Pharmacogenomics of sulfonylureas in type 2 diabetes mellitus; a systematic review

L Karkhaneh, O Tabatabaei-Malazy… - Journal of Diabetes & …, 2022 - Springer
Purpose Genetic factors have a role in response to a target medication (personalized
medicine). This study aimed to review available evidence about the relationship between …

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 …

Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case–control study and meta-analysis

M Moazzam-Jazi, L Najd-Hassan-Bonab… - Scientific Reports, 2022 - nature.com
Due to the central role in insulin secretion, the potassium inwardly-rectifying channel
subfamily J member 11 (KCNJ11) gene is one of the essential genes for type 2 diabetes …

The genetic susceptibility profile of type 2 diabetes and reflection of its possible role related to reproductive dysfunctions in the southern Indian population of …

K Irgam, BS Reddy, SG Hari, S Banapuram… - BMC Medical …, 2021 - Springer
Background The genetic association studies of type 2 diabetes mellitus (T2DM) hitherto
undertaken among the Indian populations are grossly inadequate representation of the …

[HTML][HTML] Implication of KCNJ11 and TCF7L2 gene variants for the predisposition of type 2 diabetes mellitus in West Bengal, India

B Bankura, AK Pattanayak, S Ghosh, S Guria… - Diabetes Epidemiology …, 2022 - Elsevier
Abstract Background Population-based Genome-wide association studies showed variants
in KCNJ11 and TCF7L2 genes are associated with type 2 diabetes mellitus (T2DM). Our …

Determination of individual type 2 diabetes risk profile in the North East Indian population & its association with anthropometric parameters

P Sarkar, A Bhowmick, MP Baruah… - Indian Journal of …, 2019 - journals.lww.com
Methods: DNA was extracted from blood samples of 155 patients with T2D and 100 controls.
Genotyping was performed by polymerase chain reaction-restriction fragment length …

Association between KCNJ11 E23K polymorphism and the risk of type 2 diabetes mellitus: A global meta-analysis

Y Ren, W Zhu, J Shi, A Shao, Y Cheng, Y Liu - Journal of Diabetes and its …, 2022 - Elsevier
Background Potassium inwardly rectifying channel, subfamily J member 11 (KCNJ11) is
considered to be a potential susceptible gene of type 2 diabetes mellitus (T2DM), and the …

Role of variants rs5030717 and rs5030718 of TLR4 in the risk prediction of nephropathy, hypertension and dyslipidaemia in type 2 diabetes mellitus

SA Abbas, ST Raza, SS Mir, Z Siddiqi… - British Journal of …, 2018 - Taylor & Francis
Background: Type 2 diabetes mellitus describes a metabolic disorder characterised by
prolonged elevated blood glucose that brings a risk of developing microvascular and …

[HTML][HTML] 利拉鲁肽对Kir6. 2 基因E23K 位点突变β 细胞胰岛素分泌功能的影响

庄兰艮, 金国玺, 杨青青, 胡小磊, 裴晓艳 - 中华全科医学, 2023 - zhqkyx.net
目的Kir6. 2 编码基因多态与糖尿病, 胰岛素抵抗相关, 本研究旨在探讨高糖环境下,
利拉鲁肽对Kir6. 2 基因E23K 位点突变的胰岛β 细胞胰岛素分泌功能的影响及机制. 方法以NIT …

[PDF][PDF] Updates In Common Genetic Variants May Help Guide Drug Selection For Treating Uncontrolled Diabetes

S Bazzazzadehgan, Z Shariat-Madar, F Mahdi - 2025 - preprints.org
Type 2 diabetes mellitus (T2DM) is a common, lifelong metabolic disorder. Adults with T2DM
bear a greater burden of cardiometabolic risk factors than the general population. T2DM …