Anne-laure Todeschini

Paris, France

Last Updated: 09/26/2026

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Found 17 publications

Deciphering the Impact of AKT1 Pathogenic Variants in Juvenile Granulosa Cell Tumors Using a Drosophila Model.

Deciphering the Impact of AKT1 Pathogenic Variants in Juvenile Granulosa Cell Tumors Using a Drosophila Model.

Journal: Molecular & cellular proteomics : MCP

Published: February 12, 2025

A cellular model provides insights into the pathogenicity of the oncogenic FOXL2 somatic variant p.Cys134Trp.

A cellular model provides insights into the pathogenicity of the oncogenic FOXL2 somatic variant p.Cys134Trp.

Journal: British journal of cancer

Published: May 15, 2023

The forkhead DNA-binding domain binds specific G2-rich RNA sequences.

The forkhead DNA-binding domain binds specific G2-rich RNA sequences.

Journal: Nucleic acids research

Published: March 31, 2023

FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?

FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?

Journal: The Journal of pathology

Published: May 15, 2021

Precocious Pseudo-puberty in a Two-year-old Girl, Presenting with Bilateral Ovarian Enlargement and Progressing to Unilateral Juvenile Granulosa Cell Tumour

Precocious Pseudo-puberty in a Two-year-old Girl, Presenting with Bilateral Ovarian Enlargement and Progressing to Unilateral Juvenile Granulosa Cell Tumour

Journal: Journal of clinical research in pediatric endocrinology

Published: April 14, 2021

Reply to "An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2".

Reply to "An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2".

Journal: The EMBO journal

Published: December 14, 2020

Forkhead Transcription Factors in Health and Disease.

Forkhead Transcription Factors in Health and Disease.

Journal: Trends in genetics : TIG

Published: October 02, 2020

An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes.

An exome-wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes.

Journal: Clinical genetics

Published: May 25, 2020

High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells.

High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells.

Journal: Molecular & cellular proteomics : MCP

Published: March 21, 2019

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.

Journal: EBioMedicine

Published: February 28, 2019

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.

NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex development.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 22, 2016

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Journal: Human molecular genetics

Published: July 24, 2015

Showing 1-12 of 17

Last Updated: 09/26/2026