Anne De Cian

INSERM U1154, CNRS 7196, CP26 43 Rue Cuvier 75231 Paris Cedex 05
Cuvier, 75231, France

Last Updated: 09/26/2026

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Found 26 publications

CRISPR-Cas9-mediated upregulation of utrophin ameliorates Duchenne muscular dystrophy.

CRISPR-Cas9-mediated upregulation of utrophin ameliorates Duchenne muscular dystrophy.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: October 08, 2025

Retinal organoids mirror CRISPR-Cas9 gene editing efficiency observed in vivo.

Retinal organoids mirror CRISPR-Cas9 gene editing efficiency observed in vivo.

Journal: Molecular therapy. Methods & clinical development

Published: December 26, 2024

Direct delivery of Cas9 or base editor protein and guide RNA complex enables genome editing in the retina.

Direct delivery of Cas9 or base editor protein and guide RNA complex enables genome editing in the retina.

Journal: Molecular therapy. Nucleic acids

Published: July 22, 2024

Comparative transcriptomics reveal a novel tardigrade-specific DNA-binding protein induced in response to ionizing radiation.

Comparative transcriptomics reveal a novel tardigrade-specific DNA-binding protein induced in response to ionizing radiation.

Journal: eLife

Published: July 09, 2024

Urp1 and Urp2 act redundantly to maintain spine shape in zebrafish larvae.

Urp1 and Urp2 act redundantly to maintain spine shape in zebrafish larvae.

Journal: Developmental biology

Published: August 15, 2022

De novo generation of the NPM-ALK fusion recapitulates the pleiotropic phenotypes of ALK+ ALCL pathogenesis and reveals the ROR2 receptor as target for tumor cells.

De novo generation of the NPM-ALK fusion recapitulates the pleiotropic phenotypes of ALK+ ALCL pathogenesis and reveals the ROR2 receptor as target for tumor cells.

Journal: Molecular cancer

Published: November 15, 2021

Combination of lentiviral and genome editing technologies for the treatment of sickle cell disease.

Combination of lentiviral and genome editing technologies for the treatment of sickle cell disease.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: June 15, 2021

Unraveling Ewing Sarcoma Tumorigenesis Originating from Patient-Derived Mesenchymal Stem Cells.

Unraveling Ewing Sarcoma Tumorigenesis Originating from Patient-Derived Mesenchymal Stem Cells.

Journal: Cancer research

Published: November 18, 2020

Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype.

Editing a γ-globin repressor binding site restores fetal hemoglobin synthesis and corrects the sickle cell disease phenotype.

Journal: Science advances

Published: July 30, 2019

A novel lineage of candidate pheromone receptors for sex communication in moths.

A novel lineage of candidate pheromone receptors for sex communication in moths.

Journal: eLife

Published: July 01, 2019

Cooperation, cis-interactions, versatility and evolutionary plasticity of multiple cis-acting elements underlie krox20 hindbrain regulation.

Cooperation, cis-interactions, versatility and evolutionary plasticity of multiple cis-acting elements underlie krox20 hindbrain regulation.

Journal: PLoS genetics

Published: May 25, 2018

High doses of CRISPR/Cas9 ribonucleoprotein efficiently induce gene knockout with low mosaicism in the hydrozoan Clytia hemisphaerica through microhomology-mediated deletion.

High doses of CRISPR/Cas9 ribonucleoprotein efficiently induce gene knockout with low mosaicism in the hydrozoan Clytia hemisphaerica through microhomology-mediated deletion.

Journal: Scientific reports

Published: April 10, 2018

Showing 1-12 of 26

Last Updated: 09/26/2026