Julia Hofhuis - Publications

Defining the high-translational readthrough stop codon context.

Journal: PLoS genetics

Published: March 10, 2025

Systematic and quantitative analysis of stop codon readthrough in Rett syndrome nonsense mutations.

Journal: Journal of molecular medicine (Berlin, Germany)

Published: October 13, 2023

Tissue-specific roles of peroxisomes revealed by expression meta-analysis.

Journal: Biology direct

Published: September 14, 2023

Stop Codon Context-Specific Induction of Translational Readthrough.

Journal: Biomolecules

Published: May 11, 2021

Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity.

Journal: Neurobiology of disease

Published: February 18, 2020

Dysferlin links excitation-contraction coupling to structure and maintenance of the cardiac transverse-axial tubule system.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: October 23, 2019

Dual Reporter Systems for the Analysis of Translational Readthrough in Mammals.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: April 15, 2017

Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy.

Journal: Journal of cell science

Published: October 21, 2016

The functional readthrough extension of malate dehydrogenase reveals a modification of the genetic code.

Journal: Open biology

Published: August 26, 2016

Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals.

Journal: eLife

Published: June 09, 2014