Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: POC1B[original query] |
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Analysis of catechol-O-methyltransferase gene mutation and identification of new pathogenic gene for paroxysmal kinesigenic dyskinesia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Dec . Gu Chengzhi, Li Jia, Zhu Lianhai, Lu Zhenhui, Huang Huai |
Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.
Human molecular genetics 2016 Apr 25 (7): 1447-56. Johansson Åsa, Eriksson Niclas, Lindholm Daniel, Varenhorst Christoph, James Stefan, Syvänen Ann-Christine, Axelsson Tomas, Siegbahn Agneta, Barratt Bryan J, Becker Richard C, Himmelmann Anders, Katus Hugo A, Steg Philippe Gabriel, Storey Robert F, Wallentin Lars, |
Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.
Circulation. Cardiovascular genetics 2017 Dec 10 (6): . Salo Perttu P, Havulinna Aki S, Tukiainen Taru, Raitakari Olli, Lehtimäki Terho, Kähönen Mika, Kettunen Johannes, Männikkö Minna, Eriksson Johan G, Jula Antti, Blankenberg Stefan, Zeller Tanja, Salomaa Veikko, Kristiansson Kati, Perola Mark |
Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.
BMC medical genomics 2018 Jan 11 (1): 2. Hendry Liesl M, Sahibdeen Venesa, Choudhury Ananyo, Norris Shane A, Ramsay Michèle, Lombard Zané, |
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