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A Pizzuti

Showing results (21-30 of 117) with videos related to

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Genomics|March 1, 1997
SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene familyV Lapenta, P Chiurazzi, P van der Spek, et al.
Muscle & Nerve|March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian familiesF Capon, C Levato, S Semprini, et al.
Neurology|March 24, 2004
Focal dystonia caused by Mohr-Tranebjaerg syndrome with complete deletion of the DDP1 geneA Pizzuti, G Fabbrini, L Salehi, et al.
Science (New York, N.Y.)|May 18, 1992
Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.
Journal of Neural Transmission. Supplementum|January 1, 1995
Molecules with neurotrophic effects on the human developing mesencephalic dopaminergic neuronsV Silani, S Bernasconi, A Pizzuti, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Characterization of a new TSPY gene family member in Yq (TSPYq1)A Ratti, L Stuppia, V Gatta, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 24, 2001
Human developing motor neurons as a tool to study ALSV Silani, M Braga, A Botturi, et al.
JAMA|April 21, 1993
Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspringJ B Redman, R G Fenwick, Y H Fu, et al.
International Journal of Immunopathology and Pharmacology|April 10, 2010
Giant scrotal elephantiasis: an idiopathic caseC Dianzani, F Gaspardini, P Persichetti, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
The Q121 PC-1 variant and obesity have additive and independent effects in causing insulin resistanceL Frittitta, R Baratta, D Spampinato, et al.
Pageof 12

Showing results (21-30 of 117) with videos related to

Sort By:
Pageof 12
Genomics|March 1, 1997
SMT3A, a human homologue of the S. cerevisiae SMT3 gene, maps to chromosome 21qter and defines a novel gene familyV Lapenta, P Chiurazzi, P van der Spek, et al.
Muscle & Nerve|March 1, 1996
Deletion analysis of SMN and NAIP genes in spinal muscular atrophy Italian familiesF Capon, C Levato, S Semprini, et al.
Neurology|March 24, 2004
Focal dystonia caused by Mohr-Tranebjaerg syndrome with complete deletion of the DDP1 geneA Pizzuti, G Fabbrini, L Salehi, et al.
Science (New York, N.Y.)|May 18, 1992
Triplet repeat mutations in human diseaseC T Caskey, A Pizzuti, Y H Fu, et al.
Journal of Neural Transmission. Supplementum|January 1, 1995
Molecules with neurotrophic effects on the human developing mesencephalic dopaminergic neuronsV Silani, S Bernasconi, A Pizzuti, et al.
Cytogenetics and Cell Genetics|April 25, 2000
Characterization of a new TSPY gene family member in Yq (TSPYq1)A Ratti, L Stuppia, V Gatta, et al.
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|July 24, 2001
Human developing motor neurons as a tool to study ALSV Silani, M Braga, A Botturi, et al.
JAMA|April 21, 1993
Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspringJ B Redman, R G Fenwick, Y H Fu, et al.
International Journal of Immunopathology and Pharmacology|April 10, 2010
Giant scrotal elephantiasis: an idiopathic caseC Dianzani, F Gaspardini, P Persichetti, et al.
The Journal of Clinical Endocrinology and Metabolism|December 12, 2001
The Q121 PC-1 variant and obesity have additive and independent effects in causing insulin resistanceL Frittitta, R Baratta, D Spampinato, et al.
Pageof 12