Phosphorylation of specific sets of tau isoforms reflects different neurofibrillary degeneration processes.
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Comparative biochemistry of tau in progressive supranuclear palsy, corticobasal degeneration, FTDP-17 and Pick's diseaseThe peptidylprolyl cis/trans-isomerase Pin1 modulates stress-induced dephosphorylation of Tau in neurons. Implication in a pathological mechanism related to Alzheimer diseaseAlzheimer's disease-like tau neuropathology leads to memory deficits and loss of functional synapses in a novel mutated tau transgenic mouse without any motor deficits.Progressive supranuclear palsy misdiagnosed as Parkinson's disease: a case report and review of literature.Sequencing of peptides phosphorylated on serines and threonines by post-source decay in matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.Guadeloupean parkinsonism: a cluster of progressive supranuclear palsy-like tauopathy.Pathological, clinical and genetic heterogeneity in progressive supranuclear palsy.REVIEW: tau protein pathology in Alzheimer's disease and related disorders.Neurofibrillary tangle parkinsonian disorders--tau pathology and tau genetics.Progressive supranuclear palsy (Steele-Richardson-Olszewski disease).Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism.Cerebrospinal fluid brain-derived proteins in the diagnosis of Alzheimer's disease and Creutzfeldt-Jakob disease.Pseudohyperphosphorylation has differential effects on polymerization and function of tau isoforms.Stable-tau overexpression in human neuroblastoma cells: an open door for explaining neuronal death in tauopathies.Non-Alzheimer's disease dementias: anatomic, clinical, and molecular correlates.Corticotropin-releasing factor receptor-dependent effects of repeated stress on tau phosphorylation, solubility, and aggregation.Parkinsonism and impaired axonal transport in a mouse model of frontotemporal dementiaMilestones in atypical and secondary Parkinsonisms.Tau accumulation in the retina promotes early neuronal dysfunction and precedes brain pathology in a mouse model of Alzheimer's disease.Differential assembly of human tau isoforms in the presence of arachidonic acid.Comparison of extent of tau pathology in patients with frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17), frontotemporal lobar degeneration with Pick bodies and early onset Alzheimer's disease.The complex relationship between soluble and insoluble tau in tauopathies revealed by efficient dephosphorylation and specific antibodies.Rapid Tau Protein Dephosphorylation and Differential Rephosphorylation during Cardiac Arrest-Induced Cerebral Ischemia and Reperfusion
P2860
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P2860
Phosphorylation of specific sets of tau isoforms reflects different neurofibrillary degeneration processes.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年学术文章
@wuu
1998年学术文章
@zh
1998年学术文章
@zh-cn
1998年学术文章
@zh-hans
1998年学术文章
@zh-my
1998年学术文章
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1998年學術文章
@yue
1998年學術文章
@zh-hant
name
Phosphorylation of specific se ...... illary degeneration processes.
@en
Phosphorylation of specific se ...... illary degeneration processes.
@nl
type
label
Phosphorylation of specific se ...... illary degeneration processes.
@en
Phosphorylation of specific se ...... illary degeneration processes.
@nl
prefLabel
Phosphorylation of specific se ...... illary degeneration processes.
@en
Phosphorylation of specific se ...... illary degeneration processes.
@nl
P2093
P2860
P1433
P1476
Phosphorylation of specific se ...... illary degeneration processes.
@en
P2093
Bussière T
Caillet-Boudin ML
Delacourte A
Mailliot C
Sergeant N
P2860
P304
P356
10.1016/S0014-5793(98)00910-7
P407
P577
1998-08-01T00:00:00Z