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Fatima Bosch

Has grant

Catedrática de Universidad

Universitat Autònoma de Barcelona (UAB)

Spain

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Recent Grants

Grant: Open

Towards the first cure for patients suffering from Idiopathic Pulmonary Fibrosis

Open Date: 2024-12-01

Close Date: 2026-12-01

Grant: Open

Innovative preclinical developments to treat metabolic diseases by gene therapy (QMet)

Open Date: 2024-09-01

Close Date: 2027-08-01

Grant: Open

EUROPEAN RARE DISEASES RESEARCH ALLIANCE (ERDERA)

Open Date: 2024-09-01

Close Date: 2031-08-01

Grant: Open

Enhancing and Evolving INFRAFRONTIER Disease Modelling Capacity to Enable Breakthrough Research (INFRAPLUS)

Open Date: 2024-06-01

Close Date: 2027-05-01

Grant: Close

Development of a novel gene therapy for the treatment of Idiopathic Fibrosis.

Open Date: 2022-05-01

Close Date: 2025-09-01

Articles (11)

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2026

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2025

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2025

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2025

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2024

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2024

Year:

2024

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2023

Year:

2023

Year:

2023

Year:

2023

Collaborators (12)

Pierre-Damien Denechaud

Tenure researcher

Institut des Maladies Métaboliques et Cardiovasculaires

FRANCE

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Laia Vilà

Profesora lectora

University of Barcelona

SPAIN

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Dominique Langin

Professor

Université Paul Sabatier

FRANCE

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Peter Kovacs

Leipzig University

GERMANY

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Anna Pujol

Head of Transgenic Animal Unit - Associated Teacher

Universitat Autònoma de Barcelona

SPAIN

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Joel Schick

Group Leader

Helmholtz Zentrum München Deutsches Forschungszentrum für Umwelt und Gesundheit

GERMANY

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Etienne Mouisel

Associate Professor

Université de Toulouse

FRANCE

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Giuseppe Ronzitti

Researcher

INSERM

FRANCE

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Hadi Al-Hasani

Heinrich Heine University Düsseldorf

GERMANY

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Guillaume Pavlovic

Head of Unit, Genetic Engineering and Model Validation

Institut Clinique de la Souris - ICS - IGBMC - CELPHEDIA

FRANCE

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Ana Carretero

Profesor Titular de Universidad

Universitat Autònoma de Barcelona (UAB)

SPAIN

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Cheryl Ackert-Bicknell

Associate Professor

University of Colorado Hospital

UNITED STATES

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Fatima Bosch

Research Interests

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Recent Grants

Articles (11)

AAV-mediated FGF21 gene therapy promotes health span extension by whole-body tissue-specific adaptations

Nuclear hormone-sensitive lipase regulates adipose tissue mass and adipocyte metabolism.

A myotropic AAV vector combined with skeletal muscle <i>cis</i>-regulatory elements improve glycogen clearance in mouse models of Pompe disease.

Rat models of musculoskeletal lysosomal storage disorders and their role in pre-clinical evaluation of gene therapy approaches

Reversion of metabolic dysfunction-associated steatohepatitis by skeletal muscle-directed FGF21 gene therapy

Treatment of infantile-onset Pompe disease in a rat model with muscle-directed AAV gene therapy

Gene Therapy for Diabetes

Overexpressing high levels of human vaspin limits high fat diet-induced obesity and enhances energy expenditure in a transgenic mouse.

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development.

Arginine reprograms metabolism in liver cancer via RBM39

Integrated gene expression profiles reveal a transcriptomic network underlying the thermogenic response in adipose tissue

Collaborators (12)

Pierre-Damien Denechaud

Laia Vilà

Dominique Langin

Peter Kovacs

Anna Pujol

Joel Schick

Etienne Mouisel

Giuseppe Ronzitti

Hadi Al-Hasani

Guillaume Pavlovic

Ana Carretero

Cheryl Ackert-Bicknell

Make your next move.

Fatima Bosch

Research Interests

Explore related searches

Recent Grants

Articles (11)

AAV-mediated FGF21 gene therapy promotes health span extension by whole-body tissue-specific adaptations

Nuclear hormone-sensitive lipase regulates adipose tissue mass and adipocyte metabolism.

A myotropic AAV vector combined with skeletal muscle &lt;i&gt;cis&lt;/i&gt;-regulatory elements improve glycogen clearance in mouse models of Pompe disease.

Rat models of musculoskeletal lysosomal storage disorders and their role in pre-clinical evaluation of gene therapy approaches

Reversion of metabolic dysfunction-associated steatohepatitis by skeletal muscle-directed FGF21 gene therapy

Treatment of infantile-onset Pompe disease in a rat model with muscle-directed AAV gene therapy

Gene Therapy for Diabetes

Overexpressing high levels of human vaspin limits high fat diet-induced obesity and enhances energy expenditure in a transgenic mouse.

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development.

Arginine reprograms metabolism in liver cancer via RBM39

Integrated gene expression profiles reveal a transcriptomic network underlying the thermogenic response in adipose tissue

Collaborators (12)

Pierre-Damien Denechaud

Laia Vilà

Dominique Langin

Peter Kovacs

Anna Pujol

Joel Schick

Etienne Mouisel

Giuseppe Ronzitti

Hadi Al-Hasani

Guillaume Pavlovic

Ana Carretero

Cheryl Ackert-Bicknell

Make your next move.

A myotropic AAV vector combined with skeletal muscle <i>cis</i>-regulatory elements improve glycogen clearance in mouse models of Pompe disease.