ライフサイエンスコーパス: intersegmental

1 nhibition of blood cell circulation via both intersegmental and axial vessels demonstrating that VEGF

2 egmental vessels, decreased proliferation of intersegmental and axial vessels, and hypersprouting in

3 eters, such as gait, tarsal positioning, and intersegmental and left-right coordination for wild type

4 reaching requires integration of segmental, intersegmental, and supraspinal input to propriospinal a

5 In contrast, the dorsal aortae and intersegmental arteries caudal to the heart were grossly

6 mens, as did the anterior cardinal veins and intersegmental arteries.

7 rvations indicate that LCNs of lamina I form intersegmental as well as interlaminar connections and m

8 cic wing nerve, indicating that they collate intersegmental as well as local information.

9 three different systems, intrasegmental and intersegmental as well as supraspinal, are exclusively g

10 project dorsally, which creates a cumulative intersegmental bias to dorsally located spinal neurons.

11 for notochord differentiation and for proper intersegmental blood vessel (ISV) formation.

12 owire electrodes in ipsilateral segments and intersegmental boundaries with a 250 micrometer mediolat

13 anscription of genes involved in positioning intersegmental boundaries.

14 e to long muscle fibers that are anchored to intersegmental boundaries.

15 ComInt 1s function as hub neurons in the intersegmental circuit that synchronizes distributed mic

16 Evx1 V0 interneurons are locally projecting intersegmental commissural neurons.

17 theory analysis, we identify an alternative intersegmental connection pattern producing realistic st

18 rmation about the contribution of individual intersegmental connections to the stable phase lag.

19 urons) did not demonstrate short, ascending, intersegmental connections.

20 twork with ascending-only or descending-only intersegmental connections.

21 is spontaneously active and that blocking an intersegmental connective uncoupled swimmeret activity o

22 for the DNA homology search process termed 'intersegmental contact sampling', in which the intrinsic

23 A cellular model of the intersegmental coordinating circuit that also produces t

24 in the context of alternative models of the intersegmental coordinating circuit.

25 Intersegmental coordination can in fact be achieved by s

26 of measuring limb movement that can decouple intersegmental coordination from morphology and posture.

27 rdings unequivocally demonstrate that active intersegmental coordination occurs in leeches with sever

28 le command neuron that is also vital for the intersegmental coordination of a locomotor behavior.

29 we evaluate the role of sensory feedback in intersegmental coordination using both behavioral and ph

30 (1) Intersegmental coordination varied considerably with ste

31 blockade, we observed a significant loss of intersegmental coordination.

32 is both necessary and sufficient for normal intersegmental coordination.

33 re > 3, P < .001) bilateral, unilateral, and intersegmental correlations in the ventral horns, dorsal

34 taneous nerves (DCNs) evokes the nociceptive intersegmental cutaneus trunci muscle (CTM) reflex.

35 -stroke movements that have a characteristic intersegmental difference in phase.

36 keletal system were included: limb geometry, intersegmental dynamics, and the force-length/velocity p

37 rotated spatial reference frame and altered intersegmental dynamics, did not interfere with each oth

38 ating hindgut, invaginating salivary glands, intersegmental grooves, and developing tracheae.

39 Our results suggest that intersegmental hopping contributes to enzymatic processi

40 Intersegmental hopping is possibly used by other sequenc

41 by DNA looping, a phenomenon we designate as intersegmental hopping.

42 The role of intersegmental influences was tested by severing connect

43 her CNS ganglia, thereby providing extensive intersegmental innervation for the 33 CNS ganglia compri

44 perate best with either all or none of their intersegmental inputs.

45 ieved by sensory feedback alone, without the intersegmental interactions conveyed by the nerve cord.

46 llator circuit via electrical junctions; (3) intersegmental interactions, according to theoretical an

47 of spinal motor neurons, intrasegmental and intersegmental interactions, recurrent inhibition, and d

48 All three types of intersegmental interneurons have branches in the anterio

49 al interneurons and three types of ascending intersegmental interneurons in the locust metathoracic g

50 Three types of intersegmental interneurons that originate in each abdom

51 ell types of the embryonic CNS: motoneurons, intersegmental interneurons, local interneurons, glia an

52 are efferent neurons, local interneurons, or intersegmental interneurons, recognizable as such by the

53 ly measure the affinity and kinetics of this intersegmental jumping by the ETS-family transcription f

54 ously, are nonetheless strongly modulated by intersegmental jumping in heterogeneous site environment

55 through a nonspecific-like intermediate, 2) intersegmental jumping is rate-limited by dissociation f

56 r, these pathways could produce the observed intersegmental lags, coordination between phases, and st

57 spinal, superficial lateral and superficial intersegmental lymphatics.

58 re, we study the formation of the Drosophila intersegmental motor nerve (ISN).

59 while synaptic strength profiles define the intersegmental motor phase progression realized.

60 zinc-finger protein that is induced when the intersegmental muscles (ISMs) of the moth Manduca sexta

61 The intersegmental muscles (ISMs) of the tobacco hawkmoth Ma

62 roliferation, and in the programmed death of intersegmental muscles after adult eclosion in the tobac

63 Intersegmental muscles undergoing programmed cell death

64 parate bundles, the segmental nerve (SN) and intersegmental nerve (ISN).

65 sophila Abl tyrosine kinase functions in the intersegmental nerve b (ISNb) motor choice point pathway

66 al growth cone arrest phenotype for axons of intersegmental nerve b (ISNb).

67 Fasiclin II expressing motor neurons in the intersegmental nerve B branch.

68 Previous genetic studies of intersegmental nerve b development have identified sever

69 eptor-tyrosine phosphatase Dlar suggest that intersegmental nerve b guidance requires the integration

70 cribed here shed new light on both local and intersegmental network function in this model system.

71 demonstration of distinct intrasegmental and intersegmental nociceptive heat and touch processing cir

72 f ISV sprouts to migrate correctly along the intersegmental, normally laminin-rich regions.

73 hat can be obtained from a given knot by one intersegmental passage.

74 estigate how the topological consequences of intersegmental passages depend on the geometry of the DN

75 ware of all possible topological outcomes of intersegmental passages occurring within a given knot ty

76 d in an anterior to posterior direction with intersegmental phase delays appropriate for crawling.

77 Although appropriate intersegmental phase delays were always absent, when one

78 ration and maintenance of posterior-directed intersegmental phase delays, we induced fictive crawling

79 their outputs are synchronized with a stable intersegmental phase difference of 0.25, an example of m

80 dinating circuit that also produces the same intersegmental phase has been proposed.

81 rent phases of the swim cycle and determined intersegmental phase lags by comparing the delay between

82 eceptor generated during swimming can change intersegmental phase lags of leech ganglia in a phase-de

83 onal mechanisms in nervous systems that keep intersegmental phase lags the same at different frequenc

84 een shown to play different roles in setting intersegmental phase lags.

85 These stretch receptors may set the optimal intersegmental phases during swimming movement in intact

86 vation law, in most cases a "flow-equalizing intersegmental pressure", which is different from the pr

87 The intersegmental pressure, induced to equalize the flow ra

88 to perform intersegmental transfer with the intersegmental searching ability of Pol beta being at le

89 ollows that the dorsal abdominal muscles are intersegmental, spanning from one anterior domain to the

90 es) produced this sex pheromone in the sixth intersegmental sternal glands of their abdomens.

91 known coordinating neurons and hypothesized intersegmental synaptic connections.

92 To isolate intersegmental target binding in a functionally defined

93 erging of the two elements is constrained by intersegmental torques such that initiation and performa

94 haplotype V exhibited diminished sliding and intersegmental transfer abilities but was able to jump a

95 h jumping can compensate for deficiencies in intersegmental transfer and suggest that APOBEC3H haplot

96 The rates of intersegmental transfer are strongly dependent on the sa

97 Intersegmental transfer between DNA segments that are tr

98 lowed us to observe and measure the rates of intersegmental transfer by AAG.

99 It has been difficult to detect intersegmental transfer experimentally; therefore, we de

100 ultidomain protein and provide evidence that intersegmental transfer involves a ternary intermediate,

101 th indicate that the two domains use both an intersegmental transfer mechanism, which does not involv

102 ate encounter by using sliding, jumping, and intersegmental transfer movements.

103 dundancy in the contributions of jumping and intersegmental transfer to mutagenic efficiency.

104 Pol beta also was able to perform intersegmental transfer with the intersegmental searchin

105 arize a model that includes a combination of intersegmental transfer, short-distance one-dimensional

106 DNA, but we find that it is not required for intersegmental transfer.

107 , this argues against the bridging model for intersegmental transfer.

108 site, jumping may be a common mechanism for intersegmental transfer.

109 rget site search by DNA-binding proteins via intersegmental translocation.

110 euronal activity was determined by the known intersegmental travel time and estimated delay time betw

111 the translation or splicing of pld1 impaired intersegmental vessel (ISV) development.

112 current with arteriovenous specification and intersegmental vessel (ISV) sprouting, processes regulat

113 One intersegmental vessel (ISV) sprouts from the aorta, runs

114 biomarker for cardiac looping defects), and intersegmental vessel area within freshly hatched live e

115 GF receptor-2 kinase inhibitor had a similar intersegmental vessel defect suggesting that knockdown o

116 knockdown in developing zebrafish results in intersegmental vessel defects caused by a perturbed dire

117 own of miR-10 led to premature truncation of intersegmental vessel growth in the trunk of zebrafish l

118 zed by a concentration-dependent decrease in intersegmental vessel lumen and a large tail-vessel conf

119 ed in CNS and ocular hemorrhages, defects in intersegmental vessel patterning, and increased vascular

120 knockdown zebrafish embryos show defects in intersegmental vessel sprouting in the trunk.

121 t manifests intact arterial gene expression, intersegmental vessel sprouting, and HSC gene expression

122 In the perlecan morphants, primary intersegmental vessel sprouts, which develop through ang

123 uring the initial stages of tubulogenesis in intersegmental vessels (ISVs) in the embryo.

124 MCs migrating from the DA or emerging around intersegmental vessels (ISVs) preferentially covered art

125 knockdown in zebrafish impeded sprouting of intersegmental vessels and diminished the directionality

126 bition caused increased sprouting and longer intersegmental vessels and exacerbated tip cell migratio

127 head circulation, absence of circulation in intersegmental vessels and in the dorsal longitudinal an

128 f dll4 and subsequent excessive sprouting of intersegmental vessels and reduction in dorsal aorta dia

129 Zebrafish intersegmental vessels correspond to mammalian capillary

130 gos, results in elimination or disruption of intersegmental vessels in a majority of embryos.

131 DYVE-D3, was found to inhibit the growth of intersegmental vessels in the zebrafish vasculature.

132 depletion of FMNL3 retards elongation of the intersegmental vessels in zebrafish.

133 Intersegmental vessels of somites failed to reach the do

134 Finally, we use single-cell analysis of intersegmental vessels undergoing lumen formation to dem

135 severely reduced vascular development of the intersegmental vessels was observed with doses of the s1

136 acterized by both reduced vascularization in intersegmental vessels, decreased proliferation of inter

137 ebrafish embryos delayed the angiogenesis of intersegmental vessels.

138 ion eliminated the tip cell branching in the intersegmental vessels.

139 loping vascular structures, particularly the intersegmental vessels.

140 ion of endothelial cells during formation of intersegmental vessels.

141 ts, most notably impaired circulation in the intersegmental vessels.