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P Gambetti

Showing results (121-130 of 203) with videos related to

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The Journal of Biological Chemistry|November 14, 1997
Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutationN Singh, G Zanusso, S G Chen, et al.
Neurology|April 1, 1996
Fatal familial insomnia: behavioral and cognitive featuresR Gallassi, A Morreale, P Montagna, et al.
The Journal of Biological Chemistry|August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseasesS G Chen, D B Teplow, P Parchi, et al.
The American Journal of Pathology|August 10, 2000
Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brainS Capellari, P Parchi, C M Russo, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1992
Abnormal sympathetic skin responses in thalamic lesionsP Montagna, P Cortelli, P Avoni, et al.
Brain Research|October 27, 1987
Carbon disulfide axonopathy. Another experimental model characterized by acceleration of neurofilament transport and distinct changes of axonal sizeM Pappolla, R Penton, H S Weiss, et al.
Neurology|March 1, 1992
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178R Medori, P Montagna, H J Tritschler, et al.
British Medical Bulletin|October 1, 1993
Fatal familial insomnia and the widening spectrum of prion diseasesP Gambetti, R Petersen, L Monari, et al.
The Journal of Biological Chemistry|August 7, 1999
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion proteinG Zanusso, R B Petersen, T Jin, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1995
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulationE Sforza, P Montagna, P Tinuper, et al.
Pageof 21

Showing results (121-130 of 203) with videos related to

Sort By:
Pageof 21
The Journal of Biological Chemistry|November 14, 1997
Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutationN Singh, G Zanusso, S G Chen, et al.
Neurology|April 1, 1996
Fatal familial insomnia: behavioral and cognitive featuresR Gallassi, A Morreale, P Montagna, et al.
The Journal of Biological Chemistry|August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseasesS G Chen, D B Teplow, P Parchi, et al.
The American Journal of Pathology|August 10, 2000
Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brainS Capellari, P Parchi, C M Russo, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1992
Abnormal sympathetic skin responses in thalamic lesionsP Montagna, P Cortelli, P Avoni, et al.
Brain Research|October 27, 1987
Carbon disulfide axonopathy. Another experimental model characterized by acceleration of neurofilament transport and distinct changes of axonal sizeM Pappolla, R Penton, H S Weiss, et al.
Neurology|March 1, 1992
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178R Medori, P Montagna, H J Tritschler, et al.
British Medical Bulletin|October 1, 1993
Fatal familial insomnia and the widening spectrum of prion diseasesP Gambetti, R Petersen, L Monari, et al.
The Journal of Biological Chemistry|August 7, 1999
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion proteinG Zanusso, R B Petersen, T Jin, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1995
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulationE Sforza, P Montagna, P Tinuper, et al.
Pageof 21