[HTML][HTML] Association of a transcription factor 21 gene polymorphism with hypertension

T Fujimaki, M Oguri, H Horibe, K Kato… - Biomedical …, 2015 - spandidos-publications.com
Various loci and genes that confer susceptibility to coronary artery disease (CAD) have been
identified mainly in Caucasian populations by genome‑wide association studies (GWASs) …

Transforming growth factor-β1 gene+ 869T/C, but not+ 915G/C polymorphism is associated with essential hypertension in a Chinese patient cohort

B Xi, Q Wang, H Pan - Molecular biology reports, 2012 - Springer
Many studies have suggested that transforming growth factor-β1 (TGF-β1) gene might be
involved in the development of hypertension. However, results have been inconsistent. In …

Linkage analysis of a region on chromosome 2 with essential hypertension in Chinese families

D Zhu, W Huang, H Wang, M Xiong, S Chu… - Chinese medical …, 2002 - mednexus.org
Objective To verify the linkage of the candidate regions identified in a previous study
(markers D2S168, D2S151, D2S142 on chromosome 2) with hypertension in Chinese …

Association between CACNB2 gene polymorphisms and essential hypertension

Q Sun, X Wang, Y Huang, Y Hu, J Tang… - Zhonghua yi xue yi …, 2013 - europepmc.org
Objective To assess the association between single nucleotide polymorphisms (SNPs) of
calcium channel β 2 subunit (CACNB2) gene and essential hypertension (EH) in ethnic Han …

Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study

F Frau, R Zaninello, E Salvi, MF Ortu, D Braga… - …, 2014 - Future Medicine
Background: Essential hypertension arises from the combined effect of genetic and
environmental factors. A pharmacogenomics approach could help to identify additional …

[HTML][HTML] Association of rs1137101 with hypertension and type 2 diabetes mellitus of Mongolian and Han Chinese

KY Zhao, ML Yuan, YN Wu, HW Cui… - World Journal of …, 2022 - ncbi.nlm.nih.gov
BACKGROUND Hypertension (HTN) and type 2 diabetes mellitus (T2DM) are often
coincident, and each condition is considered a risk factor for the other. Both occur frequently …

The role of NOS3 (rs2070744) and GNB3 (rs5443) genes' polymorphisms in endothelial dysfunction pathway and carotid intima-media thickness in hypertensive …

A Sydorchuk, L Sydorchuk, A Gutnitska… - General Physiology …, 2023 - search.ebscohost.com
The mechanisms orchestrating the balance between nitric oxide and endothelium-derived
contracting factors, and genetic predisposition to endothelial dysfunction in hypertensive …

[HTML][HTML] The contributory role of angiotensin receptor-like 1 gene multiple polymorphisms in hypertension among northeastern Han Chinese

R Liu, H Zhao, Y Wang, Y Wang, C Lu, Y Xiao, N Jia… - PloS one, 2014 - journals.plos.org
Background and Objective Via direct sequencing, we have recently identified six common
polymorphisms in angiotensin receptor-like 1 (AGTRL1) gene, and found only two …

[PDF][PDF] Risk of type 2 diabetes mellitus and cardiovascular complications in KCNJ11, HHEX and SLC30A8 genetic polymorphisms carriers: a case-control study

TD Aka, U Saha, SA Shati, MA Aziz, M Begum… - Heliyon, 2021 - cell.com
Background Type 2 diabetes mellitus (T2DM) and cardiovascular disease (CVD) are two
deadly diseases caused by the complex interaction of multiple genetic loci, lifestyle and …

An exploration of gene‐gene interactions and their effects on hypertension

Y Meng, S Groth, JR Quinn… - International journal of …, 2017 - Wiley Online Library
Hypertension tends to perpetuate in families and the heritability of hypertension is estimated
to be around 20–60%. So far, the main proportion of this heritability has not been found by …