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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 rons also connect with each other to form an intersegmental circuit and regulate their own wave-like
16 ated muscle relaxation can be realized by an intersegmental circuit that regulates its own patterned
17     ComInt 1s function as hub neurons in the intersegmental circuit that synchronizes distributed mic
18  Evx1 V0 interneurons are locally projecting intersegmental commissural neurons.
19  theory analysis, we identify an alternative intersegmental connection pattern producing realistic st
20 rmation about the contribution of individual intersegmental connections to the stable phase lag.
21 urons) did not demonstrate short, ascending, intersegmental connections.
22 twork with ascending-only or descending-only intersegmental connections.
23 is spontaneously active and that blocking an intersegmental connective uncoupled swimmeret activity o
24 y, multisensory integration, left-right, and intersegmental connectivity and motor circuits for cilia
25 ting to the importance of cell-type-specific intersegmental connectivity patterns and recruitment of
26  for the DNA homology search process termed 'intersegmental contact sampling', in which the intrinsic
27                      A cellular model of the intersegmental coordinating circuit that also produces t
28  in the context of alternative models of the intersegmental coordinating circuit.
29                                              Intersegmental coordination can in fact be achieved by s
30 of measuring limb movement that can decouple intersegmental coordination from morphology and posture.
31 rdings unequivocally demonstrate that active intersegmental coordination occurs in leeches with sever
32 le command neuron that is also vital for the intersegmental coordination of a locomotor behavior.
33  we evaluate the role of sensory feedback in intersegmental coordination using both behavioral and ph
34                                          (1) Intersegmental coordination varied considerably with ste
35                       Lower body kinematics, intersegmental coordination, and electromyography (EMG)
36  blockade, we observed a significant loss of intersegmental coordination.
37  is both necessary and sufficient for normal intersegmental coordination.
38 re > 3, P < .001) bilateral, unilateral, and intersegmental correlations in the ventral horns, dorsal
39 taneous nerves (DCNs) evokes the nociceptive intersegmental cutaneus trunci muscle (CTM) reflex.
40  certain degree of rotational freedom of the intersegmental D-A axes that is crucial for efficient TA
41 -stroke movements that have a characteristic intersegmental difference in phase.
42 keletal system were included: limb geometry, intersegmental dynamics, and the force-length/velocity p
43  rotated spatial reference frame and altered intersegmental dynamics, did not interfere with each oth
44 locomotion, providing new interpretations of intersegmental excitatory and inhibitory connectivity, a
45                 Our results suggest that the intersegmental feedback neurons coordinate contraction o
46 ating hindgut, invaginating salivary glands, intersegmental grooves, and developing tracheae.
47                     Our results suggest that intersegmental hopping contributes to enzymatic processi
48                                              Intersegmental hopping is possibly used by other sequenc
49 by DNA looping, a phenomenon we designate as intersegmental hopping.
50                                  The role of intersegmental influences was tested by severing connect
51 her CNS ganglia, thereby providing extensive intersegmental innervation for the 33 CNS ganglia compri
52 perate best with either all or none of their intersegmental inputs.
53 ieved by sensory feedback alone, without the intersegmental interactions conveyed by the nerve cord.
54 llator circuit via electrical junctions; (3) intersegmental interactions, according to theoretical an
55  of spinal motor neurons, intrasegmental and intersegmental interactions, recurrent inhibition, and d
56                           All three types of intersegmental interneurons have branches in the anterio
57 al interneurons and three types of ascending intersegmental interneurons in the locust metathoracic g
58                               Three types of intersegmental interneurons that originate in each abdom
59 ell types of the embryonic CNS: motoneurons, intersegmental interneurons, local interneurons, glia an
60 are efferent neurons, local interneurons, or intersegmental interneurons, recognizable as such by the
61 ly measure the affinity and kinetics of this intersegmental jumping by the ETS-family transcription f
62 ously, are nonetheless strongly modulated by intersegmental jumping in heterogeneous site environment
63  through a nonspecific-like intermediate, 2) intersegmental jumping is rate-limited by dissociation f
64 r, these pathways could produce the observed intersegmental lags, coordination between phases, and st
65  Loss of plxnd1 is associated with misguided intersegmental lymphatic vessel growth and aberrant faci
66  spinal, superficial lateral and superficial intersegmental lymphatics.
67          Individual scolopidia attach to the intersegmental membrane between pedicel and flagellum of
68 exion and return neck movements to calculate intersegmental motor control (MC), defined as the differ
69 re, we study the formation of the Drosophila intersegmental motor nerve (ISN).
70  while synaptic strength profiles define the intersegmental motor phase progression realized.
71 zinc-finger protein that is induced when the intersegmental muscles (ISMs) of the moth Manduca sexta
72                                          The intersegmental muscles (ISMs) of the tobacco hawkmoth Ma
73 roliferation, and in the programmed death of intersegmental muscles after adult eclosion in the tobac
74                                              Intersegmental muscles undergoing programmed cell death
75 parate bundles, the segmental nerve (SN) and intersegmental nerve (ISN).
76 sophila Abl tyrosine kinase functions in the intersegmental nerve b (ISNb) motor choice point pathway
77 al growth cone arrest phenotype for axons of intersegmental nerve b (ISNb).
78  Fasiclin II expressing motor neurons in the intersegmental nerve B branch.
79                  Previous genetic studies of intersegmental nerve b development have identified sever
80 eptor-tyrosine phosphatase Dlar suggest that intersegmental nerve b guidance requires the integration
81 cribed here shed new light on both local and intersegmental network function in this model system.
82 demonstration of distinct intrasegmental and intersegmental nociceptive heat and touch processing cir
83 f ISV sprouts to migrate correctly along the intersegmental, normally laminin-rich regions.
84 hat can be obtained from a given knot by one intersegmental passage.
85 estigate how the topological consequences of intersegmental passages depend on the geometry of the DN
86 ware of all possible topological outcomes of intersegmental passages occurring within a given knot ty
87 d in an anterior to posterior direction with intersegmental phase delays appropriate for crawling.
88                         Although appropriate intersegmental phase delays were always absent, when one
89 ration and maintenance of posterior-directed intersegmental phase delays, we induced fictive crawling
90 their outputs are synchronized with a stable intersegmental phase difference of 0.25, an example of m
91 dinating circuit that also produces the same intersegmental phase has been proposed.
92 rent phases of the swim cycle and determined intersegmental phase lags by comparing the delay between
93 eceptor generated during swimming can change intersegmental phase lags of leech ganglia in a phase-de
94 onal mechanisms in nervous systems that keep intersegmental phase lags the same at different frequenc
95 een shown to play different roles in setting intersegmental phase lags.
96 twork in which connectivity is determined by intersegmental phase relationships among interneurons an
97  These stretch receptors may set the optimal intersegmental phases during swimming movement in intact
98 vation law, in most cases a "flow-equalizing intersegmental pressure", which is different from the pr
99                                          The intersegmental pressure, induced to equalize the flow ra
100                                        While intersegmental relationships were largely conserved over
101                                Surprisingly, intersegmental relationships were not driven solely by p
102                                              Intersegmental RNA-RNA interactions are thought to media
103                          To explore putative intersegmental RNA-RNA relationships, we quantified simi
104  to perform intersegmental transfer with the intersegmental searching ability of Pol beta being at le
105 ollows that the dorsal abdominal muscles are intersegmental, spanning from one anterior domain to the
106 ct spinocerebellar pathways as well as local intersegmental spinal circuits using genetic tools in bo
107 es) produced this sex pheromone in the sixth intersegmental sternal glands of their abdomens.
108 duced sex pheromone from the 5(th) and 6(th) intersegmental sternal glands of virgin queens.
109  known coordinating neurons and hypothesized intersegmental synaptic connections.
110                                   To isolate intersegmental target binding in a functionally defined
111                                         Mean intersegmental time (MIT = PT/DC), diagnostic completene
112 erging of the two elements is constrained by intersegmental torques such that initiation and performa
113 haplotype V exhibited diminished sliding and intersegmental transfer abilities but was able to jump a
114 h jumping can compensate for deficiencies in intersegmental transfer and suggest that APOBEC3H haplot
115                                 The rates of intersegmental transfer are strongly dependent on the sa
116                                              Intersegmental transfer between DNA segments that are tr
117 lowed us to observe and measure the rates of intersegmental transfer by AAG.
118 wed us to estimate the size and frequency of intersegmental transfer events that occur through transi
119              It has been difficult to detect intersegmental transfer experimentally; therefore, we de
120 ultidomain protein and provide evidence that intersegmental transfer involves a ternary intermediate,
121 th indicate that the two domains use both an intersegmental transfer mechanism, which does not involv
122 ate encounter by using sliding, jumping, and intersegmental transfer movements.
123 dundancy in the contributions of jumping and intersegmental transfer to mutagenic efficiency.
124           We attribute the tension effect to intersegmental transfer which is hindered by DNA stretch
125            Pol beta also was able to perform intersegmental transfer with the intersegmental searchin
126 arize a model that includes a combination of intersegmental transfer, short-distance one-dimensional
127 s, as well as to bypass protein barriers via intersegmental transfer.
128 DNA, but we find that it is not required for intersegmental transfer.
129 , this argues against the bridging model for intersegmental transfer.
130  site, jumping may be a common mechanism for intersegmental transfer.
131 rget site search by DNA-binding proteins via intersegmental translocation.
132       Activated A02j neurons exhibit quicker intersegmental transmission in activity that enables fas
133 euronal activity was determined by the known intersegmental travel time and estimated delay time betw
134                                              Intersegmental tree similarity differed between subtype
135 the translation or splicing of pld1 impaired intersegmental vessel (ISV) development.
136 current with arteriovenous specification and intersegmental vessel (ISV) sprouting, processes regulat
137                                          One intersegmental vessel (ISV) sprouts from the aorta, runs
138  biomarker for cardiac looping defects), and intersegmental vessel area within freshly hatched live e
139 GF receptor-2 kinase inhibitor had a similar intersegmental vessel defect suggesting that knockdown o
140 knockdown in developing zebrafish results in intersegmental vessel defects caused by a perturbed dire
141 own of miR-10 led to premature truncation of intersegmental vessel growth in the trunk of zebrafish l
142 zed by a concentration-dependent decrease in intersegmental vessel lumen and a large tail-vessel conf
143 ed in CNS and ocular hemorrhages, defects in intersegmental vessel patterning, and increased vascular
144  knockdown zebrafish embryos show defects in intersegmental vessel sprouting in the trunk.
145 t manifests intact arterial gene expression, intersegmental vessel sprouting, and HSC gene expression
146           In the perlecan morphants, primary intersegmental vessel sprouts, which develop through ang
147 ac troponin) reduced EC proliferation in the intersegmental vessels (ISVs) compared to controls expos
148 uring the initial stages of tubulogenesis in intersegmental vessels (ISVs) in the embryo.
149 MCs migrating from the DA or emerging around intersegmental vessels (ISVs) preferentially covered art
150 arkers demonstrated defective development of intersegmental vessels (ISVs), subintestinal vessels (SI
151  knockdown in zebrafish impeded sprouting of intersegmental vessels and diminished the directionality
152 bition caused increased sprouting and longer intersegmental vessels and exacerbated tip cell migratio
153  head circulation, absence of circulation in intersegmental vessels and in the dorsal longitudinal an
154 f dll4 and subsequent excessive sprouting of intersegmental vessels and reduction in dorsal aorta dia
155                                    Zebrafish intersegmental vessels correspond to mammalian capillary
156 gos, results in elimination or disruption of intersegmental vessels in a majority of embryos.
157  DYVE-D3, was found to inhibit the growth of intersegmental vessels in the zebrafish vasculature.
158 depletion of FMNL3 retards elongation of the intersegmental vessels in zebrafish.
159                                              Intersegmental vessels of somites failed to reach the do
160      Finally, we use single-cell analysis of intersegmental vessels undergoing lumen formation to dem
161 severely reduced vascular development of the intersegmental vessels was observed with doses of the s1
162 acterized by both reduced vascularization in intersegmental vessels, decreased proliferation of inter
163 ts, most notably impaired circulation in the intersegmental vessels.
164 ebrafish embryos delayed the angiogenesis of intersegmental vessels.
165 ion eliminated the tip cell branching in the intersegmental vessels.
166 loping vascular structures, particularly the intersegmental vessels.
167 ion of endothelial cells during formation of intersegmental vessels.

 
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