ライフサイエンスコーパス: ciliated

1 upregulated late, when most cells were fully ciliated.

2 y motility, and airways fail to become fully ciliated.

3 gets GFP to lipid rafts if the cells are not ciliated.

4 estor of bilaterians was probably a benthic, ciliated acoelomate worm with a single opening into an e

5 Using primary human ciliated airway epithelial (HAE) cell cultures, the only

6 or (CFTR) gene that is normally expressed in ciliated airway epithelial cells and the submucosal glan

7 tious virus could be used to deliver CFTR to ciliated airway epithelium derived from CF patients, we

8 pithelium, whereas the tracheal cells form a ciliated airway epithelium.

9 consisting mostly of a lumen layer of multi-ciliated and a layer of Keratin-5-positive basal cells.

10 termediate cells, reduced proportions of SAE ciliated and basal cells, markedly abnormal SAE and alve

11 suggest a role for beta-catenin in basal to ciliated and basal to Clara-like cell differentiation.

12 with wild type, and fewer basal stem cells, ciliated and Clara cells.

13 nt differentiation in vitro, generating both ciliated and goblet cell lineages.

14 cell is differentiated at a stage similar to ciliated and microvillous olfactory neurons.

15 H7N9) virus budded from the surfaces of both ciliated and mucin-secretory cells.

16 f Mks1 and Mks3 in IMCD3 cells induced multi-ciliated and multi-centrosomal phenotypes.

17 cell shape, cell density, and the pattern of ciliated and nonciliated cells did not occur in the peri

18 isted of a layered epithelium structure with ciliated and nonciliated cells on its apical surface.

19 differentiated airway epithelium composed of ciliated and nonciliated cells.

20 n to noncontiguous or small clumps of apical ciliated and occasional nonciliated epithelial cells, ap

21 axis globally, but the nature of this cue in ciliated and other epithelia remains poorly understood.

22 Clara cells, together with ciliated and pulmonary neuroendocrine cells, make up the

23 thelium of the lung is composed of polarized ciliated and secretory cells maintained by basal stem/pr

24 asal cells, the stem/progenitor cells of the ciliated and secretory cells that are central to pulmona

25 dostratified epithelium of the lung contains ciliated and secretory luminal cells and basal stem/prog

26 n lung are lined by an epithelium made up of ciliated and secretory luminal cells and undifferentiate

27 basal cell carcinomas (BCCs) are frequently ciliated, and we test the role of cilia in BCC by condit

28 nd release a majority of their HA onto their ciliated apical surfaces to form a heavy chain hyalurona

29 uprymna scolopes, resulting in regression of ciliated appendages similar to that triggered by infecti

30 n less regression of the infection-promoting ciliated appendages, leading to this propensity for supe

31 Ciliated ASI sensory neurons are required for TGF-beta-m

32 hmw is implicated in the motility of ciliated auditory sensory neurons and, in the testis, is

33 The trapezoidal ciliated band (CB) of the postgastrular sea urchin embry

34 m the stomodeal region of the oral ectoderm, ciliated band cells and cells from the endoderm/ectoderm

35 We also observe a reduction in the number of ciliated beta-cells along with misregulated ciliary/basa

36 yl receptor sequences of a type expressed on ciliated bronchial epithelial cells and on epithelia wit

37 Primary ciliated bronchial epithelial cells were exposed to 5% c

38 clusion bodies (ICI) have been identified in ciliated bronchial epithelium of Kawasaki disease (KD) p

39 activation of Bmp4 that inhibited Clara and ciliated, but not basal cell differentiation.

40 cumulate at the centrosome/basal body in non-ciliated, but not ciliated, cells.

41 e adenosine to signal in a paracrine faction ciliated cell A(2b) receptors to activate ion/water secr

42 e higher in WD-PBECs, coincident with higher ciliated cell contents, cell sloughing, and slightly com

43 norrhoeae contribute to the inflammation and ciliated cell death associated with gonorrhea and pelvic

44 induce inflammatory cytokine production and ciliated cell death in human fallopian tubes.

45 on after naphthalene-mediated Clara-like and ciliated cell depletion.

46 tment, while it's expression correlated with ciliated cell development and decreased along with incre

47 epithelial cell fate by inhibiting Clara and ciliated cell differentiation and activating Uchl1, a ma

48 airway epithelial cell fate, Fgf10 prevents ciliated cell differentiation and promotes basal cell di

49 mponents associated with either secretory or ciliated cell fate commitment.

50 ch acts when commitment to a ciliated or non-ciliated cell fate occurs in proximal progenitors, silen

51 ubsequently differentiate into secretory and ciliated cell lineages.

52 cell death, whereas H3N2 and EV-D68 induced ciliated cell loss and tissue integrity disruption.

53 increased mucous cell numbers and decreased ciliated cell numbers.

54 e grown to goblet or normally differentiated ciliated cell phenotype at air-liquid interface in the p

55 eceptors and to the transition zone in other ciliated cell types and that cilia are present in these

56 theoretical framework to conduct a census of ciliated cell types, create structural maps, and resolve

57 lene-mediated depletion of the secretory and ciliated cell types, the two basal cell pools coordinate

58 In most ciliated cell types, tubulin is modified by glycylation,

59 Importantly, ciliated cell-specific cAMP production (estimated by FRE

60 tein kinase (PKA) subunits expressed under a ciliated cell-specific promoter) in response to increase

61 re derived from mice expressing GFP from the ciliated-cell specific FOXJ1 promoter (FOXJ1:GFP).

62 (Aqp5 and Sftpc), Clara cells (Scgb1a1) and ciliated cells (Foxj1) in E18.5 lungs.

63 t eventually differentiate into post-mitotic ciliated cells .

64 By contrast, Il-6 null mice regenerate fewer ciliated cells and an increased number of secretory cell

65 e airway epithelial cell types, Clara cells, ciliated cells and basal cells, and activated UCHL1, a m

66 RVs, RSV-B, and HCoV-OC43 infected ciliated cells and caused no major cell death, whereas H

67 summarize current knowledge regarding airway ciliated cells and cilia, how they function to maintain

68 erentiating deep layer cell types, including ciliated cells and neurons.

69 on in both cultures was restricted to apical ciliated cells and occasional nonciliated cells but not

70 basal cell fate by driving the generation of ciliated cells and preventing the production of Clara-li

71 oid morphogenesis and the differentiation of ciliated cells and reduces the expression of both notch

72 e human influenza viruses primarily infected ciliated cells and replicated efficiently, whereas a hig

73 green fluorescent protein (GFP) to cilia of ciliated cells and targets GFP to lipid rafts if the cel

74 n of asymmetry-called Kupffer's vesicle (KV)-ciliated cells are asymmetrically positioned along the a

75 rectional non-cell-autonomous cues to orient ciliated cells as they differentiate, thus playing a cri

76 e human airway epithelium is the presence of ciliated cells bearing motile cilia, specialized cell su

77 it remained unclear how the distribution of ciliated cells becomes asymmetric during KV development.

78 ear and unambiguous evidence to suggest that ciliated cells can become goblet cells using immunoelect

79 V is asymmetric along the AP axis, with more ciliated cells densely packed into the anterior region.

80 ective ablation of CTNNB1 from the oviductal ciliated cells did not affect embryo transport, possibly

81 that govern the scattering of flagellated or ciliated cells from solid surfaces.

82 22G variants infected a higher proportion of ciliated cells in cultures of human airway epithelium th

83 Thus, motile ciliated cells in general might use a similar cellular c

84 ngth and with a reduction of the fraction of ciliated cells in Npc1-deficient mouse brains and the hu

85 onic development and contribute to Clara and ciliated cells in the adult lung.

86 n increase in mucous cells and a decrease in ciliated cells in the airway.

87 or different functions: basal, secretory and ciliated cells in the conducting airways and type II and

88 syncytial virus (RSV) naturally infects the ciliated cells in the human airway epithelium.

89 n protein is enriched in cytosolic puncta in ciliated cells in zebrafish embryos.

90 shape changes that mediate tight packing of ciliated cells into the anterior pole.

91 We also show that wild-type ciliated cells located at a mutant clone border reorient

92 response leads to the death and sloughing of ciliated cells of the Fallopian tube.

93 ion and motility specifically in a subset of ciliated cells of the mouse COA (posterior notochord, PN

94 Retinas and ciliated cells of these zebrafish morphants were analyze

95 To produce directed flow, ciliated cells orient along a common planar axis in a di

96 Gas8 knockdown in ciliated cells reduces Smo signaling activity and ciliar

97 ike epithelium with basal cells and immature ciliated cells surrounded by smooth muscle and myofibrob

98 urprisingly, we also found a region of multi-ciliated cells that line the posterior dorsal pole of th

99 only assembled in terminally differentiating ciliated cells through the acentriolar pathway to trigge

100 nds on secretory cells (club and goblet) and ciliated cells to produce and transport mucus.

101 ucted an RNAi-based screen in Drosophila non-ciliated cells to test for cilium-independent loss-of-fu

102 rock2b knockdown altered the AP placement of ciliated cells without affecting cilia number or length.

103 nstrate a direct conversion of club cells to ciliated cells without proliferation, meeting a conserva

104 almost exclusively expressed in a subset of ciliated cells, a strong indicator of cilia-related func

105 KIAA0556 is expressed almost exclusively in ciliated cells, and the worm and human KIAA0556 proteins

106 rn that appeared to originate primarily with ciliated cells, but lateral spread from the base of the

107 , structural and functional abnormalities of ciliated cells, decreased number of secretoglobin (SCGB1

108 protein is enriched in the apical domain of ciliated cells, in close proximity to the apical actin c

109 rate luminal cells, including differentiated ciliated cells, in the absence of stroma.

110 In ciliated cells, including bovine and Xenopus laevis rod

111 addition to using this homology to attach to ciliated cells, it activates human neonatal regulatory B

112 and lineage differentiation (ss-tubulin IV+ ciliated cells, MUC5AC+ goblet cells, p63 + basal cells)

113 on by smoke and alcohol was only observed in ciliated cells, not basal bronchial epithelium.

114 tube, gastrocoel roof plate, epidermal multi-ciliated cells, otic vesicles, and kidneys.

115 t CEP290 localizes to the transition zone in ciliated cells, precisely to the region of Y-linkers bet

116 the proximal region of cilia in dividing and ciliated cells, respectively.

117 ss of club cells, with a concomitant gain in ciliated cells, under homeostatic conditions without inc

118 amphioxus frontal eye is composed of simple ciliated cells, unlike vertebrate rods and cones, which

119 In ciliated cells, we observe localization of recombinant C

120 (alpha2,6-linked) receptors predominated on ciliated cells, whereas avian-like (alpha2,3-linked) rec

121 ylases ccp2, ccp5, and ccp6 are expressed in ciliated cells, whereas ccp1 expression is restricted to

122 and showed airways populated essentially by ciliated cells, with an increase in neuroendocrine cells

123 docking during the differentiation of airway ciliated cells.

124 ted view of planar polarization of the brain ciliated cells.

125 al body of primary cilia in human and murine ciliated cells.

126 e show that two PCP signals are operating in ciliated cells.

127 reas its ligand EGF is induced by smoking in ciliated cells.

128 process causes an increase in the number of ciliated cells.

129 t proteins B and C, without affecting airway ciliated cells.

130 t cell metaplasia, and the loss of Clara and ciliated cells.

131 ury, PNECs can contribute to Clara cells and ciliated cells.

132 ed with the expression of ttll3 and ttll6 in ciliated cells.

133 with generation of differentiated Clara and ciliated cells.

134 ith the normal AP asymmetric distribution of ciliated cells.

135 14ECs) function as progenitors for Clara and ciliated cells.

136 to DNA damage when compared with neighboring ciliated cells.

137 y receptors Sstr5 and Htr7, respectively, in ciliated cells.

138 h was previously thought to contain only non-ciliated cells.

139 d ciliary length and a reduced percentage of ciliated cells.

140 ing of ciliogenesis, and the accumulation of ciliated cells.

141 o samples of live human bronchial epithelial ciliated cells.

142 nal differentiation program and convert into ciliated cells.

143 d produce differentiated secretory cells and ciliated cells.

144 he other expresses c-myb and directly yields ciliated cells.

145 ntrosome/basal body in non-ciliated, but not ciliated, cells.

146 al microscopy on stained sections visualized ciliated chondrocytes.

147 lB exhibit dysfunction in sperm flagella and ciliated dendrites of chordotonal organs that mediate he

148 rosine hydroxylase immunoreactive) that bore ciliated dendrites penetrating the epithelium.

149 velopment, Notch signaling occurs within the ciliated, differentiating cells of the first few supraba

150 component of the horizontal velocity at the ciliated edge generates a 2D fluid velocity field with a

151 The coordinated movement of the ciliated edge is represented as a continuous envelope im

152 g the micro-bead velocity measurement at the ciliated edge.

153 to the fluid at a finite distance above the ciliated edge.

154 Ciliated endings display neuron-type-specific patterns o

155 ntial polycystin (TRPP) complex localizes to ciliated endings of C. elegans male-specific sensory neu

156 istinct, neuron-type-specific elaboration of ciliated endings of different olfactory neuron types in

157 OIG-8 protein localizes to ciliated endings of these sensory neurons, and is transc

158 se hydrocephalus or prevent the formation of ciliated ependymal cells but caused defects in their dif

159 that Prdm16 is required for the formation of ciliated ependymal cells in the lateral ventricle.

160 This and their ciliated epidermis have led some to propose relationship

161 identified a role for Lgl2 in development of ciliated epithelia in Kupffer's vesicle, which directs l

162 ted fluid flow, as seen, for example, in the ciliated epithelia lining the respiratory airways or the

163 ed mucus along the light organ's superficial ciliated epithelia.

164 dy, we have defined such a program for multi-ciliated epithelial cells (MCCs), a cell type critical f

165 We also demonstrate that sinonasal ciliated epithelial cells express T2R14, which closely c

166 ues confirmed down-regulation of Duox in the ciliated epithelial cells lining the respiratory tract.

167 Virus replication was not observed in ciliated epithelial cells of the trachea.

168 Both macrophages and ciliated epithelial cells respond to infection by releas

169 mprising the majority of the cells, includes ciliated epithelial cells, newly identified lipophil cel

170 r by activation of phospholipase C in native ciliated epithelial cells.

171 tor critical for ciliogenesis, and a loss of ciliated epithelial cells.

172 ry response and bacterial adherence to human ciliated epithelial cultures and markedly increased viru

173 find that cobl shows enriched expression in ciliated epithelial tissues during zebrafish organogenes

174 CT) can be used to investigate injury to the ciliated epithelium in a multi-contrast setting.

175 patterning, but how this is achieved in any ciliated epithelium is unknown.

176 Here we used the ciliated epithelium of the planarian Schmidtea mediterra

177 ol to investigate injury and regeneration in ciliated epithelium.

178 ss attention has been given to injury of the ciliated epithelium.

179 capable of infecting healthy and COPD human ciliated epithelium.

180 f Dvl1, Pk2 and Vangl1 in a planar polarized ciliated epithelium.

181 To define properties of a ciliated EV-releasing cell, we performed RNA-seq on 27 G

182 d tissue M cells appear to be generated from ciliated Foxj1(+)PGRP-S(+) cells, indicative of a possib

183 ned by subtraction of the profile of the non-ciliated GFP- cells.

184 t, CaMK-II suppression results in additional ciliated hair cells and altered levels of Delta-Notch si

185 When expressed in ciliated hTERT-RPE1 human cell line, P/rd is localized t

186 ically, we found that LZTFL1 is expressed in ciliated human bronchial epithelial cells (HBECs) and it

187 rod photoreceptors using a transgene and in ciliated IMCD3 cells.

188 suggest a link between AP patterning of the ciliated Kupffer's vesicle and LR patterning of the zebr

189 e melanosome transport and disruption of the ciliated Kupffer's vesicle.

190 We propose a renewed effort to adopt ciliated land plants as models to investigate the mechan

191 uch coordination is achieved, we studied the ciliated larvae of Platynereis dumerilii, a marine annel

192 Transgenic reintroduction of Ptk7 in motile ciliated lineages prevents scoliosis in ptk7 mutants, an

193 planktonic predators also have sophisticated ciliated locomotion, behaviour and distinct development.

194 d 7 of these 22 genes with expression in the ciliated LR organizer (gastrocoel roof plate), a marked

195 er monocytes and macrophages (LysM/STAT1) or ciliated lung epithelial cells (FoxJ1/STAT1) deleted wer

196 ytes (neurosensory cells) and in statocytes (ciliated mechanosensory cells) of C. hemisphaerica, a me

197 recorded a mechanosensitive conductance in a ciliated mechanosensory neuron in vivo.

198 of ARL2BP localization at the basal body in ciliated nasal epithelial cells.

199 In the core ciliated nervous system of both males and hermaphrodites

200 Here, we show that pheromones sensed by ciliated neurons in the Caenorhabditis elegans nose alte

201 The Ciona PPE is shown to produce ciliated neurons that express genes for gonadotropin-rel

202 while DYF-11 is expressed in all C. elegans ciliated neurons, CHE-12 expression is restricted to som

203 rograms the sensory functions of a subset of ciliated neurons, independent of daf-19c.

204 involved in the development and function of ciliated neurosensory organs.

205 TTA37, V1171, and McGHS1 bind principally to ciliated NHBE cells and that their corresponding hag mut

206 y unidentified tropism of M. catarrhalis for ciliated NHBE cells.

207 irst report linking connexin function in the ciliated, node-like cells of KV with normal L-R axis dev

208 olfactory epithelium is mostly populated by ciliated olfactory sensory neurons (OSNs) and surroundin

209 suggest that Notch acts when commitment to a ciliated or non-ciliated cell fate occurs in proximal pr

210 ra cell differentiation but had no effect on ciliated or pulmonary neuroendocrine cells.

211 amb1a functions in Kupffer's vesicle (KV), a ciliated organ analogous to the mouse node, to control t

212 c fluid flow in the evolutionarily conserved ciliated organ of asymmetry (COA) and play a fundamental

213 h cell-autonomous functions in the zebrafish ciliated organ of asymmetry, Kupffer's vesicle (KV), inc

214 s7 knockdown both disrupt the formation of a ciliated organ, the Kupffers vesicle (KV), but do not di

215 Using Kupffer's vesicle as a model ciliated organ, we found that depletion of Lgl2 disrupte

216 Nearly every ciliated organism possesses three B9 domain-containing p

217 This can be a vital advantage for ciliated organisms and may be interesting to guide biolo

218 ary cilium, BBIP10 is present exclusively in ciliated organisms, and depletion of BBIP10 yields chara

219 is universally and exclusively conserved in ciliated organisms, and is required for the acetylation

220 IFT25, however, is absent from some ciliated organisms, suggesting that it may have a unique

221 y all the centrin-containing flagellated and ciliated organisms.

222 nd basal body duplication in flagellated and ciliated organisms.

223 receptor, was highly expressed in zebrafish ciliated organs and regulated ciliary structure and func

224 In zebrafish, tuba was expressed in multiple ciliated organs, and, accordingly, tuba start and splice

225 nockout, we also observed defects in several ciliated organs, including the brain (hydrocephalus), he

226 larvae 2 (lgl2) is expressed prominently in ciliated organs.

227 cells and is associated with a reduction in ciliated, ostensibly proliferation-suppressed beta cells

228 s highlighted a significantly lower level of ciliated patient cells compared to controls, confirming

229 eptor protein common to both rhabdomeric and ciliated photoreceptor cells, Prominin.

230 rominin is conserved between rhabdomeric and ciliated photoreceptor cells.

231 ays paralleling retinal degeneration seen in ciliated photoreceptors.

232 ccurs in proximal progenitors, silencing the ciliated program in the cells that will continue to expa

233 First, it is hosted by a ciliated protist, Euplotes; bacterial symbionts of cilia

234 n of cilium length, a phenomenon observed in ciliated protists [3, 4], has not been well-characterize

235 Yet, some ciliated protists do not have IFT components and, like s

236 Ciliated protists exhibit nuclear dimorphism through the

237 Moreover, various ciliated protists lack TZ components, whereas Drosophila

238 Ciliated protozoa are peculiar for their nuclear dimorph

239 zoal grazing due to the higher inhibition of ciliated protozoa as compared to bacteria when exposed t

240 Ciliated protozoa extensively remodel their somatic geno

241 Genome duality in ciliated protozoa offers a unique system to showcase the

242 Ciliated protozoa possess cellular axes reflected in the

243 rited characters are especially prominent in ciliated protozoa, in which parental noncoding RNA molec

244 pression, displays a novel mode of action in ciliated protozoa.

245 a (Escherichia coli (E. coli)) as a prey and ciliated protozoan (Paramecium caudatum) as a predator o

246 otably, unlike the heart-shaped structure of ciliated protozoan Oxytricha nova TEBPalpha-beta complex

247 ciated with the photoreceptor protein of the ciliated protozoan Stentor coeruleus (Heterotrichea; Ste

248 The giant ciliated protozoan Stentor coeruleus is re-emerging as a

249 process of programmed DNA elimination in the ciliated protozoan Tetrahymena Here, we show that the he

250 to detect and semi-quantify these NPs in the ciliated protozoan Tetrahymena thermophila as a model aq

251 ptionally active somatic macronucleus in the ciliated protozoan Tetrahymena thermophila.

252 l RNAs during the sexual reproduction of the ciliated protozoan Tetrahymena.

253 , its presence in Tetrahymena thermophila, a ciliated protozoan with seven sexes or mating types that

254 raction of Vorticella convallaria, a sessile ciliated protozoan, is completed within a few millisecon

255 Ciliated protozoans perform extreme forms of programmed

256 utionary analysis of centromeric histones in ciliated protozoans, a group that only undergoes asymmet

257 In ciliated protozoans, small RNAs (sRNAs) are integral to

258 In ciliated protozoans, small-RNA-mediated comparison of th

259 ganisms (rotifers) through dietary uptake of ciliated protozoans.

260 interactions were only evident at sites with ciliated pseudostratified columnar epithelium.

261 t infiltration than everolimus and preserved ciliated pseudostratified columnar respiratory epitheliu

262 ensitive to light has been the presence of a ciliated putative sensory cell in the close vicinity of

263 Here, we confirmed the presence of a ciliated region near the Eustachian tube orifice at the

264 rate Ccdc135 (E = 6e-78) highly expressed in ciliated respiratory epithelia and sperm, and to FAP50 (

265 Human ciliated respiratory epithelial cell cultures were infec

266 Viral antigens were localized to ciliated respiratory epithelium and cells of submucosal

267 c obstructive pulmonary disease (COPD) human ciliated respiratory epithelium was determined.

268 It specializes in infection of the ciliated respiratory epithelium, causing disease of vari

269 transcript expression in testis compared to ciliated respiratory epithelium.

270 centrosome and cilia number, including multi-ciliated respiratory-like epithelia, and longer cilia.

271 ymal layer, the node precursors form several ciliated rosette-like clusters; they then rapidly underg

272 Clara cells are non-ciliated, secretory bronchiolar epithelial cells that se

273 that two types of neuron, the amphid single-ciliated sensory neuron type K (ASK) and the male-specif

274 Here, we report that the ciliated sensory neurons (CSNs) of C. elegans express th

275 The daf-19c isoform is expressed in all ciliated sensory neurons and is necessary and sufficient

276 and that, in Drosophila, hmw is expressed in ciliated sensory neurons and spermatozoa.

277 the epidermis, intestine, body wall muscle, ciliated sensory neurons and touch receptor neurons - wh

278 lution transcriptome profile of a subtype of ciliated sensory neurons isolated from adult animals rev

279 for the undulation propagation and that the ciliated sensory neurons participated in the joint selec

280 w here that specific Caenorhabdidits elegans ciliated sensory neurons shed and release ECVs containin

281 avoidance behavior, which requires a pair of ciliated sensory neurons, the BAG neurons.

282 Photoreceptors are complex ciliated sensory neurons.

283 OFIP protein, whose sequence is conserved in ciliated species, associates with centrosome/centriole a

284 d these proteins are highly conserved across ciliated species.

285 at a transient left-right organizer (LRO), a ciliated structure where cilia play a crucial role in br

286 Developing hair cells were ciliated, suggesting that ciliogenesis was largely norma

287 verlapping domains at the apical membrane of ciliated surface cells.

288 Ciliated surfaces harbouring synchronously beating cilia

289 naive mice and were observed on their apical ciliated surfaces.

290 ovel evidence for the existence of mixing in ciliated systems, and we demonstrate that the directed t

291 s, and cilia motility is lost in a number of ciliated tissues along with a reduction in the number of

292 x2 in Xenopus is expressed preferentially in ciliated tissues, including neural tube, gastrocoel roof

293 ex members are primarily expressed in motile ciliated tissues, suggesting a conserved function in mam

294 P3 are highly regulated proteins confined to ciliated tissues.

295 tionally activated during PCP acquisition in ciliated tissues.

296 tial engagement of microbial symbionts along ciliated tissues.

297 nalling or apical docking of basal bodies in ciliated tracheal epithelial cells.

298 o and in vitro yielded basal, goblet, Clara, ciliated, type I and type II alveolar epithelial cells.

299 ep290(ko/ko) mice lack connecting cilia, and ciliated ventricular ependyma fails to mature.

300 Stat3 inhibitors reduced, the generation of ciliated vs. secretory cells from basal cells.