These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

356 related articles for article (PubMed ID: 7716548)

  • 1. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.
    Thomas PM; Cote GJ; Wohllk N; Haddad B; Mathew PM; Rabl W; Aguilar-Bryan L; Gagel RF; Bryan J
    Science; 1995 Apr; 268(5209):426-9. PubMed ID: 7716548
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy.
    Thomas PM; Wohllk N; Huang E; Kuhnle U; Rabl W; Gagel RF; Cote GJ
    Am J Hum Genet; 1996 Sep; 59(3):510-8. PubMed ID: 8751851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Pas de deux or more: the sulfonylurea receptor and K+ channels.
    Philipson LH; Steiner DF
    Science; 1995 Apr; 268(5209):372-3. PubMed ID: 7716539
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Hyperinsulinism: molecular aetiology of focal disease.
    Ryan F; Devaney D; Joyce C; Nestorowicz A; Permutt MA; Glaser B; Barton DE; Thornton PS
    Arch Dis Child; 1998 Nov; 79(5):445-7. PubMed ID: 10193261
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Adenosine diphosphate as an intracellular regulator of insulin secretion.
    Nichols CG; Shyng SL; Nestorowicz A; Glaser B; Clement JP; Gonzalez G; Aguilar-Bryan L; Permutt MA; Bryan J
    Science; 1996 Jun; 272(5269):1785-7. PubMed ID: 8650576
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Persistent hyperinsulinaemic hypoglycaemia of infancy: therapy, clinical outcome and mutational analysis.
    Meissner T; Brune W; Mayatepek E
    Eur J Pediatr; 1997 Oct; 156(10):754-7. PubMed ID: 9365062
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Further evidence for a dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy: a family with documented hyperinsulinemia in two generations.
    Hufnagel M; Eichmann D; Stieh J; Santer R
    J Clin Endocrinol Metab; 1998 Jun; 83(6):2215-6. PubMed ID: 9626165
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 18.