Ornella Cappellari

Lecturer

University of Bari Aldo Moro

Italy

Research Interests

Explore related searches

Professors in Italy

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Dr. Ornella Cappellari is a Lecturer at the University of Bari Aldo Moro in Italy. Her research focuses on Duchenne muscular dystrophy and sarcopenia, with recent articles addressing topics such as in vitro studies, gene expression normalization, and neuromuscular stimulation systems. She explores innovative therapeutic approaches and biomarkers, contributing significantly to advancements in muscular dystrophy treatment and understanding.

Articles (13)

Year:

2025

Year:

2024

Year:

2023

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (7)

Santa Cirmi

University of Messina

ITALY

View details

Capucine Trollet

FRANCE

View details

Annamaria De Luca

ITALY

View details

Andrea Aramini

Head of Research & Early Development-VP

Dompé farmaceutici SpA

ITALY

View details

Nunzio Denora

University of Bari Aldo Moro

ITALY

View details

Paola Mantuano

Tenure-track Assistant Professor (RTDb)

University of Bari Aldo Moro

ITALY

View details

Cristina Al-Khalili Szigyarto

Associated Professor

Royal Institute of Technology

SWEDEN

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Ornella Cappellari

Research Interests

Explore related searches

Contact this professor

About

Articles (13)

Patient-Oriented In Vitro Studies in Duchenne Muscular Dystrophy: Validation of a 3D Skeletal Muscle Organoid Platform

Determination of qPCR reference genes suitable for normalizing gene expression in a novel model of Duchenne muscular dystrophy, the D2-mdx mouse

Branched-Chain Amino Acids and Di-Alanine Supplementation in Aged Mice: A Translational Study on Sarcopenia

β-Dystroglycan Restoration and Pathology Progression in the Dystrophic <i>mdx</i> Mouse: Outcome and Implication of a Clinically Oriented Study with a Novel Oral Dasatinib Formulation.

A versatile system for neuromuscular stimulation and recording in the mouse model using a lightweight magnetically coupled headmount

BCAAs and Di-Alanine supplementation in the prevention of skeletal muscle atrophy: preclinical evaluation in a murine model of hind limb unloading

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the <i>mdx</i> Mouse Model and Patients.

Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate Myopathy.

BB-301: a silence and replace AAV-based vector for the treatment of oculopharyngeal muscular dystrophy.

Ultrasonography validation for early alteration of diaphragm echodensity and function in the mdx mouse model of Duchenne muscular dystrophy.

Simvastatin Treatment Does Not Ameliorate Muscle Pathophysiology in a Mouse Model for Duchenne Muscular Dystrophy.

"The Social Network" and Muscular Dystrophies: The Lesson Learnt about the Niche Environment as a Target for Therapeutic Strategies.

Cisplatin-induced skeletal muscle dysfunction: Mechanisms and counteracting therapeutic strategies

Collaborators (7)

Santa Cirmi

Capucine Trollet

Annamaria De Luca

Andrea Aramini

Nunzio Denora

Paola Mantuano

Cristina Al-Khalili Szigyarto

Make your next move.