FAQ

IER3IP1 gene

Known as: IER3IP1, IMMEDIATE-EARLY RESPONSE 3-INTERACTING PROTEIN 1, immediate early response 3 interacting protein 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2010-2017
01220102017

Papers overview

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2017
2017
IER3IP1 deficiency leads to increased β-cell death and decreased β-cell proliferation
Mutations in the gene for Immediate Early Response 3 Interacting Protein 1 (IER3IP1) cause permanent neonatal diabetes mellitus… (More)
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Review
2017
Review
2017
Microcephaly with simplified gyral pattern, epilepsy and permanent neonatal diabetes syndrome (MEDS). A new patient and review of the literature.
Microcephaly with simplified gyration, epilepsy and permanent neonatal diabetes syndrome (MEDS) is a recently described… (More)
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2014
2014
Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder.
Neonatal diabetes mellitus is known to have over 20 different monogenic causes. A syndrome of permanent neonatal diabetes along… (More)
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2011
2011
Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitors.
We describe a syndrome of primary microcephaly with simplified gyral pattern in combination with severe infantile epileptic… (More)
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2010
2010
Transcriptional regulation of IER3IP1 gene by tumor necrosis factor-alpha and Sp family proteins.
Immediate early response 3 interacting protein 1 (IER3IP1) is an endoplasmic reticulum protein with its potential cellular… (More)
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