Denis Furling

6PUBLICATIONS
48CO-AUTHORS
Medical infection agents (incl. prions)Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapy
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Publications (6)

|Sep 03, 2026
MBNL depletion drives stem cell fusion and immature myonuclear states in myotonic dystrophy type 1.

|Aug 21, 2026
Toward the clinical application of long-read sequencing in repeat-expansion disorders.

|Feb 11, 2022
Reversal of RNA toxicity in myotonic dystrophy via a decoy RNA-binding protein with high affinity for expanded CUG repeats.

Ludovic Arandel, Magdalena Matloka, Arnaud F Klein

|Mar 04, 2021
New recessive mutations in SYT2 causing severe presynaptic congenital myasthenic syndromes.

Stéphanie Bauché, Alain Sureau, Damien Sternberg

|Feb 12, 2017
Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds.

Ludovic Arandel, Micaela Polay Espinoza, Magdalena Matloka

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Frequent Collaborators

1 joint publications

Stéphanie Bauché

1 joint publications

Alain Sureau

1 joint publications

Damien Sternberg

1 joint publications

John Rendu