Angeline Gaucherot

Lyon, 69008, France

Last Updated: 09/26/2026

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Found 10 publications

Ribosome biogenesis is a therapeutic vulnerability in pediatric neuroblastoma.

Ribosome biogenesis is a therapeutic vulnerability in pediatric neuroblastoma.

Journal: Biochimie

Published: May 16, 2025

Fibrillarin-mediated ribosomal RNA maturation is a novel therapeutic vulnerability in triple-negative breast cancer.

Fibrillarin-mediated ribosomal RNA maturation is a novel therapeutic vulnerability in triple-negative breast cancer.

Journal: Breast cancer research : BCR

Published: April 22, 2025

Ribosome biogenesis is a therapeutic vulnerability in paediatric neuroblastoma.

Ribosome biogenesis is a therapeutic vulnerability in paediatric neuroblastoma.

Journal: bioRxiv : the preprint server for biology

Published: April 08, 2025

DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival.

DHX30 Coordinates Cytoplasmic Translation and Mitochondrial Function Contributing to Cancer Cell Survival.

Journal: Cancers

Published: June 11, 2021

Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance.

Alteration of ribosome function upon 5-fluorouracil treatment favors cancer cell drug-tolerance.

Journal: Nature communications

Published: May 25, 2020

Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders.

Reduced autophagy upon C9ORF72 loss synergizes with dipeptide repeat protein toxicity in G4C2 repeat expansion disorders.

Journal: The EMBO journal

Published: August 27, 2018

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences.

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences.

Journal: Nature communications

Published: August 25, 2017

A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.

A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.

Journal: Journal of assisted reproduction and genetics

Published: October 10, 2016

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.

Journal: Neuron

Published: March 24, 2016

Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.

Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.

Journal: The EMBO journal

Published: October 23, 2015

Showing 1-10 of 10

Last Updated: 09/26/2026