167 related articles for article (PubMed ID: 11228046)
1. Characterization of genes encoding the pancreatic beta-cell ATP-sensitive K+ channel in persistent hyperinsulinemic hypoglycemia of infancy in Japanese patients.
Someya T; Miki T; Sugihara S; Minagawa M; Yasuda T; Kohno Y; Seino S
Endocr J; 2000 Dec; 47(6):715-22. PubMed ID: 11228046
[TBL] [Abstract][Full Text] [Related]
2. Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.
Shyng SL; Ferrigni T; Shepard JB; Nestorowicz A; Glaser B; Permutt MA; Nichols CG
Diabetes; 1998 Jul; 47(7):1145-51. PubMed ID: 9648840
[TBL] [Abstract][Full Text] [Related]
3. ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures.
Darendeliler F; Fournet JC; Baş F; Junien C; Gross MS; Bundak R; Saka N; Günöz H
J Pediatr Endocrinol Metab; 2002; 15(7):993-1000. PubMed ID: 12199344
[TBL] [Abstract][Full Text] [Related]
4. A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
Otonkoski T; Ammälä C; Huopio H; Cote GJ; Chapman J; Cosgrove K; Ashfield R; Huang E; Komulainen J; Ashcroft FM; Dunne MJ; Kere J; Thomas PM
Diabetes; 1999 Feb; 48(2):408-15. PubMed ID: 10334322
[TBL] [Abstract][Full Text] [Related]
5. Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.
Tanizawa Y; Matsuda K; Matsuo M; Ohta Y; Ochi N; Adachi M; Koga M; Mizuno S; Kajita M; Tanaka Y; Tachibana K; Inoue H; Furukawa S; Amachi T; Ueda K; Oka Y
Diabetes; 2000 Jan; 49(1):114-20. PubMed ID: 10615958
[TBL] [Abstract][Full Text] [Related]
6. Engineering a glucose-responsive human insulin-secreting cell line from islets of Langerhans isolated from a patient with persistent hyperinsulinemic hypoglycemia of infancy.
MacFarlane WM; Chapman JC; Shepherd RM; Hashmi MN; Kamimura N; Cosgrove KE; O'Brien RE; Barnes PD; Hart AW; Docherty HM; Lindley KJ; Aynsley-Green A; James RF; Docherty K; Dunne MJ
J Biol Chem; 1999 Nov; 274(48):34059-66. PubMed ID: 10567373
[TBL] [Abstract][Full Text] [Related]
7. Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy.
Cartier EA; Conti LR; Vandenberg CA; Shyng SL
Proc Natl Acad Sci U S A; 2001 Feb; 98(5):2882-7. PubMed ID: 11226335
[TBL] [Abstract][Full Text] [Related]
8. Mutations in the sulfonylurea receptor gene in relation to the long-term outcome of persistent hyperinsulinemic hypoglycemia of infancy.
Taguchi T; Suita S; Ohkubo K; Ono J
J Pediatr Surg; 2002 Apr; 37(4):593-8. PubMed ID: 11912517
[TBL] [Abstract][Full Text] [Related]
9. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
Verkarre V; Fournet JC; de Lonlay P; Gross-Morand MS; Devillers M; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
J Clin Invest; 1998 Oct; 102(7):1286-91. PubMed ID: 9769320
[TBL] [Abstract][Full Text] [Related]
10. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
Fournet JC; Verkarre V; De Lonlay P; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
Ann Endocrinol (Paris); 1998; 59(6):485-91. PubMed ID: 10189991
[TBL] [Abstract][Full Text] [Related]
11. An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus.
Kukuvitis A; Deal C; Arbour L; Polychronakos C
J Clin Endocrinol Metab; 1997 Apr; 82(4):1192-4. PubMed ID: 9100595
[TBL] [Abstract][Full Text] [Related]
12. Genotypes of the pancreatic beta-cell K-ATP channel and clinical phenotypes of Japanese patients with persistent hyperinsulinaemic hypoglycaemia of infancy.
Ohkubo K; Nagashima M; Naito Y; Taguchi T; Suita S; Okamoto N; Fujinaga H; Tsumura K; Kikuchi K; Ono J
Clin Endocrinol (Oxf); 2005 Apr; 62(4):458-65. PubMed ID: 15807877
[TBL] [Abstract][Full Text] [Related]
13. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas P; Ye Y; Lightner E
Hum Mol Genet; 1996 Nov; 5(11):1809-12. PubMed ID: 8923010
[TBL] [Abstract][Full Text] [Related]
14. Functional analysis of a mutant sulfonylurea receptor, SUR1-R1420C, that is responsible for persistent hyperinsulinemic hypoglycemia of infancy.
Matsuo M; Trapp S; Tanizawa Y; Kioka N; Amachi T; Oka Y; Ashcroft FM; Ueda K
J Biol Chem; 2000 Dec; 275(52):41184-91. PubMed ID: 10993895
[TBL] [Abstract][Full Text] [Related]
15. The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancy.
Thomas PM; Cote GJ; Wohllk N; Mathew PM; Gagel RF
Proc Assoc Am Physicians; 1996 Jan; 108(1):14-9. PubMed ID: 8834059
[TBL] [Abstract][Full Text] [Related]
16. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.
Dunne MJ; Kane C; Shepherd RM; Sanchez JA; James RF; Johnson PR; Aynsley-Green A; Lu S; Clement JP; Lindley KJ; Seino S; Aguilar-Bryan L
N Engl J Med; 1997 Mar; 336(10):703-6. PubMed ID: 9041101
[No Abstract] [Full Text] [Related]
17. Carriers of an inactivating beta-cell ATP-sensitive K(+) channel mutation have normal glucose tolerance and insulin sensitivity and appropriate insulin secretion.
Huopio H; Vauhkonen I; Komulainen J; Niskanen L; Otonkoski T; Laakso M
Diabetes Care; 2002 Jan; 25(1):101-6. PubMed ID: 11772909
[TBL] [Abstract][Full Text] [Related]
18. Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familial hyperinsulinism.
Partridge CJ; Beech DJ; Sivaprasadarao A
J Biol Chem; 2001 Sep; 276(38):35947-52. PubMed ID: 11457841
[TBL] [Abstract][Full Text] [Related]
19. Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.
Sharma N; Crane A; Gonzalez G; Bryan J; Aguilar-Bryan L
Kidney Int; 2000 Mar; 57(3):803-8. PubMed ID: 10720932
[TBL] [Abstract][Full Text] [Related]
20. Hyperinsulinemic hypoglycemia of infancy. Recent insights into ATP-sensitive potassium channels, sulfonylurea receptors, molecular mechanisms, and treatment.
Sperling MA; Menon RK
Endocrinol Metab Clin North Am; 1999 Dec; 28(4):695-708, vii. PubMed ID: 10609115
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
