ライフサイエンスコーパス: olfactory epithelium

1 of v2r family C, are restricted to the main olfactory epithelium.

2 neurons, the primary sensory neurons of the olfactory epithelium.

3 function and OR representation in the adult olfactory epithelium.

4 to develop a chronic BLM has focused on the olfactory epithelium.

5 BC) as the neural stem cell of the postnatal olfactory epithelium.

6 n may be among the roles of Sox2/Pax6 in the olfactory epithelium.

7 of OSNs in the olfactory placode to an aging olfactory epithelium.

8 y neurons (OSNs), which reside in the dorsal olfactory epithelium.

9 chemosensory signaling occurs outside of the olfactory epithelium.

10 reduced olfaction is due to a dysfunctional olfactory epithelium.

11 ons of the septal organ and also of the main olfactory epithelium.

12 ater becomes restricted to the ventrolateral olfactory epithelium.

13 rs extracellular space K(+) buffering in the olfactory epithelium.

14 expression in supportive cells of the nasal olfactory epithelium.

15 diated by the vomeronasal organ and the main olfactory epithelium.

16 ein and G-protein G(olf) in the cilia of the olfactory epithelium.

17 of a second family of receptors in the mouse olfactory epithelium.

18 nspire air (sniff) to convey odorants to the olfactory epithelium.

19 d end feet of the sustentacular cells of the olfactory epithelium.

20 receptor (TAAR)-like receptor in the lamprey olfactory epithelium.

21 nt embryos show impaired neurogenesis in the olfactory epithelium.

22 localize to cellular plasma membranes in the olfactory epithelium.

23 essential for antigen trafficking across the olfactory epithelium.

24 n and the enhancement of neurogenesis within olfactory epithelium.

25 val of olfactory sensory neurons in the main olfactory epithelium.

26 ll lineage commitment and development of the olfactory epithelium.

27 -deleted virus replicated efficiently in the olfactory epithelium.

28 vity cartilage and bony projections, and the olfactory epithelium.

29 ivates neural stem cells to reconstitute the olfactory epithelium.

30 n heterologous expression systems and in rat olfactory epithelium.

31 the distribution of sensory cells within the olfactory epithelium.

32 cross the extent and within the depth of the olfactory epithelium.

33 of M71 OR and beta(2)-AR expression in mouse olfactory epithelium.

34 se lineage tracing in the regenerating mouse olfactory epithelium.

35 ctory glomeruli after chemical damage of the olfactory epithelium.

36 brain and spinal cord, sensory ganglia, and olfactory epithelium.

37 is expressed in both the olfactory bulb and olfactory epithelium.

38 are thought to require interactions with the olfactory epithelium.

39 ation of GBCs is the neural stem cell of the olfactory epithelium.

40 The Dlx5-/- mutation reduces the size of the olfactory epithelium.

41 ed loss of olfactory receptor neurons of the olfactory epithelium.

42 ort of horseradish peroxidase applied to the olfactory epithelium.

43 ineage commitment and the development of the olfactory epithelium.

44 enerate multiple mature cell lineages in the olfactory epithelium.

45 ul for future studies of neurogenesis in the olfactory epithelium.

46 do not express the Galphaolf protein in the olfactory epithelium.

47 ust sexually dimorphic phenotype in the main olfactory epithelium.

48 eyond their role as odorant detectors in the olfactory epithelium.

49 ulation of sensory neurons in the mouse main olfactory epithelium.

50 DM)-ventrolateral (VL) gradient in the mouse olfactory epithelium.

51 an, and chemosensory neurons within the main olfactory epithelium.

52 tation mouse embryo and the developing mouse olfactory epithelium.

53 highly sensitive to temperature drops at the olfactory epithelium.

54 hts into the dynamics of neurogenesis in the olfactory epithelium.

55 (mOSNs), the primary sensory neurons of the olfactory epithelium.

56 ife and that odorant environment affects the olfactory epithelium.

57 ntiation of multiple other cell types in the olfactory epithelium.

58 t was indeed eliminated in the mutant mice's olfactory epithelium.

59 Here, we considered this in the main olfactory epithelium, a chemosensory structure with over

60 The adult olfactory epithelium, a site for ongoing, life-long, rob

61 f that family during the recovery of the rat olfactory epithelium after methyl bromide lesion.

62 the initial site of replication or from the olfactory epithelium after viremic spread.

63 Temperature drops at the contralateral olfactory epithelium also induced responses in the gamma

64 eas within the most ventral zone of the main olfactory epithelium, although their expression patterns

65 amily members are known to be present in the olfactory epithelium and are thought to affect olfaction

66 studies of odor-elicited responses from the olfactory epithelium and bulb in the tiger salamander, A

67 We used the olfactory system (olfactory epithelium and bulb) because its attributes ma

68 ch has been learned about odor coding in the olfactory epithelium and bulb, but little is known about

69 ystem are nestled within the recesses of the olfactory epithelium and detect diverse odorants; howeve

70 nd a neurogenin1 reporter ingressed into the olfactory epithelium and differentiated into microvillou

71 develop altered head morphology, an expanded olfactory epithelium and disorganized peripheral axons.

72 ed the expression of Pax6 and Sox2 in normal olfactory epithelium and during epithelial regeneration

73 the central and peripheral nervous systems, olfactory epithelium and endocrine pancreas.

74 establish normal connections with peripheral olfactory epithelium and help olfactory bulb recovery fr

75 mmalian homologs of which are coexpressed in olfactory epithelium and hematopoietic cells.

76 specific receptor representation in the main olfactory epithelium and in glomeruli within the olfacto

77 ining the spatial organization of the normal olfactory epithelium and in reestablishing the neuronal

78 is expressed at different levels across the olfactory epithelium and in restricted glomeruli across

79 n the olfactory nerve bundles underlying the olfactory epithelium and in the olfactory nerve layer an

80 otide exchange factor (GEF) expressed in the olfactory epithelium and in the striatum.

81 The olfactory epithelium and its projection onto the bulb ar

82 rderly projections of sensory neurons in the olfactory epithelium and may also involve chromatography

83 fic in both olfactory sensory neurons of the olfactory epithelium and mitral cells of the olfactory b

84 The volumes of the main olfactory epithelium and muscles regulating diameter of

85 gene expression, we found that the isolated olfactory epithelium and OB, but not the piriform cortex

86 and elimination of neurons within the adult olfactory epithelium and olfactory bulb allows for adapt

87 r learning-induced structural changes in the olfactory epithelium and olfactory bulb in an odorant li

88 beta-Galactosidase distribution in the olfactory epithelium and olfactory bulb in Cx36 knockout

89 the expression of connexin 36 (Cx36) in the olfactory epithelium and olfactory bulb of adult mice.

90 ined that Sall3 is expressed by cells in the olfactory epithelium and olfactory bulb.

91 on is maintained in the developing and adult olfactory epithelium and olfactory nerve.

92 stem-cell self-renewal, as documented in the olfactory epithelium and other tissues.

93 bulb (OB) receives odor information from the olfactory epithelium and relays this to the olfactory co

94 head trauma, viruses, and toxic agents, the olfactory epithelium and sectors of the olfactory bulb h

95 organs in the vertebrate head, including the olfactory epithelium and the crystalline lens of the eye

96 rom contact with all other cells between the olfactory epithelium and the glomerulus of the olfactory

97 self-renewing interfollicular epidermis, the olfactory epithelium and the intestinal crypts of Lieber

98 icrovillous sensory neurons in the zebrafish olfactory epithelium and the mouse vomeronasal organ.

99 animals uncovered parallels between the main olfactory epithelium and the vomeronasal organ in the re

100 to the sustentacular cells of the unlesioned olfactory epithelium and to the adjoining respiratory ep

101 or for SDF-1, is expressed by neurons in the olfactory epithelium and VNO.

102 ceptors and signaling components of the main olfactory epithelium and vomeronasal organ involved in p

103 expressed in sensory cells in the developing olfactory epithelium and vomeronasal organ, with both li

104 s were expressed specifically in OSNs in the olfactory epithelium, and ANO2::EGFP fusion protein loca

105 oupled receptors that detect odorants in the olfactory epithelium, and comprise the largest gene fami

106 OSNs differentiate from stem cells in the olfactory epithelium, and how the epithelium generates c

107 te buds including the epithelium of lips and olfactory epithelium, and ii) mechanosensory cells of ne

108 dorsal root ganglia, trigeminal ganglia, and olfactory epithelium, and less intense expression in the

109 Dlx5 is expressed in the olfactory placode, olfactory epithelium, and local circuit neurons of the o

110 O/E proteins are highly expressed in the olfactory epithelium, and O/E binding sites have been id

111 ell numbers, number of mature neurons in the olfactory epithelium, and reactive astrocyte numbers in

112 different patterns of deposition across the olfactory epithelium, and that these patterns are differ

113 s expressed in other tissues, such as brain, olfactory epithelium, and the inner ear, and may modulat

114 ithelium, were unaffected by blockade of the olfactory epithelium, and were independent of respiratio

115 onal distribution of ORs within zones of the olfactory epithelium appeared stable across development;

116 he only O/E family member expressed, but the olfactory epithelium appeared unaffected and olfactory m

117 tor cells residing in the basal layer of the olfactory epithelium are capable of reconstituting the n

118 Odorant receptors (ORs) in the olfactory epithelium bind to volatile small molecules le

119 We collected olfactory epithelium brushings and cerebrospinal fluid s

120 several regions of the brain, including the olfactory epithelium, bulb, peri/paraventricular nuclei,

121 involved in chloride ion accumulation in the olfactory epithelium, but it is also involved in OSN neu

122 2 expression, cadherin-4 is not found in the olfactory epithelium, but it is detected in the larval a

123 that the functional inactivation of the main olfactory epithelium, but not the vomeronasal organ, cau

124 oes compromise the integrity of parts of the olfactory epithelium by altering proliferation, neuronal

125 were investigated in the murine eye and the olfactory epithelium by analysing gene expression and di

126 Direct damage to the olfactory epithelium by inhalation of the olfactotoxin m

127 Odorants are detected in the nasal olfactory epithelium by the odorant receptor family, who

128 nerative capacity, recovery of the mammalian olfactory epithelium can fail in severely injured areas,

129 Within the olfactory epithelium, Cbr2 is a new anatomical marker fo

130 In the olfactory epithelium, CFAP69 is enriched in OSN cilia, w

131 Growing evidence suggests that the main olfactory epithelium contains a subset of olfactory sens

132 Thus, even in the adult, the olfactory epithelium contains neurons at various develop

133 Since the olfactory epithelium continues to generate new olfactory

134 symptom of AD with amyloid pathology in the olfactory epithelium correlating well to the brain patho

135 ement was observed in young and mature mouse olfactory epithelium cultures, in the dissected olfactor

136 Confocal microscopy of the olfactory epithelium detected similar amounts of virus-s

137 ck of olfactory receptor neurons in the main olfactory epithelium, developing Mash1-/-;Tattler-4+/- m

138 r required for B-cell lineage commitment and olfactory epithelium development.

139 pression of Abeta40 or Abeta42 solely in the olfactory epithelium disrupts the olfactory sensory neur

140 Each neuron in the olfactory epithelium expresses only one allele of one OR

141 rane proteins, explants from Shep1 knock-out olfactory epithelium extend neuronal processes less effi

142 iboprobes for eight odorant receptors on the olfactory epithelium from unilaterally methyl bromide-le

143 along the developmental lineage of the main olfactory epithelium-from multipotent stem cells through

144 son with the rest of the nervous system, the olfactory epithelium has an unparalleled ability to rene

145 y the vomeronasal organ, and not by the main olfactory epithelium, has recently been called into ques

146 trong expression of ABCG1 transcripts in the olfactory epithelium, hind brain, eye, and dorsal root g

147 gions with prolonged neurogenesis, e.g., the olfactory epithelium, hippocampus, basal forebrain and c

148 The olfactory epithelium houses chemosensory neurons, which

149 xcitation (SCAPE) microscopy of intact mouse olfactory epithelium, imaging ~10,000 olfactory sensory

150 th embryonic development and turnover of the olfactory epithelium in adult mice, and rosette-bearing

151 The olfactory epithelium in AQP4-null mice had identical app

152 of RT-QuIC analysis of nasal brushings from olfactory epithelium in diagnosing sporadic Creutzfeldt-

153 meruli as well as OSN cell bodies within the olfactory epithelium in freely breathing mice, we find w

154 ctory receptor neurons extend axons from the olfactory epithelium in the antenna into the brain.

155 sis maintains the neuronal population of the olfactory epithelium in the face of piecemeal neuronal t

156 ed ethmoid turbinals supporting an expansive olfactory epithelium in the nasal cavity, allowing full

157 NiV initially predominantly targeted the olfactory epithelium in the nasal turbinates.

158 ory sensory neurons in the mature Chd7(Gt/+) olfactory epithelium indicate critical roles for Chd7 in

159 s affected in CHARGE syndrome including eye, olfactory epithelium, inner ear and vascular system.

160 The olfactory epithelium is a sensory neuroepithelium that s

161 In adult mammals, the olfactory epithelium is a uniquely robust neuroprolifera

162 Ventral olfactory epithelium is at particular risk for metaplasi

163 n Lhx2-deficient mice, the morphology of the olfactory epithelium is grossly normal.

164 The olfactory epithelium is mostly populated by ciliated olf

165 Adult neurogenesis in the olfactory epithelium is often depicted as a unidirection

166 al olfactory cavity (PC), whereas a separate olfactory epithelium lies in the vomeronasal organ (VNO)

167 These odors elicit responses in the olfactory epithelium, main olfactory bulb, and olfactory

168 on of mRNA encoding Cx36 was observed in the olfactory epithelium mainly in ventral and lateral regio

169 The olfactory epithelium maintains stem and progenitor cells

170 pathways, if they are active in normal adult olfactory epithelium, may play a minor role in this tiss

171 Studies of the olfactory epithelium model system have demonstrated that

172 sumed that odorants are detected by the main olfactory epithelium (MOE) and pheromones are sensed thr

173 y distinct chemosensory structures: the main olfactory epithelium (MOE) and the vomeronasal organ (VN

174 olfactory sensory neurons (OSNs) in the main olfactory epithelium (MOE) are stimulated by volatile ch

175 The detection of odorants by the main olfactory epithelium (MOE) depends on coupling of odoran

176 The main olfactory epithelium (MOE) is an excellent model to stud

177 The main olfactory epithelium (MOE) is primarily involved in the

178 y sensory neurons (OSNs) located in the main olfactory epithelium (MOE) send their axons to glomeruli

179 etected by the vomeronasal organ or the main olfactory epithelium (MOE) trigger social behaviors in m

180 olfactory sensory neurons (OSNs) in the main olfactory epithelium (MOE), and on the coalescence of OS

181 ty: the vomeronasal organ (VNO) and the main olfactory epithelium (MOE).

182 ical role in the septal organ as in the main olfactory epithelium (MOE).

183 Pathological analysis of olfactory epithelium obtained from human COVID-19 autops

184 ATP released by the olfactory epithelium (OE) after noxious stimuli provides

185 r GFRalpha1 are prominently expressed in the olfactory epithelium (OE) and olfactory bulb (OB), but t

186 dorsomedial and ventromedial regions of the olfactory epithelium (OE) are distinguished from one ano

187 tterns of receptor expression in the ventral olfactory epithelium (OE) are mirrored in the dorsal OE.

188 Olfactory epithelium (OE) contains a population of proge

189 Neurons in the murine olfactory epithelium (OE) differ by the olfactory recept

190 Neurons in the olfactory epithelium (OE) each express a single dominant

191 velopment, axons from sensory neurons in the olfactory epithelium (OE) extend into the olfactory bulb

192 The capacity of the olfactory epithelium (OE) for lifelong neurogenesis and

193 The embryonic olfactory epithelium (OE) generates only a very few olfa

194 Neural precursors in the developing olfactory epithelium (OE) give rise to three major neuro

195 Olfactory epithelium (OE) has a lifelong capacity for ne

196 The olfactory epithelium (OE) is composed of olfactory senso

197 The vertebrate olfactory epithelium (OE) is known for its ability to re

198 The olfactory epithelium (OE) is one of the few tissues to u

199 development of the cerebral hemispheres and olfactory epithelium (OE) is severely reduced.

200 levels in the olfactory bulb (OB) following olfactory epithelium (OE) lesion in mice, and hypothesiz

201 The olfactory epithelium (OE) of mice deficient in cystic fi

202 neurons have been extensively studied in the olfactory epithelium (OE) of rodents but not in humans.

203 Mouse olfactory epithelium (OE) originates from ectodermally d

204 asia and declining neurogenesis in the aging olfactory epithelium (OE) remains unknown.

205 e characterized two precursor classes in the olfactory epithelium (OE) shortly after it becomes a dis

206 In Shh-/-embryos, ORN axons exit a single olfactory epithelium (OE) that develops centrally within

207 The ability of the olfactory epithelium (OE) to regenerate after injury is

208 The remarkable capacity of the adult olfactory epithelium (OE) to regenerate fully both neuro

209 lfactory sensory neuron (OSN) axons from the olfactory epithelium (OE) to the olfactory bulb (OB) is

210 The inflammatory status of the olfactory epithelium (OE) was assessed using histology,

211 operties of sustentacular cells (SCs) in the olfactory epithelium (OE) were investigated in tissue sl

212 spatially restricted manner in the mammalian olfactory epithelium (OE), and this patterning probably

213 on globose basal cells (GBCs) of the rodent olfactory epithelium (OE), are described.

214 D1 is expressed in embryonic and adult mouse olfactory epithelium (OE), as well as during epithelial

215 y stem/progenitor cells is a hallmark of the olfactory epithelium (OE), beginning at the placodal sta

216 In the olfactory epithelium (OE), generation of new neurons by

217 if another neurogenic tissue, the peripheral olfactory epithelium (OE), might also exhibit changes af

218 In vertebrate olfactory epithelium (OE), neurogenesis proceeds continu

219 In the olfactory epithelium (OE), odorant receptor stimulation

220 emonstrated a reduced number of cells in the olfactory epithelium (OE), resulting in a thinner neuron

221 S was expressed in developing neurons in the olfactory epithelium (OE), while in the adult its expres

222 ly controlled manner specifically within the olfactory epithelium (OE).

223 system, and they have also been observed in olfactory epithelium (OE).

224 ctivation of resident macrophages within the olfactory epithelium (OE).

225 to identify possible sources of apoE in the olfactory epithelium (OE).

226 tor, enzyme PLC140, are present in the squid olfactory epithelium (OE).

227 fluences neuron development in the postnatal olfactory epithelium (OE).

228 icantly to tissue regeneration in the murine olfactory epithelium (OE).

229 ate gyrus (DG), olfactory bulb (OB), and the olfactory epithelium (OE).

230 s, the horizontal basal cells (HBCs), in the olfactory epithelium (OE).

231 ially expressed in the developing and mature olfactory epithelium (OE): Axons elaborated by ventral a

232 but consistently through ventral and lateral olfactory epithelium (OE); and 3) projects to just two t

233 09 single cells from the retina and the main olfactory epithelium of adult and newborn mice.

234 ssessed the expression of this marker in the olfactory epithelium of adult mice.

235 The olfactory epithelium of fish contains three intermingled

236 ly, this analysis also revealed that, in the olfactory epithelium of Mash1-/- animals, there is an ov

237 A protein that is found in the main olfactory epithelium of mice ensures that odour-sensing

238 general systems and in the model system, the olfactory epithelium of mouse.

239 ed ribosome immunoprecipitation of mRNA from olfactory epithelium of odor-stimulated mice followed by

240 actory epithelium cultures, in the dissected olfactory epithelium of rodents, and in live conscious d

241 e of microvillous sensory neurons within the olfactory epithelium of zebrafish embryos.

242 ire olfactory system, driving neurons in the olfactory epithelium, olfactory bulb (OB), and cortex.

243 radon progeny Polonium-210 ((210)Po) in the olfactory epithelium, olfactory bulb, frontal lobe, and

244 Cadherin-2 is expressed in the olfactory epithelium, olfactory nerve, and olfactory bul

245 Here, we show that, in the mouse olfactory epithelium, olfactory receptor (OR) genes are

246 risingly, there was no evidence of PrP(d) in olfactory epithelium or olfactory nerve fascicles at any

247 expressing Cre in peripheral neurons of the olfactory epithelium or the retina reveals widespread, p

248 y bulb had higher (210)Po levels than either olfactory epithelium (p = 0.071), frontal lobe (p < 0.00

249 have found the expression of Ggamma13 in the olfactory epithelium, particularly in the cilia of the O

250 mixture information appears to occur in the olfactory epithelium prior to transmission of odor infor

251 Persistent neurogenesis in the olfactory epithelium provides a unique model to study ne

252 The continuous replacement of neurons in the olfactory epithelium provides an advantageous model for

253 That the stem cells of the olfactory epithelium reproduce the organization of the o

254 Neurogenesis in the zebrafish olfactory epithelium requires the bHLH proneural transcr

255 Olfactory sensory neurons (OSNs) in the main olfactory epithelium respond to environmental odorants.

256 Permanent zinc sulfate lesion of the olfactory epithelium resulted in a selective loss of the

257 ort of horseradish peroxidase applied to the olfactory epithelium revealed numerous axons of olfactor

258 ng to define a detailed map of the postnatal olfactory epithelium, revealing cell fate potentials and

259 n this preliminary study, RT-QuIC testing of olfactory epithelium samples obtained from nasal brushin

260 eaction showed that they were transcribed in olfactory epithelium (SORB, SORF, all SVR and Sasa CaSR

261 y aquatic larvae of Xenopus laevis, the main olfactory epithelium specialized for sensing water-borne

262 olfactory sensory neurons (OSNs) in the main olfactory epithelium starting from embryonic stage 11.5

263 harmacologically induced degeneration of the olfactory epithelium, suggesting that it is intrinsicall

264 nd olfactory sensory neuron formation in the olfactory epithelium, suggesting that the loss of CHD7 m

265 des induce large EOG responses in the rodent olfactory epithelium, suggesting that these compounds ac

266 suggests that olfactory receptor neurons and olfactory epithelium supporting cells may share a common

267 As a tissue of choice, we selected trout olfactory epithelium that has been previously suggested

268 ged into the adult "air nose," whereas a new olfactory epithelium, the adult "water nose," forms in t

269 urocrine tissues as diverse as the lens, the olfactory epithelium, the inner ear, the cranial sensory

270 of OAs with supporting cells throughout the olfactory epithelium, the lamina propria, the fila olfac

271 s are expressed in nearly all neurons of the olfactory epithelium, the vomeronasal organ, the septal

272 In the zebrafish olfactory epithelium, three morphologically distinct olf

273 e tuned the neurophysiologic response of the olfactory epithelium to ethanol odor at some expense to

274 ion of retroviral vectors into the embryonic olfactory epithelium to study the ORs' contribution to a

275 id cells provided a route of spread from the olfactory epithelium to TG neurons, while SSMs blocked s

276 now be obtained based on the global from the olfactory epithelium to the OB glomerular activity patte

277 ensory neurons (OSNs) project axons from the olfactory epithelium to the OB, where they form spherica

278 olfactory nerve (ON) and then grow from the olfactory epithelium to the olfactory bulb (OB), enter t

279 Axonal projections from the olfactory epithelium to the olfactory bulb are organized

280 These neurons extend their axons from the olfactory epithelium to the olfactory bulb located at th

281 veral subsystems that project axons from the olfactory epithelium to the olfactory bulb.

282 neurons (OSNs) project their axons from the olfactory epithelium toward the olfactory bulb (OB) in a

283 lso shown that air pollution can contact the olfactory epithelium, translocate to the olfactory bulb,

284 ion was also found in the developing retina, olfactory epithelium, trigeminal ganglion, and hair foll

285 ource external to the body and stimulate the olfactory epithelium upon inhalation through the nares (

286 re designed to enable direct delivery to the olfactory epithelium using a refillable nasal atomizer t

287 Moreover, within the main olfactory epithelium, v2r genes are expressed in a basal

288 ring development, expression of NCS-1 in the olfactory epithelium was localized in the dendritic knob

289 ature and mature OSNs coexisting in the same olfactory epithelium, we sought to use this unique syste

290 d as a spatial activation pattern across the olfactory epithelium, when odor is drawn into the nose t

291 ing odorant molecules to the portions of the olfactory epithelium where they are best detected.

292 tau aggregates in the Bowman's glands of the olfactory epithelium, which holds potential for an endos

293 The sense of smell is mediated by the olfactory epithelium, which is composed of a mosaic patt

294 I odorant receptors located in zone 1 of the olfactory epithelium, which projects to the dorsal aspec

295 periodontium, rostral periodontium, tongue, olfactory epithelium, whisker pads and brainstem.

296 n, which constitutes approximately 1% of the olfactory epithelium, will provide new insights into the

297 induces oxidative stress and inflammation in olfactory epithelium with concomitant effects on brain.

298 Chemical ablation of the olfactory epithelium with dichlobenil or physical separa

299 to facilitate the rapid repopulation of the olfactory epithelium with mature neurons during normal c

300 lots correlated loss of KLF7 activity in the olfactory epithelium with significant downregulation of