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Jérémie Vitte

Showing results (1-10 of 6) with videos related to

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Advances in Experimental Medicine and Biology|March 13, 2010
Spinal muscular atrophyJérémie Vitte, Ruben Attali, Nasim Warwar, et al.
Journal of Neuropathology and Experimental Neurology|August 20, 2010
Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson diseaseJérémie Vitte, Sabine Traver, André Maués De Paula, et al.
Journal of Neuro-Oncology|May 15, 2016
An allograft mouse model for the study of hearing loss secondary to vestibular schwannoma growthNicolas-Xavier Bonne, Jérémie Vitte, Fabrice Chareyre, et al.
The American Journal of Pathology|August 25, 2007
Refined characterization of the expression and stability of the SMN gene productsJérémie Vitte, Coralie Fassier, Francesco D Tiziano, et al.
Human Molecular Genetics|November 15, 2006
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule compositionAnne Tarrade, Coralie Fassier, Sabrina Courageot, et al.
Plos One|August 15, 2009
Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathyMargot Fournier, Jérémie Vitte, Jérôme Garrigue, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Advances in Experimental Medicine and Biology|March 13, 2010
Spinal muscular atrophyJérémie Vitte, Ruben Attali, Nasim Warwar, et al.
Journal of Neuropathology and Experimental Neurology|August 20, 2010
Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson diseaseJérémie Vitte, Sabine Traver, André Maués De Paula, et al.
Journal of Neuro-Oncology|May 15, 2016
An allograft mouse model for the study of hearing loss secondary to vestibular schwannoma growthNicolas-Xavier Bonne, Jérémie Vitte, Fabrice Chareyre, et al.
The American Journal of Pathology|August 25, 2007
Refined characterization of the expression and stability of the SMN gene productsJérémie Vitte, Coralie Fassier, Francesco D Tiziano, et al.
Human Molecular Genetics|November 15, 2006
A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule compositionAnne Tarrade, Coralie Fassier, Sabrina Courageot, et al.
Plos One|August 15, 2009
Parkin deficiency delays motor decline and disease manifestation in a mouse model of synucleinopathyMargot Fournier, Jérémie Vitte, Jérôme Garrigue, et al.
Pageof 1