Potassium inwardly-rectifying channel subfamily J member 11 (KCNJ11) gene polymorphism in Egyptian type 2 diabetic patients: a single-center study.
Abdelazem AS, Gaber OA, Hussein S, Nasr FME, M Elshorbagy EA, Ibrahim SM, Abdel-Hameed AM, Rashad MH, El-Shal AS, Abdelnabi AM.

Molecular Dynamics Simulation of Kir6.2 Variants Reveals Potential Association with Diabetes Mellitus.
Elangeeb ME, Elfaki I, Eleragi AMS, Ahmed EM, Mir R, Alzahrani SM, Bedaiwi RI, Alharbi ZM, Mir MM, Ajmal MR, Tayeb FJ, Barnawi J., Free PMC Article

An analysis of the relationship between ABCC8 and KCNJ11 gene polymorphisms and diabetic retinopathy in Turkish population.
Alp E, Doguizi S, Mutlu Icduygu F, Akgun E, Sekeroglu MA, Ozer MA.

Repurposing antidiabetic drugs for rheumatoid arthritis: results from a two-sample Mendelian randomization study.
Qin C, Diaz-Gallo LM, Tang B, Wang Y, Nguyen TD, Harder A, Lu Y, Padyukov L, Askling J, Hägg S., Free PMC Article

Sex differences of the shared genetic landscapes between type 2 diabetes and peripheral artery disease in East Asians and Europeans.
Lu Z, Zhang H, Yang Y, Zhao H.

Protection against Ischemic Heart Disease: A Joint Role for eNOS and the K(ATP) Channel.
Severino P, D'Amato A, Mancone M, Palazzuoli A, Mariani MV, Prosperi S, Myftari V, Lavalle C, Forleo GB, Birtolo LI, Caputo V, Miraldi F, Chimenti C, Badagliacca R, Maestrini V, Palmirotta R, Vizza CD, Fedele F., Free PMC Article

Risk of type 2 diabetes and KCNJ11 gene polymorphisms: a nested case-control study and meta-analysis.
Moazzam-Jazi M, Najd-Hassan-Bonab L, Masjoudi S, Tohidi M, Hedayati M, Azizi F, Daneshpour MS., Free PMC Article

Association of KCNJ11 and ABCC8 single-nucleotide polymorphisms with type 2 diabetes mellitus in a Kinh Vietnamese population.
Tran NQ, Truong SD, Ma PT, Hoang CK, Le BH, Dinh TTN, Van Tran L, Tran TV, Le LHG, Le KT, Nguyen HT, Vu HA, Mai TP, Do MD., Free PMC Article

Clinical presentation and long-term outcome of patients with KCNJ11/ABCC8 variants: Neonatal diabetes or MODY in the DPV registry from Germany and Austria.
Warncke K, Eckert A, Kapellen T, Kummer S, Raile K, Dunstheimer D, Grulich-Henn J, Woelfle J, Wenzel S, Hofer SE, Dost A, Holl RW.

The E23K Polymorphism of KCNJ11 and Diabetic Retinopathy in Northern Iran.
Alidoust L, Ajamian F, Abbaspour S, Sharafshah A, Keshavarz P., Free PMC Article

KCNJ11 and KCNQ1 Gene Polymorphisms and Placental Expression in Women with Gestational Diabetes Mellitus.
Majcher S, Ustianowski P, Malinowski D, Czerewaty M, Tarnowski M, Safranow K, Dziedziejko V, Pawlik A., Free PMC Article

Association between KCNJ11 E23K polymorphism and the risk of type 2 diabetes mellitus: A global meta-analysis.
Ren Y, Zhu W, Shi J, Shao A, Cheng Y, Liu Y.

Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of K(ATP)-Channel Neonatal Diabetes Mellitus in Vietnam National Children's Hospital.
Ngoc CTB, Dien TM, De Franco E, Ellard S, Houghton JAL, Lan NN, Thao BP, Khanh NN, Flanagan SE, Craig ME, Dung VC., Free PMC Article

Impact of KCNJ11 rs5219, UCP2 rs659366, and MTHFR rs1801133 Polymorphisms on Type 2 Diabetes: A Cross-Sectional Study.
Lapik IA, Ranjit R, Galchenko AV., Free PMC Article

Association of common genetic variants of KCNJ11 gene with the risk of type 2 diabetes mellitus.
Malekizadeh A, Rahbaran M, Afshari M, Abbasi D, Aghaei Meybodi HR, Hasanzad M.

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.
Yun JH, Yoo MG, Park JY, Lee HJ, Park SI., Free PMC Article

Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11.
Hewat TI, Yau D, Jerome JCS, Laver TW, Houghton JAL, Shields BM, Flanagan SE, Patel KA., Free PMC Article

Clinical Characteristics, Molecular Features, and Long-Term Follow-Up of 15 Patients with Neonatal Diabetes: A Single-Centre Experience.
Abali ZY, De Franco E, Karakilic Ozturan E, Poyrazoglu S, Bundak R, Bas F, Flanagan SE, Darendeliler F., Free PMC Article

Continuous spectrum of glucose dysmetabolism due to the KCNJ11 gene mutation-Case reports and review of the literature.
He B, Li X, Zhou Z.

Update of variants identified in the pancreatic β-cell K(ATP) channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes.
De Franco E, Saint-Martin C, Brusgaard K, Knight Johnson AE, Aguilar-Bryan L, Bowman P, Arnoux JB, Larsen AR, Sanyoura M, Greeley SAW, Calzada-León R, Harman B, Houghton JAL, Nishimura-Meguro E, Laver TW, Ellard S, Del Gaudio D, Christesen HT, Bellanné-Chantelot C, Flanagan SE., Free PMC Article

A computational structural biology study to understand the impact of mutation on structure-function relationship of inward-rectifier potassium ion channel Kir6.2 in human.
Gupta MK, Vadde R.

Role of the KCNJ Gene Variants in the Clinical Outcome of Type 1 Diabetes.
Blasetti A, Castorani V, Comegna L, Franchini S, Prezioso G, Provenzano M, Di Giulio C, Iannucci D, Matonti L, Tumini S, Chiarelli F, Stuppia L.

Nucleotide inhibition of the pancreatic ATP-sensitive K+ channel explored with patch-clamp fluorometry.
Usher SG, Ashcroft FM, Puljung MC., Free PMC Article

Influence of KCNJ11 gene polymorphism in T2DM of south Indian population.
Aswathi R, Viji D, Pricilla Charmine PS, Akram Husain RSR, Noorul Ameen SH, Ahmed SS, Ramakrishnan V.

Neonatal diabetes due to potassium channel mutation: Response to sulfonylurea according to the genotype.
Garcin L, Mericq V, Fauret-Amsellem AL, Cave H, Polak M, Beltrand J.