Nathalie Marissal-Bernard

Marseille, 13005, France

Last Updated: 09/26/2026

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Found 19 publications

Restoring the interplay between the endoplasmic reticulum and mitochondria by gene therapy improves Charcot-Marie-Tooth type 2A disease.

Restoring the interplay between the endoplasmic reticulum and mitochondria by gene therapy improves Charcot-Marie-Tooth type 2A disease.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: June 16, 2026

Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth.

Differential effect of Fas activation on spinal muscular atrophy motoneuron death and induction of axonal growth.

Journal: Cellular and molecular biology (Noisy-le-Grand, France)

Published: October 24, 2022

Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.

Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4H.

Journal: Brain : a journal of neurology

Published: March 25, 2022

Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cells.

Physiology of PNS axons relies on glycolytic metabolism in myelinating Schwann cells.

Journal: PloS one

Published: January 02, 2022

Astrocyte-targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast-fatigable motor units in a mouse model of amyotrophic lateral sclerosis.

Astrocyte-targeting RNA interference against mutated superoxide dismutase 1 induces motoneuron plasticity and protects fast-fatigable motor units in a mouse model of amyotrophic lateral sclerosis.

Journal: Glia

Published: September 23, 2021

Altered action potential waveform and shorter axonal initial segment in hiPSC-derived motor neurons with mutations in VRK1.

Altered action potential waveform and shorter axonal initial segment in hiPSC-derived motor neurons with mutations in VRK1.

Journal: Neurobiology of disease

Published: April 20, 2021

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.

Loss of Cajal bodies in motor neurons from patients with novel mutations in VRK1.

Journal: Human molecular genetics

Published: February 13, 2019

Altered interplay between endoplasmic reticulum and mitochondria in Charcot-Marie-Tooth type 2A neuropathy.

Altered interplay between endoplasmic reticulum and mitochondria in Charcot-Marie-Tooth type 2A neuropathy.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: January 20, 2019

PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease.

PFN2 and GAMT as common molecular determinants of axonal Charcot-Marie-Tooth disease.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: November 06, 2017

Endoplasmic reticulum and mitochondria in diseases of motor and sensory neurons: a broken relationship?

Endoplasmic reticulum and mitochondria in diseases of motor and sensory neurons: a broken relationship?

Journal: Cell death & disease

Published: June 03, 2017

Parkin functionally interacts with PGC-1α to preserve mitochondria and protect dopaminergic neurons.

Parkin functionally interacts with PGC-1α to preserve mitochondria and protect dopaminergic neurons.

Journal: Human molecular genetics

Published: August 13, 2016

Reply: Is SIGMAR1 a confirmed FTD/MND gene?

Reply: Is SIGMAR1 a confirmed FTD/MND gene?

Journal: Brain : a journal of neurology

Published: June 20, 2015

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Last Updated: 09/26/2026