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E M Valente

Showing results (21-30 of 61) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|December 19, 2001
Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian familiesA R Bentivoglio, P Cortelli, E M Valente, et al.
Archives Italiennes De Biologie|November 21, 2012
A subcellular analysis of genetic modulation of PINK1 on mitochondrial alterations, autophagy and cell deathP Lenzi, R Marongiu, A Falleni, et al.
AJNR. American Journal of Neuroradiology|August 26, 2017
Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert SyndromeF Arrigoni, R Romaniello, D Peruzzo, et al.
AJNR. American Journal of Neuroradiology|September 28, 2007
Diffusion tensor imaging in Joubert syndromeA Poretti, E Boltshauser, T Loenneker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
A Yorkshire family with adult-onset cranio-cervical primary torsion dystoniaA Münchau, E M Valente, M B Davis, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Cell Death and Differentiation|March 23, 2013
PINK1 protects against cell death induced by mitochondrial depolarization, by phosphorylating Bcl-xL and impairing its pro-apoptotic cleavageG Arena, V Gelmetti, L Torosantucci, et al.
Stem Cells International|March 2, 2026
Analysis of Primary Cilium-Bearing Human Neuroprogenitors Using Flow CytometryE De Gasperi, M De Vita, M Brusa, et al.
Pageof 7

Showing results (21-30 of 61) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|December 19, 2001
Phenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian familiesA R Bentivoglio, P Cortelli, E M Valente, et al.
Archives Italiennes De Biologie|November 21, 2012
A subcellular analysis of genetic modulation of PINK1 on mitochondrial alterations, autophagy and cell deathP Lenzi, R Marongiu, A Falleni, et al.
AJNR. American Journal of Neuroradiology|August 26, 2017
Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert SyndromeF Arrigoni, R Romaniello, D Peruzzo, et al.
AJNR. American Journal of Neuroradiology|September 28, 2007
Diffusion tensor imaging in Joubert syndromeA Poretti, E Boltshauser, T Loenneker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
A Yorkshire family with adult-onset cranio-cervical primary torsion dystoniaA Münchau, E M Valente, M B Davis, et al.
Journal of Medical Genetics|February 27, 2004
A locus for autosomal dominant keratoconus maps to human chromosome 3p14-q13F Brancati, E M Valente, A Sarkozy, et al.
American Journal of Human Genetics|March 20, 2001
Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36E M Valente, A R Bentivoglio, P H Dixon, et al.
Brain : a Journal of Neurology|September 27, 2000
A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16E M Valente, S D Spacey, G M Wali, et al.
Cell Death and Differentiation|March 23, 2013
PINK1 protects against cell death induced by mitochondrial depolarization, by phosphorylating Bcl-xL and impairing its pro-apoptotic cleavageG Arena, V Gelmetti, L Torosantucci, et al.
Stem Cells International|March 2, 2026
Analysis of Primary Cilium-Bearing Human Neuroprogenitors Using Flow CytometryE De Gasperi, M De Vita, M Brusa, et al.
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