[PDF][PDF] Sweet sixteenth for ChREBP: established roles and future goals

A Abdul-Wahed, S Guilmeau, C Postic - Cell metabolism, 2017 - cell.com
With the identification of ChREBP in 2001, our interest in understanding the molecular
control of carbohydrate sensing has surged. While ChREBP was initially studied as a master …

MondoA/ChREBP: The usual suspects of transcriptional glucose sensing; Implication in pathophysiology

P Richards, S Ourabah, J Montagne, AF Burnol… - Metabolism, 2017 - Elsevier
Identification of the Mondo glucose-responsive transcription factors family, including the
MondoA and MondoB/ChREBP paralogs, has shed light on the mechanism whereby …

The association between a Fatty Acid Binding Protein 1 (FABP1) gene polymorphism and serum lipid abnormalities in the MASHAD cohort study

M Valizadeh, M Aghasizadeh, M Nemati… - … and Essential Fatty …, 2021 - Elsevier
Introduction Dyslipidemia is a known risk factor for cardiovascular disease and is partially
determined by genetic variations in the genes involved in lipoprotein metabolism. Therefore …

Amino acid change in the carbohydrate response element binding protein is associated with lower triglycerides and myocardial infarction incidence depending on …

C Ortega-Azorín, JV Sorlí, R Estruch… - Circulation …, 2014 - Am Heart Assoc
Background—A variant (rs3812316, C771G, and Gln241His) in the MLXIPL (Max-like
protein X interacting protein-like) gene encoding the carbohydrate response element …

Association of common genetic variants with lipid traits in the Indian population

GK Walia, V Gupta, A Aggarwal, M Asghar… - PloS one, 2014 - journals.plos.org
Genome-wide association studies (GWAS) have been instrumental in identifying novel
genetic variants associated with altered plasma lipid levels. However, these quantitative trait …

Identifying genetic markers associated with susceptibility to cardiovascular diseases

H Shukla, JL Mason, A Sabyah - Advances in Medical …, 2021 - api.taylorfrancis.com
Cardiovascular diseases (CVDs), characterized by diseases of the heart and blood vessels,
are the number one cause of death globally, representing 31% of all deaths in 2015 [1]. Most …

Contextualizing genetics for regional heart failure care

P Iyngkaran, MC Thomas, R Johnson… - Current Cardiology …, 2016 - ingentaconnect.com
Congestive heart failure (CHF) is a chronic and often devastating cardiovascular disorder
with no cure. There has been much advancement in the last two decades that has seen …

[PDF][PDF] Zinc finger protein 259 (ZNF259) polymorphisms are associated with the risk of metabolic syndrome in a Han Chinese population

Y Wu, S Yu, S Wang, J Shi, Z Xu, Q Zhang, Y Fu, Y Qi… - Clin Lab, 2015 - researchgate.net
Background: Zinc finger protein 259 (ZNF259) binds to the cytoplasmic domain of epidermal
growth factor recep-tor (EGFR) in quiescent cells and contributes tolipid metabolism. This …

载脂蛋白A5 (ApoA5) 基因多态性与动脉粥样硬化性脑梗死关系的研究

洪雁, 周碧燕, 李洁, 梁智, 张千 - 中国实用神经疾病杂志, 2015 - cqvip.com
目的: 研究脑梗死患者的动脉粥样硬化程度和载脂蛋白A5 (ApoA5)‐1131T/C 和553G/T
两位点的关系. 方法选取2011‐12—2013‐12 间我院医学影像科计算机体层扫描和磁共振确诊 …

[HTML][HTML] Association study of BUD13-ZNF259 gene rs964184 polymorphism and hemorrhagic stroke risk

S Zhou, J Zhao, Z Wang, K Li, S Nie, F Gao… - … Journal of Clinical …, 2015 - ncbi.nlm.nih.gov
We aimed to evaluate the association of rs964184 of BUD13-ZNF259 gene with the risk of
hemorrhagic stroke (HS). A total of 138 HS cases and 587 controls were recruited for the …