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F Persichetti

Showing results (1-10 of 29) with videos related to

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Molecular Medicine (Cambridge, Mass.)|April 1, 1997
The genetic defect causing Huntington's disease: repeated in other contexts?J F Gusella, F Persichetti, M E MacDonald
Nucleic Acids Research|February 11, 1990
An additional HindIII polymorphism at the coagulation factor XIIIA locusC Iodice, A Novelletto, P Malaspina, et al.
Annals of Human Genetics|October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosomeF Persichetti, P Blasi, M Hammer, et al.
Human Molecular Genetics|November 25, 2000
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organellesP Hilditch-Maguire, F Trettel, L A Passani, et al.
Annals of Human Genetics|October 1, 1990
The human Y chromosome shows a low level of DNA polymorphismP Malaspina, F Persichetti, A Novelletto, et al.
Neurobiology of Disease|October 21, 1999
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segmentF Persichetti, F Trettel, C C Huang, et al.
Somatic Cell and Molecular Genetics|July 20, 1999
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteinsC C Huang, P W Faber, F Persichetti, et al.
Human Molecular Genetics|November 25, 2000
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.
Nature Genetics|August 1, 1993
Trinucleotide repeat length instability and age of onset in Huntington's diseaseM Duyao, C Ambrose, R Myers, et al.
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Molecular Medicine (Cambridge, Mass.)|April 1, 1997
The genetic defect causing Huntington's disease: repeated in other contexts?J F Gusella, F Persichetti, M E MacDonald
Nucleic Acids Research|February 11, 1990
An additional HindIII polymorphism at the coagulation factor XIIIA locusC Iodice, A Novelletto, P Malaspina, et al.
Annals of Human Genetics|October 1, 1992
Disequilibrium of multiple DNA markers on the human Y chromosomeF Persichetti, P Blasi, M Hammer, et al.
Human Molecular Genetics|November 25, 2000
Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organellesP Hilditch-Maguire, F Trettel, L A Passani, et al.
Annals of Human Genetics|October 1, 1990
The human Y chromosome shows a low level of DNA polymorphismP Malaspina, F Persichetti, A Novelletto, et al.
Neurobiology of Disease|October 21, 1999
Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segmentF Persichetti, F Trettel, C C Huang, et al.
Somatic Cell and Molecular Genetics|July 20, 1999
Amyloid formation by mutant huntingtin: threshold, progressivity and recruitment of normal polyglutamine proteinsC C Huang, P W Faber, F Persichetti, et al.
Human Molecular Genetics|November 25, 2000
Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cellsF Trettel, D Rigamonti, P Hilditch-Maguire, et al.
Nature Genetics|August 1, 1993
Trinucleotide repeat length instability and age of onset in Huntington's diseaseM Duyao, C Ambrose, R Myers, et al.
Acta Neurologica Scandinavica|April 1, 1992
HLA-linked spinocerebellar ataxia: a clinical and genetic study of large Italian kindredsM Spadaro, P Giunti, P Lulli, et al.
Pageof 3