about
Screening for known mutations in EIF2Bgenes in a large panel of patients with premature ovarian failureCree leukoencephalopathy and CACH/VWM disease are allelic at the EIF2B5 locusA yeast purification system for human translation initiation factors eIF2 and eIF2Bε and their use in the diagnosis of CACH/VWM diseaseGenes involved in leukodystrophies: a glance at glial functions.Peptidomics analysis of lymphoblastoid cell lines.Atherogenic subfractions of lipoproteins in the treatment of metabolic syndrome by physical activity and diet - the RESOLVE trial.Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive.The tumoral A genotype of the MGMT rs34180180 single-nucleotide polymorphism in aggressive gliomas is associated with shorter patients' survival.Radiotherapy plus temozolomide in elderly patients with glioblastoma: a "real-life" report.Detection of the alternative lengthening of telomeres pathway in malignant gliomas for improved molecular diagnosis.Peptidomics and proteomics studies of transformed lymphocytes from patients mutated for the eukaryotic initiation factor 2B.The long non-coding RNA HOTAIR is transcriptionally activated by HOXA9 and is an independent prognostic marker in patients with malignant glioma.Letter to the Editor: No evidence for association between the EIF2B5 gene and multiple sclerosis in French familiesHistoire naturelle des leucodystrophies avec mutation EIF2B : étude rétrospective multicentrique de 24 cas adultes[eIF2B and Cree Indian leukodystrophies]Autosomal dominant leukodystrophy and childhood ataxia with central nervous system hypomyelination syndrome[Monoclonal IgM interference with immunoturbidimetric determination of ferritin and transferrin]Exon deletion in the non-catalytic domain of eIF2Bepsilon due to a splice site mutation leads to infantile forms of CACH/VWM with severe decrease of eIF2B GEF activityDominant form of vanishing white matter-like leukoencephalopathy[Coupling proteinemia and serum protein electrophoresis: evaluation of the capillary technique (Capillarys 2, Sebia), experience from Clermont-Ferrand]Transcriptional alterations in glioma result primarily from DNA methylation-independent mechanismsChildhood Ataxia with Central Nervous System Hypomyelination / Vanishing White Matter
P50
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P50
description
researcher
@en
name
Anne Fogli
@en
Anne Fogli
@nl
type
label
Anne Fogli
@en
Anne Fogli
@nl
prefLabel
Anne Fogli
@en
Anne Fogli
@nl
P106
P31
P496
0000-0002-2651-7441