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Louis Mandel

Showing results (131-140 of 221) with videos related to

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Frontiers in Neuroscience|March 4, 2026
Correction: DYRK1A roles in human neural progenitorsJeremie Courraud, Angélique Quartier, Nathalie Drouot, et al.
Frontiers in Neuroscience|April 4, 2025
DYRK1A roles in human neural progenitorsJeremie Courraud, Angélique Quartier, Nathalie Drouot, et al.
Experimental Cell Research|August 28, 2003
NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomesBarbara Bardoni, Rob Willemsen, Ivan Jeanne Weiler, et al.
Molecular Cell|August 23, 2002
Proteases acting on mutant huntingtin generate cleaved products that differentially build up cytoplasmic and nuclear inclusionsAstrid Lunkes, Katrin S Lindenberg, Léa Ben-Haïem, et al.
The American Journal of Pathology|April 26, 2011
Increased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weaknessBelinda S Cowling, Anne Toussaint, Leonela Amoasii, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2009
Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiationVincent Marion, Corinne Stoetzel, Dominique Schlicht, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutationAndoni Echaniz-Laguna, Anne-Sophie Nicot, Sophie Carré, et al.
The Journal of Clinical Investigation|December 8, 2010
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscleKarim Hnia, Helene Tronchère, Kinga K Tomczak, et al.
Human Molecular Genetics|July 3, 2003
82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localizationBarbara Bardoni, Marie Castets, Marc-Etienne Huot, et al.
Human Molecular Genetics|October 19, 2004
Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophyAurora Pujol, Isidre Ferrer, Carme Camps, et al.
Pageof 23

Showing results (131-140 of 221) with videos related to

Sort By:
Pageof 23
Frontiers in Neuroscience|March 4, 2026
Correction: DYRK1A roles in human neural progenitorsJeremie Courraud, Angélique Quartier, Nathalie Drouot, et al.
Frontiers in Neuroscience|April 4, 2025
DYRK1A roles in human neural progenitorsJeremie Courraud, Angélique Quartier, Nathalie Drouot, et al.
Experimental Cell Research|August 28, 2003
NUFIP1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosomesBarbara Bardoni, Rob Willemsen, Ivan Jeanne Weiler, et al.
Molecular Cell|August 23, 2002
Proteases acting on mutant huntingtin generate cleaved products that differentially build up cytoplasmic and nuclear inclusionsAstrid Lunkes, Katrin S Lindenberg, Léa Ben-Haïem, et al.
The American Journal of Pathology|April 26, 2011
Increased expression of wild-type or a centronuclear myopathy mutant of dynamin 2 in skeletal muscle of adult mice leads to structural defects and muscle weaknessBelinda S Cowling, Anne Toussaint, Leonela Amoasii, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 5, 2009
Transient ciliogenesis involving Bardet-Biedl syndrome proteins is a fundamental characteristic of adipogenic differentiationVincent Marion, Corinne Stoetzel, Dominique Schlicht, et al.
Neuromuscular Disorders : NMD|September 11, 2007
Subtle central and peripheral nervous system abnormalities in a family with centronuclear myopathy and a novel dynamin 2 gene mutationAndoni Echaniz-Laguna, Anne-Sophie Nicot, Sophie Carré, et al.
The Journal of Clinical Investigation|December 8, 2010
Myotubularin controls desmin intermediate filament architecture and mitochondrial dynamics in human and mouse skeletal muscleKarim Hnia, Helene Tronchère, Kinga K Tomczak, et al.
Human Molecular Genetics|July 3, 2003
82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localizationBarbara Bardoni, Marie Castets, Marc-Etienne Huot, et al.
Human Molecular Genetics|October 19, 2004
Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophyAurora Pujol, Isidre Ferrer, Carme Camps, et al.
Pageof 23