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G Forloni

Showing results (71-80 of 93) with videos related to

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Neurology|January 15, 2003
Pure spastic paraparesis associated with a novel presenilin 1 R278K mutationA Assini, L Terreni, R Borghi, et al.
Neurobiology of Disease|January 1, 1997
A neurotoxic and gliotrophic fragment of the prion protein increases plasma membrane microviscosityM Salmona, G Forloni, L Diomede, et al.
Neurology|November 1, 1991
Long-term acetyl-L-carnitine treatment in Alzheimer's diseaseA Spagnoli, U Lucca, G Menasce, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitroF Tagliavini, F Prelli, L Verga, et al.
The European Journal of Neuroscience|September 1, 1994
A neurotoxic prion protein fragment induces rat astroglial proliferation and hypertrophyG Forloni, R Del Bo, N Angeretti, et al.
Biochemical and Biophysical Research Communications|August 16, 1993
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinC Selvaggini, L De Gioia, L Cantù, et al.
The Journal of General Virology|March 11, 2006
Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaksP L Acutis, A Bossers, J Priem, et al.
Neuropathology and Applied Neurobiology|July 23, 2020
Peripheral inflammation exacerbates α-synuclein toxicity and neuropathology in Parkinson's modelsP La Vitola, C Balducci, M Baroni, et al.
Neurobiology of Disease|August 31, 2000
Apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in rat cerebellar granule cells treated with the prion protein fragment 106-126S Thellung, T Florio, V Villa, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Neurology|January 15, 2003
Pure spastic paraparesis associated with a novel presenilin 1 R278K mutationA Assini, L Terreni, R Borghi, et al.
Neurobiology of Disease|January 1, 1997
A neurotoxic and gliotrophic fragment of the prion protein increases plasma membrane microviscosityM Salmona, G Forloni, L Diomede, et al.
Neurology|November 1, 1991
Long-term acetyl-L-carnitine treatment in Alzheimer's diseaseA Spagnoli, U Lucca, G Menasce, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|May 19, 2000
Intracellular mechanisms mediating the neuronal death and astrogliosis induced by the prion protein fragment 106-126S Thellung, T Florio, A Corsaro, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Synthetic peptides homologous to prion protein residues 106-147 form amyloid-like fibrils in vitroF Tagliavini, F Prelli, L Verga, et al.
The European Journal of Neuroscience|September 1, 1994
A neurotoxic prion protein fragment induces rat astroglial proliferation and hypertrophyG Forloni, R Del Bo, N Angeretti, et al.
Biochemical and Biophysical Research Communications|August 16, 1993
Molecular characteristics of a protease-resistant, amyloidogenic and neurotoxic peptide homologous to residues 106-126 of the prion proteinC Selvaggini, L De Gioia, L Cantù, et al.
The Journal of General Virology|March 11, 2006
Identification of prion protein gene polymorphisms in goats from Italian scrapie outbreaksP L Acutis, A Bossers, J Priem, et al.
Neuropathology and Applied Neurobiology|July 23, 2020
Peripheral inflammation exacerbates α-synuclein toxicity and neuropathology in Parkinson's modelsP La Vitola, C Balducci, M Baroni, et al.
Neurobiology of Disease|August 31, 2000
Apoptotic cell death and impairment of L-type voltage-sensitive calcium channel activity in rat cerebellar granule cells treated with the prion protein fragment 106-126S Thellung, T Florio, V Villa, et al.
Pageof 10