ライフサイエンスコーパス: cytoarchitecture

1 ments by altering the organization of the TM cytoarchitecture.

2 (KO) mice exhibit alterations in hippocampal cytoarchitecture.

3 itin ligase, causes disorganized presynaptic cytoarchitecture.

4 the actin cytoskeleton and may maintain the cytoarchitecture.

5 r maintenance of cortical actin cytoskeleton cytoarchitecture.

6 n (eGFP)-WASp fusion protein restores normal cytoarchitecture.

7 ion potential conduction, axon survival, and cytoarchitecture.

8 dual variability, which can be influenced by cytoarchitecture.

9 d on the basis of known markers and cortical cytoarchitecture.

10 hippocampal learning accompany the abnormal cytoarchitecture.

11 rat display significant variability in their cytoarchitecture.

12 ting specific changes in cell morphology and cytoarchitecture.

13 econdary because of the disruption of apical cytoarchitecture.

14 role in the development of normal cerebellar cytoarchitecture.

15 kable neurotransmitter diversity and complex cytoarchitecture.

16 ay have roles associated with maintenance of cytoarchitecture.

17 d at several levels in regulating aspects of cytoarchitecture.

18 e function is largely based on their complex cytoarchitecture.

19 ctural role for Mlps as components of muscle cytoarchitecture.

20 al disorders characterized by abnormal brain cytoarchitecture.

21 differ in their patterns of connectivity and cytoarchitecture.

22 genomic DNA, and manifestation of apoptotic cytoarchitecture.

23 el, the nob retina appeared to have a normal cytoarchitecture.

24 o muscle cell differentiation via effects on cytoarchitecture.

25 afford new approaches to the study of yeast cytoarchitecture.

26 d fertile and have grossly normal cerebellar cytoarchitecture.

27 contrast is insufficient for delineation of cytoarchitecture.

28 ibitory systems are influenced by changes in cytoarchitecture.

29 be closely tied to their unique and flexible cytoarchitecture.

30 pproximation representing the organ of Corti cytoarchitecture.

31 nt with the development of aberrant cortical cytoarchitecture.

32 ent role of CryAB in maintaining muscle cell cytoarchitecture.

33 d, more spinous, and an overall more complex cytoarchitecture.

34 in brain size and perturbations in cortical cytoarchitecture.

35 tial for muscle fiber integrity and myofiber cytoarchitecture.

36 residual hippocampal tissue with distinctive cytoarchitecture.

37 vital role in maintaining lens function and cytoarchitecture.

38 ss structural changes in cortical neurons or cytoarchitecture.

39 ogenesis and marked perturbation of cortical cytoarchitecture.

40 t was additionally distinguished by cortical cytoarchitecture.

41 g memory but not of long-term plasticity and cytoarchitecture.

42 quirement for En1/2 in the maturation of DRN cytoarchitecture.

43 activity to a variety of dipteran blastoderm cytoarchitectures.

44 ausal mutations disrupt E-cadherin-dependent cytoarchitecture, adversely affecting protein assemblies

45 test area to develop, only assuming a mature cytoarchitecture after 34 weeks.

46 of neurons not distinguished on the basis of cytoarchitecture alone, which provided a better understa

47 luding instructing cells to develop a unique cytoarchitecture, amass extensive protein synthesis mach

48 mpanied by dramatic morphological changes in cytoarchitecture and adhesion.

49 nal expression of TTA can affect hippocampal cytoarchitecture and behavior in a strain-dependent mann

50 e regulation of normal and pathological cell cytoarchitecture and behaviour.

51 tion is distinguished by dramatic changes in cytoarchitecture and cell behavior.

52 , a specialized neurogenic niche with unique cytoarchitecture and cell-cell contacts.

53 we investigated the regional differences in cytoarchitecture and cellular identities of aromatase-ex

54 The cytoarchitecture and connections of the caudal cingulate

55 Two major subregions, distinct by their cytoarchitecture and connections to other brain structur

56 Moreover, the cytoarchitecture and connectivity patterns in the proxim

57 nd to subregions of the APC distinguished by cytoarchitecture and connectivity.

58 several evolutionary changes in hippocampal cytoarchitecture and connectivity.

59 e observed focal patches of abnormal laminar cytoarchitecture and cortical disorganization of neurons

60 vulnerable neurons, leading to disruption of cytoarchitecture and degeneration of spines and neurites

61 development because of its relatively simple cytoarchitecture and developmental program.

62 nctions in concert with WASp to fine-tune DC cytoarchitecture and direct cell migration.

63 reduced reward-seeking behavior and altered cytoarchitecture and dopaminergic function in the nucleu

64 2D, monolayer cultures and displayed altered cytoarchitecture and enhanced membrane protrusive activi

65 ich contribute towards the transformation of cytoarchitecture and epithelial morphology.

66 eby epithelial polarity proteins dictate the cytoarchitecture and fate of other tissue-resident cells

67 er ear development and is critical to normal cytoarchitecture and function.

68 Influences of experience on the cytoarchitecture and functional connectivity of neurons

69 entral to the development of normal neuronal cytoarchitecture and have been suggested in previous stu

70 g is essential for the development of normal cytoarchitecture and hearing function as MEKK4 signaling

71 On the basis of cytoarchitecture and immunohistochemistry, the sensory t

72 alsin is important for maintaining cellular cytoarchitecture and integrity of cellular organelles.

73 Based on cytoarchitecture and myelin distribution, we identified

74 sing questions unique to the muscle-specific cytoarchitecture and myosin isoforms.

75 The intrinsic cytoarchitecture and neurochemical organization of the n

76 oscopy and neurosphere assay the morphology, cytoarchitecture and neurogenic potential of cV-SVZ.

77 ons, including the cerebellum, showed normal cytoarchitecture and no aberrant pathology.

78 n myelination of the CNS but normal neuronal cytoarchitecture and normal myelination of the PNS.

79 Studies addressing the cytoarchitecture and organization of afferent input to t

80 mM versus 6.4+/-0.3 mM, p=0.009) with islet cytoarchitecture and pancreatic mass of islet beta-cells

81 The cytoarchitecture and placement of pulleys suggest that t

82 imately promote adaptive changes in myofiber cytoarchitecture and protein composition.

83 turally homologized to nonhuman species with cytoarchitecture and receptor architecture: pregenual (p

84 y but does play an indispensable role in the cytoarchitecture and refractive quality of the lens.

85 v-GFP-FRNK) and examined its effects on NRVM cytoarchitecture and signaling.

86 These tissue blocks retain their cytoarchitecture and support productive infection of var

87 ized histologically by disorganized cortical cytoarchitecture and thus, we hypothesized that expressi

88 of intracellular calcium is crucial for lens cytoarchitecture and transparency, however, the identity

89 Exactly how the exquisite cytoarchitecture and underlying circuitry becomes establ

90 es operate at each stage to change the spine cytoarchitecture and, in doing so, alter its function.

91 lopment, where cellular spatial composition (cytoarchitecture) and dynamics are hypothesized to be li

92 GVHD, thereby damaging thymic stromal cells, cytoarchitecture, and function.

93 ase Rho is a novel regulator of T lymphocyte cytoarchitecture, and functional Rho is required for ver

94 nship between keratin mutation, keratinocyte cytoarchitecture, and hypersensitivity to trauma.

95 th intracingulate connections, the location, cytoarchitecture, and ligand binding studies demonstrate

96 expression of chondrocyte markers, abnormal cytoarchitecture, and loss of proteoglycan matrix.

97 ing defects observed in keratin IF bundling, cytoarchitecture, and mitochondria are partially restore

98 ualization of myelinated fiber arrangements, cytoarchitecture, and projection fields of afferent fibe

99 Although cortical layering, cytoarchitecture, and proteome were found to be largely

100 The disruption of DRN cytoarchitecture appears to result from a defect in seco

101 e, we provide evidence that aspects of local cytoarchitecture are associated with aspects of global m

102 lterations of integrin-mediated adhesion and cytoarchitecture are central to development, wound heali

103 ly-L-proline binding activity and to disrupt cytoarchitecture as effectively as ZmPRO4.

104 relates well with the subsequent gradient of cytoarchitecture as well as the pattern of retinotectal

105 ata show that many aspects of abnormal brain cytoarchitecture can be prevented by manipulating a sing

106 rrespond well to microstructural borders and cytoarchitecture cannot be visualized in a living brain

107 initiation depends on tissue-intrinsic local cytoarchitectures, causing tumors to consistently origin

108 ls from mechanical stress, keratins regulate cytoarchitecture, cell growth, proliferation, apoptosis,

109 have been associated with the maintenance of cytoarchitecture, cellular differentiation and maturatio

110 ouse NF-M KSP repeats does not affect axonal cytoarchitecture, challenging the conventional viewpoint

111 phenotype was accompanied by changes in the cytoarchitecture characterized by ectopic expression of

112 dent based on available information on their cytoarchitecture, chemoarchitecture, molecular signature

113 scriptions of the heterogeneity of human ACC cytoarchitecture, connections, and functions, especially

114 Based on analysis of cytoarchitecture, connections, and immunocytochemical ma

115 ed of three distinct cortical areas based on cytoarchitecture, connectivity, and neurophysiological r

116 ippiensis, using a variety of methodologies: cytoarchitecture (cresyl violet), histochemistry (peanut

117 T cell cytoarchitecture differs dramatically depending on wheth

118 position was associated with cortical axonal cytoarchitecture disruption and increased neurodegenerat

119 leton and may regulate changes of lymphocyte cytoarchitecture during polarization and extravasation.

120 rast, the mutant ND4 disrupted mitochondrial cytoarchitecture, elevated reactive oxygen species, indu

121 collection of subnuclei delineated by gross cytoarchitecture features; however, there has yet to be

122 olecular markers as a powerful complement to cytoarchitecture for neocortical layer and cell-type com

123 s of the layer-dependent pattern of cortical cytoarchitecture, gene expression, and neuronal differen

124 investigated whether the unique human islet cytoarchitecture had functional implications.

125 Over the past few years the cytoarchitecture has been a focus of study for familial

126 e), the age where differences in hippocampal cytoarchitecture have previously been observed, for diff

127 ion of keratin IFs to structural support and cytoarchitecture in basal layer keratinocytes of the epi

128 benzimide staining identified the developing cytoarchitecture in coronal and tangential sections of G

129 ty is responsible for maintaining epithelial cytoarchitecture in efferent ductules and the reabsorpti

130 vations of the dynamics of three-dimensional cytoarchitecture in highly photosensitive specimens such

131 y that properly engrafted without disrupting cytoarchitecture in immunocompetent recipients.

132 ctures is instrumental in maintaining proper cytoarchitecture in many tissues.

133 ession patterns were related to the evolving cytoarchitecture in mice at birth (P0) and in adulthood,

134 ed less severe ataxia with normal cerebellar cytoarchitecture in stg-BDNF mice than the original stg

135 Disturbed junctional cytoarchitecture in subjects with desmosomal mutations c

136 teleosts, nucleus medialis has a distinctive cytoarchitecture in that most of its somata are confined

137 ained RA (robust nucleus of the arcopallium) cytoarchitecture in the presence of aromatase inhibitors

138 (CNS) in ts1-infected mice, preserves normal cytoarchitecture in the thymus, and delays paralysis, th

139 Examination of the cytoarchitecture in this cortical region (reminiscent of

140 polarity proteins, molecular determinants of cytoarchitecture, in malignant melanoma.

141 First, analysis of mSCN and vSCN cytoarchitecture indicated that the mSCN is similar in l

142 in dramatic perturbations in organ of Corti cytoarchitecture: instead of two pillar cells, there are

143 that occur in the context of complex tissue cytoarchitecture is critical for deciphering the mechani

144 Qualitative studies show that the ACC cytoarchitecture is heterogeneous, but there are few qua

145 evelopment and long-term consequences on the cytoarchitecture is largely unstudied.

146 Since DR cytoarchitecture is organized with respect to the midlin

147 Some mutants survive but their cerebellum cytoarchitecture is profoundly altered.

148 No changes were observed in pancreatic islet cytoarchitecture, islet size, or alpha-cell number.

149 Its impressive cytoarchitecture led to the long standing belief that it

150 2 and VLDLR exhibit severely perturbed brain cytoarchitecture, limiting the utility of these mice for

151 trate that mutant desmin alters myofibrillar cytoarchitecture, markedly disrupts the lateral sarcomer

152 rial sets of adjacent sections processed for cytoarchitecture, myeloarchitecture, acetylcholinesteras

153 ent of the human hippocampus, we studied the cytoarchitecture, myeloarchitecture, and neuronal morpho

154 nd scientific approach to the brain, linking cytoarchitecture, neurophysiology and cerebral localizat

155 Our framework enables quantification of cytoarchitecture NSC dynamics and may have implications

156 , quantification of the seemingly stochastic cytoarchitecture of beta cells in an islet requires math

157 and elicits an attending perturbation in the cytoarchitecture of both human and rodent cells.

158 The aim of this study is to describe the cytoarchitecture of canine V-SVZ (cV-SVZ), to assess its

159 In this study, we compared the cortical cytoarchitecture of four cortical areas in adult hearing

160 The cytoarchitecture of human islets has been examined, focu

161 mbryo are driven by intricate changes to the cytoarchitecture of individual cells.

162 al whisker map, whereas postsynaptically the cytoarchitecture of layer IV neurons was altered as spin

163 coincident with establishment of the unique cytoarchitecture of lens fiber cells.

164 o capture the in-focus and three-dimensional cytoarchitecture of metal-impregnated cells.

165 resent report we describe the prevalence and cytoarchitecture of molecular-layer heterotopia in C57BL

166 -1(-/-) embryos were used to analyze the 3-D cytoarchitecture of motor, commissural, and sensory axon

167 l mechanism that regulates the integrity and cytoarchitecture of neuroepithelial progenitors.

168 " Here we provide a detailed analysis of the cytoarchitecture of neurogenic complexes in adult spiny

169 Our data suggest that the cytoarchitecture of neurogenic niches and the tempo of n

170 that septin 11 plays important roles in the cytoarchitecture of neurons, including dendritic arboriz

171 We examined the cytoarchitecture of pars principalis, the largest cellul

172 The cytoarchitecture of retinas from control and dfw2J mice

173 molecule 95 (PSD95), a core component in the cytoarchitecture of synapses.

174 sumption of an HFD has a major impact on the cytoarchitecture of the arcuate nucleus in vulnerable su

175 The cytoarchitecture of the auditory area changes in a stepw

176 t cell-cell adhesive interactions within the cytoarchitecture of the bone marrow microenvironment.

177 Here, the cytoarchitecture of the brain of adult amphioxus Branchi

178 try and electron microscopy, and the overall cytoarchitecture of the brain was studied by Ekhart et a

179 ace, and allowing the formation of a defined cytoarchitecture of the brain.

180 w no detectable morphological defects in the cytoarchitecture of the brain.

181 death, resulting in no gross changes in the cytoarchitecture of the brains of these mice.

182 nt arising from a global perturbation of the cytoarchitecture of the cell.

183 Although the overall cytoarchitecture of the cerebellum appeared normal in th

184 atomical basis of schizophrenia involves the cytoarchitecture of the cerebral cortex, but the phenoty

185 ionally links these elements to preserve the cytoarchitecture of the germline cells.

186 Here, we examined the cytoarchitecture of the greater pneumotaxic center and i

187 nipulations in a preparation where the gross cytoarchitecture of the hippocampus is preserved.

188 to examine the developmental patterns in the cytoarchitecture of the human cerebral cortex from birth

189 Here we describe the cytoarchitecture of the human SVZ at the lateral ganglio

190 (HEC) brain slice culture that maintains the cytoarchitecture of the intact brain.

191 data across multiple studies on the cortical cytoarchitecture of the macaque cortex with information

192 e of this study was to examine in detail the cytoarchitecture of the MON in the goldfish using Golgi

193 nal KO mice, show major abnormalities in the cytoarchitecture of the neocortex and cerebellum and die

194 However, abnormalities in the cytoarchitecture of the neocortex, most pronounced in th

195 g by SPRY2 is essential for establishing the cytoarchitecture of the organ of Corti and for hearing.

196 l" cochlear amplifier mechanism based on the cytoarchitecture of the organ of Corti and using the tim

197 on and proliferation, which leads to altered cytoarchitecture of the postnatal brain in a gene-dose-d

198 We describe the cytoarchitecture of the sensory trigeminal complex, the

199 t migrates to and substantially disrupts the cytoarchitecture of the skin, which results in progressi

200 At E16-17 the cytoarchitecture of the VMH became recognizable by Nissl

201 as early as embryonic day 13 (E13) when the cytoarchitecture of the VMH was not recognizable by Niss

202 The overall cytoarchitecture of the young adult brain appears normal

203 c ability to integrate and contribute to the cytoarchitecture of these same organs.

204 e documented for the first time the detailed cytoarchitecture of these zones, and propose a model of

205 nce has been confirmed in numerous taxa, the cytoarchitecture of this region has not been extensively

206 nt function in the development of the normal cytoarchitecture of this structure.

207 Alternate sections were processed for Nissl cytoarchitecture or acetylcholinesterase chemoarchitectu

208 in DD mice were not attributable to aberrant cytoarchitecture or glutamate density.

209 Subpopulations of Kenyon cells, distinct in cytoarchitecture, position, and immunohistochemical trai

210 mea) is characterized by a relatively normal cytoarchitecture posteriorly with an abrupt transition t

211 sharp than normal, consistent with deficient cytoarchitecture, probably due in part to reduced number

212 causes loss of the pinwheels, disrupted SVZ cytoarchitecture, proliferation and depletion of the nor

213 void of matrix and exhibits markedly altered cytoarchitecture, proliferative capacity, and degree of

214 neurons and that its absence disrupts barrel cytoarchitecture, reduces asymmetrical orientation of sp

215 cquisition of labelled neural structures and cytoarchitecture reference in the same brain greatly fac

216 S-matured MoDCs are characterized by altered cytoarchitecture, resembling immature MoDCs, lower expre

217 cent labeling and confocal microscopy of the cytoarchitecture revealed that the viral nucleocapsids a

218 Furthermore, quantitative analysis of cytoarchitecture revealed that visual and motor circuits

219 Despite an apparent normal VMH cytoarchitecture, sf-1 heterozygous (+/-) mice exhibited

220 Cytoarchitecture showed that areas d32/p32 have a dysgra

221 ese cell movements are dependent upon intact cytoarchitecture, since the pharmacological disruption o

222 g Lewis (LEW) rats, exhibited a disrupted DG cytoarchitecture, slices of three other rat strains, inc

223 Alteration of neocortical cytoarchitecture, such as disruption of the highly elong

224 l populations in regions with well-developed cytoarchitecture, such as the stratum radiatum and strat

225 ing loss of Purkinje cells (PCs) and altered cytoarchitecture suggesting a developmental etiology for

226 s accompanied by the assembly of a polarized cytoarchitecture that provides the basis for directional

227 mesangial cells to create three-dimensional cytoarchitecture that underlies cellular differentiation

228 genesis mode prefigures the highly divergent cytoarchitectures that are seen in extant species.

229 x, the hippocampal dentate gyrus, appears by cytoarchitecture to be missing.

230 rylation of S257 is required for the correct cytoarchitecture to develop, as cells transfected with Z

231 s known about how patterning genes influence cytoarchitecture to drive changes in cell shape.

232 In comparing the forebrain cytoarchitecture to the pattern of cell type-specific st

233 Given the conservation of the epithelial cytoarchitecture, tumorigenesis may be generally initiat

234 te lineage cells in a three-dimensional (3D) cytoarchitecture using human cerebral cortical spheroids

235 Because of their longevity and in vivo-like cytoarchitecture, we conclude that slice cultures may be

236 o examine the early determinants of cortical cytoarchitecture, we deleted specific neuronal classes i

237 No qualitative differences in cytoarchitecture were observed between the schizophrenic

238 ectable, although the nonspecific changes in cytoarchitecture were still apparent.

239 from maize pollen for their ability to alter cytoarchitecture when microinjected into living plant ce

240 rogate microenvironments of complex neuronal cytoarchitectures, where different subdomains encounter

241 ibited delayed acquisition of early striatal cytoarchitecture with aberrant expression of progressive

242 The entorhinal cortex has a unique cytoarchitecture with large stellate neurons in layer II

243 to layers, and the alignment of postsynaptic cytoarchitecture with the afferent inputs.

244 metabolic function and preservation of islet cytoarchitecture, with reconstitution of rich intrainsul