Giulio Cossu

Max Delbrück Center — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

84h-index29.3kcitations389works2.72yr avg
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Research Topics

Muscle Physiology and Disorders(192), Tissue Engineering and Regenerative Medicine(106), Mesenchymal stem cell research(67), Pluripotent Stem Cells Research(56), Congenital heart defects research(34)

Publications388 total

Mini-agrin prevents calcium leakage and restores the dystrophin complex
2025Open Access
<i>Slit1</i> -a MET target gene in the embryonic limbs, prevents premature differentiation during mammalian myogenesis
2025
TNAP expressing adventitial pericytes contribute to myogenesis during foetal development
Vascular Pharmacology·2025· 1 citedOpen Access
Author Correction: Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
EMBO Molecular Medicine·2024Open Access
Standing the test of COVID-19: charting the new frontiers of medicine
Frontiers in Science·2024· 10 citedOpen Access
Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy
EMBO Molecular Medicine·2024· 5 citedOpen Access
ICSOS 2023 Authors Index
2023Open Access
Potency assays and biomarkers for cell-based advanced therapy medicinal products
Frontiers in Immunology·2023· 26 citedOpen Access
Mesoangioblasts at 20: From the embryonic aorta to the patient bed
Frontiers in Genetics·2023· 10 citedOpen Access
Cost and availability of novel cell and gene therapies
EMBO Reports·2023· 30 citedOpen Access
The Transcriptional Regulator Prdm1 Is Essential for the Early Development of the Sensory Whisker Follicle and Is Linked to the Beta-Catenin First Dermal Signal
Biomedicines·2022· 9 citedOpen Access
The contracture-in-a-well. An in vitro model distinguishes bulk and interfacial processes of irreversible (fibrotic) cell-mediated contraction
Biomaterials Advances·2022· 5 citedOpen Access
Challenges in cell transplantation for muscular dystrophy
Experimental Cell Research·2021· 11 cited
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle
MDC Repository (Max-Delbrueck-Center for Molecular Medicine)·2021· 1 citedOpen Access
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle
Frontiers in Genetics·2021· 23 citedOpen Access
Inclusivity and diversity: Integrating international perspectives on stem cell challenges and potential
Stem Cell Reports·2021· 24 citedOpen Access
Transient reprogramming of postnatal cardiomyocytes to a dedifferentiated state
PLoS ONE·2021· 10 citedOpen Access
Merosin deficient congenital muscular dystrophy type 1A: An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands
Neuromuscular Disorders·2021· 6 citedOpen Access
Adenoviral Mediated Delivery of OSKM Factors Induces Partial Reprogramming of Mouse Cardiac Cells In Vivo
Advanced Therapeutics·2020· 15 citedOpen Access
Challenges and potential in regenerative medicine: A joint report from EASAC and FEAM
2020· 4 cited
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Frequent Co-authors

Maurilio Sampaolesi(11), Rossana Tonlorenzi(10), Yvan Torrente(10), Shahragim Tajbakhsh(7), Margaret Buckingham(7), Roberto Bottinelli(7), Maria Gabriella Cusella De Angelis(6), A Innocenzi(6), Giuseppe D’Antona(6), Laura Perani(5), Beatriz G. Gálvez(5), Francesco Saverio Tedesco(5), Ugo Borello(5), Marcello Coletta(4), Arianna Dellavalle(4), Enrico Tagliafico(4), Graziella Messina(4), Paolo Bianco(4), Silvia Brunelli(4), Robert G. Kelly(4)