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1 xons, small dendrites, dendritic spines, and synaptic boutons).
2 erneurons were contacted by several types of synaptic bouton.
3 he soma affect neurotransmitter release from synaptic boutons.
4 ion of enlarged intraluminal vesicles within synaptic boutons.
5 formed with abundant, highly ramified, small synaptic boutons.
6 Ns and INs mingled with dense collections of synaptic boutons.
7      Fmr1 dramatically lowers DCV numbers in synaptic boutons.
8 isualized fusing with the plasma membrane of synaptic boutons.
9  encounters with presynaptic growth cones or synaptic boutons.
10  of DVAP-33A tightly modulates the number of synaptic boutons.
11 is dependent on fasciclin II localization at synaptic boutons.
12 ivity levels results in an altered number of synaptic boutons.
13 utamatergic NMJs, and that Wg is secreted by synaptic boutons.
14 l overexpression results in fewer and larger synaptic boutons.
15 s that traverse the lateral margin of select synaptic boutons.
16 vantage of FM1-43 as a fluorescent marker of synaptic boutons.
17 n increase in the density of GABA-containing synaptic boutons.
18  as well as formation of ectopic mossy fiber synaptic boutons.
19 ribution to the signalling in the individual synaptic boutons.
20  presynaptic function at the level of single synaptic boutons.
21 erved using light microscopy corresponded to synaptic boutons.
22  neuronal surface with increasing numbers of synaptic boutons.
23 as olfactory cilia, insect antennae, or even synaptic boutons.
24 ile filopodia as well as in later-stabilized synaptic boutons.
25  mutant larvae have also a reduced number of synaptic boutons.
26 was found within mossy fiber axons and giant synaptic boutons.
27 lity can cluster spatially within individual synaptic boutons.
28 s and the electrophysiological properties of synaptic boutons.
29  with lysosome markers in soma, neurites and synaptic boutons.
30 ion of p62 in neurons and muscles, and fewer synaptic boutons.
31 nd colocalize extracellularly in surrounding synaptic boutons.
32 atellite" budding from larval motor terminus synaptic boutons.
33 ger proportion of the open conformation than synaptic boutons.
34 of medial NTS found immunoreactive OT within synaptic boutons.
35 in synaptic boutons as well as the number of synaptic boutons.
36 ansmitter release sites housed in a chain of synaptic boutons.
37 f Limk leads to stunted terminals with fewer synaptic boutons.
38  to a sparser microtubule array in axons and synaptic boutons.
39 ity to rapidly boost neuropeptide content in synaptic boutons.
40 ed by collapsing the H+ gradient in type III synaptic boutons.
41 ttached functional excitatory and inhibitory synaptic boutons.
42  vesicles, indicating that they are probably synaptic boutons.
43 ires only a postsynaptic neuron and attached synaptic boutons.
44 s revealed that FLN90 is present surrounding synaptic boutons.
45  was formed mainly by synapses with multiple synaptic boutons.
46 nsport, suggesting localization primarily in synaptic boutons.
47 types of synapses on terminal and en passant synaptic boutons.
48 arger synaptic size and increased numbers of synaptic boutons.
49 etically with the BMP pathway, and at mutant synaptic boutons, a key component of this pathway, phosp
50 aboration (overgrowth, overbranching, excess synaptic boutons), accumulation of development-arrested
51 urprising difference in the vulnerability of synaptic boutons after axotomy, which depend on cell-typ
52                             Small excitatory synaptic boutons also were labeled in the MML; by contra
53 ; there is a large increase in the number of synaptic boutons, an elaboration of the synaptic branchi
54 These markers clearly recognized puncta-like synaptic boutons and both signals were well overlapped.
55 to be concentrated in the region surrounding synaptic boutons and consequently enlarges the membrane
56 mbine single-cell dye labeling of individual synaptic boutons and counterstaining of the entire nervo
57 hat motor neuron terminals failed to develop synaptic boutons and cytoskeletal abnormalities arose, i
58 ent, we identified beag, a mutant with fewer synaptic boutons and decreased neurotransmitter release.
59 e is a significant decrease in the number of synaptic boutons and extent of synaptic arborization, as
60 strictions that normally separate individual synaptic boutons and is necessary to achieve the normal
61  pathway interfere with the formation of new synaptic boutons and lead to aberrant synaptic structure
62 PTP-NP tyrosine phosphatase, is expressed on synaptic boutons and may participate in the regulation o
63 inar distribution of the dendritic trees and synaptic boutons and the number of synapses formed by a
64  are identified as neuronal varicosities and synaptic boutons and the rods as short segments of axons
65 development; in its absence, there are fewer synaptic boutons and there is a decrease in synaptic str
66 xons were reconstructed, and the morphology, synaptic boutons, and projection pattern of each axon we
67 al processes, and inhibits Ca(2+) entry into synaptic boutons, and we can reverse this by controlled
68 d that gold particles were restricted to pre-synaptic boutons, and were present mainly on the membran
69                      As the first functional synaptic boutons appeared in these cultures, numerous fi
70 es in total axonal length and the density of synaptic boutons are present in layer V pyramidal neuron
71 es the formation of microtubule loops within synaptic boutons as well as the number of synaptic bouto
72 cles and reported transmission at individual synaptic boutons, as well as secretion and fusion pore '
73  II antisera labeled regions associated with synaptic boutons at both larval and adult stages.
74 unction prevents the normal proliferation of synaptic boutons at glutamatergic neuromuscular junction
75 the CNS neuropil and to a variable subset of synaptic boutons at neuromuscular junctions (NMJs).
76 rate remains to be clarified, targets SVs to synaptic boutons at rest and might be outpaced by activi
77 scade that stimulated the development of new synaptic boutons at the Drosophila larval neuromuscular
78 rons can rapidly induce the outgrowth of new synaptic boutons at the larval neuromuscular junction (N
79 led expansions revealed that they were large synaptic boutons bearing asymmetric synapses.
80 LG and which is dynamically expressed during synaptic bouton budding.
81 peptidergic vesicles are immobile in resting synaptic boutons but become mobile after seconds of stim
82 calolide B or photobleaching DCVs entering a synaptic bouton by retrograde transport.
83  results successfully showed that Drosophila synaptic boutons can be quantified and thus we can exami
84  morphological transition of growth cones to synaptic boutons characterizes synaptogenesis.
85 hoton imaging of cortical axons to show that synaptic boutons come and go, just like spines.
86 al relationship of 133 anterogradely labeled synaptic boutons conveying CS or US information on retro
87     Furthermore, ultrastructural analysis of synaptic boutons demonstrated the presence of multivesic
88 ated Purkinje cells with functional adherent synaptic boutons, demonstrating the presynaptic locus of
89 d' digital neurite atlas, and estimating the synaptic bouton density along the axons for a mouse brai
90    The epac1-cAMP sensor (camps) response in synaptic boutons depends on extracellular Ca(2+) and rya
91 s and show that Eps15 is required for proper synaptic bouton development and normal levels of synapti
92 s have overgrown dendritic trees with larger synaptic boutons, developmental defects in pruning, and
93       Interestingly, the number of GABAergic synaptic boutons did not increase during this time, indi
94 ons and may participate in the regulation of synaptic bouton endocytosis.
95  acutely activate integrin signaling, induce synaptic bouton enlargement, and increase postsynaptic g
96  convergent inputs comprising interdigitated synaptic boutons evoke self-contained synaptic responses
97 s linked to the transient enlargement of the synaptic boutons, followed by a sustained increase in co
98                                   During new synaptic bouton formation, synapsin redistributed upon s
99                                     Finally, synaptic boutons from single-labeled axons of glycinergi
100  Two different markers were used to identify synaptic boutons: GFP marking with a synaptotagmin (Syt)
101                            The small size of synaptic boutons has hampered efforts to define the dyna
102 her then localized to the plasma membrane of synaptic boutons, immunolabeling for the DOR was intrace
103 er of synapses per neuron formed by multiple synaptic boutons in comparison to sham-MC.
104 e the ability of motor neurons to extend new synaptic boutons in correlation to muscle growth.
105  of synaptic vesicle recycling at individual synaptic boutons in hippocampal cell cultures derived fr
106 led that PTP-NP-2 is abundantly expressed on synaptic boutons in primary neurons.
107  strongly concentrated in a subpopulation of synaptic boutons in the CNS neuropil and to a variable s
108  in somata in the inner nuclear layer and in synaptic boutons in the inner plexiform layer.
109 ger and extensive, it was chosen to quantify synaptic boutons in the neuronal culture.
110                                The number of synaptic boutons in wild type neurons increased by 27% b
111 ack Endophilin fail to take up FM1-43 dye in synaptic boutons, indicating an inability to retrieve sy
112 pecially in the increased formation of fine, synaptic "bouton-like" structures, in which both TrkA an
113 ject from the unaffected hemisphere and form synaptic bouton-like structures in the denervated half o
114 F transection produced also a higher loss of synaptic boutons, mainly at the dendritic level.
115 zed by an increase in the number of multiple synaptic boutons (MSBs), i.e., presynaptic axon terminal
116 ry interest were synapses formed by multiple synaptic boutons (MSBs), which have recently been found
117 lar junctions (NMJs), resulting in increased synaptic bouton number and branch formation.
118 overexpression caused a dramatic increase in synaptic bouton number and changes in synapse structure.
119 overexpression of Shank result in defects in synaptic bouton number and maturation.
120  synaptic development, including controlling synaptic bouton number and the ability to bud new varico
121 strophic morphology and marked reductions in synaptic bouton numbers.
122  of microglomeruli each comprising the large synaptic bouton of a projection neuron (PN) from the ant
123 ide evidence that zinc is sequestered within synaptic boutons of a subpopulation of retinal ganglion
124   We conclude that the protein is present in synaptic boutons of axons with different neurochemical p
125            We determined that FM1-43-labeled synaptic boutons of csp mutant neuromuscular junctions f
126 esulted in a reduction of pY816 in axons and synaptic boutons of hippocampal mossy fibers, thereby im
127 unoreactivity was increased in axons but not synaptic boutons of mossy fibers in ZnT3 knockout mice t
128 ormal accumulation of mitochondria in distal synaptic boutons of NMJs.
129 nce of vesicle exocytosis and endocytosis in synaptic boutons of rat cerebellar granule cells.
130 ansporter currents because the small size of synaptic boutons precludes direct recordings.
131                             We find that the synaptic boutons show both chemical synaptic structures
132  synapses also show a profound overgrowth of synaptic boutons, similar to known Drosophila endocytoti
133 ors are not due to presynaptic retraction of synaptic boutons, since other presynaptic components are
134 ns downstream of presynaptic PDK1 to control synaptic bouton size, active zone number, and synaptic f
135 ves the transformation of a growth cone into synaptic boutons specialized for transmitter release.
136                   As synapses grow, existing synaptic boutons stretch apart and new boutons insert be
137                                 In addition, synaptic bouton structure at motor nerve terminals is al
138 re, small synaptic vesicles in glutamatergic synaptic boutons, studied with synaptophluorin, are as a
139 al surface and had fewer and less pronounced synaptic boutons, suggesting they prioritize efficient a
140    An analysis of 250 anterogradely labelled synaptic boutons (taken from layers 2/3) indicated that
141 rt of mitochondria to NMJs, the structure of synaptic boutons, the organization of presynaptic microt
142 umber of synaptic vesicles in an area of the synaptic bouton thought to contain the reserve vesicle p
143 strate that the UPS functions locally within synaptic boutons to acutely control levels of presynapti
144 ed feature of imac mutants is the failure of synaptic boutons to form.
145 ds beyond the perisomatic chemical GABAergic synaptic boutons to the distal AIS, lacks both sodium ch
146  endocytosis, Eps15 moves from the center of synaptic boutons to the periphery in response to synapti
147 s grow wider after high-frequency AP firing: synaptic boutons undergo a rapid enlargement, which is m
148 ronous release is tied to calcium entry into synaptic boutons via P/Q type calcium channels, whereas
149  the density of immunogold particles per pre-synaptic bouton were almost 50% lower than in younger ra
150                                   Functional synaptic boutons were identified with FM1-43-based digit
151 ly axo-spinous synapses, as well as multiple synaptic boutons were increased in the perilesion cortex
152            Horizontal patchy connections and synaptic boutons were labeled by injections of the neuro
153 , the morphological characteristics of their synaptic boutons were measured and assessed at the elect
154    Using an image analysis software Image J, synaptic boutons were quantified on the basis of the siz
155 ss than 10 axonal vesicles occurring between synaptic boutons, were stable at 30 minutes but markedly
156 ts was formed mainly by synapses with single synaptic boutons, whereas in the ischemia EC and sham EC
157 ng causes motoneuron terminals to have fewer synaptic boutons, whereas increased neuronal activity re
158 ma-motoneurons were apposed by S- and F-type synaptic boutons, whereas only alpha-motoneurons demonst
159 ifferentiation, and are restricted to type I synaptic boutons, which mediate fast, excitatory glutama
160 Evoked activity induces Wnt1/Wg release from synaptic boutons, which stimulates both a postsynaptic D
161 mutant neurons reveal enlarged and irregular synaptic boutons with dense accumulation of synaptic ves
162 c and anatomical features, such as the large synaptic boutons with which they often terminate.

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