Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion (Q33391087)

26 July 2017

title

Mutations in UCP2 in congenital hyperinsulinism reveal a role for regulation of insulin secretion (English)

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Christine Bellanné-Chantelot

26 July 2017

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1 reference

Fredéric Bouillaud

3

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5

object named as

Christine Bellanné-Chantelot

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26 July 2017

8

Pascale de Lonlay

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26 July 2017

author name string

M Mar González-Barroso

1

1 reference

26 July 2017

Irina Giurgea

2

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26 July 2017

Andrea Anedda

4

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26 July 2017

Laurence Hubert

6

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26 July 2017

Yves de Keyzer

7

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26 July 2017

Daniel Ricquier

9

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26 July 2017

language of work or name

English

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publication date

9 December 2008

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26 July 2017

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26 July 2017

volume

3

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26 July 2017

issue

12

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26 July 2017

page(s)

e3850

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Creative Commons Attribution 4.0 International

26 July 2017

copyright license

start time

9 December 2008

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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12 December 2020

Neonatal Hyperinsulinemic Hypoglycemia: Heterogeneity of the Syndrome and Keys for Differential Diagnosis1

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12 December 2020

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

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12 December 2020

Uncoupling protein-2 contributes significantly to high mitochondrial proton leak in INS-1E insulinoma cells and attenuates glucose-stimulated insulin secretion

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12 December 2020

Uncoupling protein 2, in vivo distribution, induction upon oxidative stress, and evidence for translational regulation

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0003850

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DOI

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26 July 2017

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26 July 2017

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