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1                                          The cytoarchitectural abnormalities in the neocortex of pren
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
4                              The presence of cytoarchitectural abnormalities that may reflect such pe
5                                     No major cytoarchitectural abnormalities were apparent in the stg
6 mouse mutation causing ataxia and cerebellar cytoarchitectural abnormalities, including hypoplasia, f
7  In particular, there are several reports of cytoarchitectural alterations in anterior cingulate and
8         We uncover widespread and cumulative cytoarchitectural alterations in the dentate gyrus durin
9 c nuclear degeneration and other generalized cytoarchitectural alterations, 2) enzymatic detection of
10  cultures [< or = 6 days in vitro (DIV)] and cytoarchitectural analyses of mutant mice have been used
11  vasoactive intestinal polypeptide (VIP) and cytoarchitectural analysis of the suprachiasmatic nuclei
12                The resulting cell-type-level cytoarchitectural analysis revealed novel features of ab
13 rom the surrounding medial striatum based on cytoarchitectural and chemical neuroanatomical criteria.
14 amplified in protein data were reflective of cytoarchitectural and functional variation between brain
15                                        Nissl cytoarchitectural and MAP-2 immunocytochemical evidence
16                                              Cytoarchitectural and neurochemical studies demonstrate
17                     Converging evidence from cytoarchitectural and neuroimaging measurements underlie
18             A distal-to-proximal gradient of cytoarchitectural and neuronal morphologic maturity is s
19 aralleled the maturational gradients seen in cytoarchitectural and neuronal morphologic studies.
20                               We conducted a cytoarchitectural and ultrastructural study in complete
21                                The essential cytoarchitectural appearance of the hippocampal subfield
22 rs arose in a disease course and exhibited a cytoarchitectural appearance reminiscent of human follic
23                             We conclude that cytoarchitectural area 6Va in the marmoset is similar to
24 ipital cortex, a region corresponding to the cytoarchitectural area V5/MT+ was activated in the anoph
25                                   Columns in cytoarchitectural areas located at some distance from on
26                                The classical cytoarchitectural areas of the neocortex are composed of
27   The mammalian neocortex is subdivided into cytoarchitectural areas with distinct connectivity, gene
28                                 The leftward cytoarchitectural asymmetry and highly varied topography
29 njection sites was reconstructed relative to cytoarchitectural borders.
30 ns of gene expression is the extent to which cytoarchitectural boundaries within the hippocampus are
31  the hippocampus corresponding to predefined cytoarchitectural boundaries, which could be confirmed b
32 gh glucose exhibit aberrant maturational and cytoarchitectural cellular changes, implicating cellular
33 ent reorganization coincides with additional cytoarchitectural changes and the onset of re-epithelial
34 of relatively circumscribed and often subtle cytoarchitectural changes in neuronal density and inhibi
35 d of neural progenitor proliferation induces cytoarchitectural changes in the embryonic neocortex.
36             Our data highlight that synaptic cytoarchitectural changes occur early in AD and they may
37 This topography is accompanied by changes in cytoarchitectural characteristics, raising the question
38   However, recapitulating the structural and cytoarchitectural complexities of native tissues in vitr
39 indicate that, under natural conditions, the cytoarchitectural complexity of neurons in the mushroom
40 andular stomach, the mucosa of which has low cytoarchitectural complexity with a spiral arrangement o
41 females receiving exogenous testosterone, no cytoarchitectural component was asymmetrical.
42 -based phenotyping approach to reexamine the cytoarchitectural consequences of Reelin deficiency, usi
43                                              Cytoarchitectural defects in the cochlea of digenic hete
44 A2/CA1 borders and agrees well with previous cytoarchitectural definitions of CA2.
45 or complex instrumentations, preservation of cytoarchitectural details, optimized confocal microscopy
46                                              Cytoarchitectural differences between human and mouse ha
47 LC-beta1 or mGluR5 dramatically disrupts the cytoarchitectural differentiation of 'barrels' in the mo
48            This reduction coincides with the cytoarchitectural differentiation of the telencephalon i
49       In line with extensive vacuolation and cytoarchitectural disintegration, the numbers of synapse
50 ocortical layering, and profound hippocampal cytoarchitectural disorganization.
51 l cells, showed no alterations in density or cytoarchitectural distribution in NFL KO mice at 5 month
52 indings do not replicate previous reports of cytoarchitectural disturbances in the entorhinal cortex
53 igated the consequences of these AGT-induced cytoarchitectural disturbances on indices of DA function
54                       However, understanding cytoarchitectural dynamics of this process has been limi
55 y, using unbiased stereological methods, two cytoarchitectural estimates of the SDApc's structure, ne
56 atelets is capable of producing the hallmark cytoarchitectural features associated with activation.
57 hods to directly translate three-dimensional cytoarchitectural features from labeled tissues into mat
58    Area borders and island location based on cytoarchitectural features in the mediotemporal lobe wer
59                                        Other cytoarchitectural features of schizophrenia which are of
60                       We also noted that the cytoarchitectural features of the median eminence became
61                           The development of cytoarchitectural features of the MGB was examined in ra
62 These caudal areas contain histochemical and cytoarchitectural features that resemble the shell and c
63 an anatomically distinct region based on its cytoarchitectural features.
64 emporale (part of Brodmann's area 22), has a cytoarchitectural homolog, area Tpt, in Old World monkey
65 ory in supporting the integral balance among cytoarchitectural infrastructure, ion-homeostasis and vi
66 ells, contributing to the maintenance of the cytoarchitectural integrity of the retina.
67 muscle indicating a requirement for Mef2A in cytoarchitectural integrity.
68 cle potentially playing a role in regulating cytoarchitectural integrity.
69 ward volumetric asymmetry of area Tpt at the cytoarchitectural level.
70 t for higher cognition in which a variety of cytoarchitectural, neuronal morphometric, and innervatio
71 igin and cellular behaviors underpinning the cytoarchitectural organization of the mes and r1, howeve
72 rvival, apoptosis evasion, angiogenesis, and cytoarchitectural organization.
73  link macroscopic anatomical and microscopic cytoarchitectural parcellations.
74 ic asymmetry by volumetric assessment of the cytoarchitectural profile of area Tpt.
75 c IP causes dramatic alterations in specific cytoarchitectural proteins and demonstrate alterations i
76                                   Defects of cytoarchitectural proteins can cause left ventricular no
77 oanatomic feature, cortical layer, and brain cytoarchitectural region in the Conel data.
78 fore the developmental patterns of different cytoarchitectural regions are not distinguishable from o
79 al of cMyBP-C and occurs before the onset of cytoarchitectural remodeling in tamoxifen-treated cMyBP-
80 in Drosophila and mammals requires extensive cytoarchitectural remodeling, the elimination of many or
81 ed signaling complexes that are important in cytoarchitectural reorganization.
82 uthors conclude that a specific, sex-related cytoarchitectural SDApc parameter shows left-right asymm
83 ) are critical for organizing functional and cytoarchitectural sex differences in these subnuclei, a
84             GFAP-/- astrocytes had a reduced cytoarchitectural stability as evidenced by less abundan
85  bat auditory cortex may require symmetrical cytoarchitectural structure.
86                                              Cytoarchitectural studies indicate cellular abnormalitie
87 identified in nonhuman primates and in human cytoarchitectural studies.
88   We studied the afferent connections of two cytoarchitectural subdivisions of the caudolateral front
89                    Sertoli cells provide the cytoarchitectural support and microenvironment necessary
90         A cortical area defined in classical cytoarchitectural terms may belong to more than one and
91  associated with the appearance of apoptotic cytoarchitectural traits.
92 e from lesion studies suggests that, despite cytoarchitectural uniformity within the hippocampus, inf

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