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1 astic activation of only one OR allele in an olfactory sensory neuron.
2 g the expression of one odorant receptor per olfactory sensory neuron.
3 resumed that the olfactory placode forms all olfactory sensory neurons.
4 properties of TAARs when expressed in native olfactory sensory neurons.
5 uces amyloid beta production, exclusively in olfactory sensory neurons.
6 hase of optogenetically driven activation of olfactory sensory neurons.
7 code, where they are specified shortly after olfactory sensory neurons.
8 ctivator of the unfolded protein response in olfactory sensory neurons.
9 hat express channelrhodopsin-2 in all of the olfactory sensory neurons.
10 GC-D is expressed in a special group of olfactory sensory neurons.
11 ural stem cells and down-regulated in mature olfactory sensory neurons.
12 eptors, inhibiting the basal spike firing in olfactory sensory neurons.
13 rant receptors expressed in the cilia of the olfactory sensory neurons.
14 mulation in the cytoplasm of differentiating olfactory sensory neurons.
15 , and are best studied in photoreceptors and olfactory sensory neurons.
16 ay be due, in part, to prolonged survival of olfactory sensory neurons.
17 cilia also occurs in auditory hair cells and olfactory sensory neurons.
18 ocalized in the dendritic knobs and axons of olfactory sensory neurons.
19 rant-induced signaling in photoreceptors and olfactory sensory neurons.
20 crete modules receiving input from idiotypic olfactory sensory neurons.
21 function found almost exclusively in mature olfactory sensory neurons.
22 ion required for the formation of functional olfactory sensory neurons.
23 o transport in native mammalian tissue using olfactory sensory neurons.
24 Expression of human APPsw exclusively in olfactory sensory neurons also perturbs connectivity wit
25 heterologous expression, in both Drosophila olfactory sensory neurones and in human embryonic kidney
27 , we examined the 3D nuclear organization of olfactory sensory neurons and determined the positions o
29 s in the OE extend beyond that of defects in olfactory sensory neurons and may include alterations in
31 fly brain, including three subpopulations of olfactory sensory neurons and projection neurons (PNs).
32 ion channels mediate sensory transduction in olfactory sensory neurons and retinal photoreceptor cell
35 ecifically expressed in newly differentiated olfactory sensory neurons and their axons during develop
36 ection neurons receive odor information from olfactory sensory neurons and transmit it to higher brai
37 sly by capturing the population of activated olfactory sensory neurons and using expression profiling
38 We observed smaller olfactory bulbs, reduced olfactory sensory neurons, and disorganized epithelial u
39 (BBSome) as bona fide constituents of IFT in olfactory sensory neurons, and show that they exist in 1
40 f normal patterns of spontaneous activity in olfactory sensory neurons, and we uncover some of the me
42 ew studies report how discrete identities of olfactory sensory neurons are converted into a spatial m
49 elial cells, neuroepithelial taste cells, or olfactory sensory neurons at chemosensory mucosal surfac
53 lfactory bulb, where they envelop bundles of olfactory sensory neuron axons in a manner distinct from
54 organization of the cytoskeleton changed as olfactory sensory neuron axons moved from the ONLo to th
56 n the terminals of hippocampal mossy fibers, olfactory sensory neuron axons, and growth cones of prim
58 ys originating from a discrete population of olfactory sensory neurons but fail to document any synap
60 posed to modulate the odorant sensitivity of olfactory sensory neurons by inhibiting activation of cy
70 t these concepts are essentially ignored for olfactory sensory neurons, despite the analogies that ar
72 Remarkably, this odor-evoked inhibition of olfactory sensory neurons elicited by itself a full rang
80 ng these is the popular notion that a single olfactory sensory neuron expresses a single odorant rece
83 genes ( approximately 1,400 in mouse), each olfactory sensory neuron expresses one, and only one, of
88 oid neuropil structures formed by axons from olfactory sensory neurons expressing the same olfactory
89 alcium imaging recordings of dissociated rat olfactory sensory neurons, expressing the recombinant OR
90 te Netrins as the only known attractants for olfactory sensory neurons, first drawing OR111-7-express
91 tic protein gene expression, suggesting that olfactory sensory neurons follow an intrinsic program of
92 lfactory system suggests that the peripheral olfactory sensory neurons form synaptic connections befo
93 ulator of neural stem cell proliferation and olfactory sensory neuron formation in the olfactory epit
96 hunger modulates the sensitivity of specific olfactory sensory neurons in Drosophila and facilitates
98 ribe a functionally segregated population of olfactory sensory neurons in the fruitfly, Drosophila me
99 rant-induced, activity-dependent survival of olfactory sensory neurons in the main olfactory epitheli
100 ion of neural stem cells and regeneration of olfactory sensory neurons in the mature Chd7(Gt/+) olfac
102 e virus gains access to the CNS by infecting olfactory sensory neurons in the nasal mucosa of mice.
104 actory epithelium revealed numerous axons of olfactory sensory neurons in the right hemisphere of 27
105 ponse profile and the axonal identity of the olfactory sensory neurons in which they are expressed.
106 contribution of the cranial neural crest to olfactory sensory neurons in zebrafish and provide impor
107 r-evoked inhibition and excitation in single olfactory sensory neurons increases the odor-coding capa
108 or exposure to acetophenone, a ligand of M72 olfactory sensory neurons, increases the strength of M72
112 eceptor DAF-2, functionally switched the AWC olfactory sensory neuron into an interneuron in the salt
113 s the direct transduction of the activity of olfactory sensory neurons into motor response, whereas t
116 eparated by less than 1 mm [1], and a single olfactory sensory neuron is sufficient for near-normal g
117 receptor (OR) genes in the mouse genome, an olfactory sensory neuron is thought to express only one
121 We also found that in these mice, the mature olfactory sensory neuron layer is reduced, and that olfa
124 tional landscapes of Dnmt3a-deficient mature olfactory sensory neurons (mOSNs), the primary sensory n
126 r association with the continually generated olfactory sensory neurons, OEG have attracted interest f
127 ral vector to transiently introduce OMP into olfactory sensory neurons of adult OMP-null mice and, us
132 its distribution was axonal-specific in both olfactory sensory neurons of the olfactory epithelium an
133 was unexpected because amino acid-sensitive olfactory sensory neurons of Xenopus commonly function i
135 The odor response properties of a mammalian olfactory sensory neuron (OSN) are determined by the tig
136 dy, we test the hypothesis that Tnc inhibits olfactory sensory neuron (OSN) axon growth in the develo
137 mechanisms contribute to the specificity of olfactory sensory neuron (OSN) axon innervation of the o
138 ) are thought to be critical determinants of olfactory sensory neuron (OSN) axon targeting and organi
140 or receptors (ORs) play an important role in olfactory sensory neuron (OSN) axon targeting/coalescenc
141 at allowed us to simultaneously label single olfactory sensory neuron (OSN) axonal arbors and their p
144 R) are strongly implicated in coalescence of olfactory sensory neuron (OSN) axons and the formation o
148 precise role of the ion transporter NKCC1 in olfactory sensory neuron (OSN) chloride accumulation has
150 receptor (OR) genes in the mouse genome, an olfactory sensory neuron (OSN) is thought to express one
152 ttern likely results from both the intrinsic olfactory sensory neuron (OSN) sensitivity and the sorpt
154 etized mice, the physiological activation of olfactory sensory neuron (OSN) terminals reliably trigge
157 orting into a GFP+ sample enriched in mature olfactory sensory neurons (OSNs) and a GFP- sample enric
158 te the interaction of odorous compounds with olfactory sensory neurons (OSNs) and influence the guida
159 unoreactive glutamate levels were highest in olfactory sensory neurons (OSNs) and mitral cells, the p
160 ribe a functionally segregated population of olfactory sensory neurons (OSNs) and projection neurons
161 ion waveforms and examined spike patterns of olfactory sensory neurons (OSNs) and projection neurons
162 hat can induce neurotransmitter release from olfactory sensory neurons (OSNs) and reduces the total t
164 h FAF1 is specifically expressed in immature olfactory sensory neurons (OSNs) and show that overexpre
165 y epithelium is mostly populated by ciliated olfactory sensory neurons (OSNs) and surrounding sustent
174 Here we show that Or47b-and Or88a-expressing olfactory sensory neurons (OSNs) detect the fly-produced
176 odel of odor coding in which a population of olfactory sensory neurons (OSNs) expressing a single OR
179 pecialized olfactory subsystem that includes olfactory sensory neurons (OSNs) expressing the receptor
180 n-promoting effect of synthetic cVA requires olfactory sensory neurons (OSNs) expressing the receptor
181 in mammals is the convergence of axons from olfactory sensory neurons (OSNs) expressing the same odo
183 mmalian and insect olfactory systems is that olfactory sensory neurons (OSNs) expressing the same uni
186 retinoic acid-inactivating enzyme Cyp26B1 in olfactory sensory neurons (OSNs) forms a dorsomedial (DM
189 tein (SNMP), is expressed in a population of olfactory sensory neurons (OSNs) implicated in pheromone
190 plete convergence when Mecp2 is deficient in olfactory sensory neurons (OSNs) in an otherwise wild-ty
193 icity also affects the input to the MOB from olfactory sensory neurons (OSNs) in the glomerular layer
194 We show that Atf5 is highly expressed in olfactory sensory neurons (OSNs) in the main olfactory e
196 In contrast to the widely held view that olfactory sensory neurons (OSNs) in the main olfactory e
197 orant receptor (OR) genes across millions of olfactory sensory neurons (OSNs) in the main olfactory e
201 implicated in establishing the topography of olfactory sensory neurons (OSNs) in the olfactory bulb (
205 Input to the central nervous system from olfactory sensory neurons (OSNs) is modulated presynapti
208 sions: (1) a main olfactory system, in which olfactory sensory neurons (OSNs) located in the main olf
209 dor molecules are transduced by thousands of olfactory sensory neurons (OSNs) located in the nasal ca
210 ctory behaviors are processed by first-order olfactory sensory neurons (OSNs) of the Drosophila larva
214 is a natural biosensor since its peripheral olfactory sensory neurons (OSNs) respond to the external
215 in olfactory epithelium contains a subset of olfactory sensory neurons (OSNs) responding to pheromone
216 is composed of multiple cell types including olfactory sensory neurons (OSNs) that are readily replac
217 2,000 glomeruli, each receiving inputs from olfactory sensory neurons (OSNs) that express a specific
219 n olfactory bulb receives axonal inputs from olfactory sensory neurons (OSNs) that express the same o
222 by the activation of a subset of ORs and the olfactory sensory neurons (OSNs) that express them.
223 screen for cilial membrane proteins of mouse olfactory sensory neurons (OSNs) that identified all the
224 detect odorous chemicals through specialized olfactory sensory neurons (OSNs) that transduce odorants
225 factory epithelium continues to generate new olfactory sensory neurons (OSNs) throughout life, we inv
226 he core determinant of identity for axons of olfactory sensory neurons (OSNs) to coalesce into glomer
227 s (ORs) function in the guidance of axons of olfactory sensory neurons (OSNs) to glomeruli in the olf
228 is not known how M3-Rs affect the ability of olfactory sensory neurons (OSNs) to respond to odours.
229 G-protein-coupled olfactory receptors on the olfactory sensory neurons (OSNs) triggers a signaling ca
230 of the mammalian olfactory system, with new olfactory sensory neurons (OSNs) wiring into highly orga
233 adenylyl cyclase 3 (AC3), is coexpressed in olfactory sensory neurons (OSNs) with poly-N-acetyllacto
234 onally cooperate to provide individual mouse olfactory sensory neurons (OSNs) with the cell surface d
235 o flow-cytometrically sorted pools of mature olfactory sensory neurons (OSNs), and finally arriving a
236 was expressed in basal precursors, immature olfactory sensory neurons (OSNs), and olfactory ensheath
237 in and reporter are particularly abundant in olfactory sensory neurons (OSNs), and specific BBS8 anti
239 ery mRNA detected in samples of mature mouse olfactory sensory neurons (OSNs), immature OSNs, and the
240 ually dimorphic neural coding of odorants by olfactory sensory neurons (OSNs), primary sensory neuron
242 These rhythms are dependent on clocks in olfactory sensory neurons (OSNs), suggesting that odoran
243 The olfactory epithelium (OE) is composed of olfactory sensory neurons (OSNs), sustentacular supporti
245 nose, odorants are detected on the cilia of olfactory sensory neurons (OSNs), where a cAMP-mediated
246 C]GV1-57, that appears to specifically label olfactory sensory neurons (OSNs), which are essential fo
248 the dorsal OB is determined by two types of olfactory sensory neurons (OSNs), which reside in the do
249 osophila olfactory system, odorants activate olfactory sensory neurons (OSNs), which stimulate projec
267 by the odorant receptors on the membrane of olfactory sensory neurons, plays a vital role in their h
270 n 2 (Nrp2), is known to mediate targeting of olfactory sensory neurons (primary neurons), to the post
273 effect on cell proliferation in the OE or on olfactory sensory neurons projecting to the OB, but indu
274 ACE1 null mice have axon guidance defects in olfactory sensory neuron projections to glomeruli in the
276 An important mechanism by which vertebrate olfactory sensory neurons rapidly adapt to odorants is f
277 ry sensory neuron layer is reduced, and that olfactory sensory neurons show increased rate of cell de
280 eir own expression and the patterning of the olfactory sensory neurons' synaptic connections in the b
288 ich a fluorescent reporter selectively marks olfactory sensory neurons that have been activated recen
289 ry interneurons and of synaptic terminals of olfactory sensory neurons (the primary sensory neurons o
291 ues are recognized by receptors expressed on olfactory sensory neurons, the primary sensory neurons o
292 EET blocks electrophysiological responses of olfactory sensory neurons to attractive odors in Anophel
293 tly of the number of odor components, to any olfactory sensory neuron type with a response curve that
294 th great precision by the axons of different olfactory sensory neuron types and act as functional uni
295 is phenotype is caused by ciliary defects of olfactory sensory neurons, we examined mice with deletio
296 ry epithelium (OE) generates only a very few olfactory sensory neurons when the basic helix-loop-heli
297 cyclase transduction system in the cilia of olfactory sensory neurons, which is the site of odorant
298 duction of tph-1 by functional regulation of olfactory sensory neurons, which underscores the importa
299 ry inputs to individual glomeruli, we loaded olfactory sensory neurons with a Ca(2+) indicator and me
300 utilized the genetically labeled murine M72 olfactory sensory neurons with the green fluorescent pro
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