Xavier Calvet-Suarez

Barcelona, CT, Spain

Last Updated: 09/26/2026

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Found 34 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

Strategy for drug repurposing in fibroadipogenic replacement during muscle wasting: application to duchenne muscular dystrophy.

Strategy for drug repurposing in fibroadipogenic replacement during muscle wasting: application to duchenne muscular dystrophy.

Journal: Frontiers in cell and developmental biology

Published: October 03, 2024

Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy.

Single cell RNA sequencing of human FAPs reveals different functional stages in Duchenne muscular dystrophy.

Journal: Frontiers in cell and developmental biology

Published: March 11, 2024

Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progression.

Decoding the muscle transcriptome of patients with late-onset Pompe disease reveals markers of disease progression.

Journal: Brain : a journal of neurology

Published: February 27, 2024

Imaging mass cytometry analysis of Becker muscular dystrophy muscle samples reveals different stages of muscle degeneration.

Imaging mass cytometry analysis of Becker muscular dystrophy muscle samples reveals different stages of muscle degeneration.

Journal: Scientific reports

Published: April 21, 2023

Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations.

Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations.

Journal: Cell death & disease

Published: March 22, 2023

Nintedanib Reduces Muscle Fibrosis and Improves Muscle Function of the Alpha-Sarcoglycan-Deficient Mice.

Nintedanib Reduces Muscle Fibrosis and Improves Muscle Function of the Alpha-Sarcoglycan-Deficient Mice.

Journal: Biomedicines

Published: September 09, 2022

Reduced Number of Thymoma CTLA4-Positive Cells Is Associated With a Higher Probability of Developing Myasthenia Gravis.

Reduced Number of Thymoma CTLA4-Positive Cells Is Associated With a Higher Probability of Developing Myasthenia Gravis.

Journal: Neurology(R) neuroimmunology & neuroinflammation

Published: September 07, 2022

BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients.

BNIP3 Is Involved in Muscle Fiber Atrophy in Late-Onset Pompe Disease Patients.

Journal: The American journal of pathology

Published: February 07, 2022

Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands.

Clinical and genetic features of a large homogeneous cohort of oculopharyngeal muscular dystrophy patients from the Canary Islands.

Journal: European journal of neurology

Published: November 25, 2021

Autoantibody screening in Guillain-Barré syndrome.

Autoantibody screening in Guillain-Barré syndrome.

Journal: Journal of neuroinflammation

Published: July 14, 2021

Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.

Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy.

Journal: Brain : a journal of neurology

Published: May 19, 2021

Showing 1-12 of 34

Last Updated: 09/26/2026