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Showing results (201-210 of 212) with videos related to

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Molecular Phylogenetics and Evolution|March 5, 2018
Complex taxonomy of the 'brush tail' peregrine earthworm Pontoscolex corethrurusS Taheri, S James, V Roy, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Plos Genetics|April 20, 2026
Dominance modifiers at the Arabidopsis self-incompatibility locus retain proto-miRNA features and act through non-canonical pathwaysRita A Batista, Eléonore Durand, Monika Mörchen, et al.
Autophagy|December 9, 2014
Autophagy in osteoblasts is involved in mineralization and bone homeostasisMarie Nollet, Sabine Santucci-Darmanin, Véronique Breuil, et al.
Journal of Cachexia, Sarcopenia and Muscle|August 16, 2025
Sepsis Induces Long-Term Muscle and Mitochondrial Dysfunction due to Autophagy Disruption Amenable by Urolithin AAlexandre Pierre, Raphael Favory, Benoit Brassart, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
Annals of Neurology|June 14, 2008
De novo LMNA mutations cause a new form of congenital muscular dystrophySusana Quijano-Roy, Blaise Mbieleu, Carsten G Bönnemann, et al.
Human Gene Therapy|December 22, 2004
Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophyNorma B Romero, Serge Braun, Olivier Benveniste, et al.
Experimental Hematology & Oncology|December 10, 2023
ProNGF promotes brain metastasis through TrkA/EphA2 induced Src activation in triple negative breast cancer cellsJulien Cicero, Sarah Trouvilliez, Martine Palma, et al.
Soft Matter|February 13, 2023
Steering self-organisation through confinementNuno A M Araújo, Liesbeth M C Janssen, Thomas Barois, et al.
Pageof 22

Showing results (201-210 of 212) with videos related to

Sort By:
Pageof 22
Molecular Phylogenetics and Evolution|March 5, 2018
Complex taxonomy of the 'brush tail' peregrine earthworm Pontoscolex corethrurusS Taheri, S James, V Roy, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Plos Genetics|April 20, 2026
Dominance modifiers at the Arabidopsis self-incompatibility locus retain proto-miRNA features and act through non-canonical pathwaysRita A Batista, Eléonore Durand, Monika Mörchen, et al.
Autophagy|December 9, 2014
Autophagy in osteoblasts is involved in mineralization and bone homeostasisMarie Nollet, Sabine Santucci-Darmanin, Véronique Breuil, et al.
Journal of Cachexia, Sarcopenia and Muscle|August 16, 2025
Sepsis Induces Long-Term Muscle and Mitochondrial Dysfunction due to Autophagy Disruption Amenable by Urolithin AAlexandre Pierre, Raphael Favory, Benoit Brassart, et al.
Brain : a Journal of Neurology|June 22, 2014
Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophySophie Nicole, Amina Chaouch, Torberg Torbergsen, et al.
Annals of Neurology|June 14, 2008
De novo LMNA mutations cause a new form of congenital muscular dystrophySusana Quijano-Roy, Blaise Mbieleu, Carsten G Bönnemann, et al.
Human Gene Therapy|December 22, 2004
Phase I study of dystrophin plasmid-based gene therapy in Duchenne/Becker muscular dystrophyNorma B Romero, Serge Braun, Olivier Benveniste, et al.
Experimental Hematology & Oncology|December 10, 2023
ProNGF promotes brain metastasis through TrkA/EphA2 induced Src activation in triple negative breast cancer cellsJulien Cicero, Sarah Trouvilliez, Martine Palma, et al.
Soft Matter|February 13, 2023
Steering self-organisation through confinementNuno A M Araújo, Liesbeth M C Janssen, Thomas Barois, et al.
Pageof 22