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151 related items for PubMed ID: 10567373

  • 1. 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 26; 274(48):34059-66. PubMed ID: 10567373
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  • 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 26; 47(7):1145-51. PubMed ID: 9648840
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  • 3. 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 26; 47(6):715-22. PubMed ID: 11228046
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  • 4. Sulfonylurea receptor 1 and Kir6.2 expression in the novel human insulin-secreting cell line NES2Y.
    Macfarlane WM, O'Brien RE, Barnes PD, Shepherd RM, Cosgrove KE, Lindley KJ, Aynsley-Green A, James RF, Docherty K, Dunne MJ.
    Diabetes; 2000 Jun 26; 49(6):953-60. PubMed ID: 10866047
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  • 5. 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 26; 48(2):408-15. PubMed ID: 10334322
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  • 6. 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 26; 49(1):114-20. PubMed ID: 10615958
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  • 7. 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 06; 336(10):703-6. PubMed ID: 9041101
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  • 9. 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 06; 25(1):101-6. PubMed ID: 11772909
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  • 10. 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 27; 98(5):2882-7. PubMed ID: 11226335
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  • 13. 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 27; 108(1):14-9. PubMed ID: 8834059
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  • 14. 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 01; 102(7):1286-91. PubMed ID: 9769320
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  • 17. The structure and function of the ATP-sensitive K+ channel in insulin-secreting pancreatic beta-cells.
    Miki T, Nagashima K, Seino S.
    J Mol Endocrinol; 1999 Apr 01; 22(2):113-23. PubMed ID: 10194514
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  • 18. Sur1 knockout mice. A model for K(ATP) channel-independent regulation of insulin secretion.
    Seghers V, Nakazaki M, DeMayo F, Aguilar-Bryan L, Bryan J.
    J Biol Chem; 2000 Mar 31; 275(13):9270-7. PubMed ID: 10734066
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  • 20. 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 29; 275(52):41184-91. PubMed ID: 10993895
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