Valerie Drouet

Dam, Dif
Arpajon, 91297, France

Last Updated: 09/26/2026

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Found 11 publications

Time-resolved near backscatter imaging system on Laser MegaJoule.

Time-resolved near backscatter imaging system on Laser MegaJoule.

Journal: The Review of scientific instruments
Published: November 01, 2022

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Journal: Frontiers in neurology
Published: July 26, 2017

AXIN deficiency in human and mouse hepatocytes induces hepatocellular carcinoma in the absence of β-catenin activation.

AXIN deficiency in human and mouse hepatocytes induces hepatocellular carcinoma in the absence of β-catenin activation.

Journal: Journal of hepatology
Published: July 21, 2017

Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.

Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.

Journal: Genome biology
Published: June 17, 2016

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease.

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease.

Journal: Annals of neurology
Published: November 27, 2015

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Journal: American journal of human genetics
Published: November 16, 2015

Generation of Mice with Hepatocyte-Specific Conditional Deletion of Notum.

Generation of Mice with Hepatocyte-Specific Conditional Deletion of Notum.

Journal: PloS one
Published: October 15, 2015

LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis.

LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis.

Journal: PloS one
Published: July 28, 2015

Synaptojanin 1 mutation in Parkinson's disease brings further insight into the neuropathological mechanisms.

Synaptojanin 1 mutation in Parkinson's disease brings further insight into the neuropathological mechanisms.

Journal: BioMed research international
Published: July 09, 2014

Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells.

Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells.

Journal: PloS one
Published: April 15, 2014

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

Journal: Movement disorders : official journal of the Movement Disorder Society
Published: December 03, 2013
Showing 1-11 of 11

Last Updated: 09/26/2026