(Q24322771)

Eukaryotic translation initiation factor 2B subunit delta

1 reference

Eukaryotic translation initiation factor 2B subunit gamma

1 reference

Eukaryotic translation initiation factor 2B subunit beta

1 reference

guanyl-nucleotide exchange factor activity

1 reference

0 references

Enrico Bertini

5

0 references

Anne Fogli

object named as

Anne Fogli

1

1 reference

ORCID Public Data File 2021

author name string

Raphael Schiffmann

2

0 references

Lynne Hugendubler

3

0 references

Patricia Combes

4

0 references

Diana Rodriguez

6

0 references

Scot R Kimball

7

0 references

Odile Boespflug-Tanguy

European Journal of Human Genetics

8

0 references

language of work or name

English

0 references

publication date

July 2004

0 references

published in

0 references

volume

12

0 references

page(s)

561-6

0 references

issue

7

0 references

cites work

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Childhood ataxia with diffuse central nervous system hypomyelination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

A new leukoencephalopathy with vanishing white matter.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Increased density of oligodendrocytes in childhood ataxia with diffuse central hypomyelination (CACH) syndrome: neuropathological and biochemical study of two cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Leukoencephalopathy among native Indian infants in northern Quebec and Manitoba

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

A severe variant of childhood ataxia with central hypomyelination/vanishing white matter leukoencephalopathy related to EIF21B5 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Cree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Ovarian failure related to eukaryotic initiation factor 2B mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Identification of domains and residues within the epsilon subunit of eukaryotic translation initiation factor 2B (eIF2Bepsilon) required for guanine nucleotide exchange reveals a novel activation function promoted by eIF2B complex formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Mammalian stress granules represent sites of accumulation of stalled translation initiation complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Eukaryotic initiation factor 2B (eIF2B).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Brain abnormalities, defective meiotic chromosome synapsis and female subfertility in HSF2 null mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

Role of translation initiation factor eIF-2B in the regulation of protein synthesis in mammalian cells

21 January 2018

2 references

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

21 January 2018

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

7 January 2021

The effect of genotype on the natural history of eIF2B-related leukodystrophies.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

7 January 2021

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

7 January 2021

Initiation of protein synthesis in a cell-free system prepared from rat hepatocytes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

7 January 2021

Initiation factor eIF2 alpha phosphorylation in stress responses and apoptosis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201189

7 January 2021