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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

377 related items for PubMed ID: 9648840

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24. Compound heterozygosity for the common sulfonylurea receptor mutations can cause mild diazoxide-sensitive hyperinsulinism.
    Dekel B, Lubin D, Modan-Moses D, Quint J, Glaser B, Meyerovitch J.
    Clin Pediatr (Phila); 2002 Apr; 41(3):183-6. PubMed ID: 11999683
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. MgADP antagonism to Mg2+-independent ATP binding of the sulfonylurea receptor SUR1.
    Ueda K, Inagaki N, Seino S.
    J Biol Chem; 1997 Sep 12; 272(37):22983-6. PubMed ID: 9287292
    [Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. 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 12; 22(2):113-23. PubMed ID: 10194514
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Regulation of cloned ATP-sensitive K channels by phosphorylation, MgADP, and phosphatidylinositol bisphosphate (PIP(2)): a study of channel rundown and reactivation.
    Ribalet B, John SA, Weiss JN.
    J Gen Physiol; 2000 Sep 12; 116(3):391-410. PubMed ID: 10962016
    [Abstract] [Full Text] [Related]

  • 31. Differential nucleotide regulation of KATP channels by SUR1 and SUR2A.
    Masia R, Enkvetchakul D, Nichols CG.
    J Mol Cell Cardiol; 2005 Sep 12; 39(3):491-501. PubMed ID: 15893323
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Increased ATPase activity produced by mutations at arginine-1380 in nucleotide-binding domain 2 of ABCC8 causes neonatal diabetes.
    de Wet H, Rees MG, Shimomura K, Aittoniemi J, Patch AM, Flanagan SE, Ellard S, Hattersley AT, Sansom MS, Ashcroft FM.
    Proc Natl Acad Sci U S A; 2007 Nov 27; 104(48):18988-92. PubMed ID: 18025464
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Severe congenital hyperinsulinism caused by a mutation in the Kir6.2 subunit of the adenosine triphosphate-sensitive potassium channel impairing trafficking and function.
    Marthinet E, Bloc A, Oka Y, Tanizawa Y, Wehrle-Haller B, Bancila V, Dubuis JM, Philippe J, Schwitzgebel VM.
    J Clin Endocrinol Metab; 2005 Sep 27; 90(9):5401-6. PubMed ID: 15998776
    [Abstract] [Full Text] [Related]

  • 36. 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 27; 25(1):101-6. PubMed ID: 11772909
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.
    Henwood MJ, Kelly A, Macmullen C, Bhatia P, Ganguly A, Thornton PS, Stanley CA.
    J Clin Endocrinol Metab; 2005 Feb 27; 90(2):789-94. PubMed ID: 15562009
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 19.