Cargando…

Association of KCNJ11 rs5219 gene polymorphism with type 2 diabetes mellitus in a population of Syria: a case-control study

BACKGROUND: Type 2 diabetes mellitus is believed to be a polygenic disorder that develops as a result of a complex interaction between multiple genes and environmental factors. KCNJ11 gene encodes a Kir6.2 protein which forms the inner section of the potassium channels in pancreatic beta cells. Seve...

Descripción completa

Detalles Bibliográficos
Autores principales:	Makhzoom, Osama, Kabalan, Younes, AL-Quobaili, Faizeh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2019
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567472/ https://www.ncbi.nlm.nih.gov/pubmed/31195986 http://dx.doi.org/10.1186/s12881-019-0846-3

Ejemplares similares

Impact of KCNJ11 rs5219, UCP2 rs659366, and MTHFR rs1801133 Polymorphisms on Type 2 Diabetes: A Cross-Sectional Study
por: Lapik, Irina Alexandrovna, et al.
Publicado: (2021)

Association of eNOS (G894T, rs1799983) and KCNJ11 (E23K, rs5219) gene polymorphism with coronary artery disease in North Indian population
por: Raza, Syed Tasleem, et al.
Publicado: (2021)

KCNJ11: Genetic Polymorphisms and Risk of Diabetes Mellitus
por: Haghvirdizadeh, Polin, et al.
Publicado: (2015)

Association between KCNJ11 rs5219 variant and alcohol consumption on the effect of insulin secretion in a community-based Korean cohort: a 12-year follow-up study
por: Yun, Ji Ho, et al.
Publicado: (2021)

Diabetes Insipidus due to Metastases of Undiagnosed Lung Cancer: A Case Report from Syria
por: Alali, Ibrahim, et al.
Publicado: (2023)

Plasma amyloid β levels in Alzheimer’s disease and cognitively normal controls in Syrian population
por: Manafikhi, Rafah, et al.
Publicado: (2021)

Congenital hypothyroidism: a five-year retrospective study at Children's University Hospital, Damascus, Syria
por: Saoud, Mariam, et al.
Publicado: (2019)

Independent case-control study in KCNJ11 gene polymorphism with Type 2 diabetes Mellitus
por: Alqadri, Nada
Publicado: (2022)

KCNJ11 and KCNQ1 Gene Polymorphisms and Placental Expression in Women with Gestational Diabetes Mellitus
por: Majcher, Sandra, et al.
Publicado: (2022)

Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population
por: Tran, Nam Quang, et al.
Publicado: (2022)

The relationship between papillary thyroid carcinoma and preoperative TSH level: A cross-sectional study from Syria
por: Shahrokh, Marjan, et al.
Publicado: (2023)

Correlation between KCNQ1 and KCNJ11 gene polymorphisms and type 2 and post-transplant diabetes mellitus in the Asian Indian population
por: Khan, Imran Ali, et al.
Publicado: (2015)

The E23K Polymorphism of KCNJ11 and Diabetic Retinopathy in Northern Iran
por: Alidoust, L., et al.
Publicado: (2022)

An analysis of the association between a polymorphism of KCNJ11 and diabetic retinopathy in a Chinese Han population
por: Liu, Nai-Jia, et al.
Publicado: (2015)

Hyperinsulinaemic hypoglycaemia and diabetes mellitus due to dominant ABCC8/KCNJ11 mutations
por: Kapoor, R. R., et al.
Publicado: (2011)

Quantitative Assessment of the Effect of KCNJ11 Gene Polymorphism on the Risk of Type 2 Diabetes
por: Qiu, Ling, et al.
Publicado: (2014)

Identifying the association between single nucleotide polymorphisms in KCNQ1, ARAP1, and KCNJ11 and type 2 diabetes mellitus in a Chinese population
por: Li, Yiping, et al.
Publicado: (2020)

Case report: Neonatal diabetes mellitus caused by KCNJ11 mutation presenting with intracranial hemorrhage
por: Wu, Bo, et al.
Publicado: (2023)

Psychiatric morbidity in children with KCNJ11 neonatal diabetes
por: Bowman, P., et al.
Publicado: (2016)

A novel mutation KCNJ11 R136C caused KCNJ11-MODY
por: Chen, Yaning, et al.
Publicado: (2021)

Study on the correlation between KCNJ11 gene polymorphism and metabolic syndrome in the elderly
por: Jiang, Fan, et al.
Publicado: (2017)

Association of polymorphic markers of genes FTO, KCNJ11, CDKAL1, SLC30A8, and CDKN2B with type 2 diabetes mellitus in the Russian population
por: Nikitin, Aleksey G., et al.
Publicado: (2017)

Successful sulfonylurea treatment in a patient with permanent neonatal diabetes mellitus with a novel KCNJ11 mutation
por: Ahn, Sung Yeon, et al.
Publicado: (2015)

ADIPOQ,KCNJ11 and TCF7L2 polymorphisms in type 2 diabetes in Kyrgyz population: A case‐control study
por: Isakova, Jainagul, et al.
Publicado: (2018)

Forecasting future prevalence of type 2 diabetes mellitus in Syria
por: Al Ali, Radwan, et al.
Publicado: (2013)

Association of KCNJ11 (E23K) gene polymorphism with susceptibility to type 2 diabetes in Iranian patients
por: Rastegari, Ali, et al.
Publicado: (2015)

Effect of laparoscopic mini-gastric bypass versus laparoscopic sleeve gastrectomy on hypertension and dyslipidemia in obese type 2 diabetes mellitus patients
por: Ahmad, Wassim B., et al.
Publicado: (2023)

A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes
por: Gole, Evangelia, et al.
Publicado: (2018)

Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case–control study and meta-analysis
por: Moazzam-Jazi, Maryam, et al.
Publicado: (2022)

Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes
por: Babiker, Tarig, et al.
Publicado: (2016)

Role of GNB3, NET, KCNJ11, TCF7L2 and GRL genes single nucleotide polymorphism in the risk prediction of type 2 diabetes mellitus
por: Rizvi, Saliha, et al.
Publicado: (2016)

Risk of type 2 diabetes mellitus and cardiovascular complications in KCNJ11, HHEX and SLC30A8 genetic polymorphisms carriers: A case-control study
por: Aka, Tutun Das, et al.
Publicado: (2021)

SUN-278 Neonatal Diabetes in an Infant with Heterozygous Mutation in KCNJ11 Gene
por: Kota, Archana, et al.
Publicado: (2019)

Transient Neonatal Diabetes due to a Mutation in KCNJ11 in a Child with Klinefelter Syndrome
por: Dahl, Amanda R., et al.
Publicado: (2018)

STK11 rs2075604 Polymorphism Is Associated with Metformin Efficacy in Chinese Type 2 Diabetes Mellitus
por: Li, Qingchu, et al.
Publicado: (2017)

Association of rs10830962 polymorphism with gestational diabetes mellitus risk in a Chinese population
por: Xie, Kaipeng, et al.
Publicado: (2019)

Successful Treatment of Diabetic Ketoacidosis and Hyperglycemic Hyperosmolar Status in an Infant with KCNJ11-Related Neonatal Diabetes Mellitus via Continuous Renal Replacement Therapy
por: Chen, Ting, et al.
Publicado: (2018)

Association of Genetic Variants of KCNJ11 and KCNQ1 Genes with Risk of Type 2 Diabetes Mellitus (T2DM) in the Indian Population: A Case-Control Study
por: Khan, Vasiuddin, et al.
Publicado: (2020)

Changing the Treatment of Permanent Neonatal Diabetes Mellitus from Insulin to Glibenclamide in a 4-Month-Old Infant with KCNJ11 Activating Mutation
por: Ilkhanipoor, Homa, et al.
Publicado: (2013)

Mutational analysis of KCNJ11 in Chinese elderly essential hypertensive patients
por: Li, Jia-Yue, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_05kq0hstbqn9ok2l9u9jlo7rr5