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Biochemical and Biophysical Research Communications
|
May 16, 1994
Soluble amyloid beta-protein is a marker of Alzheimer amyloid in brain but not in cerebrospinal fluid
M Tabaton, M G Nunzi, R Xue, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1991
Ultrastructural localization of beta-amyloid, tau, and ubiquitin epitopes in extracellular neurofibrillary tangles
M Tabaton, S Cammarata, G Mancardi, et al.
The American Journal of Pathology
|
March 1, 1989
Selective presence of ubiquitin in intracellular inclusions
V Manetto, F W Abdul-Karim, G Perry, et al.
Archives of Neurology
|
September 1, 1973
Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria
S DiMauro, D L Schotland, E Bonilla, et al.
FEBS Letters
|
June 16, 1997
Heterogeneity of water-soluble amyloid beta-peptide in Alzheimer's disease and Down's syndrome brains
C Russo, T C Saido, L M DeBusk, et al.
Neurology
|
August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study
C M Bütefisch, P Gambetti, L Cervenakova, et al.
Journal of Neuropathology and Experimental Neurology
|
March 1, 1986
Electron microscopic localization of Alzheimer neurofibrillary tangle components recognized by an antiserum to paired helical filaments
G Perry, D J Selkoe, B R Block, et al.
The Journal of Biological Chemistry
|
September 6, 2000
The chaperone protein BiP binds to a mutant prion protein and mediates its degradation by the proteasome
T Jin, Y Gu, G Zanusso, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
B B Worrall, S T Herman, S Capellari, et al.
Acta Neuropathologica
|
February 7, 1998
Familial parkinsonism and dementia with ballooned neurons, argyrophilic neuronal inclusions, atypical neurofibrillary tangles, tau-negative astrocytic fibrillary tangles, and Lewy bodies
T Mizutani, T Inose, S Nakajima, et al.
Page
of 21
Search research articles
Search
Showing results (111-120 of 203) with videos related to
Sort By:
Page
of 21
Biochemical and Biophysical Research Communications
|
May 16, 1994
Soluble amyloid beta-protein is a marker of Alzheimer amyloid in brain but not in cerebrospinal fluid
M Tabaton, M G Nunzi, R Xue, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 15, 1991
Ultrastructural localization of beta-amyloid, tau, and ubiquitin epitopes in extracellular neurofibrillary tangles
M Tabaton, S Cammarata, G Mancardi, et al.
The American Journal of Pathology
|
March 1, 1989
Selective presence of ubiquitin in intracellular inclusions
V Manetto, F W Abdul-Karim, G Perry, et al.
Archives of Neurology
|
September 1, 1973
Progressive ophthalmoplegia, glycogen storage, and abnormal mitochondria
S DiMauro, D L Schotland, E Bonilla, et al.
FEBS Letters
|
June 16, 1997
Heterogeneity of water-soluble amyloid beta-peptide in Alzheimer's disease and Down's syndrome brains
C Russo, T C Saido, L M DeBusk, et al.
Neurology
|
August 23, 2000
Inherited prion encephalopathy associated with the novel PRNP H187R mutation: a clinical study
C M Bütefisch, P Gambetti, L Cervenakova, et al.
Journal of Neuropathology and Experimental Neurology
|
March 1, 1986
Electron microscopic localization of Alzheimer neurofibrillary tangle components recognized by an antiserum to paired helical filaments
G Perry, D J Selkoe, B R Block, et al.
The Journal of Biological Chemistry
|
September 6, 2000
The chaperone protein BiP binds to a mutant prion protein and mediates its degradation by the proteasome
T Jin, Y Gu, G Zanusso, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 16, 1999
Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease
B B Worrall, S T Herman, S Capellari, et al.
Acta Neuropathologica
|
February 7, 1998
Familial parkinsonism and dementia with ballooned neurons, argyrophilic neuronal inclusions, atypical neurofibrillary tangles, tau-negative astrocytic fibrillary tangles, and Lewy bodies
T Mizutani, T Inose, S Nakajima, et al.
Page
of 21