Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.
about
A mouse model of human hyperinsulinism produced by the E1506K mutation in the sulphonylurea receptor SUR1.Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.Differentiating sodium-glucose co-transporter-2 inhibitors in development for the treatment of type 2 diabetes mellitus.Review of insulin-dependent and insulin-independent agents for treating patients with type 2 diabetes mellitus and potential role for sodium-glucose co-transporter 2 inhibitors.Complementing insulin therapy to achieve glycemic control.A new familial form of a late-onset, persistent hyperinsulinemic hypoglycemia of infancy caused by a novel mutation in KCNJ11.
P2860
Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
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2011年论文
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2011年论文
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name
Relative expression of a domin ...... of congenital hyperinsulinism.
@ast
Relative expression of a domin ...... of congenital hyperinsulinism.
@en
type
label
Relative expression of a domin ...... of congenital hyperinsulinism.
@ast
Relative expression of a domin ...... of congenital hyperinsulinism.
@en
prefLabel
Relative expression of a domin ...... of congenital hyperinsulinism.
@ast
Relative expression of a domin ...... of congenital hyperinsulinism.
@en
P2093
P2860
P356
P1433
P1476
Relative expression of a domin ...... of congenital hyperinsulinism
@en
P2093
Carmit Avnon Ziv
David H Zangen
Efrat Laiba
Ruth Shemer
Sharona Tunovsky-Babaey
Show-Ling Shyng
P2860
P304
P356
10.2337/DB11-0984
P407
P577
2011-11-21T00:00:00Z