Virginie Steunou

Paris, 75013, France

Last Updated: 09/26/2026

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Found 11 publications

RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitis.

RIPK1 inhibition reduces biliary injury and fibrosis in primary sclerosing cholangitis.

Journal: Science advances
Published: December 17, 2025

Adipocyte-specific Mlkl knockout mitigates obesity-induced metabolic dysfunction by enhancing mitochondrial functions.

Adipocyte-specific Mlkl knockout mitigates obesity-induced metabolic dysfunction by enhancing mitochondrial functions.

Journal: Cell death & disease
Published: April 03, 2025

Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.

Insights from the genetic characterization of central precocious puberty associated with multiple anomalies.

Journal: Human reproduction (Oxford, England)
Published: July 29, 2020

Increasing knowledge in IGF1R defects: lessons from 35 new patients.

Increasing knowledge in IGF1R defects: lessons from 35 new patients.

Journal: Journal of medical genetics
Published: May 29, 2019

Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders.

Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders.

Journal: Science advances
Published: July 30, 2018

Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome.

Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome.

Journal: The Journal of clinical endocrinology and metabolism
Published: September 28, 2017

Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.

Exhaustive methylation analysis revealed uneven profiles of methylation at IGF2/ICR1/H19 11p15 loci in Russell Silver syndrome.

Journal: Journal of medical genetics
Published: November 15, 2014

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.

Extensive investigation of the IGF2/H19 imprinting control region reveals novel OCT4/SOX2 binding site defects associated with specific methylation patterns in Beckwith-Wiedemann syndrome.

Journal: Human molecular genetics
Published: June 12, 2014

IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinoma.

IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinoma.

Journal: PloS one
Published: February 18, 2014

Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation.

Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation.

Journal: Human mutation
Published: January 29, 2014

Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b.

Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b.

Journal: Human mutation
Published: January 24, 2013
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Last Updated: 09/26/2026