Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: PAFAH1B2[original query] |
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Exclusion of the alpha2 subunit of platelet-activating factor acetylhydrolase 1b (PAFAH1B2) as a prothrombotic gene in a protein C-deficient kindred and population-based case-control sample. Thrombosis and haemostasis 2007 Sep 98 (3): 587-92. Hasstedt Sandra J, Scott Bruce T, Rosendaal Frits R, Callas Peter W, Vossen Carla Y, Long George L, Bovill Edwin |
Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2).
The Journal of biological chemistry 2013 Apr 288 (17): 11940-8. Zhou Gang, Marathe Gopal K, Hartiala Jaana, Hazen Stanley L, Allayee Hooman, Tang W H Wilson, McIntyre Thomas |
Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.
American journal of human genetics 2014 Feb 94 (2): 223-32. Peloso Gina M, Auer Paul L, Bis Joshua C, Voorman Arend, Morrison Alanna C, Stitziel Nathan O, Brody Jennifer A, Khetarpal Sumeet A, Crosby Jacy R, Fornage Myriam, Isaacs Aaron, Jakobsdottir Johanna, Feitosa Mary F, Davies Gail, Huffman Jennifer E, Manichaikul Ani, Davis Brian, Lohman Kurt, Joon Aron Y, Smith Albert V, Grove Megan L, Zanoni Paolo, Redon Valeska, Demissie Serkalem, Lawson Kim, Peters Ulrike, Carlson Christopher, Jackson Rebecca D, Ryckman Kelli K, Mackey Rachel H, Robinson Jennifer G, Siscovick David S, Schreiner Pamela J, Mychaleckyj Josyf C, Pankow James S, Hofman Albert, Uitterlinden Andre G, Harris Tamara B, Taylor Kent D, Stafford Jeanette M, Reynolds Lindsay M, Marioni Riccardo E, Dehghan Abbas, Franco Oscar H, Patel Aniruddh P, Lu Yingchang, Hindy George, Gottesman Omri, Bottinger Erwin P, Melander Olle, Orho-Melander Marju, Loos Ruth J F, Duga Stefano, Merlini Piera Angelica, Farrall Martin, Goel Anuj, Asselta Rosanna, Girelli Domenico, Martinelli Nicola, Shah Svati H, Kraus William E, Li Mingyao, Rader Daniel J, Reilly Muredach P, McPherson Ruth, Watkins Hugh, Ardissino Diego, , Zhang Qunyuan, Wang Judy, Tsai Michael Y, Taylor Herman A, Correa Adolfo, Griswold Michael E, Lange Leslie A, Starr John M, Rudan Igor, Eiriksdottir Gudny, Launer Lenore J, Ordovas Jose M, Levy Daniel, Chen Y-D Ida, Reiner Alexander P, Hayward Caroline, Polasek Ozren, Deary Ian J, Borecki Ingrid B, Liu Yongmei, Gudnason Vilmundur, Wilson James G, van Duijn Cornelia M, Kooperberg Charles, Rich Stephen S, Psaty Bruce M, Rotter Jerome I, O'Donnell Christopher J, Rice Kenneth, Boerwinkle Eric, Kathiresan Sekar, Cupples L Adrien |
Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians. Journal of lipid research 2015 Dec . Gombojav Bayasgalan, Lee Soo Ji, Kho Minjung, Song Yun-Mi, Lee Kayoung, Sung Jooh |
Clinical Phenotypes Associated to Engrailed 2 Gene Alterations in a Series of Neuropediatric Patients. Frontiers in neuroanatomy 2018 8 12 61. Carratala-Marco Francisco, Andreo-Lillo Patricia, Martinez-Morga Marta, Escamez-Martínez Teresa, Botella-López Arancha, Bueno Carlos, Martinez Salvad |
A Genome-Wide Association Study of Metabolic Syndrome in the Taiwanese Population. Nutrients 2024 1 16 (1): . Chih-Yi Ho, Jia-In Lee, Shu-Pin Huang, Szu-Chia Chen, Jiun-Hung Ge |
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- Page last updated:Apr 29, 2024
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