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F Persichetti

Showing results (11-20 of 29) with videos related to

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Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Human Molecular Genetics|July 1, 1994
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Somatic Cell and Molecular Genetics|March 1, 1994
Mouse Huntington's disease gene homolog (Hdh)G T Barnes, M P Duyao, C M Ambrose, et al.
Experimental Neurology|April 1, 1997
Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneuronsC M Kosinski, J H Cha, A B Young, et al.
Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.
Human Molecular Genetics|January 1, 1994
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Huntington's diseaseJ F Gusella, S McNeil, F Persichetti, et al.
Molecular Medicine (Cambridge, Mass.)|May 1, 1995
Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeatF Persichetti, C M Ambrose, P Ge, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|September 1, 1993
The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite lociC Jodice, M Frontali, F Persichetti, et al.
American Journal of Human Genetics|June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia IC Jodice, P Malaspina, F Persichetti, et al.
Human Molecular Genetics|July 1, 1994
Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Brain : a Journal of Neurology|December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic studyM Frontali, M Spadaro, P Giunti, et al.
Somatic Cell and Molecular Genetics|March 1, 1994
Mouse Huntington's disease gene homolog (Hdh)G T Barnes, M P Duyao, C M Ambrose, et al.
Experimental Neurology|April 1, 1997
Huntingtin immunoreactivity in the rat neostriatum: differential accumulation in projection and interneuronsC M Kosinski, J H Cha, A B Young, et al.
Journal of Molecular Evolution|December 1, 1995
Recurrent simple tandem repeat mutations during human Y-chromosome radiation in Caucasian subpopulationsB M Ciminelli, F Pompei, P Malaspina, et al.
Human Molecular Genetics|January 1, 1994
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington diseaseA Novelletto, F Persichetti, G Sabbadini, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Huntington's diseaseJ F Gusella, S McNeil, F Persichetti, et al.
Molecular Medicine (Cambridge, Mass.)|May 1, 1995
Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeatF Persichetti, C M Ambrose, P Ge, et al.
Pageof 3