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1 th both speed and accuracy in the Drosophila olfactory system.
2 relevant physiological input to the Xenopus olfactory system.
3 initial stages of signal transduction in the olfactory system.
4 ork with this architecture in the Drosophila olfactory system.
5 differentiation of CSPs in the A. lineolatus olfactory system.
6 re, we investigated this issue in the insect olfactory system.
7 t dynamics we here use a model of the locust olfactory system.
8 ning of this sensory-motor transition in the olfactory system.
9 initial site of synaptic integration in the olfactory system.
10 rons (OSNs) form the primary elements of the olfactory system.
11 rst stage of sensory processing in the mouse olfactory system.
12 s translated into perceived intensity by the olfactory system.
13 ing already at the first synapse of the main olfactory system.
14 maintain circadian rhythms in the mammalian olfactory system.
15 the nervous system, including the peripheral olfactory system.
16 th of which are key components of the insect olfactory system.
17 issue in the locust (Schistocerca americana) olfactory system.
18 nt insights into the assembly of the nascent olfactory system.
19 Glomeruli are functional units in the olfactory system.
20 in olfactory system but not in the accessory olfactory system.
21 key molecular and anatomical features of the olfactory system.
22 an important site of integration in the fly olfactory system.
23 s underlying ORN diversity in the Drosophila olfactory system.
24 ature neurons of both the main and accessory olfactory system.
25 uron (PN) target selection in the Drosophila olfactory system.
26 l organization of glomeruli in the zebrafish olfactory system.
27 ition requires the visual system but not the olfactory system.
28 ial for an endoscopic diagnosis of AD in the olfactory system.
29 tors in the development of this facet of the olfactory system.
30 of activity may represent information in the olfactory system.
31 ceptors, and at long range, by affecting the olfactory system.
32 y experience at various stages of the insect olfactory system.
33 ts exhibit FXGs in mature axons in the adult olfactory system.
34 d how such mechanisms are implemented in the olfactory system.
35 al cavity likely reflects a highly sensitive olfactory system.
36 precise wiring and function of the mammalian olfactory system.
37 eptor in the function and development of the olfactory system.
38 art by a vasopressin system intrinsic to the olfactory system.
39 ositional repulsion depends primarily on the olfactory system.
40 a code can be read by neural circuits of the olfactory system.
41 imary afferent connections in the Drosophila olfactory system.
42 he initial signal transformation site of the olfactory system.
43 is ability is particularly important for the olfactory system.
44 ons we directly test this idea in the locust olfactory system.
45 re plasticity in the gross morphology of the olfactory system.
46 sensing has been attributed to any mammalian olfactory system.
47 ns in the first brain relay of the fruit fly olfactory system.
48 bout how experience changes circuitry in the olfactory system.
49 have acted as axonal guidepost cells in the olfactory system.
50 lar cues for natural behavior in a mammalian olfactory system.
51 ding of information processing in the insect olfactory system.
52 lecular relationship between single and dual olfactory systems.
53 ed in most mammals by the main and accessory olfactory systems.
54 he neural crest and placodes to the otic and olfactory systems.
55 in the mouse retina and in the mouse and fly olfactory systems.
56 t and early functioning of the gustatory and olfactory systems.
57 combine information from both the taste and olfactory systems.
58 nriched for genes associated with immune and olfactory systems.
59 chanosensitivity may be a general feature in olfactory systems.
60 to be functionally expressed in several non-olfactory systems.
61 e new complex patterns, as they arise in the olfactory system?
62 ed four critical developmental stages of the olfactory system: 3rd instar larval (prepatterning), 8 h
63 Albeit located in parallel partitions of the olfactory system, 5-HT largely elicited MC excitation in
64 here we demonstrate that, in the adult mouse olfactory system, a 1-week-long exposure to an artificia
66 aling mechanism by which interneurons of the olfactory system act as directors for the activity-depen
67 roplasticity, we investigated the effects of olfactory system activation on neurotransmitter (NT) exp
68 is also evidence for asymmetry in the human olfactory system, although evidence in non-human animal
69 ophila antennal lobe, the first relay in the olfactory system and a model circuit for understanding o
70 ur, a response pathway through the accessory olfactory system and a new role for vomeronasal organ si
71 t the ACo is reciprocally connected with the olfactory system and basal forebrain, as well as with th
72 tiation of crypt cells in development of the olfactory system and demonstrated that this type of cell
73 niquely detailed description of a vertebrate olfactory system and highlight anatomically distinct par
74 s of metal-induced neurotoxicity of the fish olfactory system and identify novel miRNA biomarkers of
75 onounced sexual dimorphism of the peripheral olfactory system and its representation in higher brain
76 is required for amino acid detection by the olfactory system and suggest that it plays a role in the
77 strates for acid detection in the Drosophila olfactory system and support a labelled-line mode of aci
78 irst validated trans-Tango in the Drosophila olfactory system and then implemented it in the gustator
81 arly and severely in cerebral regions of the olfactory system, and they have also been observed in ol
82 he main olfactory system (MOS) and accessory olfactory system (AOS) detect and process pheromonal sti
87 onclusion, axonal regeneration in the locust olfactory system appears to be possible, precise, and fa
88 primary sensory receptive field maps of the olfactory system are exquisitely organized and respond d
90 meronasal organ (VNO), part of the accessory olfactory system, are important for pheromone detection.
91 d serotonergic neurons within the Drosophila olfactory system as a model to establish a framework for
93 s use various biological components from the olfactory system as sensing elements, possessing great c
95 ent of the visual, auditory, vestibular, and olfactory systems, attributable to profound defects in s
97 rally assumed wiring principle in vertebrate olfactory systems, axons of single receptor neurons of X
101 arbor in mature sensory neurons in the main olfactory system but not in the accessory olfactory syst
102 is highly expressed in the developing mouse olfactory system, but its expression is downregulated po
104 on classes is essential for functions of the olfactory system, but the underlying mechanisms that gen
105 e addressed this question in the adult mouse olfactory system by combining odor discrimination studie
107 OBPs contribute to the sensitivity of the olfactory system by transporting odorants through the se
108 phagocytosis by OECs in the developing mouse olfactory system by utilizing two transgenic reporter li
110 ur work provides evidence that the mammalian olfactory system can read temporal patterns, and suggest
112 tly it has been suggested that damage to the olfactory system (CN I) decreases the ability to taste;
113 ir body, no teeth, poor vision, and an acute olfactory system, comprise the only placental order (Pho
114 at Ts65Dn mice demonstrate an abnormality in olfactory system connectivity, a defect in the refinemen
117 for the development and function of the main olfactory system, contributing to the development and al
119 udy demonstrated that the in vivo biomimetic olfactory system could provide novel approaches to enhan
120 t that hormonal modulation of the peripheral olfactory system could underlie differences in how males
122 Coding of information in the peripheral olfactory system depends on two fundamental : interactio
125 onasal organ, a sensory structure within the olfactory system, detects chemical signals that affect s
127 y Fezf1 and Fezf2 as important regulators of olfactory system development and sensory neuron identity
128 lfactory bulb (OB), but their importance for olfactory system development is completely unknown.
129 unpredicted degree of similarity between the olfactory system development of vertebrates and that of
134 ion produces rhythmic activity in the entire olfactory system, driving neurons in the olfactory epith
140 that odor evidence integration in the human olfactory system enhances discrimination on a two-altern
141 in olfaction and suggest that the peripheral olfactory system, especially the central zone, may be st
146 cusses the role of active sensing in shaping olfactory system function at multiple levels and draws p
147 ry oscillations are a ubiquitous hallmark of olfactory system function in animals, direct evidence fo
148 tion profoundly shapes nearly all aspects of olfactory system function, from the distribution of odor
149 e first station of sensory processing in the olfactory system, GABAergic interneuron signaling shapes
151 nformation processing in the mouse accessory olfactory system guides the expression of social behavio
152 lopmental programs underlying the Drosophila olfactory system harbor a disproportionate amount of int
159 However, the maximum temporal resolution of olfactory systems has not been accurately determined.
160 h the numerical simplicity of the Drosophila olfactory system, has produced rapid gains in our unders
161 odorants will interact with receptors in the olfactory system have achieved a success rate of 70%.
163 xamples from the mouse retina and Drosophila olfactory system, I present worked examples illustrating
166 at the antennal lobe, the first relay of the olfactory system in insects and analog to the olfactory
167 ays formed by mitral and tufted cells of the olfactory system in mice and characterized the emergence
168 anization of sensory cells in the peripheral olfactory system in mice for better odor detection.
169 yloid-beta (Abeta) deposition throughout the olfactory system in mice that overexpress a mutated form
171 e role of sensory systems, in particular the olfactory system, in the detection and perception of cue
172 This arrangement is much like the fly's olfactory system, in which afferents target uniquely ide
173 that DEET targets multiple components of the olfactory system, including OBPs and odorant receptors.
174 undantly expressed genes related to the moth olfactory system, including those encoding the olfactory
175 The need to breathe links the mammalian olfactory system inextricably to the respiratory rhythms
178 erception of these odors within the mosquito olfactory system involves the interplay of odorant-bindi
180 m and demonstrate that the Drosophila larval olfactory system is a powerful model in which to underst
182 ides novel insight into the way in which the olfactory system is affected in CNS demyelinating diseas
183 ling, these results imply that the mammalian olfactory system is capable of very high transient infor
186 Axon targeting during the development of the olfactory system is not always accurate, and numerous ax
189 attern of underlying pathology affecting the olfactory system is shown to be complex, involving multi
193 rlying odor representations in the mammalian olfactory system is strongly patterned by respiratory be
194 Together, these results suggest that the rat olfactory system is symmetric, with highly lateralized o
196 ctory nucleus (AON), a component of the main olfactory system, is a cortical region that processes ol
198 rneurons, partially instructed by the larval olfactory system laid down during embryogenesis, pattern
201 c OR expression, but also elucidates how the olfactory system maximizes and maintains the diversity o
203 ts show a similar level of complexity of the olfactory system morphology of small and large wasps.
204 Recent studies indicate that both the main olfactory system (MOS) and accessory olfactory system (A
206 wn whether AD-related alterations in central olfactory system neural activity, as measured by functio
210 v2r expression pattern in main and accessory olfactory system of amphibians presents an excellent opp
212 relationship between two transmitters in the olfactory system of C. elegans, showing that a neuropept
216 e deutocerebral neurons" (CSDns), within the olfactory system of Drosophila Specifically, we determin
217 Taking advantage of the well-characterized olfactory system of Drosophila, we derive a simple quant
221 ng with temperature sensitivity found in the olfactory system of mice and Xenopus laevis tadpoles, a
227 ptional profiles in the adult and developing olfactory system of the six species suggest the possibil
228 ene expression during the development of the olfactory system of two specialist Drosophila species to
229 associated with such transformations in the olfactory system of zebrafish, a small vertebrate that o
230 atus, has one of the most acute and eclectic olfactory systems of all mosquito species hitherto studi
233 utations that compromise the function of the olfactory system on the development of anxiety-like beha
235 n inhibitory circuit motif in the Drosophila olfactory system, parallel inhibition, which differs fro
238 e are congenitally anosmic and have abnormal olfactory system physiology, additionally Karstensen et
239 the largely feedforward organization of the olfactory system precludes reconstruction using standard
240 red piriform cortex, an integral part of the olfactory system, processes odor information relayed by
241 ssue of Neuron by Cury and Uchida in the rat olfactory system provides evidence that such patterns co
242 nstrate that during early development of the olfactory system, radial glia play an important role in
244 ensory processing circuits in the visual and olfactory systems receive input from complex, rapidly ch
248 er of vital behaviors, the components of the olfactory system responsible for assigning meaning to od
250 ional explanation to account for patterns of olfactory system scaling in vertebrates, the primacy of
259 Here we describe a feedforward model of the olfactory system that achieves both strong compression a
261 s (OBPs) are small soluble proteins found in olfactory systems that are capable of binding several ty
262 parasitic nematodes have evolved specialized olfactory systems that likely contribute to appropriate
263 information is encoded and processed in the olfactory system, the functional connectivity within and
266 tructural correlates of developing and adult olfactory systems, the paucity of information available
267 The coevolution of the OR repertoire and the olfactory system therefore reveals general principles of
269 been proposed: that DEET interferes with the olfactory system to block host odour recognition and tha
271 s of information transmission may enable the olfactory system to efficiently identify and localize od
272 r, and highlight the dynamic capacity of the olfactory system to engage both object-level and compone
273 athway that regulates the sensitivity of the olfactory system to odor concentrations, demonstrating t
282 ptically suppressed the first synapse of the olfactory system via GABAB receptors on sensory terminal
283 ala's anatomical proximity to the peripheral olfactory system, we combined high-resolution fMRI with
284 processed, transformed, and stored within an olfactory system, we examined the anatomy of the input r
286 Using in vivo brain electroporation of the olfactory system, we show that the transmembrane form of
287 neuronal populations have been gained in the olfactory system where rich spatio-temporal dynamics is
288 del system for studying sparse coding in the olfactory system, where this format is important for acc
289 wer fundamental questions about noise in the olfactory system: Where does spontaneous activity origin
290 neurons (the primary sensory neurons of the olfactory system, which provide the initial olfactory in
291 fixed neural architecture of the vertebrate olfactory system, which requires that new olfactory rece
292 ty can occur in the periphery of adult mouse olfactory system, which should improve odor detection an
293 issues in the context of the mouse accessory olfactory system, which specializes in detection of chem
294 ated neural pathways, the main and accessory olfactory systems, which are specialized to detect odors
295 entities is particularly timely in the human olfactory system, whose structural differences from nonp
299 urogenesis is a key feature of the mammalian olfactory system, with new olfactory sensory neurons (OS
300 the nerve is anatomically independent of the olfactory system, with two major cell populations within
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