Valentine Mosbach
Lyon, France
Last Updated: 09/26/2026
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Found 10 publications
Partial Bypass of Frataxin Deficiency by ISCU M141I Restores Cytosolic and Nuclear Fe-S Cluster Assembly.
Journal: bioRxiv : the preprint server for biology
Published: September 29, 2025
Partial bypass of frataxin deficiency by ISCU M141I restores cytosolic and nuclear Fe-S cluster assembly.
Journal: Cell death and differentiation
Published: September 18, 2025
A multiple animal and cellular models approach to study frataxin deficiency in Friedreich Ataxia.
Journal: Biochimica et biophysica acta. Molecular cell research
Published: March 01, 2024
Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.
Journal: Brain : a journal of neurology
Published: July 18, 2022
Resection and repair of a Cas9 double-strand break at CTG trinucleotide repeats induces local and extensive chromosomal deletions.
Journal: PLoS genetics
Published: December 06, 2019
Trinucleotide repeat instability during double-strand break repair: from mechanisms to gene therapy.
Trinucleotide repeat instability during double-strand break repair: from mechanisms to gene therapy.
Journal: Current genetics
Published: April 30, 2018
A fast, sensitive and cost-effective method for nucleic acid detection using non-radioactive probes.
A fast, sensitive and cost-effective method for nucleic acid detection using non-radioactive probes.
Journal: Biology methods & protocols
Published: March 13, 2018
TALEN-Induced Double-Strand Break Repair of CTG Trinucleotide Repeats.
Journal: Cell reports
Published: February 27, 2017
Highly specific contractions of a single CAG/CTG trinucleotide repeat by TALEN in yeast.
Journal: PloS one
Published: November 13, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026