Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation-Reference-Cited by-同舟云学术

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Impaired EIF2S3 function associated with a novel phenotype of X-linked hypopituitarism with glucose dysregulation

Published:2019-04 Issue: Volume:42 Page:470-480
ISSN:2352-3964
Container-title:EBioMedicine
language:en
Short-container-title:EBioMedicine

Author:

Gregory Louise C.,Ferreira Carolina B.,Young-Baird Sara K.,Williams Hywel J.,Harakalova Magdalena,van Haaften Gijs,Rahman Sofia A.,Gaston-Massuet Carles,Kelberman Daniel,GOSgene ,Qasim Waseem,Camper Sally A.,Dever Thomas E.,Shah Pratik,Robinson Iain C.A.F.,Dattani Mehul T.

Funder

Great Ormond Street Hospital (GOSH) charity

Medical Research Foundation

MRC/Wellcome Trust

National Institute for Health Research

Biomedical Research Centre

Intramural Research Program

Postdoctoral Research Associate

National Institute of General Medical Sciences

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference32 articles.

1. Molecular mechanism of scanning and start codon selection in eukaryotes;Hinnebusch;Microbiol Mol Biol Rev,2011

2. GTP hydrolysis controls stringent selection of the AUG start codon during translation initiation in Saccharomyces cerevisiae;Huang;Genes Dev,1997

3. Mutations in GCD11, the structural gene for eIF-2 gamma in yeast, alter translational regulation of GCN4 and the selection of the start site for protein synthesis;Dorris;EMBO J,1995

4. MEHMO (mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly, obesity), a novel syndrome: assignment of disease locus to xp21.1-p22.13;Steinmuller;Eur J Hum Genet,1998

5. eIF2gamma mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation;Borck;Mol Cell,2012

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