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Results: 9

1.

Polymorphisms of the SUR1 (ABCC8) and Kir6.2 (KCNJ11) genes predict the conversion from impaired glucose tolerance to type 2 diabetes. The Finnish Diabetes Prevention Study.

Laukkanen O, Pihlajamäki J, Lindström J, Eriksson J, Valle TT, Hämäläinen H, Ilanne-Parikka P, Keinänen-Kiukaanniemi S, Tuomilehto J, Uusitupa M, Laakso M; Finnish Diabetes Prevention Study Group.

J Clin Endocrinol Metab. 2004 Dec;89(12):6286-90.

PMID:
15579791
[PubMed - indexed for MEDLINE]
2.

Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.

Gloyn AL, Siddiqui J, Ellard S.

Hum Mutat. 2006 Mar;27(3):220-31. Review.

PMID:
16416420
[PubMed - indexed for MEDLINE]
3.

Genetics of type 2 diabetes mellitus and other specific types of diabetes; its role in treatment modalities.

Kota SK, Meher LK, Jammula S, Kota SK, Modi KD.

Diabetes Metab Syndr. 2012 Jan-Mar;6(1):54-8. doi: 10.1016/j.dsx.2012.05.014. Epub 2012 Jul 4. Review.

PMID:
23014256
[PubMed - indexed for MEDLINE]
4.

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.

Flanagan SE, Clauin S, Bellanné-Chantelot C, de Lonlay P, Harries LW, Gloyn AL, Ellard S.

Hum Mutat. 2009 Feb;30(2):170-80. doi: 10.1002/humu.20838. Review.

PMID:
18767144
[PubMed - indexed for MEDLINE]
5.

Towards selective Kir6.2/SUR1 potassium channel openers, medicinal chemistry and therapeutic perspectives.

Hansen JB.

Curr Med Chem. 2006;13(4):361-76. Review.

PMID:
16475928
[PubMed - indexed for MEDLINE]
6.

[Congenital hyperinsulinism in newborn and infant].

Giurgea I, Ribeiro MJ, Boddaert N, Touati G, Robert JJ, Saudubray JM, Jaubert F, Bellanné-Chantelot C, Brunelle F, Nihoul-Fékété C, de Lonlay P.

Arch Pediatr. 2005 Nov;12(11):1628-35. Epub 2005 Sep 28. Review. French.

PMID:
16198094
[PubMed - indexed for MEDLINE]
7.

Permanent neonatal diabetes due to activating mutations in ABCC8 and KCNJ11.

Edghill EL, Flanagan SE, Ellard S.

Rev Endocr Metab Disord. 2010 Sep;11(3):193-8. doi: 10.1007/s11154-010-9149-x. Review.

PMID:
20922570
[PubMed - indexed for MEDLINE]
8.

[Neonatal diabetes: a disease linked to multiple mechanisms].

Flechtner I, Vaxillaire M, Cavé H, Froguel P, Polak M.

Arch Pediatr. 2007 Nov;14(11):1356-65. Epub 2007 Oct 10. Review. French.

PMID:
17931842
[PubMed - indexed for MEDLINE]
9.

[The rare syndromic forms of monogenic diabetes in childhood].

Zmysłowska A, Bodalski J, Młynarski W.

Pediatr Endocrinol Diabetes Metab. 2008;14(1):41-3. Review. Polish.

PMID:
18577346
[PubMed - indexed for MEDLINE]
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