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1 the spiking or postsynaptic activity of the granular cells.
2 suppression of normal osmotic regulation in granular cells.
3 hippocampal CA3 pyramidal and dentate gyrus granular cells.
4 540, was found elevated in the cytoplasm of granular cells.
5 lamellar body exocytosis from the uppermost granular cells, a process that is upregulated following
6 thway was used to study the relation between granular cell activity and the resultant fMRI response i
7 r cells determine the fMRI response, whereas granular cell activity-related mechanisms control the fM
8 d a major population of large and moderately granular cells and a minor population of small and agran
9 nd young neuronal progeny, but not in mature granular cells and astrocytes, in the subgranular zone o
10 he cerebellar cortex IGF-IR mRNA is found in granular cells and IGF-I stimulation is mitogenic and pr
11 es revealed that both mRNAs are expressed in granular cells and plasmatocytes, the primary classes of
12 A1-CA4 pyramidal neurons of the hippocampus, granular cells and Purkinje neurons of the cerebellum, a
13 wing lesion of the hippocampal dentate gyrus granular cells by intradentate colchicine injection.
14 t cell types of RCC (i.e., clear cell, mixed granular cell/clear cell, and sarcomatoid types) but als
15 incompletely secreted lamellar bodies within granular cells, demonstrable not only by several morphol
16 tability, signaling cascades upstream of the granular cells determine the fMRI response, whereas gran
17 hese early investigators recognised distinct granular cells Ehrlich's use of stains was a landmark co
18 process involves a reduction in reverberant granular cell excitation that is induced by PW deflectio
19 ad high-grade spindle cell areas and one had granular cell histology in addition to the clear cell ar
21 tracellular matrix and the transformation of granular cells into corneocytes, in an SP- and Casp-14-d
22 NA is tightly coupled to the differentiated (granular cell) keratinocyte phenotype in vivo and in vit
23 past their normal stopping site at the inner granular cell layer (GCL), and became misplaced in the o
24 A slight reduction of cell survival in the granular cell layer (GCL)/SGZ was observed in young anim
26 s, transplanted cells that integrated in the granular cell layer differentiated into cells characteri
30 stem cells in the subgranular zone (SGZ) and granular cell layer of the dentate gyrus compared to bot
31 ctive cells are mispositioned throughout the granular cell layer of the dentate gyrus during developm
34 ice resulted in impaired neurogenesis at the granular cell layer of the olfactory bulb and the DG in
35 e cells, multifocal thinning of the external granular cell layer, and loss of neurons in the deep cer
36 e of flaking and thickened skin, loss of the granular cell layer, prominent elongation of rete pegs w
37 showed selective infection of the cerebellar granular cell layer, with preservation of Purkinje cells
41 xpression in epidermis is most pronounced in granular cell layers, and although the surface pH of NHE
43 ly choreographed sequence of events in which granular cells lose their nuclei and become desiccated c
47 sed at relatively low levels in Purkinje and granular cells of cerebellum and in neuronal cells of ce
48 ] and NE occurred more frequently in MTLE in Granular Cells of DG and Pyramidal Layer [P=0.052 and 0.
49 trations were higher in NTLE vs. MTLE in the Granular Cells of DG and the Pyramidal Layer (CA1 subfie
50 arge phosphoprotein that is expressed in the granular cells of epidermis where it is localized in ker
54 expression was absent in the renin-secreting granular cells of the juxtaglomerular apparatus and the
55 rocyanine 540 permeability in differentiated granular cells parallels the changes in membrane permeab
56 tured basal keratinocytes to the spinous and granular cell phenotypes seen in the skin can be stimula
62 ant pathway fibers monosynaptically activate granular cells, so variations in population spike latenc
64 have labeled general cell types rather than granular cell subpopulations, and they do not explain th
65 m, CB and CR cells were co-localized in some granular cell subsets in laterodorsal and dorsolateral r
68 ral cell types including the above-mentioned granular cells, thick-smooth dendrite cells, and large m
72 ) performed functional experiments on coarse granular cells using a warm stage microscopic technique
73 About 70% of the oligonucleotide-permeable granular cells were viable as verified by a mitochondria
74 was expressed in the proliferating external granular cells, with occassional staining in the molecul
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