Somatic gain-of-function mutations in BUD13 promote oncogenesis by disrupting Fbw7 function
Somatic mutations occurring on key enzymes are extensively studied and targeted therapies
are developed with clinical promises. However, context-dependent enzyme function through …
are developed with clinical promises. However, context-dependent enzyme function through …
Influence of multiple apolipoprotein AI and B genetic variations on insulin resistance and metabolic syndrome in obstructive sleep apnea
X Li, Z Fu, H Xu, J Zou, H Zhu, Z Li, K Su, D Huai… - Nutrition & …, 2020 - Springer
Background The relationships between apolipoprotein AI (APOA-I), apolipoprotein B (APOB)
with insulin resistance, metabolic syndrome (MetS) are unclear in OSA. We aimed to …
with insulin resistance, metabolic syndrome (MetS) are unclear in OSA. We aimed to …
[HTML][HTML] Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis
J Zhao, X Wu, S Nie, X Gao, J Sun, K Li… - Clinical …, 2017 - ncbi.nlm.nih.gov
Objective CDKN2B-AS1 polymorphisms were shown to associate with the risk of stroke in
European. The goal of this study was to evaluate the contribution of CDKN2B-AS1 …
European. The goal of this study was to evaluate the contribution of CDKN2B-AS1 …
Polymorphisms in genes that affect the variation of lipid levels in a Brazilian pediatric population with sickle cell disease: rs662799 APOA5 and rs964184 ZPR1
TNS Valente-Frossard, NRC Cruz, FO Ferreira… - Blood Cells, Molecules …, 2020 - Elsevier
This cross-sectional study investigated associations between SNPs in metabolizing lipid
genes, alpha-thalassemia and laboratory parameters in two forms of sickle cell disease …
genes, alpha-thalassemia and laboratory parameters in two forms of sickle cell disease …
The ZPR1 genotype predicts myocardial infarction in patients with familial hypercholesterolemia
Background The rs964184 variant in the ZPR1 gene has been associated with blood lipids
and cardiovascular disease risk in the general population through genome-wide association …
and cardiovascular disease risk in the general population through genome-wide association …
ALDH2 rs671 Polymorphism Likely a Risk Factor for Hemorrhagic Stroke: A Hospital-Based Study
S Zhang, W Luo, T Pan, J Xie, Z Xu… - International Journal of …, 2023 - Taylor & Francis
Background Hypertension is the main risk factor for hemorrhagic stroke. Aldehyde
dehydrogenase 2 (ALDH2) may inhibit the occurrence of hypertension by anti-oxidative …
dehydrogenase 2 (ALDH2) may inhibit the occurrence of hypertension by anti-oxidative …
[PDF][PDF] Impact of gender and age on the association of the BUD13-ZNF259 rs964184 polymorphism with coronary heart disease.
X Xu, Y Li, Y Huang, H Ye, L Han, H Ji… - Anatolian Journal of …, 2018 - jag.journalagent.com
Objective: Coronary heart disease (CHD) is the most common cause of death worldwide.
This study aimed to validate the association of the rs964184 polymorphism with the CHD …
This study aimed to validate the association of the rs964184 polymorphism with the CHD …