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F Persichetti

Showing results (21-30 of 29) with videos related to

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Neurobiology of Disease|December 1, 1994
Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brainsF Persichetti, J Srinidhi, L Kanaley, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Neurobiology of Disease|June 1, 1996
Differential expression of normal and mutant Huntington's disease gene allelesF Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics|July 31, 2007
Factors associated with HD CAG repeat instability in Huntington diseaseV C Wheeler, F Persichetti, S M McNeil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 1, 1997
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatumR J Ferrante, C A Gutekunst, F Persichetti, et al.
RNA Biology|August 12, 2015
SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translationS Zucchelli, D Cotella, H Takahashi, et al.
Cytogenetics and Cell Genetics|January 1, 1995
CEPH consortium map of chromosome 14D W Cox, G D Billingsley, A E Bale, et al.
Science (New York, N.Y.)|July 21, 1995
Inactivation of the mouse Huntington's disease gene homolog HdhM P Duyao, A B Auerbach, A Ryan, et al.
Veterinary Parasitology, Regional Studies and Reports|April 28, 2019
Corrigendum to "Cross-sectional survey on Tritrichomonas foetus infection in Italian cats" [Vet. Parasitol. Reg. Stud. Rep.] 6C (2016) 14-19]F Veronesi, A L Gazzonis, E Napoli, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Neurobiology of Disease|December 1, 1994
Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brainsF Persichetti, J Srinidhi, L Kanaley, et al.
American Journal of Human Genetics|August 1, 1993
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locusT J Kwiatkowski, H T Orr, S Banfi, et al.
Neurobiology of Disease|June 1, 1996
Differential expression of normal and mutant Huntington's disease gene allelesF Persichetti, L Carlee, P W Faber, et al.
Journal of Medical Genetics|July 31, 2007
Factors associated with HD CAG repeat instability in Huntington diseaseV C Wheeler, F Persichetti, S M McNeil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 1, 1997
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatumR J Ferrante, C A Gutekunst, F Persichetti, et al.
RNA Biology|August 12, 2015
SINEUPs: A new class of natural and synthetic antisense long non-coding RNAs that activate translationS Zucchelli, D Cotella, H Takahashi, et al.
Cytogenetics and Cell Genetics|January 1, 1995
CEPH consortium map of chromosome 14D W Cox, G D Billingsley, A E Bale, et al.
Science (New York, N.Y.)|July 21, 1995
Inactivation of the mouse Huntington's disease gene homolog HdhM P Duyao, A B Auerbach, A Ryan, et al.
Veterinary Parasitology, Regional Studies and Reports|April 28, 2019
Corrigendum to "Cross-sectional survey on Tritrichomonas foetus infection in Italian cats" [Vet. Parasitol. Reg. Stud. Rep.] 6C (2016) 14-19]F Veronesi, A L Gazzonis, E Napoli, et al.
Pageof 3