
| Polymorphism rs7214723 in CAMKK1: a new genetic variant associated with cardiovascular diseases. Bioscience reports 2021 6 41 (7): . Beghi Sofia, Cavaliere Francesca, Manfredini Matteo, Ferrarese Sandro, Corazzari Claudio, Beghi Cesare, Buschini Annamar |
| The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms. Neurobiology of disease 2021 May 155 105394. Hidalgo Sergio, Campusano Jorge M, Hodge James J |
| APOE alleles are associated with sex-specific structural differences in brain regions affected in Alzheimer's disease and related dementia. PLoS biology 2022 12 20 (12): e3001863. Savignac Chloé, Villeneuve Sylvia, Badhwar AmanPreet, Saltoun Karin, Shafighi Kimia, Zajner Chris, Sharma Vaibhav, Gagliano Taliun Sarah A, Farhan Sali, Poirier Judes, Bzdok Dani |
| Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease. Brain : a journal of neurology 2023 5 . Amélie Pinard, Wenlei Ye, Stuart M Fraser, Jill A Rosenfeld, Pavel Pichurin, Scott E Hickey, Dongchuan Guo, Alana C Cecchi, Maura L Boerio, Stéphanie Guey, Chaker Aloui, Kwanghyuk Lee, Markus Kraemer, Saleh Omar Alyemni, , Michael J Bamshad, Deborah A Nickerson, Elisabeth Tournier-Lasserve, Shozeb Haider, Sheng Chih Jin, Edward R Smith, Kristopher T Kahle, Lily Yeh Jan, Mu He, Dianna M Milewi |
| Hailey-Hailey Disease is Associated with Diabetes: A Population-based Cohort Study, Clinical Cohort Study, and Pedigree Analysis. Acta dermato-venereologica 2023 11 103 adv10436. Philip Curman, William Jebril, Carmella Evans-Molina, Etty Bachar-Wikstrom, Henrik Larsson, Martin Cederlöf, Jakob D Wikstr |
| Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation. Clinical immunology (Orlando, Fla.) 2023 1 247 109236. Lin Yung-Feng, Lee Wen-I, Ho Ching-Huang, Chen Shih-Hsiang, Hsu Mei-Hsin, Wu Ren-Chin, Lee Wan-Fang, Jaing Tang-Her, Huang Jing-Long, Tsai Shih-Fe |
- Page last reviewed:Feb 1, 2024
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