Damien Plassard

Illkirch-graffenstaden, France

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 29 publications

Profiling of desmoid tumors reveals frequent mutations in chromatin-remodeling genes and identifies an Immune-myogenic subtype.

Profiling of desmoid tumors reveals frequent mutations in chromatin-remodeling genes and identifies an Immune-myogenic subtype.

Journal: European journal of cancer (Oxford, England : 1990)
Published: January 11, 2026

TASP1-mediated cleavage of REV3L enhances the activity of DNA polymerase ζ in mammalian cells.

TASP1-mediated cleavage of REV3L enhances the activity of DNA polymerase ζ in mammalian cells.

Journal: Nature communications
Published: October 01, 2025

RBMX functional retrocopy safeguards brain development in a species-dependent context.

RBMX functional retrocopy safeguards brain development in a species-dependent context.

Journal: Brain : a journal of neurology
Published: September 11, 2025

Cdkn2a/p16Ink4a loss impairs Spatial memory independently of Alzheimer's-associated genetic pathways in young adult mice.

Cdkn2a/p16Ink4a loss impairs Spatial memory independently of Alzheimer's-associated genetic pathways in young adult mice.

Journal: Cellular and molecular life sciences : CMLS
Published: July 08, 2025

MiT fusions, TSC1-TSC2 divergence, and stem-like programs reveal distinct origins and vulnerabilities in PEComa.

MiT fusions, TSC1-TSC2 divergence, and stem-like programs reveal distinct origins and vulnerabilities in PEComa.

Journal: Nature communications
Published: May 28, 2025

Gene-specific transcript buffering revealed by perturbation of coactivator complexes.

Gene-specific transcript buffering revealed by perturbation of coactivator complexes.

Journal: Science advances
Published: March 19, 2025

GGC repeat expansions within new open reading frames are translated into toxic polyglycine proteins in oculopharyngodistal myopathy.

GGC repeat expansions within new open reading frames are translated into toxic polyglycine proteins in oculopharyngodistal myopathy.

Journal: Nature genetics
Published: February 28, 2025

Compromised retinoic acid receptor beta expression accelerates the onset of motor, cellular and molecular abnormalities in a mouse model of Huntington's disease.

Compromised retinoic acid receptor beta expression accelerates the onset of motor, cellular and molecular abnormalities in a mouse model of Huntington's disease.

Journal: Neurobiology of disease
Published: November 11, 2024

Hippocampal Astrocyte Morphology Follows an Unexpected Trajectory With Age in a Transgenic Rodent Model of Tauopathy.

Hippocampal Astrocyte Morphology Follows an Unexpected Trajectory With Age in a Transgenic Rodent Model of Tauopathy.

Journal: Glia
Published: September 13, 2024

Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.

Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability.

Journal: American journal of human genetics
Published: July 22, 2024

Gene-specific RNA homeostasis revealed by perturbation of coactivator complexes.

Gene-specific RNA homeostasis revealed by perturbation of coactivator complexes.

Journal: bioRxiv : the preprint server for biology
Published: February 14, 2024

Dysregulated expression of cholesterol biosynthetic genes in Alzheimer's disease alters epigenomic signatures of hippocampal neurons.

Dysregulated expression of cholesterol biosynthetic genes in Alzheimer's disease alters epigenomic signatures of hippocampal neurons.

Journal: Neurobiology of disease
Published: December 29, 2023
Showing 1-12 of 29

Last Updated: 09/26/2026