about
Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs.Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy.RNA pathogenesis via Toll-like receptor-activated inflammation in expanded repeat neurodegenerative diseases.Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases.The emerging genetic landscape of cerebral palsy.Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease.Modeling and analysis of repeat RNA toxicity in Drosophila.Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autism.Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyGenetic or Other Causation Should Not Change the Clinical Diagnosis of Cerebral PalsyTargeted resequencing identifies genes with recurrent variation in cerebral palsyNon-self mutation: double-stranded RNA elicits antiviral pathogenic response in a Drosophila model of expanded CAG repeat neurodegenerative diseasesErratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyDefinition and diagnosis of cerebral palsy in genetic studies: a systematic review
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P50
description
onderzoeker
@nl
researcher, ORCID id # 0000-0003-0345-9944
@en
name
Clare L van Eyk
@ast
Clare L van Eyk
@en
Clare L van Eyk
@nl
type
label
Clare L van Eyk
@ast
Clare L van Eyk
@en
Clare L van Eyk
@nl
prefLabel
Clare L van Eyk
@ast
Clare L van Eyk
@en
Clare L van Eyk
@nl
P106
P31
P496
0000-0003-0345-9944