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J Ghiso

Showing results (51-60 of 116) with videos related to

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Annals of Neurology|April 13, 2000
Inclusion body myositis, muscle blood vessel and cardiac amyloidosis, and transthyretin Val122Ile alleleV Askanas, W K Engel, R B Alvarez, et al.
Neurology|October 1, 1992
Amyloidoma of the CNS. II. Immunohistochemical and biochemical studyR G Vidal, J Ghiso, G Gallo, et al.
The Biochemical Journal|November 24, 1999
Functional and structural properties of lipid-associated apolipoprotein J (clusterin)M Calero, T Tokuda, A Rostagno, et al.
Annals of the New York Academy of Sciences|May 20, 2000
A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementiaJ Ghiso, R Vidal, A Rostagno, et al.
Biochemical and Biophysical Research Communications|March 30, 1990
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding proteinM Haltia, F Prelli, J Ghiso, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrilsL G Goldfarb, P Brown, M Haltia, et al.
Neuroscience Letters|March 15, 1996
Blood-brain barrier uptake of the 40 and 42 amino acid sequences of circulating Alzheimer's amyloid beta in guinea pigsC L Martel, J B Mackic, J G McComb, et al.
Biochemical and Biophysical Research Communications|December 15, 1986
In vitro formation of amyloid fibrils from two synthetic peptides of different lengths homologous to Alzheimer's disease beta-proteinE M Castaño, J Ghiso, F Prelli, et al.
The Journal of Experimental Medicine|December 1, 1990
Mutation in gelsolin gene in Finnish hereditary amyloidosisE Levy, M Haltia, I Fernandez-Madrid, et al.
Brain Research|November 29, 1991
Isolation and amino terminal sequence of beta-trace, a novel protein from human cerebrospinal fluidA P Kuruvilla, G M Hochwald, J Ghiso, et al.
Pageof 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
Annals of Neurology|April 13, 2000
Inclusion body myositis, muscle blood vessel and cardiac amyloidosis, and transthyretin Val122Ile alleleV Askanas, W K Engel, R B Alvarez, et al.
Neurology|October 1, 1992
Amyloidoma of the CNS. II. Immunohistochemical and biochemical studyR G Vidal, J Ghiso, G Gallo, et al.
The Biochemical Journal|November 24, 1999
Functional and structural properties of lipid-associated apolipoprotein J (clusterin)M Calero, T Tokuda, A Rostagno, et al.
Annals of the New York Academy of Sciences|May 20, 2000
A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementiaJ Ghiso, R Vidal, A Rostagno, et al.
Biochemical and Biophysical Research Communications|March 30, 1990
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding proteinM Haltia, F Prelli, J Ghiso, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Synthetic peptides corresponding to different mutated regions of the amyloid gene in familial Creutzfeldt-Jakob disease show enhanced in vitro formation of morphologically different amyloid fibrilsL G Goldfarb, P Brown, M Haltia, et al.
Neuroscience Letters|March 15, 1996
Blood-brain barrier uptake of the 40 and 42 amino acid sequences of circulating Alzheimer's amyloid beta in guinea pigsC L Martel, J B Mackic, J G McComb, et al.
Biochemical and Biophysical Research Communications|December 15, 1986
In vitro formation of amyloid fibrils from two synthetic peptides of different lengths homologous to Alzheimer's disease beta-proteinE M Castaño, J Ghiso, F Prelli, et al.
The Journal of Experimental Medicine|December 1, 1990
Mutation in gelsolin gene in Finnish hereditary amyloidosisE Levy, M Haltia, I Fernandez-Madrid, et al.
Brain Research|November 29, 1991
Isolation and amino terminal sequence of beta-trace, a novel protein from human cerebrospinal fluidA P Kuruvilla, G M Hochwald, J Ghiso, et al.
Pageof 12