Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: PPP3CA[original query] |
---|
Polymorphisms in the calcineurin genes are associated with the training responsiveness of cardiac phenotypes in Chinese young adults. European journal of applied physiology 2010 Nov 110 (4): 761-7. He Zi-Hong, Hu Yang, Li Yan-Chun, Bao Da-Peng, Ruiz Jonatan R, Lucia Alejand |
Fine mapping of calcineurin (PPP3CA) gene reveals novel alternative splicing patterns, association of 5'UTR trinucleotide repeat with addiction vulnerability, and differential isoform expression in Alzheimer's disease. Substance use & misuse 2010 Sep 45 (11): 1809-26. Chiocco Matthew J, Zhu Xuguang, Walther Donna, Pletnikova Olga, Troncoso Juan C, Uhl George R, Liu Qing-Ro |
Are calcineurin genes associated with endurance phenotype traits? European journal of applied physiology 2010 Jun 109 (3): 359-69. He Zi-Hong, Hu Yang, Wang Hai-Yan, Li Yan-Chun, Lu Ying-Li, Zhang Li, Bao Ba-Peng, Ruiz Jonatan R, Lucia Alejand |
Are calcineurin genes associated with athletic status? A function, replication study. Medicine and science in sports and exercise 2011 Aug 43 (8): 1433-40. He Zi-Hong, Hu Yang, Li Yan-Chun, Yvert Thomas, Santiago Catalina, Gómez-Gallego Félix, Ruiz Jonatan R, Lucia Alejand |
Investigation of two Wnt signalling pathway single nucleotide polymorphisms in a breast cancer-affected Australian population. Twin research and human genetics : the official journal of the International Society for Twin Studies 2011 Dec 14 (6): 562-7. Gabrovska Plamena N, Smith Robert A, Haupt Larisa M, Griffiths Lyn |
AMD-associated genes encoding stress-activated MAPK pathway constituents are identified by interval-based enrichment analysis. PloS one 2013 8 (8): e71239. SanGiovanni John Paul, Lee Phil |
A genome-wide association study of anorexia nervosa.
Molecular psychiatry 2014 Oct 19 (10): 1085-94. Boraska V, Franklin C S, Floyd J A B, Thornton L M, Huckins L M, Southam L, Rayner N W, Tachmazidou I, Klump K L, Treasure J, Lewis C M, Schmidt U, Tozzi F, Kiezebrink K, Hebebrand J, Gorwood P, Adan R A H, Kas M J H, Favaro A, Santonastaso P, Fernández-Aranda F, Gratacos M, Rybakowski F, Dmitrzak-Weglarz M, Kaprio J, Keski-Rahkonen A, Raevuori A, Van Furth E F, Slof-Op 't Landt M C T, Hudson J I, Reichborn-Kjennerud T, Knudsen G P S, Monteleone P, Kaplan A S, Karwautz A, Hakonarson H, Berrettini W H, Guo Y, Li D, Schork N J, Komaki G, Ando T, Inoko H, Esko T, Fischer K, Männik K, Metspalu A, Baker J H, Cone R D, Dackor J, DeSocio J E, Hilliard C E, O'Toole J K, Pantel J, Szatkiewicz J P, Taico C, Zerwas S, Trace S E, Davis O S P, Helder S, Bühren K, Burghardt R, de Zwaan M, Egberts K, Ehrlich S, Herpertz-Dahlmann B, Herzog W, Imgart H, Scherag A, Scherag S, Zipfel S, Boni C, Ramoz N, Versini A, Brandys M K, Danner U N, de Kovel C, Hendriks J, Koeleman B P C, Ophoff R A, Strengman E, van Elburg A A, Bruson A, Clementi M, Degortes D, Forzan M, Tenconi E, Docampo E, Escaramís G, Jiménez-Murcia S, Lissowska J, Rajewski A, Szeszenia-Dabrowska N, Slopien A, Hauser J, Karhunen L, Meulenbelt I, Slagboom P E, Tortorella A, Maj M, Dedoussis G, Dikeos D, Gonidakis F, Tziouvas K, Tsitsika A, Papezova H, Slachtova L, Martaskova D, Kennedy J L, Levitan R D, Yilmaz Z, Huemer J, Koubek D, Merl E, Wagner G, Lichtenstein P, Breen G, Cohen-Woods S, Farmer A, McGuffin P, Cichon S, Giegling I, Herms S, Rujescu D, Schreiber S, Wichmann H-E, Dina C, Sladek R, Gambaro G, Soranzo N, Julia A, Marsal S, Rabionet R, Gaborieau V, Dick D M, Palotie A, Ripatti S, Widén E, Andreassen O A, Espeseth T, Lundervold A, Reinvang I, Steen V M, Le Hellard S, Mattingsdal M, Ntalla I, Bencko V, Foretova L, Janout V, Navratilova M, Gallinger S, Pinto D, Scherer S W, Aschauer H, Carlberg L, Schosser A, Alfredsson L, Ding B, Klareskog L, Padyukov L, Courtet P, Guillaume S, Jaussent I, Finan C, Kalsi G, Roberts M, Logan D W, Peltonen L, Ritchie G R S, Barrett J C, , Estivill X, Hinney A, Sullivan P F, Collier D A, Zeggini E, Bulik C |
Distinct patterns of somatic genome alterations in lung adenocarcinomas and squamous cell carcinomas. Nature genetics 2016 May . Campbell Joshua D, Alexandrov Anton, Kim Jaegil, Wala Jeremiah, Berger Alice H, Pedamallu Chandra Sekhar, Shukla Sachet A, Guo Guangwu, Brooks Angela N, Murray Bradley A, Imielinski Marcin, Hu Xin, Ling Shiyun, Akbani Rehan, Rosenberg Mara, Cibulskis Carrie, Ramachandran Aruna, Collisson Eric A, Kwiatkowski David J, Lawrence Michael S, Weinstein John N, Verhaak Roel G W, Wu Catherine J, Hammerman Peter S, Cherniack Andrew D, Getz Gad, , Artyomov Maxim N, Schreiber Robert, Govindan Ramaswamy, Meyerson Matth |
DISC1 as a Possible Genetic Contribution to Opioid Dependence in a Polish Sample. Journal of studies on alcohol and drugs 2016 Mar 77 (2): 220-6. Fudalej Sylwia, Jakubczyk Andrzej, Kopera Maciej, Piwonski Jerzy, Bielecki Wojciech, Drygas Wojciech, Wasilewska Krystyna, Ilgen Mark, Bohnert Amy, Barry Kristen, Ploski Rafal, Blow Frederic C, Wojnar Marc |
Association of the PPP3CA c.249G>A variant with clinical outcomes of tacrolimus-based therapy in kidney transplant recipients. Pharmacogenomics and personalized medicine 2017 10 101-106. Salgado Patricia C, Genvigir Fabiana Dv, Felipe Claudia R, Tedesco-Silva Helio, Medina-Pestana Jose O, Doi Sonia Q, Hirata Mario H, Hirata Rosario |
Polymorphisms in mTOR and Calcineurin Signaling Pathways Are Associated With Long-Term Clinical Outcomes in Kidney Transplant Recipients. Frontiers in pharmacology 2018 9 1296. Campos-Salazar Antony Brayan, Genvigir Fabiana Dalla Vecchia, Felipe Claudia Rosso, Tedesco-Silva Helio, Medina-Pestana José, Monteiro Gabriela Vieira, Basso Rodrigo de Gouveia, Cerda Alvaro, Hirata Mario Hiroyuki, Hirata Rosario Dominguez Cres |
Convergent functional genomics of cocaine misuse in humans and animal models. The American journal of drug and alcohol abuse 2019 8 46 (1): 22-30. Forero Diego A, González-Giraldo Yei |
Differential expression of genes related to calcineurin and mTOR signaling and regulatory miRNAs in peripheral blood from kidney recipients under tacrolimus-based therapy. Annals of translational medicine 2020 11 8 (17): 1051. Bonezi Vivian, Genvigir Fabiana Dalla Vecchia, Salgado Patrícia de Cássia, Felipe Claudia Rosso, Tedesco-Silva Helio, Medina-Pestana José Osmar, Cerda Alvaro, Doi Sonia Quateli, Hirata Mario Hiroyuki, Hirata Rosario Dominguez Cres |
PPP3CA truncating variants clustered in the regulatory domain cause early-onset refractory epilepsy. Clinical genetics 2021 5 100 (2): 227-233. Panneerselvam Sugi, Wang Julia, Zhu Wenmiao, Dai Hongzheng, Pappas John G, Rabin Rachel, Low Karen J, Rosenfeld Jill A, Emrick Lisa, Xiao Rui, Xia Fan, Yang Yaping, Eng Christine M, Anderson Anne, Chau Vann, Soler-Alfonso Claudia, Streff Haley, Lalani Seema R, Mercimek-Andrews Saadet, , , Bi Weim |
Deletion mutation within the goat PPP3CA gene identified by GWAS significantly affects litter size. Reproduction, fertility, and development 2021 4 33 (7): 476-483. Bai Yangyang, Li Jie, Zhu Haijing, Liu Jinwang, Dong Shuwei, Li Longping, Qu Lei, Chen Hong, Song Xiaoyue, Lan Xianyo |
CD8+ cell somatic mutations in multiple sclerosis patients and controls-Enrichment of mutations in STAT3 and other genes implicated in hematological malignancies. PloS one 2021 12 16 (12): e0261002. Valori Miko, Jansson Lilja, Tienari Pentti |
Development and Verification of the Hypoxia- and Immune-Associated Prognostic Signature for Pancreatic Ductal Adenocarcinoma. Frontiers in immunology 2021 10 12 728062. Chen Dongjie, Huang Hui, Zang Longjun, Gao Wenzhe, Zhu Hongwei, Yu Xi |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: