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EIF2B5 gene
Known as:
EIF2B5
, EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 5
, EIF2Bepsilon
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This gene plays a role in the initiation of protein biosynthesis.
National Institutes of Health
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Related topics
Related topics
15 relations
Childhood Ataxia with Central Nervous System Hypomyelinization
EIF2B1 gene
EIF2B1 protein, human
EIF2B2 gene
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Narrower (1)
EIF2B5 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Vanishing white matter disease with a novel EIF2B5 mutation: A 10-year follow-up
Gonca Bektaş
,
G. Yeşil
,
Melis Ulak Özkan
,
Edibe Pembegül Yıldız
,
T. A. Uzunhan
,
M. Çalışkan
Clinical neurology and neurosurgery (Dutch…
2018
Corpus ID: 49431208
2017
2017
[Association between homozygous c.318A>GT mutation in exon 2 of the EIF2B5 gene and the infantile form of vanishing white matter leukoencephalopathy].
C. Esmer
,
Gabriela Blanco Hernández
,
Víctor M Saavedra Alanís
,
Jorge Guillermo Reyes Vaca
,
A. Bravo Oro
Boletín Médico del Hospital Infantil de México
2017
Corpus ID: 11371994
2016
2016
Use of focused exome sequencing in adult-onset leukodystrophy to identify new genes and mutations
Wei-Jia Zhang
,
David S. Lynch
,
Rossella Falcone
,
D. Hughes
,
A. Pittman
,
H. Houlden
The Lancet
2016
Corpus ID: 54418816
2015
2015
Infantile onset Vanishing White Matter disease associated with a novel EIF2B5 variant, remarkably long life span, severe epilepsy, and hypopituitarism
April L. Woody
,
D. T. Hsieh
,
Harkirtin K. McIver
,
L. P. Thomas
,
L. Rohena
American Journal of Medical Genetics. Part A
2015
Corpus ID: 26133678
Vanishing White Matter disease (VWM) is an inherited progressive leukoencephalopathy caused by mutations in the genes EIF2B1–5…
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2015
2015
No evidence for a role of Ile587Val polymorphism of EIF2B5 gene in multiple sclerosis in Kashmir Valley of India
Insha Zahoor
,
R. Asimi
,
E. Haq
Journal of Neurological Sciences
2015
Corpus ID: 21883861
2014
2014
Novel mutations identified in EIF2B5 gene in Kashmiri patients as susceptibility factor for multiple sclerosis.
Insha Zahoor
,
Zeenat Hamid
,
R. Asimi
,
E. Haq
Indian Journal of Biochemistry & Biophysics
2014
Corpus ID: 19453801
White matter disease refers to a set of diseases that affect the white matter of the brain and all of which have different…
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2010
2010
Ectopic expression of eIF2Bepsilon in rat skeletal muscle rescues the sepsis-induced reduction in guanine nucleotide exchange activity and protein synthesis.
A. P. Tuckow
,
T. Vary
,
S. Kimball
,
L. Jefferson
American Journal of Physiology. Endocrinology and…
2010
Corpus ID: 25802417
Eukaryotic initiation factor 2B (eIF2B) is a guanine nucleotide exchange factor (GEF) whose activity is both tightly regulated…
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2010
2010
Ectopic expression of eIF 2 B ε in rat skeletal muscle rescues the sepsis-induced reduction in guanine nucleotide exchange activity and protein synthesis
A. P. Tuckow
,
T. Vary
,
S. Kimball
,
L. Jefferson
2010
Corpus ID: 1391688
Tuckow AP, Vary TC, Kimball SR, Jefferson LS. Ectopic expression of eIF2Bε in rat skeletal muscle rescues the sepsis-induced…
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Highly Cited
2004
Highly Cited
2004
Structure of the Catalytic Fragment of Translation Initiation Factor 2B and Identification of a Critically Important Catalytic Residue*
T. Boesen
,
S. S. Mohammad
,
G. Pavitt
,
G. Andersen
Journal of Biological Chemistry
2004
Corpus ID: 29111392
Eukaryotic initiation factor (eIF) 2B catalyzes the nucleotide activation of eIF2 to its active GTP-bound state. The exchange…
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Highly Cited
2000
Highly Cited
2000
Identification of Domains and Residues within the ɛ Subunit of Eukaryotic Translation Initiation Factor 2B (eIF2Bɛ) Required for Guanine Nucleotide Exchange Reveals a Novel Activation Function…
E. Gomez
,
G. Pavitt
Molecular and Cellular Biology
2000
Corpus ID: 35004676
ABSTRACT Eukaryotic translation initiation factor 2B (eIF2B) is the guanine nucleotide exchange factor for protein synthesis…
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