Monica Suelves

Badalona, CT 08916, Spain

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 18 publications

HDAC11 deficiency improves muscle phenotype in a Duchenne muscular dystrophy murine model by reducing inflammation and fibrosis.

HDAC11 deficiency improves muscle phenotype in a Duchenne muscular dystrophy murine model by reducing inflammation and fibrosis.

Journal: Life sciences
Published: January 22, 2025

HDAC11 deficiency regulates age-related muscle decline and sarcopenia.

HDAC11 deficiency regulates age-related muscle decline and sarcopenia.

Journal: GeroScience
Published: January 03, 2025

Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.

Erratum: Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.

Journal: iScience
Published: December 30, 2024

AntimiR treatment corrects myotonic dystrophy primary cell defects across several CTG repeat expansions with a dual mechanism of action.

AntimiR treatment corrects myotonic dystrophy primary cell defects across several CTG repeat expansions with a dual mechanism of action.

Journal: Science advances
Published: October 09, 2024

Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.

Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.

Journal: iScience
Published: July 10, 2023

An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation.

An Integrative Analysis of DNA Methylation Pattern in Myotonic Dystrophy Type 1 Samples Reveals a Distinct DNA Methylation Profile between Tissues and a Novel Muscle-Associated Epigenetic Dysregulation.

Journal: Biomedicines
Published: April 22, 2022

Characterization of RAN Translation and Antisense Transcription in Primary Cell Cultures of Patients with Myotonic Dystrophy Type 1.

Characterization of RAN Translation and Antisense Transcription in Primary Cell Cultures of Patients with Myotonic Dystrophy Type 1.

Journal: Journal of clinical medicine
Published: October 30, 2021

HDAC11: a multifaceted histone deacetylase with proficient fatty deacylase activity and its roles in physiological processes.

HDAC11: a multifaceted histone deacetylase with proficient fatty deacylase activity and its roles in physiological processes.

Journal: The FEBS journal
Published: January 22, 2021

Loss of HDAC11 accelerates skeletal muscle regeneration in mice.

Loss of HDAC11 accelerates skeletal muscle regeneration in mice.

Journal: The FEBS journal
Published: March 24, 2020

HDAC11 is a novel regulator of fatty acid oxidative metabolism in skeletal muscle.

HDAC11 is a novel regulator of fatty acid oxidative metabolism in skeletal muscle.

Journal: The FEBS journal
Published: October 30, 2019

MacroH2A1.1 regulates mitochondrial respiration by limiting nuclear NAD+ consumption.

MacroH2A1.1 regulates mitochondrial respiration by limiting nuclear NAD+ consumption.

Journal: Nature structural & molecular biology
Published: March 07, 2017

Muscle cell identity requires Pax7-mediated lineage-specific DNA demethylation.

Muscle cell identity requires Pax7-mediated lineage-specific DNA demethylation.

Journal: BMC biology
Published: February 05, 2016
Showing 1-12 of 18

Last Updated: 09/26/2026