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2 ltered, supporting the view that hippocampal cytoarchitectural abnormalities may be part of the cereb
3 valuated the extent of postnatal recovery of cytoarchitectural abnormalities previously observed in t
6 mouse mutation causing ataxia and cerebellar cytoarchitectural abnormalities, including hypoplasia, f
8 In particular, there are several reports of cytoarchitectural alterations in anterior cingulate and
10 inform on the contribution of MDD-associated cytoarchitectural alterations to the symptomatology and
11 c nuclear degeneration and other generalized cytoarchitectural alterations, 2) enzymatic detection of
12 cultures [< or = 6 days in vitro (DIV)] and cytoarchitectural analyses of mutant mice have been used
13 vasoactive intestinal polypeptide (VIP) and cytoarchitectural analysis of the suprachiasmatic nuclei
15 rom the surrounding medial striatum based on cytoarchitectural and chemical neuroanatomical criteria.
16 ls for mimicking some three-dimensional (3D) cytoarchitectural and functional aspects of the brain.
17 ese findings provide causal insight into the cytoarchitectural and functional organization of the tha
18 amplified in protein data were reflective of cytoarchitectural and functional variation between brain
20 nt study provides a detailed analysis of the cytoarchitectural and myeloarchitectural organization of
26 te acquisition of HD organoids, confirmed by cytoarchitectural and transcriptional defects leading to
28 characterizing molecular, cellular, spatial, cytoarchitectural, and organoid-wide properties from flu
30 rs arose in a disease course and exhibited a cytoarchitectural appearance reminiscent of human follic
32 ipital cortex, a region corresponding to the cytoarchitectural area V5/MT+ was activated in the anoph
35 The mammalian neocortex is subdivided into cytoarchitectural areas with distinct connectivity, gene
36 incorporates tools for analyses relative to cytoarchitectural areas, including statistical propertie
41 ns of gene expression is the extent to which cytoarchitectural boundaries within the hippocampus are
42 the hippocampus corresponding to predefined cytoarchitectural boundaries, which could be confirmed b
44 gh glucose exhibit aberrant maturational and cytoarchitectural cellular changes, implicating cellular
45 ent reorganization coincides with additional cytoarchitectural changes and the onset of re-epithelial
46 of relatively circumscribed and often subtle cytoarchitectural changes in neuronal density and inhibi
47 d of neural progenitor proliferation induces cytoarchitectural changes in the embryonic neocortex.
49 This topography is accompanied by changes in cytoarchitectural characteristics, raising the question
50 However, recapitulating the structural and cytoarchitectural complexities of native tissues in vitr
51 indicate that, under natural conditions, the cytoarchitectural complexity of neurons in the mushroom
52 andular stomach, the mucosa of which has low cytoarchitectural complexity with a spiral arrangement o
53 nd that CITKI/KI and CITFS/FS organoids lost cytoarchitectural complexity, transitioning from pseudos
56 erm behavioral, molecular, bioenergetic, and cytoarchitectural consequences of postnatal fluoxetine (
57 -based phenotyping approach to reexamine the cytoarchitectural consequences of Reelin deficiency, usi
59 ng retinogenesis leads to persistent retinal cytoarchitectural defects, ranging from focal lesions wi
61 or complex instrumentations, preservation of cytoarchitectural details, optimized confocal microscopy
62 tion, to examine the molecular, cellular and cytoarchitectural development of the human fetal cortex
64 r study showed that the dominant axis of MTL cytoarchitectural differentiation follows the iso-to-all
65 LC-beta1 or mGluR5 dramatically disrupts the cytoarchitectural differentiation of 'barrels' in the mo
69 l cells, showed no alterations in density or cytoarchitectural distribution in NFL KO mice at 5 month
70 indings do not replicate previous reports of cytoarchitectural disturbances in the entorhinal cortex
71 igated the consequences of these AGT-induced cytoarchitectural disturbances on indices of DA function
73 y, using unbiased stereological methods, two cytoarchitectural estimates of the SDApc's structure, ne
74 atelets is capable of producing the hallmark cytoarchitectural features associated with activation.
76 hods to directly translate three-dimensional cytoarchitectural features from labeled tissues into mat
77 Area borders and island location based on cytoarchitectural features in the mediotemporal lobe wer
82 These caudal areas contain histochemical and cytoarchitectural features that resemble the shell and c
83 We then determined its associations with (i) cytoarchitectural features using histological atlases by
89 emporale (part of Brodmann's area 22), has a cytoarchitectural homolog, area Tpt, in Old World monkey
90 ory in supporting the integral balance among cytoarchitectural infrastructure, ion-homeostasis and vi
91 exin-B2 activity is critical for maintaining cytoarchitectural integrity of the developing neuroepith
97 ogy(1-3) provide exquisite three-dimensional cytoarchitectural maps but lack probabilistic labels thr
98 t for higher cognition in which a variety of cytoarchitectural, neuronal morphometric, and innervatio
99 igin and cellular behaviors underpinning the cytoarchitectural organization of the mes and r1, howeve
103 le-cell resolution and uncovered a series of cytoarchitectural patterning events that are critical fo
108 c IP causes dramatic alterations in specific cytoarchitectural proteins and demonstrate alterations i
111 fore the developmental patterns of different cytoarchitectural regions are not distinguishable from o
112 al of cMyBP-C and occurs before the onset of cytoarchitectural remodeling in tamoxifen-treated cMyBP-
113 in Drosophila and mammals requires extensive cytoarchitectural remodeling, the elimination of many or
115 uthors conclude that a specific, sex-related cytoarchitectural SDApc parameter shows left-right asymm
116 ) are critical for organizing functional and cytoarchitectural sex differences in these subnuclei, a
117 dy revealed a differential 4D spatiotemporal cytoarchitectural signature inferred by non-Gaussian dif
122 We studied the afferent connections of two cytoarchitectural subdivisions of the caudolateral front
126 rous brain disorders, and exhibits a gradual cytoarchitectural transition from six-layered parahippoc
127 cytoarchitecturally heterogenous, containing cytoarchitectural types that are variably specialized fo
128 e from lesion studies suggests that, despite cytoarchitectural uniformity within the hippocampus, inf