ライフサイエンスコーパス: granular layer

1 ructed a large-scale 3D network model of the granular layer.

2 coincident with misshaped nuclei within the granular layer.

3 whereas PTH2R was detected in the spinous to granular layer.

4 the more differentiated keratinocytes of the granular layer.

5 ecular layers, oriented perpendicular to the granular layer.

6 hen granule cell axons are stimulated in the granular layer.

7 r lipid composition and cell adhesion in the granular layer.

8 only scattered cellular staining within the granular layer.

9 SEZ) and early postnatal cerebellar external granular layer.

10 epidermis of human skin, particularly in the granular layer.

11 s into the intercellular spaces of the upper granular layer.

12 ttern in the junction of stratum corneum and granular layers.

13 onal staining in the molecular, and internal granular layers.

14 elates with the atrophy of the molecular and granular layers.

15 solution of cell-cell junctions in the upper granular layers.

16 the highest similarity in supragranular and granular layers.

17 ised the majority of stimulus information in granular layers.

18 ty correlate with the synaptic distance from granular layers.

19 ng increased tension and TJ stability in the granular layer 2.

20 motor cortex (M1) emphasize its lack of the granular layer 4 (L4) typical of sensory cortices.

21 a TEs composed of three layers: an outermost granular layer, a middle primary wall composed of a mesh

22 res of BA22/TA were the presence of distinct granular layers, a prominent, jagged layer IIIc, and a d

23 ly in the protoplasmic islet in the internal granular layer after the third postnatal week.

24 In addition, a granular layer and a low-density zone typifying the peri

25 je somata and dendrites, neurons in internal granular layer and dentate nucleus, and neuronal element

26 d the most posterior end of GC and overlying granular layer and encompassed an area provisionally ref

27 of granule neuron precursors in the external granular layer and glial precursor cells throughout the

28 cant in the stellate and basket cells of the granular layer and Golgi cells of the molecular layer.

29 al weeks (g.w.), PV appeared in the external granular layer and in a few Purkinje cells at 11 g.w., a

30 ve cells occurred in clusters throughout the granular layer and reached their highest reactivity by P

31 ermis characterized by complete absence of a granular layer and stratum corneum.

32 ranule cells (NeuN-positive) in the internal granular layer and the migrating granule cells did not e

33 e to skin models resulted in the loss of the granular layer and thinning of the epidermis and stratum

34 Conversely, LIMK1 is expressed in the upper granular layers and phosphorylates and inhibits cofilin.

35 ggrin processing, reduced lamellar bodies in granular layers and significantly altered lipid composit

36 ispersed widely before entering the internal granular layer, and a rostral pathway along the cerebell

37 the external granular layer to the internal granular layer, and lack of excitatory inputs triggers t

38 onsisting of three distinct stages: spinous, granular layer, and stratum corneum.

39 ing must take place through a surface porous granular layer, and that layer must be composed of grain

40 e subpial stream is replaced by the external granular layer, and the NTZ organizes into distinct DCN

41 l pattern of lamination and lack an internal granular layer, and those with more complex laminar arch

42 tive koniocellular LGN influence on V1 supra-granular layers, and they indicate comparable capacities

43 with patterns previously derived from supra-granular-layers, and produced stimulation-induced spatia

44 es such as the main olfactory bulb (internal granular layer), anterior olfactory nucleus, and deep la

45 In long-term cultures, the granular layer appeared well preserved and the UBC axons

46 itatory input, consisting of output from the granular layer (approximately 25 ms), exogenous input to

47 network that hints for the first time at the granular layer as a major determinant of cerebellar bloo

48 that the lack of recurrent excitation in the granular layer as commonly required in traditional reser

49 c-fos expression throughout the ipsilateral granular layer as well as in Purkinje cell nuclei.

50 A3 and ephrin-A5 is observed in the external granular layer between the posterior and anterior lobes.

51 Within the granular layer, both receptors were expressed in the cyt

52 ume of the molecular layer by 24% and of the granular layer by 22% in comparison with controls.

53 Therefore, granular layer capillaries are controlled by the balance

54 ification of new cell types including a deep granular layer cell that relays sensory information from

55 eterious action is intrinsic to the external granular layer cell.

56 layed barrier formation as embryos, enlarged granular layer cells and corneocytes, and a morphologica

57 of basal cells, stratum spinosum cells, and granular layer cells were all stained uniformly, but not

58 The confinement of SULT2B1b to the granular layer coincides with this being the area with t

59 that the predominant AP-1 heterodimer in the granular layer consists of Fra-2 and JunB while a JunD a

60 l, and, at 13 g.w., the newly formed subpial granular layer contained GABA-immunoreactive cells, as w

61 ortex, affecting primarily the dentate gyrus granular layer (DG) and CA4 of the hippocampus and layer

62 ociated with the epidermal keratinocyte (KC) granular layer differentiation program.

63 human profilaggrin gene is expressed in the granular layer during the late stages of terminal differ

64 human profilaggrin gene is expressed in the granular layer during the late stages of the epidermal d

65 ebellar granule cells remain in the external granular layer (EGL) for 20-48 hr before initiating thei

66 bit the proliferation of cerebellar external granular layer (EGL) neuroblasts by mechanisms that are

67 cursor cells (GCPs), located in the external granular layer (EGL) of the cerebellum, gives rise to me

68 howed appropriate expression in the external granular layer (EGL) of the postnatal day (PN) 7 cerebel

69 n precursors (GNP) in the postnatal external granular layer (EGL), the internal granular layer formed

70 plasticity provides a dynamic control of the granular layer encoding capacity.

71 the somata of granule cells in the internal granular layer, even though these cells gave large AMPA

72 he normal pattern of suprabasal (spinous and granular layer) expression in transgenic mouse epithelia

73 e circumvented by considering other inherent granular layer features such as inverted input signals o

74 external granular layer (EGL), the internal granular layer formed normally in Smo/Smo mice and tumor

75 Fs) as well as microinjection of NMDA in the granular layer generates beam-like responses with a cent

76 pidermis is fragile, and acantholysis in the granular layer generates localized lesions, compromising

77 rCs and basolateral dendrites of GoCs in the granular layer (GL).

78 Specifically, we targeted granular layers (GL) of rat and turtle cerebella that ar

79 r layer and the mossy fiber terminals in the granular layer glomeruli in late development and during

80 Surprisingly, after entering the internal granular layer, granule cells re-extend both their somat

81 R, but expression is restricted to the upper granular layers (i.e., no spinous layer expression).

82 contains acellular regions within the inner granular layer (igl) and ectopic, calbindin-immunoreacti

83 xternal germinal layer (EGL) to the internal granular layer (IGL) is a crucial process in the develop

84 pment by affecting cerebellar size, internal granular layer (IGL) thickness, and Purkinje cell (PC) d

85 ressing cells are restricted to the internal granular layer (IGL), but that the BDNF protein is prese

86 Lateral area 29 (29l) has a dense granular layer II-IV and undifferentiated layers V and V

87 evated concentrations of D2 receptors in the granular layer in isocortical regions of the temporal lo

88 ration of their progenies in the hippocampus granular layer in vivo.

89 Here we show that a granular layer interneuron, called the unipolar brush ce

90 e cells, which migrate from the hilus to the granular layer, interneurons traverse this layer in the

91 of structural proteins of the upper spinous/granular layers (involucrin, profilaggrin-filaggrin, lor

92 However, the granular layer is a region with variable metabolic deman

93 ion of KCs from basal epidermal layer to the granular layer is accompanied by marked differences in n

94 he average GCP proliferation in the external granular layer is progressively slower as development pr

95 In sensory cortex, layer 4 (the granular layer) is the target of ascending pathways.

96 ed to originate from the external cerebellar granular layer, it is reasonable to postulate that IGF-I

97 vestigated whether a frontal area that lacks granular layer IV, supplementary eye field, exhibits fea

98 t low-frequency oscillations observed in the granular layer may provide a reference for repetitive EP

99 aw skin, marked attenuation of the epidermal granular layer, mild acanthosis, and orthokeratotic hype

100 molecular layer and medium-size soma of the granular layer (most likely Golgi cells).

101 Granular layer network modeling indicates that phase dis

102 stem-level models and detailed models of the granular layer network.

103 Interneurons or granular layer neurons and some glial cells express NR2C

104 Here, we show, in the granular layer of acute rat cerebellar slices, that capi

105 ere we demonstrate that GFAP(+) cells of the granular layer of cerebellum express GABArho subunits du

106 ilaggrin is expressed in the differentiating granular layer of epidermis and other stratified epithel

107 es (n = 4) immunostained keratohyalin in the granular layer of human epidermis and also showed some r

108 models, and, moreover, was localized to the granular layer of keratinocytes as seen in psoriasis in

109 skin, whereas weak signal was present in the granular layer of newborn and adult skin.

110 ed multipotent progenitors into the external granular layer of newborn meander tail mice (gene symbol

111 ly isolated and propagated from the external granular layer of newborn wild-type mouse cerebellum, co

112 velopment when reimplanted into the external granular layer of normal mice.

113 into the deep cerebellar tissue or external granular layer of postnatal day 4/5 rats to label dividi

114 each mystacial whisker is represented in the granular layer of primary somatosensory (SI) cortex by a

115 The traditional view of the external granular layer of the cerebellar cortex giving rise to i

116 f the choroid plexus, meninges, and external granular layer of the cerebellum and in columns of cells

117 1 is essential for proper development of the granular layer of the cerebellum and the hair cells of t

118 They project in the granular layer of the cerebellum and the medial reticula

119 llular volume fraction and tortuosity of the granular layer of the cerebellum were determined from me

120 s a type of glutamatergic interneuron in the granular layer of the cerebellum.

121 erebrum and MeCP2(lo )neurons highest in the granular layer of the cerebellum.

122 alleja, the olfactory bulb, and the internal granular layer of the cerebellum.

123 of MSCs also were found within the external granular layer of the cerebellum.

124 cells predicted to give rise to the external granular layer of the cerebellum.

125 n also decreased Fos immunoreactivity in the granular layer of the dentate gyrus of the hippocampus b

126 of the CA1-CA3 pyramidal cell layer and the granular layer of the dentate gyrus.

127 l cells of the ventricular zone and external granular layer of the developing cerebellar cortex.

128 ic murine model expressing human KLK5 in the granular layer of the epidermis (Tg-KLK5).

129 ld guide expression of specific genes in the granular layer of the epidermis and could be useful in g

130 expression of SULT2B1b was localized to the granular layer of the epidermis similar to that of filag

131 III of the vagal lobe and in the superficial granular layer of the lateral subnucleus of the commissu

132 matergic interneuron that is enriched in the granular layer of the mammalian vestibulocerebellum and

133 y absent neuronal population in the internal granular layer of the mature meander tail anterior lobe.

134 eizures are generated intracortically in the granular layer of the neocortex.

135 en (PM-Scl), which has been localized to the granular layer of the nucleolus and to distinct nucleocy

136 clude the anterior olfactory nucleus and the granular layer of the olfactory bulb.

137 The superficial granular layer of the rostral AVCN and the medial sheet

138 SRC3 was detected in the suprabasal and granular layer of the skin, similar to cathelicidin expr

139 lencephalic area, the glomerular region, the granular layer of the valvula cerebelli, the nucleus dif

140 class of neurons recently identified in the granular layer of the vestibulocerebellum, receive excit

141 gnals were detected in the upper spinous and granular layers of reepithelializing keratinocytes and i

142 oriens of the hippocampus, the molecular and granular layers of the cerebellum, and the molecular lay

143 vglut1 is prominent in granular layers of the cerebellum, habenula, preglomerul

144 cytes is restricted to the upper spinous and granular layers of the epidermis of IBS patients, wherea

145 er of cellular excitation, in the mitral and granular layers of the OB and in the piriform cortex (PC

146 ecrease of these sites occurred in hilar and granular layers of the ventral dentate gyrus.

147 an primates and assessed the effect on supra-granular layers of V1 that project to higher visual cort

148 ctive electrical current inflow in the supra-granular layers of V1.

149 are in the more differentiated (spinous and granular) layers of the epidermis, with little expressio

150 of rhythmic neuronal activity in the input (granular) layers of V1, adaptation caused a pronounced i

151 their axon arbors are either confined to the granular layer or proliferate in both the granular and g

152 etinal rod outer segments and the cerebellar granular layer possessed masked glucuronyl 3-SO4 that be

153 retroviral labeling of cells in the external granular layer produced only granule neurons in the inte

154 types included granule cells of the internal granular layer, Purkinje cells, Golgi cells, and molecul

155 ith recurrent models in which neurons in the granular layer receive intracortical inputs from nearby

156 twork context--whereas neurons in the input (granular) layers showed virtually no correlated variabil

157 separated parallel fibres were activated by granular layer stimulation, the EPSC prolongation produc

158 fect for parallel fibre stimulation than for granular layer stimulation.

159 of binding was significantly greater in the granular layer than in the molecular layer.

160 skin, with higher expressions in spinous and granular layers than in the basal layer.

161 anglionic eminence and via a massive subpial granular layer that may also supply some GABAergic inter

162 y in recently generated cells in the dentate granular layer, the subventricular zone, the olfactory b

163 s and stratum corneum layers, variability in granular layer thickness, and parakeratosis in some regi

164 form that they acquire while traversing the granular layer to finally assume an adult-like pyramidal

165 ature during its migration from the external granular layer to the internal granular layer, and lack

166 iting premature apoptosis in the spinous and granular layers to promote conification, and promoting t

167 ed to increased spike-timing precision among granular layer V1 neurons as well.

168 al pulvinar after LGN lesion activated supra-granular layer V1 neurons.

169 ggrin expression by 24 h, this marker of the granular layer was induced in a smaller subset of HPV ty

170 d highly differentiated keratinocytes of the granular layer were hr-negative.

171 gy is constitutively active in the epidermal granular layer where by electron microscopy we identifie

172 ytes migrate through the epidermis up to the granular layer where, on terminal differentiation, they

173 l they reach the deep strata of the internal granular layer, where they become rounded again and form

174 The granular layer, which mainly consists of granule and Gol

175 network of feedforward excitation within the granular layer, which may amplify vestibular signals and

176 in the parabasal prickle cell layer and the granular layer, while differentiated keratinocytes displ

177 Ectosplenial area 26 has a granular layer with few large pyramidal neurons below.

178 eased numbers of small dense granules in the granular layer with few or no surrounding keratin bundle

179 circuit by stimulating the prefrontal infra-granular-layers with patterns previously derived from su