Chantal Sellier

Illkirch-graffenstaden, France

Last Updated: 09/26/2026

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Found 28 publications

Author Correction: FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosis.

Author Correction: FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosis.

Journal: Nature neuroscience

Published: July 16, 2026

FUS controls muscle differentiation through phase separation-mediated recruitment of the transcription factors MEF2 and ETV5.

FUS controls muscle differentiation through phase separation-mediated recruitment of the transcription factors MEF2 and ETV5.

Journal: The EMBO journal

Published: November 05, 2025

CREB3 gain of function variants protect against ALS.

CREB3 gain of function variants protect against ALS.

Journal: Nature communications

Published: May 09, 2024

C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?

C9ORF72 hexanucleotide repeat expansion: From ALS and FTD to a broader pathogenic role?

Journal: Revue neurologique

Published: March 20, 2024

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Journal: Nature communications

Published: December 04, 2023

Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Integrative genetic analysis illuminates ALS heritability and identifies risk genes.

Journal: Nature communications

Published: August 08, 2021

De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.

De Novo Frameshift Variants in the Neuronal Splicing Factor NOVA2 Result in a Common C-Terminal Extension and Cause a Severe Form of Neurodevelopmental Disorder.

Journal: American journal of human genetics

Published: December 30, 2019

FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosis.

FUS-mediated regulation of acetylcholine receptor transcription at neuromuscular junctions is compromised in amyotrophic lateral sclerosis.

Journal: Nature neuroscience

Published: May 17, 2019

Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders.

Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders.

Journal: The EMBO journal

Published: August 27, 2018

Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers.

Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers.

Journal: Acta neuropathologica communications

Published: July 27, 2018

Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.

Repeat-associated non-AUG (RAN) translation and other molecular mechanisms in Fragile X Tremor Ataxia Syndrome.

Journal: Brain research

Published: December 05, 2017

Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy.

Daunorubicin reduces MBNL1 sequestration caused by CUG-repeat expansion and rescues cardiac dysfunctions in a Drosophila model of myotonic dystrophy.

Journal: Disease models & mechanisms

Published: October 16, 2017

Showing 1-12 of 28

Last Updated: 09/26/2026