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1 ink many regions of the protocerebrum to the calyces.
2 s represent zones of afferent endings in the calyces.
3 t in processes originating from the necks of calyces.
4 er processes, intramacular nerve fibers, and calyces.
5 rom afferent nerve fibers and basal parts of calyces.
6  retrograde catheter to the renal pelvis and calyces.
7  both slow and rapid forms of endocytosis at calyces.
8 dy, including a giant neuron innervating the calyces.
9 c insects its mushroom bodies possess robust calyces.
10 eruli that characterize insect mushroom body calyces.
11 ntennal lobes and attenuation or loss of the calyces.
12 te as those of mushroom bodies equipped with calyces.
13 f the two Kenyon cell populations of the two calyces.
14 ecover anthocyanins from Hibiscus sabdariffa calyces.
15  of the pedunculus and the basal ring of the calyces.
16 d the organization of their terminals in the calyces.
17 control), agave DF (ADF) or ADF with jamaica calyces (ADF-JC).
18 5.67% total anthocyanins were recovered from calyces after double extractions, and the content increa
19          The expression of h-alpha-synA53Tin calyces also inhibited vesicle replenishment to the read
20                  Recordings from dissociated calyces and afferent endings revealed large K+ conductan
21 roductive late summer mothers had smaller MB calyces and ALs than foundresses.
22 pectively), lobulated kidneys with prominent calyces and diabetes mellitus (diagnosed at ages 33 and
23             We measured the volume of the MB calyces and peduncle, antennal lobes (AL), optic lobes (
24 an cause renal scarring, distortion of renal calyces and pelvic, ureteric strictures, stenosis, urina
25 transitional epithelium that lines the renal calyces and pelvis, ureters, and bladder.
26 leviated by the polyphenols found in roselle calyces and sweet basil leaves.
27  responsible of the intense red color of the calyces, and have potential as natural colorants for foo
28 tency (jitter) was increased in VCN neurons, calyces, and MNTB neurons of -/- mice compared with +/+
29 the lateral protocerebrum, the mushroom body calyces, and the lobula complex.
30 s from adjacent Kenyon cell dendrites in the calyces are adjacent in the lobes even after their polar
31  and intrinsic neurons (Kenyon cells) in the calyces are arranged according to polar coordinates.
32  of the lateral protocerebrum, mushroom body calyces are buried deep within it with their columns ext
33 se to MACs and synapses and hypothesize that calyces are composed of multiple activity modules, each
34 orescent tracer injections revealed that the calyces are exclusively supplied by visual neurons from
35 alin, though the overall architecture of the calyces are very different.
36 cies that generally lack antennal lobes, the calyces are vestigial or absent.
37 ushroom bodies, the primary input region, or calyces, are predominantly supplied by olfactory project
38                     Feedback pathways to the calyces arise from satellite neuropils adjacent to the m
39 stibular periphery, staining was observed in calyces around type I hair cells, at the synaptic pole o
40 gonia, featuring highly inflated, five-lobed calyces, as a newly identified species of the derived, d
41  SV release in postnatal day (P) 16-19 mouse calyces, as their release properties resemble mature cal
42 ded whole-cell responses from hair cells and calyces at room temperature and body temperature.
43 plies sparse immunoreactive processes to the calyces' basal ring, collar, and lip.
44 med before P2) downregulate Sox2 and acquire calyces between P0 and P14.
45  Inhibition of GABAergic signaling in the MB calyces, but not in the lobes, impairs patterning discri
46 senting one of three concentric zones of the calyces, called the lip, collar, and basal ring.
47             A region immediately beneath the calyces, called the neck, is invaded by these neurons as
48 ches that were presynaptic to type II cells, calyces, calyceal processes, and other nerve fibers in t
49 n of nicotine induced inward currents in the calyces capable of generating action potentials that ove
50                                          The calyces, columns, and especially the gyri show DC0 immun
51 t mushroom bodies possesses a pair of simple calyces comprising two populations of Kenyon cells, the
52 tional and structural data showed that young calyces could form within 2 d, well before the onset of
53 rinary tract, namely the ureter, pelvis, and calyces, could be depicted with radiography.
54                   At early time points, many calyces enclosed Sox2-labeled hair cells, while some Sox
55                  We show that rat vestibular calyces express an unusual mix of voltage-gated Na and K
56                                              Calyces express presynaptic glycine receptors whose acti
57 y 11 (P11), and before the onset of hearing, calyces expressed high levels of ionotropic GABA(A) rece
58 alization and distention of the nondependent calyces for definitive renal access with an 18-gauge 5-F
59 ergic feedback neurons from the lobes to the calyces for nonelemental learning.
60  The ATP-independent endocytosis occurred at calyces from postnatal days 8-15, suggesting its existen
61 patches excised from the nonsynaptic face of calyces, GABA and glycine evoked single-channel currents
62                          Results showed that calyces had 1) vesiculated, spine-like processes that in
63  time of the receptor potential and (2) some calyces had nonquantal transmission with little synaptic
64 s even after their polar arrangements in the calyces have been transformed to rectilinear arrangement
65                    A drink made with roselle calyces (Hibiscus sabdariffa) and sweet basil leaves (Oc
66 ch in fructans and insoluble DF, and jamaica calyces (Hibiscus sabdariffa), which is rich in DF and p
67              Here we show that lesions of MB calyces impair ants' visual navigation to a remembered f
68 esses invades all zones of the mushroom body calyces in Periplaneta.
69 ke structures characterize the mushroom body calyces in the brains of certain species of insects; we
70 g type I HCs first lacked and later regained calyces in the recovery, but not the nonrecovery, group.
71 nsgenically or dialyzed in the short term in calyces, inhibited two of the most common forms of endoc
72               Afferent terminals segment the calyces into discrete zones, I, II, III, and IIIA, which
73 ted release time course found in posthearing calyces is not known.
74 ding to volume of patient's renal pelvis and calyces, maximum 60 mg per instillation) via retrograde
75  dilatation of the ureter, renal pelvis, and calyces might be seen.
76                    We report the presence in calyces of an atypical arrangement of subcellular organe
77 naptic afferents, which grow rapidly to form calyces of Held and to establish mono-innervation betwee
78                     These data indicate that calyces of Held follow a noncanonical program to establi
79                 Here we confirm that RRPs at calyces of Held from 14 to 21 day old mice have a fixed
80 neity in release probability for more mature calyces of Held nerve terminals.
81 axonal endings of bushy cells at MNTB cells (calyces of Held), and MNTB neurons of Kcna1-null (-/-) m
82 Interestingly, the parent cell bodies of the calyces of Held, the globular bushy cells of the cochlea
83  as their release properties resemble mature calyces of Held.
84 rminating in large synaptic endings known as calyces of Held.
85                             In addition, the calyces of Hymenoptera receive substantial direct input
86 that are comparable to those observed in the calyces of insect mushroom bodies and which characterize
87 ganization of afferent neurons supplying the calyces of the cockroach Periplaneta americana.
88             We describe visual inputs to the calyces of the mushroom bodies of the honeybee Apis mell
89 nnections between the antennal lobes and the calyces of the mushroom bodies.
90 ex (MGC) and send an axon from the AL to the calyces of the mushroom body (CA) as well as the lateral
91 eral protocerebrum and, collaterally, to the calyces of the mushroom body.
92 rve fibers and their large afferent endings (calyces) on type I hair cells branch.
93                    Convergence of developing calyces onto postsynaptic targets, indicative of competi
94                                         When calyces or ciliary neurons were labeled en mass with neu
95 glutamate release probability for adult-like calyces (P30-P34).
96    We found that essentially all vesicles in calyces participated in recycling, challenging the small
97     Dried and milled eggplant fruit peel and calyces (PC) and mesocarp, placenta and core (Mes) were
98 tional plan of the insect mushroom body into calyces, peduncle, and lobes is maintained, as is the ar
99 ry beta4 Na(+) channel subunit into immature calyces (postnatal day 5-6) induced an increase in I(NaR
100                   In immature hair cells and calyces (postnatal days (P)1-P4), tuning sharpened at ea
101 to be higher olfactory centers because their calyces receive abundant collaterals of projection neuro
102  synaptically released glutamate at immature calyces, resulting in significant desensitization.
103 croscopy data of immature and mature labeled calyces reveal that mitochondrial volumes are increased
104             Presynaptically, Mir-183/96(dko) calyces show an increase in release-ready synaptic vesic
105 postnatal ages (15-17 d after birth) LES rat calyces showed prolonged spike latencies, indicative of
106 uilana alone, or in combination with jamaica calyces, shows promising potential as a bioactive ingred
107 corporation of sweet basil leaves to roselle calyces slightly decreased the vitamin C and lycopene co
108 patterns, while neurons contacted by complex calyces (stalks and >20 swellings) providing stronger sy
109    We discovered that morphologically simple calyces (stalks and <=10 swellings) providing weaker syn
110 rain possesses a mushroom body equipped with calyces supplied by olfactory projection neurons.
111      Kenyon cells providing dendrites to the calyces supply a pedunculus and lobes divided into subdi
112 d NL, whereas trkB is expressed in the nerve calyces surrounding NM neurons and in the ventral, but n
113 potassium channels nor the afferent synaptic calyces that distinguish mature type I hair cells from t
114                                 The afferent calyces that innervate type I hair cell, and the basolat
115 ques to record currents in large presynaptic calyces that midbrain neurons form on ciliary neurons.
116 orm large cup-shaped postsynaptic terminals (calyces) that envelope the basolateral surfaces of type
117 ilar at P13 in the parent-cell bodies of the calyces, the bushy cells of the cochlear nucleus.
118            No other sensory inputs reach the calyces, thereby showing a complete switch of calyx moda
119 polar arrangements of their dendrites in the calyces to laminar arrangements of their terminals in th
120 -to-one signal transmission from presynaptic calyces to postsynaptic MNTB neurons and induced extra p
121 -to-one signal transmission from presynaptic calyces to postsynaptic MNTB neurons.
122 ncy signal transmission from the presynaptic calyces to the postsynaptic medial nucleus of the trapez
123         Axons from the annular zones of both calyces together provide a sleeve of axons that ensheath
124 sive asynchronous release in Cplx1-deficient calyces triggered aberrant action potentials in their ta
125 in the striola failed to develop the complex calyces typical of these cells.
126               Subsequent lesioning of the MB calyces using procaine hydrochloride injection caused an
127 er-order cognitive processing (mushroom body calyces) versus peripheral sensory processing (optic and
128                  Endocytosis at dynamin 1 KO calyces was the same as in wild type after weak stimuli,
129  the morphological complexity of presynaptic calyces, we characterized the intrinsic excitability of
130  predominantly at single active zones in rat calyces, we found that single active zones contained 5-2
131 ic diameter of greater than 3 cm and dilated calyces, we lean more towards surgical intervention.
132                                 While normal calyces were able to fire APs without failures at impres
133 iteria were developed to classify cells when calyces were not present, as in cultures and neonatal or
134 gth of dendrites in the collar region of the calyces were strongly correlated with worker age, but wh
135  this study, commercially available hibiscus calyces were subjected to ethanolic-aqueous extraction a
136 ures at impressive rates of up to 1 kHz, LES calyces were unable to do so.
137 pally after infusion of its dried sepals and calyces, which are usually discarded.
138                    In contrast, labeling the calyces with a water-soluble dye by diffusion through th
139 ain sensory input regions are large, doubled calyces with modality-specific, distinct sensory neuropi

 
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