Valerie Risson

CNRS 5310, INSERM U121, Faculté De Médecine Lyon Est
Lyon, 69008, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Characterisation of a Missense Variant of the Alström Syndrome Centrosome and Basal Body Associated Protein (ALMS1) Gene Associated with Cardiomyopathy Using Induced Pluripotent Stem Cells.

Characterisation of a Missense Variant of the Alström Syndrome Centrosome and Basal Body Associated Protein (ALMS1) Gene Associated with Cardiomyopathy Using Induced Pluripotent Stem Cells.

Journal: Genes

Published: December 08, 2025

Human organoids and their clinical promise in the neuromuscular field

Human organoids and their clinical promise in the neuromuscular field

Journal: Medecine sciences : M/S

Published: November 28, 2025

Delivery of Prime editing in human stem cells using pseudoviral NanoScribes particles.

Delivery of Prime editing in human stem cells using pseudoviral NanoScribes particles.

Journal: Nature communications

Published: June 11, 2024

LSD1 controls a nuclear checkpoint in Wnt/β-Catenin signaling to regulate muscle stem cell self-renewal.

LSD1 controls a nuclear checkpoint in Wnt/β-Catenin signaling to regulate muscle stem cell self-renewal.

Journal: Nucleic acids research

Published: September 13, 2022

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.

Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy.

Journal: Brain : a journal of neurology

Published: July 18, 2022

Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.

Expanding the phenotypic variability of MORC2 gene mutations: From Charcot-Marie-Tooth disease to late-onset pure motor neuropathy.

Journal: Human mutation

Published: February 14, 2022

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.

Journal: Acta neuropathologica

Published: February 01, 2022

Evidence of a dual mechanism of action underlying the anti-proliferative and cytotoxic effects of ammonium-alkyloxy-stilbene-based α7- and α9-nicotinic ligands on glioblastoma cells.

Evidence of a dual mechanism of action underlying the anti-proliferative and cytotoxic effects of ammonium-alkyloxy-stilbene-based α7- and α9-nicotinic ligands on glioblastoma cells.

Journal: Pharmacological research

Published: August 05, 2021

MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis.

MACF1 controls skeletal muscle function through the microtubule-dependent localization of extra-synaptic myonuclei and mitochondria biogenesis.

Journal: eLife

Published: May 18, 2021

Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons.

Modeling Charcot-Marie-Tooth Disease In Vitro by Transfecting Mouse Primary Motoneurons.

Journal: Journal of visualized experiments : JoVE

Published: January 22, 2019

Genome editing in primary cells and in vivo using viral-derived Nanoblades loaded with Cas9-sgRNA ribonucleoproteins.

Genome editing in primary cells and in vivo using viral-derived Nanoblades loaded with Cas9-sgRNA ribonucleoproteins.

Journal: Nature communications

Published: December 11, 2017

A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.

A transgenic mouse expressing CHMP2Bintron5 mutant in neurons develops histological and behavioural features of amyotrophic lateral sclerosis and frontotemporal dementia.

Journal: Human molecular genetics

Published: February 05, 2016

Showing 1-12 of 15

Last Updated: 09/26/2026