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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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Human Genome Epidemiology Literature Finder|Home|PHGKB
Human Genome Epidemiology Literature Finder
Last data update: Jan 25, 2025
. (Total: 235671Documents)
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Cardiovascular Diseases and GNB3[original query]
[A cross-racial analysis on the susceptible gene polymorphisms of salt-sensitive hypertension].
Zhonghua xin xue guan bing za zhi 2010 Oct 38 (10): 943-8.
Lu Jia-peng, Zhang Ling, Wang W
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[DISTRIBUTION OF GENOTYPES OF C825T POLYMORPHISM ß3-SUBUNIT G-PROTEIN GENE IN PATIENTS WITH ARTERIAL HYPERTENSION ACCORDING THE DEGREE OF OBESITY].
Georgian medical news 0 (244-245): 36-40.
Moiseyenko I, Prystupa L, Garbuzova V, Pogorielova O, Opolonskaya
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Cardiovascular diseases-related GNB3 C825T polymorphism has a significant sex-specific effect on serum soluble E-selectin levels.
Journal of inflammation (London, England) 2016 13 39.
Gbadoe Kokoè Mélinda, Berdouzi Nazha, Aguiñano Alex-Ander Aldasoro, Ndiaye Ndeye Coumba, Visvikis-Siest Soph
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Association of G-protein beta3 subunit gene C825T polymorphism with cardiac and cerebrovascular events in Chinese hypertensive patients.
Clinical and experimental hypertension (New York, N.Y. : 1993) 2017 Jan 1-5.
Zhu Weiwei, Li Jing, Sun Xipeng, Hua
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Comprehensive insight into functional interaction between GNB3 C825T and eNOS T-786C, G894T gene polymorphisms and association with susceptibility to diabetic erectile dysfunction.
Andrology 2018 Aug .
Ben Khedher M R, Abid M, Jamoussi K, Hammami
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Association of metabolic syndrome components with the genotypes of the ?825? polymorphism in the g protein ?3-subunit gene (GNB3).
Wiadomosci lekarskie (Warsaw, Poland : 1960) 2018 11 71 (7): 1242-1249.
Prystupa Lyudmyla N, Moiseyenko Irina O, Garbuzova Victoria Yu, Kmyta Vladyslava V, Dudchenko Irina
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The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population.
PloS one 2020 6 15 (6): e0234547.
Soltész Beáta, Pikó Péter, Sándor János, Kósa Zsigmond, Ádány Róza, Fiatal Szilv
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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