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2 esolution and corresponding atomic models of paired helical and straight filaments from the brain of
3 ates and becomes hyperphosphorylated forming paired helical and straight filaments, which can further
8 isease (AD), immunohistochemistry of WT1 and paired helical filament (PHF) in serial sections was car
10 formation of amyloid fibrils displaying the paired helical filament (PHF) morphology characteristic
11 Ser 262 is phosphorylated extensively in paired helical filament (PHF) tau from Alzheimer's disea
12 m the progressive pattern of neuropathology [paired helical filament (PHF)-tau and amyloid-beta] in A
13 r AV-1451 exhibits high binding affinity for paired helical filament (PHF)-tau pathology in Alzheimer
17 idue amino-acid sequence, referred to as the paired helical filament 6 (PHF6), which may play an impo
18 ide (Abeta) concentration, Abeta deposition, paired helical filament formation, cerebrovascular amylo
22 ur phosphospecific probes also revealed that paired helical filament preparations exhibited phospho-t
23 ognizing independent phospho-epitopes in the paired helical filament proteins (PHF) found in AD brain
25 ylated at the same amino acid residues as AD paired helical filament tau (PHFtau), but they exhibited
26 vasive analyses in cortical regions in which paired helical filament tau accumulation is expected in
27 vasive analyses in cortical regions in which paired helical filament tau accumulation is expected in
28 d in clinical studies) provides estimates of paired helical filament tau burden in good correlation w
29 d in clinical studies) provides estimates of paired helical filament tau burden in good correlation w
30 t analysis, Tau-nY29 detects soluble tau and paired helical filament tau from severely affected Alzhe
33 ripts of SORL1 and ABCA7 was associated with paired helical filament tau tangle density, and the expr
36 e phosphorylation site consistently found in paired helical filament tau, serine 413, is modified by
37 global pathology score, and as amyloid load, paired helical filament tau-positive (PHFtau) tangle den
39 n have the deposition of Alzheimer's disease paired helical filament type hyperphosphorylated tau.
41 was a significant decrease in the density of paired helical filament-1-positive neurons in the immuni
42 vidence for hyperphosphorylated tau protein (paired helical filament-I tau), which has been associate
46 h wt mice, prominent inner retinal Abeta and paired helical filament-tau, and decreased retinal gangl
47 ain tau pathology in the form of tangles and paired helical filament-tau-containing neurites in Alzhe
48 t et al reports that antibodies generated to paired helical filaments (AMY antibodies) unexpectedly l
49 bodies which recognize phosphorylated tau in paired helical filaments (AT8 and PHF-1) show positive i
53 hosphorylated and accumulates in the form of paired helical filaments (PHF) in the brains of patients
56 orylation is implicated in the biogenesis of paired helical filaments (PHF) seen in Alzheimer's disea
59 drated tau 2-19 and collagen I and insoluble paired helical filaments (PHFs) and collagen I of weak h
60 ng of tau protein leads to the generation of paired helical filaments (PHFs) and neurofibrillary tang
61 generation of muscle fibers characterized by paired helical filaments (PHFs) composed of phosphorylat
62 s the neurofibrillary tangle, which contains paired helical filaments (PHFs) composed of the microtub
63 o determine if the high phosphate content of paired helical filaments (PHFs) in Alzheimer's disease (
64 ion of human Alzheimer high-molecular-weight paired helical filaments (PHFs) in the dentate gyrus of
66 lzheimer disease (AD) is the accumulation of paired helical filaments (PHFs) of hyperphosphorylated m
69 table aggregates leading to the formation of paired helical filaments (PHFs) which deposit into neuro
70 specific serine/threonine residues found in paired helical filaments (PHFs), and its expression is u
72 that phosphorylated tau, like that found in paired helical filaments (PHFs), does not promote microt
79 tion and vacuolated muscle fibers containing paired helical filaments and 6- to 10-nm fibrils, both r
81 at in Alzheimer's disease, the copresence of paired helical filaments and Abeta-amyloidosis indicates
82 he formation and/or stabilization of NFT and paired helical filaments and provide a model system to i
83 ation of isolated tau filaments demonstrated paired helical filaments and ribbon-like structures.
84 ylated tau (P-tau) in the form of tangles of paired helical filaments and/or straight filaments is on
85 nd beta-amyloid precursor protein, and their paired helical filaments are composed of phosphorylated
86 idely regarded as the principal component of paired helical filaments comprising Alzheimer neurofibri
87 ly hyperphosphorylated tau polymers known as paired helical filaments constitute one of the major cha
89 recognition of the role of proteoglycans in paired helical filaments formation makes proteoglycans o
90 ments by a method used for the extraction of paired helical filaments from Alzheimer's disease brain.
93 ongly binds to tau lesions primarily made of paired helical filaments in Alzheimer brains (eg, intran
94 mentia through its deposition in the form of paired helical filaments in Alzheimer's disease neurofib
95 We document the first case of tauopathy with paired helical filaments in an aged chimpanzee (Pan trog
96 phosphorylated tau is the major component of paired helical filaments in neurofibrillary lesions asso
97 tau (microtubule-binding protein that forms paired helical filaments in neurons of the Alzheimer's d
98 s disease (AD) and accumulates as tangles of paired helical filaments in neurons undergoing degenerat
100 eadily bound thioflavin-S, a dye that stains paired helical filaments in the histochemical diagnosis
101 ociated protein tau is found aggregated into paired helical filaments in the intraneuronal neurofibri
102 cytochemistry, including colocalization with paired helical filaments in the neuropil and perikarya.
104 s dysfunction and aggregation into insoluble paired helical filaments is involved in the pathogenesis
105 otein tau that is the major component of the paired helical filaments observed in Alzheimer's disease
106 s of Alzheimer disease (AD), are composed of paired helical filaments of abnormally hyperphosphorylat
111 of neuritic plaques (NPs) and from the 24 nm paired helical filaments of neurofibrillary tangles (NFT
112 tau is the major structural component of the paired helical filaments present in the brains of Alzhei
113 mbling straight filaments or Pronase-treated paired helical filaments raises fundamental questions co
114 nds pathological hyperphosphorylated tau and paired helical filaments tau directly but not non-phosph
115 were highly correlated with neuritic plaque, paired helical filaments tau neurofibrillary tangle and
116 SP), tau proteins assemble into straight and paired helical filaments that form intraneuronal deposit
117 nds microtubules, and self-assembles to form paired helical filaments that likely contribute to neuro
118 ormation of either sarkosyl-insoluble tau or paired helical filaments was not induced by Abeta42.
119 lary tangles consisted of tau-immunoreactive paired helical filaments with a diameter and helical per
122 phorylated tau is the principal component of paired helical filaments, a pathological hallmark of Alz
123 , amyloid-beta immunoreactive filaments, and paired helical filaments, all of which are pathological
125 curred on material in close proximity to the paired helical filaments, but never was on the paired he
126 endent epitope of tau in Alzheimer's disease paired helical filaments, demonstrates positivity in the
127 n IBM muscle and AD brain phenotypes include paired helical filaments, hyperphosphorylated tau protei
128 rus neurons showed cytoplasmic inclusions of paired helical filaments, P-tau aggregates characteristi
129 specific Serine/Threonine residues found in paired helical filaments, suggesting its role in tauopat
130 onoclonal antibody Alz50 much like authentic paired helical filaments, suggesting that the conformati
132 demonstrates two novel components of the IBM paired helical filaments, which may lead to better under
149 osphorylated form, aggregates into insoluble paired-helical filaments (PHFs) in Alzheimer's disease (
152 with three microtubule-binding repeats form paired helical-like filaments under physiological condit
153 ons, where oxidation may contribute to final paired helical morphology, but is not a necessary prereq
157 and C634 to C651 and is composed of two base paired helical regions that flank a phylogenetically con
159 euron loss, intracytoplasmic tau aggregates, paired helical tau filaments, increased 4R tau messenger
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