ライフサイエンスコーパス: labyrinth

1 and prevented the formation of the placental labyrinth.

2 ith a thin and poorly vascularized placental labyrinth.

3 othelial cells specifically in the placental labyrinth.

4 can also exist as an entity confined to the labyrinth.

5 lial cells in the cochlea and the vestibular labyrinth.

6 structuring of the otocyst to form a complex labyrinth.

7 ntained numerous maternal blood pools in the labyrinth.

8 le of TF in the maintenance of the placental labyrinth.

9 ant for regeneration/repair in the mammalian labyrinth.

10 tyly), and dysmorphogenesis of the placental labyrinth.

11 a of the crista ampullaris of the vestibular labyrinth.

12 oietic markers, and localize to the vascular labyrinth.

13 uclear inflammatory cells into the placental labyrinth.

14 ormation normally provided by the vestibular labyrinth.

15 otransmitters were found only in the carotid labyrinth.

16 d with trophoblastic cells in the interphase labyrinth.

17 nonsensory elements of the adult membranous labyrinth.

18 al embryos, as well as in E13.5 yolk sac and labyrinth.

19 lation of the neurosensory epithelium in one labyrinth.

20 ion of the spongiotrophoblast layer into the labyrinth.

21 ased size and malformation of the membranous labyrinth.

22 opology of the accessible part of a chemical labyrinth.

23 molecule to pass through the given chemical labyrinth.

24 iadne is the legendary Minoan goddess of the Labyrinth.

25 native splice forms in the HCs of vestibular labyrinth.

26 lve fine anatomic detail in vitro, as in the labyrinth.

27 ed defective vasculogenesis in the placental labyrinth, a collapsed endocardium, and impaired vessel

28 loss of the diploid spongiotrophoblasts and labyrinth and an expansion of the polyploid giant cell l

29 PRV transport from the vestibular labyrinth and cervical muscles also resulted in CNS infe

30 ions of separate retrograde tracers into the labyrinth and into the floccular and ventral parafloccul

31 chymal remodeling that forms the mature bony labyrinth and regulates inductive signaling mechanisms i

32 A knockout mice made earlier, that displayed labyrinth and yolk sac-specific defects, but our finding

33 ual reconstructions of plesiosaur endosseous labyrinths and the first large-scale, quantitative study

34 blood vessels failed to invade the placental labyrinth, and in the embryo proper, where defective blo

35 model implementing these feedbacks, circles, labyrinths, and islands form when sorting dominates; pol

36 from the two labyrinths even though a single labyrinth appeared capable of signalling 3-D head motion

37 he aorta, pulmocutaneous artery, and carotid labyrinth appears to reflect a phylogenetic transition b

38 cells and a severe disruption of the normal labyrinth architecture in the placenta.

39 roscopy analysis revealed that this aberrant labyrinth architecture was associated with disrupted bas

40 ymphatic duct and swelling of the membranous labyrinth are common features in Gbx2-/- inner ears.

41 g the development of the membranous and bony labyrinths are largely unknown.

42 These smaller labyrinths are well described by a family of patterns th

43 imaeroid specializations, including the otic labyrinth arrangement and the brain space configuration

44 lium of the otic pit, otocyst and membranous labyrinth as they underwent morphogenesis.

45 PLET1 expression in trophoblast cells of the labyrinth, as well as in spongiotrophoblast and glycogen

46 ouse model with noise-induced cochlear blood-labyrinth-barrier (CBLB) injury, we examined the effects

47 Unlike the placental labyrinth, basement membranes and vasculogenesis were no

48 interface, as well as a severe disruption of labyrinth branching morphogenesis.

49 morphogenesis, widespread penetration of the labyrinth by spongiotrophoblasts, and abnormal distribut

50 here we produce tortuous thermal paths (i.e. labyrinths) by introducing slits to control the impact o

51 er ear revealed a collapse of the membranous labyrinth, consistent with a critical role for NKCC1 in

52 A mature inner ear is a complex labyrinth containing multiple sensory organs and nonsens

53 mics of the inner ear fluids, and membranous labyrinth deformability.

54 hat the proper organization of the placental labyrinth depends on coordinated inter-endothelial repul

55 s in neural tube closure, abnormal placental labyrinth development associated with loss of epithelial

56 irmed that lethality was due to a failure of labyrinth development, and this correlates exactly with

57 d for monosynaptic input from the vestibular labyrinth, direct projection to the oculomotor nucleus a

58 Transient inactivation of the intact labyrinth elicited the lateralized behaviour described b

59 eg muscles receive equal inputs from the two labyrinths even though a single labyrinth appeared capab

60 Sauropterygian labyrinth evolution is therefore correlated closely with

61 The HAI-1(-/-) placental labyrinth exhibited a complete failure of vascularizatio

62 ibited reduced fetal vessel branching in the labyrinth, failed SA remodeling and reendothelialization

63 inating individual canal input from the left labyrinth following right nVIII block, which indicated t

64 chorionic trophoblasts and enabled placental labyrinth formation and development to term.

65 spongiotrophoblast layer, and an absence of labyrinth formation causing an improper vascularization

66 nt1), which regulates BCT cell integrity and labyrinth formation.

67 roaches, many questions remain, and the bony labyrinth has shown considerable potential for the phylo

68 Lesions of the entire vestibular labyrinth have been shown to severely alter VIIIth nerve

69 edictions for the critical curves separating labyrinth, hybrid and hexagonal phases.

70 rin-2 labeling of structures in the cortical labyrinth in a pattern similar to that of the Na(+)-Ca2+

71 ibly inactivating the intact contra-lesional labyrinth in compensating animals through superfusion of

72 accumulation of endolymph in the membranous labyrinth in the inner ear.

73 munoreactivity was present in the vestibular labyrinth, in stromal cells underneath the non-immunorea

74 arent in the otic capsule and the membranous labyrinth, including ectopic and fused sensory patches.

75 the firing of vestibular afferents from each labyrinth independently and measured the resulting balan

76 In addition, the vascular labyrinth is disorganized, with thickening of the matern

77 Efferent innervation of the vestibular labyrinth is known to be cholinergic.

78 , the endolymphatic duct, and the membranous labyrinth is poorly developed.

79 The placental labyrinth is the interface for gas and nutrient exchange

80 ex organ rudiment, the developing membranous labyrinth, is initiated.

81 The placental labyrinth (L) had a higher sO2 than the junctional zone

82 l portion of the placenta, in particular the labyrinth (LA), displays strong overlapping expression o

83 also developed abnormally, showing a thinner labyrinth lacking embryonic erythrocytes and blood vesse

84 oliferation and increase in apoptosis in the labyrinth layer and both unchanged in the junctional zon

85 ys postcoitum as nearly complete loss of the labyrinth layer and significant reduction of the spongio

86 entas display lack of vascularization of the labyrinth layer as well as increased rates of apoptosis,

87 The labyrinth layer failed to form properly in the majority

88 n of placental morphogenesis at the stage of labyrinth layer formation and occurs in the absence of o

89 emonstrated a drastic disorganization of the labyrinth layer in the placenta of Rb-deficient embryos,

90 subset of trophoblast within the chorion and labyrinth layer of the mouse placenta.

91 nd that the ESX1 protein is expressed in the labyrinth layer of the placenta in vivo, where its subce

92 ssed in the syncytiotrophoblast cells of the labyrinth layer of the placenta, and the epithelial cell

93 condarily causing collapse of the underlying labyrinth layer.

94 , most notably in the spongiotrophoblast and labyrinth layers.

95 erstitial (epithelial) cells in type-II, and labyrinth-like infolding structures opening towards the

96 common feature of all transfer cells is the labyrinth-like wall-in-growth (WIG) that increases the p

97 ffects of increasingly aquatic lifestyles on labyrinth morphology among marine reptiles.

98 Finally, aspects of endosseous labyrinth morphology are remarkably similar between dive

99 it septation, neural tube closure, placental labyrinth morphology, lung lobe septation, hair growth,

100 After formation of the membranous labyrinth, Nor-1 expression in the vestibule is limited

101 rs superior of the otocyst to form a complex labyrinth of cavities and ducts is blocked, as indicated

102 le ectodermal patch, the inner ear becomes a labyrinth of chambers housing six to eight sensory organ

103 al thickening called the otic placode into a labyrinth of chambers which house sensory organs that se

104 e vertebrate inner ear consists of a complex labyrinth of epithelial cells that is surrounded by a bo

105 the inner ear is sculpted into this complex labyrinth of fluid-filled ducts punctuated by their asso

106 earch in this area can provide glimpses of a labyrinth of genetic architectures that have rarely been

107 on the vestibular hair cells located in the labyrinth of the dogfish Scyliorhinus canicula, and find

108 The membranous labyrinth of the inner ear establishes a precise geometr

109 egulate the concentration of iron within the labyrinth of the inner ear, which might indirectly tune

110 which collectively constitute the membranous labyrinth of the inner ear.

111 surface area of the exchange barrier in the labyrinth of the mouse placenta to be reduced and thickn

112 ect attention at navigating the multifaceted labyrinth of the neurohormonal model that has led to the

113 glutamate immunoreactivity in the vestibular labyrinth of the oyster toadfish by using whole end orga

114 GFP expression at E11.5 to E13.5 in both the labyrinth of the placenta and the yolk sac.

115 showed high expression of TCblR/CD320 in the labyrinth of the placenta, embryonic brain, and spinal c

116 SP9/MKP-4 in the trophoblast giant cells and labyrinth of the placenta.

117 cellular flux of interstitial fluid into the labyrinth of the salivary duct.

118 ize themselves into a carefully sculpted, 3D labyrinth of vessels that regulate blood flow throughout

119 ing whether a molecule can traverse chemical labyrinths of channels, tunnels, and buried cavities usu

120 First, the membranous labyrinths of mouse inner ears ranging from 10.25 to 17

121 Paint-filled membranous labyrinths of Otx1-/- mutants showed an absence of the l

122 bryonic vasculature and heart, the placental labyrinths of these embryos exhibited aberrant alignment

123 the inner ear by paint-filling of membranous labyrinths of Whl/+ embryos.

124 ones that can pass through a given chemical labyrinth or screen chemical labyrinths to identify thos

125 ells are closely related to the basal lamina labyrinths or fractones derived from subependymal microg

126 It has osteological correlates of a labyrinth organ, which in extant climbing perches gives

127 ng electrode placed unilaterally on the bony labyrinth overlying the posterior canal (PC).

128 ause it is impractical to test each molecule/labyrinth pair using computationally expensive methods,

129 nism underlying development of the placental labyrinth, particularly in terms of its endothelial orga

130 We conclude that both labyrinths provide independent estimates of head motion

131 The labyrinths range from straight nanobeams with a complete

132 towards the midgestational expansion of the labyrinth region while maintaining the thin layer of tro

133 Orientation of the osseous labyrinth relative to the long axis of the skull was dif

134 entrally compact, anteroposteriorly elongate labyrinths, resembling those of crocodylians.

135 motor output because stimulation of just one labyrinth revealed a power law relationship between stim

136 Antigenic targets of autoimmunity within the labyrinth seem to be diverse.

137 w that Capreolinae are more variable in bony labyrinth shape than Cervinae and confirm for the first

138 contrast, plesiosaurs have compact, bulbous labyrinths, sharing some features with those of sea turt

139 used to look for acoustic neuromas, abnormal labyrinth signal intensity or enhancement, and brain dis

140 ilic deposits in the cochlear and vestibular labyrinths, similar to protein aggregation in well-known

141 Differences in relative labyrinth size among sauropterygians correspond to locom

142 mong plesiosaurs coincide with reductions of labyrinth size, paralleling the evolutionary history of

143 ns form a pair of chiral enantiomeric gyroid labyrinths (srs nets) over a broad range of compositions

144 promised after destruction of the vestibular labyrinths, suggesting that the extraretinal signals nee

145 f the olfactory apparatus and the endosseous labyrinth suggests that olfaction, hearing, and equilibr

146 ective placentas, with significantly reduced labyrinth surface area and blood vessel vascularization.

147 [5, 6] placodonts have proportionally larger labyrinths than actively swimming taxa (i.e., all other

148 have been located previously in the carotid labyrinth, the aortic arch, and the pulmocutaneous arter

149 nic ectoderm, as well as in the yolk sac and labyrinth tissues that form later.

150 The relative contributions of each labyrinth to behavior, as well as how the brain recovers

151 tance of the conformal perilymph-filled bony labyrinth to pressure changes and to high frequency soun

152 given chemical labyrinth or screen chemical labyrinths to identify those that allow a given molecule

153 We identified an Epcam(hi) labyrinth trophoblast progenitor (LaTP) in mouse placent

154 xpressed markers of both junctional zone and labyrinth trophoblast subtypes in a manner comparable to

155 lacenta that at a clonal level generates all labyrinth trophoblast subtypes, syncytiotrophoblasts I a

156 rtension and liver damage, promoted abnormal labyrinth vascularization in the placenta, and decreased

157 duced definitive erythropoiesis in placental labyrinth vasculature.

158 ta ampullaris, and the membranous vestibular labyrinth was collapsed.

159 in these regions that give rise to the bony labyrinth was complementary to TR expression in the sens

160 Additionally, the volume fraction of the labyrinth was reduced, as was the surface area for mater

161 gus nerve, whereas only cells in the carotid labyrinth were innervated by the glossopharyngeal nerve.

162 s influenced the evolution of the endosseous labyrinth, which houses the vestibular sensory organ of

163 eficiency in the arterioles of the placental labyrinth, which leads first to flow reversal in the umb

164 Any perturbation in the structure of the labyrinth will undoubtedly lead to functional deficits.

165 formation of a uniform sheet of cells into a labyrinth with multiple cell types.

166 rocess involves distortion of the membranous labyrinth with the formation of endolymphatic hydrops.

167 The labyrinths within the gyroid film are densely packed and

168 Signals from the bilateral vestibular labyrinths work in tandem to generate robust estimates o

169 -derived cell subtypes in the junctional and labyrinth zones of the placenta.