Human Genome Epidemiology Literature Finder
Records 1 - 22 (of 22 Records) |
Query Trace: ATP2A2[original query] |
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Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular psychiatry 2001 Jan 6 (1): 92-7. Jacobsen N J, Franks E K, Elvidge G, Jones I, McCandless F, O'Donovan M C, Owen M J, Craddock |
Alterations in the ATP2A2 gene in correlation with colon and lung cancer. Cancer genetics and cytogenetics 2006 Dec 171 (2): 105-11. Korosec Branka, Glavac Damjan, Rott Tomaz, Ravnik-Glavac Met |
A724A polymorphism of sarco(endo)plasmic reticulum Ca2+-ATPase 2 (SERCA2) in hypertensive patients. Clinical chemistry and laboratory medicine : CCLM / FESCC 2007 45 (4): 467-70. Kiec-Wilk Beata, Dembinska-Kiec Aldona, Olszanecka Agnieszka, Bodzioch Marek, Schmitz Gerd, Kawecka-Jaszcz Kali |
ATP2A3 gene is involved in cancer susceptibility. Cancer genetics and cytogenetics 2009 Jan 188 (2): 88-94. Korosec Branka, Glavac Damjan, Volavsek Metka, Ravnik-Glavac Met |
[Role of the M235T (c.704c>T) polymorphism of angiotensynogen gene as well as A724A (c.2171G>A) polymorphism of SERCA2a gene in ethiopathogenesis of left ventricular hypertrophy in essential hypertension]. Przegla?d lekarski 2010 67 (3): 151-6. Kie?-Wilk Beata, Olszanecka Agnieszka, Miko?ajczyk Magdalena, Kawecka-Jaszcz Kali |
Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes. Physiological genomics 2011 Sep 43 (17): 981-92. Windelinckx An, De Mars Gunther, Huygens Wim, Peeters Maarten W, Vincent Barbara, Wijmenga Cisca, Lambrechts Diether, Aerssens Jeroen, Vlietinck Robert, Beunen Gaston, Thomis Martine A |
Role of genetic polymorphisms of ion channels in the pathophysiology of coronary microvascular dysfunction and ischemic heart disease. Basic research in cardiology 2013 Nov 108 (6): 387. Fedele Francesco, Mancone Massimo, Chilian William M, Severino Paolo, Canali Emanuele, Logan Suzanna, De Marchis Maria Laura, Volterrani Maurizio, Palmirotta Raffaele, Guadagni Fiorel |
Common genetic variants in selected Ca²? signaling genes and the risk of appropriate ICD interventions in patients with heart failure. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2013 Dec 38 (3): 169-77. Francia Pietro, Adduci Carmen, Ricotta Agnese, Stanzione Rosita, Sensini Isabella, Uccellini Arianna, Frattari Alessandra, Balla Cristina, Cotugno Maria, Cappato Riccardo, Rubattu Speranza, Volpe Massi |
Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling. Cardiovascular research 2015 Aug . Lozano-Velasco Estefanía, Hernández-Torres Francisco, Daimi Houria, Serra Selma A, Herraiz Adela, Hove-Madsen Leif, Aránega Amelia, Franco Die |
Intellectual disability and cognitive ability in Darier disease: Swedish nation-wide study. The British journal of dermatology 2015 Jul 173 (1): 155-8. Cederlöf M, Karlsson R, Larsson H, Almqvist C, Magnusson P K E, Nordlind K, Landén M, Lichtenstein |
Darier disease in Israel: combined evaluation of genetic and neuropsychiatric aspects. The British journal of dermatology 2015 Oct . Dodiuk-Gad R P, Cohen-Barak E, Khayat M, Milo H, Amariglio-Diskin L, Danial-Faran N, Sah M, Ziv M, Shani-Adir A, Amichai B, Zlotogorski A, Borochowitz Z, Rozenman D, Shalev |
Novel mutations in Darier disease and association to self-reported disease severity. PloS one 2017 10 12 (10): e0186356. Leong Ivone U S, Stuckey Alexander, Ahanian Tara, Cederlöf Martin, Wikstrom Jakob |
Novel West syndrome candidate genes in a Chinese cohort. CNS neuroscience & therapeutics 2018 4 24 (12): 1196-1206. Peng Jing, Wang Ying, He Fang, Chen Chen, Wu Li-Wen, Yang Li-Fen, Ma Yu-Ping, Zhang Wen, Shi Zi-Qing, Chen Chao, Xia Kun, Guo Hui, Yin Fei, Pang N |
Genotype-phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2018 10 177 (8): 717-726. Gordon-Smith Katherine, Green Elaine, Grozeva Detelina, Tavadia Sherine, Craddock Nick, Jones Li |
Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits.
European journal of human genetics : EJHG 2019 Jan . van Setten Jessica, Verweij Niek, Mbarek Hamdi, Niemeijer Maartje N, Trompet Stella, Arking Dan E, Brody Jennifer A, Gandin Ilaria, Grarup Niels, Hall Leanne M, Hemerich Daiane, Lyytikäinen Leo-Pekka, Mei Hao, Müller-Nurasyid Martina, Prins Bram P, Robino Antonietta, Smith Albert V, Warren Helen R, Asselbergs Folkert W, Boomsma Dorret I, Caulfield Mark J, Eijgelsheim Mark, Ford Ian, Hansen Torben, Harris Tamara B, Heckbert Susan R, Hottenga Jouke-Jan, Iorio Annamaria, Kors Jan A, Linneberg Allan, MacFarlane Peter W, Meitinger Thomas, Nelson Christopher P, Raitakari Olli T, Silva Aldana Claudia T, Sinagra Gianfranco, Sinner Moritz, Soliman Elsayed Z, Stoll Monika, Uitterlinden Andre, van Duijn Cornelia M, Waldenberger Melanie, Alonso Alvaro, Gasparini Paolo, Gudnason Vilmundur, Jamshidi Yalda, Kääb Stefan, Kanters Jørgen K, Lehtimäki Terho, Munroe Patricia B, Peters Annette, Samani Nilesh J, Sotoodehnia Nona, Ulivi Sheila, Wilson James G, de Geus Eco J C, Jukema J Wouter, Stricker Bruno, van der Harst Pim, de Bakker Paul I W, Isaacs Aar |
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 |
Whole exome sequencing improves mutation detection in Hailey-Hailey disease. The Journal of dermatology 2021 4 48 (7): 989-992. Wang Zhe, Wang Zhenzhen, Sun Lele, Yu Xueping, Pang Zheng, Liu Hong, Zhang Fur |
Proteomic Characterization of a Candidate Polygenic Driver of Metabolism in Non-small Cell Lung Cancer. Journal of molecular biology 2022 May 434 (13): 167636. Badr Heba, Blutrich Ron, Chan Kaitlin, Tong Jiefei, Taylor Paul, Zhang Wen, Kafri Ran, Röst Hannes L, Tsao Ming-Sound, Moran Michael |
Subcellular compartmentalization of STIM1 for the distinction of Darier disease from Hailey-Hailey disease. Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG 2022 11 20 (12): 1613-1619. Stanisz Hedwig, Mitteldorf Christina, Janning Helena, Bennemann Anette, Schön Michael P, Frank Jor |
Association of Somatic ATP2A2 Damaging Variants With Grover Disease. JAMA dermatology 2023 5 . Devin Seli, Katharine T Ellis, Mohamad Goldust, Khadim Shah, Ronghua Hu, Jing Zhou, Jennifer M McNiff, Keith A Choa |
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced genetics (Hoboken, N.J.) 2023 3 4 (1): 2200013. Estrella Elicia, Rockowitz Shira, Thorne Marielle, Smith Pressley, Petit Jeanette, Zehnder Veronica, Yu Richard N, Bauer Stuart, Berde Charles, Agrawal Pankaj B, Beggs Alan H, Gharavi Ali G, Kunkel Louis, Brownstein Catherine |
Whole-Exome Sequencing Reveals Mutational Signature of Hypertrophic Cardiomyopathy. International journal of general medicine 2023 10 16 4617-4628. Xi-Qin Wang, Fang Yuan, Bao-Rui |
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- Page last updated:Apr 16, 2024
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