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1 Rosenthal fibers (RF), intra-astrocytic hyaline inclusio
2 Rosenthal fibers and eosinophilic granular bodies were o
3 Rosenthal's canal (RC) extended to between 560 and 650 d
6 udy further the effects of elevated GFAP and Rosenthal fibers per se, independent of mutations, we pe
10 presence of eosinophilic inclusions known as Rosenthal fibers (RFs) within astrocytes, and is caused
11 d by cytoplasmic protein aggregates known as Rosenthal fibers along with variable degrees of leukodys
17 rized by cytoplasmic inclusion bodies called Rosenthal fibers (RFs), which contain GFAP, small heat s
18 s characterized by protein inclusions called Rosenthal fibers within astrocyte cell bodies and proces
19 low-cost "do-it-yourself" air filter (Corsi-Rosenthal Box; CR Box) on indoor air concentrations of 4
20 class averages, efficiency/angular coverage, Rosenthal-Henderson plots and local/global 3D reconstruc
21 , cerebellum, and spinal cord) and decreased Rosenthal fibers in olfactory bulb, hippocampus, corpus
22 with GFAP-R76H and -R236H mutations develop Rosenthal fibers, the hallmark protein aggregates observ
26 njections of Neurobiotin (NB) were made into Rosenthal's canal, labeling a small cluster of cells in
28 hy adult controls and 25 outpatients meeting Rosenthal-National Institute of Mental Health criteria f
30 e increases in GFAP, and the accumulation of Rosenthal fibers, cytoplasmic protein inclusions contain
32 thology with GFAP aggregation in the form of Rosenthal fibers, widespread astrogliosis, and white mat
33 lead to protein aggregation and formation of Rosenthal fibers, complex astrocytic inclusions that con
34 orms of Alexander disease is the presence of Rosenthal fibers, cytoplasmic inclusions in astrocytes t
36 at promote GFAP accumulation and the role of Rosenthal fibers (RFs) in the disease process remain unk
38 justment users reported higher satisfaction (Rosenthal r = -0.4; 95% CI, -0.6 to -0.1) and longer dai
40 teins, and ubiquitinated proteins are termed Rosenthal fibers and characterize Alexander disease, a l
42 the predictive and construct validity of the Rosenthal et al. diagnosis of winter seasonal affective
44 of spiral ganglion neurons (SGNs) within the Rosenthal's canal and of SGN projections toward both the
45 95% CI, -0.6 to -0.1) and longer daily use (Rosenthal r = -0.3; 95% CI, -0.5 to 0.0) compared with t
47 rophic' morphology, cytoplasmic vacuolation, Rosenthal fibres and associated stress protein markers.
49 ide formal proof linking GFAP mutations with Rosenthal fibers and oxidative stress, and correlate gli
50 ne is generated and immediately reacted with Rosenthal's complex to produce the corresponding zircona
51 n of spiral ganglion (SG) cell somata within Rosenthal's canal demonstrated a mean of approximately 5