Nicolas Levy

Saclay, 91190, France

Last Updated: 09/26/2026

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Found 179 publications

Identifying Therapeutic Targets for Amyotrophic Lateral Sclerosis Through Modeling of Multi-Omics Data.

Identifying Therapeutic Targets for Amyotrophic Lateral Sclerosis Through Modeling of Multi-Omics Data.

Journal: International journal of molecular sciences

Published: May 05, 2025

Nucleoporin NUP210L and BAF-paralogue BAF-L redundantly ensure nuclear integrity and manchette microtubule organisation in mouse spermatids.

Nucleoporin NUP210L and BAF-paralogue BAF-L redundantly ensure nuclear integrity and manchette microtubule organisation in mouse spermatids.

Journal: Human molecular genetics

Published: April 24, 2025

Author Correction: Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.

Author Correction: Mutations in ACTRT1 and its enhancer RNA elements lead to aberrant activation of Hedgehog signaling in inherited and sporadic basal cell carcinomas.

Journal: Nature medicine

Published: February 06, 2025

Voltage-Gated Ion Channel Compensatory Effect in DEE: Implications for Future Therapies.

Voltage-Gated Ion Channel Compensatory Effect in DEE: Implications for Future Therapies.

Journal: Cells

Published: September 09, 2024

Inhibition of poly(ADP-Ribosyl)ation reduced vascular smooth muscle cells loss and improves aortic disease in a mouse model of human accelerated aging syndrome.

Inhibition of poly(ADP-Ribosyl)ation reduced vascular smooth muscle cells loss and improves aortic disease in a mouse model of human accelerated aging syndrome.

Journal: Cell death & disease

Published: May 13, 2024

The Molecular Landscape of Premature Aging Diseases Defined by Multilayer Network Exploration.

The Molecular Landscape of Premature Aging Diseases Defined by Multilayer Network Exploration.

Journal: Advanced biology

Published: March 10, 2024

A Dysferlin Exon 32 Nonsense Mutant Mouse Model Shows Pathological Signs of Dysferlinopathy.

A Dysferlin Exon 32 Nonsense Mutant Mouse Model Shows Pathological Signs of Dysferlinopathy.

Journal: Biomedicines

Published: April 01, 2023

A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities.

A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities.

Journal: American journal of medical genetics. Part A

Published: December 21, 2022

Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care.

Objective Evaluation of Clinical Actionability for Genes Involved in Myopathies: 63 Genes with a Medical Value for Patient Care.

Journal: International journal of molecular sciences

Published: June 29, 2022

Transient posterior subcapsular cataract in a type 1 diabetic girl

Transient posterior subcapsular cataract in a type 1 diabetic girl

Journal: Journal francais d'ophtalmologie

Published: June 13, 2022

Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49.

Novel Exon-Skipping Therapeutic Approach for the DMD Gene Based on Asymptomatic Deletions of Exon 49.

Journal: Genes

Published: June 07, 2022

HINT1 neuropathy: Expanding the genotype and phenotype spectrum.

HINT1 neuropathy: Expanding the genotype and phenotype spectrum.

Journal: Clinical genetics

Published: June 02, 2022

Showing 1-12 of 179

Last Updated: 09/26/2026