Veronica Nobile

Rome, 00168, Italy

Last Updated: 09/26/2026

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Found 15 publications

FMR1 RNA interaction with DNMT1 blocks DNA methylation at the FMR1 locus.

FMR1 RNA interaction with DNMT1 blocks DNA methylation at the FMR1 locus.

Journal: NAR molecular medicine

Published: September 09, 2025

Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders.

Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders.

Journal: International journal of molecular sciences

Published: January 22, 2024

Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway.

Rutin Protects Fibroblasts from UVA Radiation through Stimulation of Nrf2 Pathway.

Journal: Antioxidants (Basel, Switzerland)

Published: March 11, 2023

Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals.

Age-Dependent Dysregulation of APP in Neuronal and Skin Cells from Fragile X Individuals.

Journal: Cells

Published: November 06, 2022

Ribosomal RACK1 Regulates the Dendritic Arborization by Repressing FMRP Activity.

Ribosomal RACK1 Regulates the Dendritic Arborization by Repressing FMRP Activity.

Journal: International journal of molecular sciences

Published: July 13, 2022

Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype.

Mother and Daughter Carrying of the Same Pathogenic Variant in FGFR2 with Discordant Phenotype.

Journal: Genes

Published: May 15, 2022

Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?

Mechanisms of the FMR1 Repeat Instability: How Does the CGG Sequence Expand?

Journal: International journal of molecular sciences

Published: April 10, 2022

Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Co-Occurrence of Fragile X Syndrome with a Second Genetic Condition: Three Independent Cases of Double Diagnosis.

Journal: Genes

Published: October 20, 2021

DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome.

DNA Methylation, Mechanisms of FMR1 Inactivation and Therapeutic Perspectives for Fragile X Syndrome.

Journal: Biomolecules

Published: December 15, 2020

Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization.

Infantile Liver Failure Syndrome 1 associated with a novel variant of the LARS1 gene: Clinical, genetic, and functional characterization.

Journal: Clinical genetics

Published: September 11, 2020

Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families.

Reversion to Normal of FMR1 Expanded Alleles: A Rare Event in Two Independent Fragile X Syndrome Families.

Journal: Genes

Published: January 17, 2020

Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene.

Altered mitochondrial function in cells carrying a premutation or unmethylated full mutation of the FMR1 gene.

Journal: Human genetics

Published: September 18, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026