ライフサイエンスコーパス: glandular

1 nts presented with ulceroglandular (37%) and glandular (25%) forms of tularemia, followed by pneumoni

2 rafts at the apical membrane of surface and glandular airway epithelium.

3 TSC values in normal glandular and adipose breast tissue were 35 mmol/kg +/-

4 tion has been further investigated, both for glandular and extraglandular manifestations of the disea

5 SIgA is transported across glandular and mucosal epithelial cells into external sec

6 t for the similar gene networks found in the glandular and respiratory organs of both insects and cru

7 st squares mean ADCs (x 10(-3) mm(2)/sec) in glandular and stromal benign prostatic hyperplasia were

8 were measured in transition zone cancers and glandular and stromal benign prostatic hyperplasia.

9 g allowed clear visualization of endometrial glandular and stromal regions within tissue samples.

10 hospholipid composition compared with normal glandular and stromal tissue.

11 ) is a pathologic proliferation of prostatic glandular and stromal tissues; a variety of growth facto

12 s a progressive age-related proliferation of glandular and stromal tissues; various growth factors an

13 nduction of chemoattractants, cytokines, and glandular apoptosis in males and females.

14 Disruption of glandular architecture associates with poor clinical out

15 ve invasion while retaining their epithelial glandular architecture with an inward apical pole deline

16 cal data analysis applied to prostate cancer glandular architecture.

17 ds with hollow lumen, which resembles normal glandular architectures in vivo.

18 rity, reticular basement membrane thickness, glandular area, expression of markers of activation of a

19 Glandular atrophy and a positive CagA status are determi

20 t solid glandular structures and evidence of glandular atrophy and necrotizing vasculitis.

21 , two methylation markers (MYOD1 and RUNX3), glandular atypia, and TP53 mutation status.

22 th high classification accuracy consisted of glandular atypia, P53 abnormality, and Aurora kinase A p

23 n between an animal's olfactory cues and its glandular bacterial communities.

24 ensions system, the MGD for a 5-cm-thick 50% glandular breast is 2.50 mGy, which is less than the Mam

25 Distinguishing tumor from normal glandular breast tissue is an important step in breast-c

26 ether they affect (18)F-FDG uptake in normal glandular breast tissue.

27 iated with an altered migration pattern from glandular buds (cellular aggregates) to epithelial cell

28 Many human glandular cancers metastasize along nerve tracts, but th

29 to the impairment of acinar cells, the major glandular cells of protein, salt secretion, and fluid mo

30 Abnormalities were defined as atypical glandular cells, atypical squamous cells of undetermined

31 t for focal active colitis with regenerative glandular changes and neural hyperplasia.

32 tween the epithelium and Brunner glands with glandular coexpression of ErbB2, which is normally restr

33 ue fibers, with minimal presence of fatty or glandular components.

34 modalities for breasts of varying sizes and glandular compositions.

35 numbers of stem cells located in the base of glandular crypts.

36 In Sjogren's Syndrome (SS), inherent glandular defects, autoimmunity, and mononuclear cell in

37 ons such as Sjogren's syndrome can result in glandular destruction and hyposalivation.

38 rk that is important for single cells during glandular development and the early stages of breast can

39 e was unable to inhibit neonatal endometrial glandular development in Wnt7a-Cre(+)PR(f/-) mice.

40 signaling pathways, which play key roles in glandular development, branching and homeostasis.

41 (i.e., micropapillary, sarcomatoid, squamous/glandular differentiation, etc.), management guidelines

42 For squamous/glandular differentiation, nested variant, and other rar

43 the genomic program associated with prostate glandular differentiation, we identified acini-like PCA

44 ecular processes that can promote epithelial glandular disruption.

45 ectra models to compute and compare the mean glandular dose (MGD) resulting from both imaging modalit

46 Mean glandular dose for DR photon counting was significantly

47 The average glandular dose for screening examinations was 1.49 mGy.

48 The mean glandular dose for the breast simulated by 4.5 cm of PMM

49 The average glandular dose was 39% lower in s2D/DBT versus digital m

50 Mean glandular dose was calculated for DR photon counting and

51 The mean glandular dose was estimated to be in the range of 1.8-2

52 MATERIAL/METHODS: Image quality and mean glandular doses were measured and compared for 47 mammog

53 the mouse uterus increased both uterine horn/glandular duct dilation and hydrosalpinx.

54 at the uterine horn dilation correlates with glandular duct dilation detected microscopically followi

55 ss, the chlamydial induction of uterine horn/glandular duct dilation may be used to evaluate plasmid-

56 t required for the induction of uterine horn/glandular duct dilation.

57 the number of cross sections of the dilated glandular ducts counted under microscopy.

58 The dilated glandular ducts pushed the uterine horn lumen to closure

59 leading to inflammation and dilation of the glandular ducts.

60 but not PI3K modulators, rescued colorectal glandular dysmorphogenesis of PTEN deficiency.

61 gs is produced by a combination of lymph and glandular emission, with pigmentary cell filtering in th

62 ndantly expressed in the uterine luminal and glandular epithelia as well as in the conceptus trophect

63 Many glandular epithelia develop from multipotent basal stem

64 Glandular epithelia, including the mammary and prostate

65 luding the functionally distinct luminal and glandular epithelia, to maintain uterine cycling.

66 contribute to a loss of tissue structure in glandular epithelia.

67 box A2 (FOXA2) is uniquely expressed in the glandular epithelial (GE) cells of the uterus, and condi

68 icrobes interact with host mucins lining the glandular epithelial cells and trigger inflammation.

69 We used glandular epithelial cells in a three-dimensional cultur

70 nderstand how HCMV is replicating within the glandular epithelial cells so that it might be possible

71 Chlamydial infection was detected in the glandular epithelial cells, potentially leading to infla

72 ymphocytes, autoantibodies, interferons, and glandular epithelial cells.

73 in the intersection zone between luminal and glandular epithelial compartments.

74 is essential to maintain lineage fidelity in glandular epithelial stem cells.

75 herpesvirus that persistently replicates in glandular epithelial tissue.

76 gene expression profile of a human prostate glandular epithelial tissue.

77 ds of the uterus and a critical regulator of glandular epithelium (GE) differentiation, development,

78 ribution of alpha6beta4E within normal human glandular epithelium and its regulation and effect on ce

79 Virus replicated in glandular epithelium and lymphatic endothelium in the de

80 loss of the entire endometrium (luminal and glandular epithelium and stroma) and inner circular but

81 wild-type control mice, and the fraction of glandular epithelium in lesions from Tgfb1-null mice was

82 ke spheroids that mimic numerous features of glandular epithelium in vivo, such as acinar morphogenes

83 unique localization of mast cells within the glandular epithelium of NPs and showed that mast cells i

84 all the 3 proteases were abundant within the glandular epithelium of NPs but were not found in normal

85 and migrates along the apical surface of the glandular epithelium toward the proximal end of the glan

86 like structures, including organized luminal/glandular epithelium, stroma, vascularized mucosa and tw

87 osed mice were posteriorized and had reduced glandular epithelium.

88 l cysts comprise the structural units of the glandular epithelium.

89 mation ability and transformation of the SCJ glandular epithelium.

90 gulation of cellular polarity of endometrial glandular epithelium.

91 d CD8(+) T and CD21(+) B lymphocytes but not glandular epithelium.

92 hread cells during the transition from thick glandular exudate to ultradilute material.

93 lls, increased symmetric stem cell division, glandular fission, and more rapid stem cell lineage trac

94 s well as unstimulated whole- and stimulated glandular flow rates (P < 0.05).

95 Aside from its activity in promoting glandular fluid secretion, however, it is unclear whethe

96 3R) plays a pivotal role in the induction of glandular fluid secretions.

97 processes including tissue morphogenesis and glandular formation.

98 a compressed thickness of 6.0 cm and a 14.3% glandular fraction, a DBT acquisition resulted in an 83%

99 h a compressed thickness of 5.0 cm and a 50% glandular fraction, a DBT acquisition resulted in an onl

100 explore the pathogenic mechanisms related to glandular function, microbial and immune parameters in t

101 Intercellular communication is essential for glandular functions and tissue homeostasis.

102 tion, leaving the forestomach almost intact (glandular gastrectomy [GG]) and compared subsequent meta

103 ompletely eliminates estrogen production, on glandular gene expression and histology in male and fema

104 The glandular hairs of the fossils are restricted to the lea

105 rity field is provided by the orientation of glandular hairs on the inner surface of the trap.

106 on in transgenic N. tabacum was localized to glandular heads.

107 ption factor is a master regulator of normal glandular homeostasis in the prostate, as well as growth

108 To determine whether altered glandular homeostasis occurs before the onset of autoimm

109 diverse plants, yet their interactions with glandular hosts rarely are incorporated into broad ecolo

110 artments, which alters turnover kinetics and glandular hyperplasia.

111 e to study unstimulated whole and stimulated glandular (i.e., parotid and submandibular) saliva flow

112 NK cells also modulated the type of glandular inflammation after infection, as they prevente

113 Dysfunction occurred before glandular inflammation, suggesting that a soluble mediat

114 o subsets with distinct disease activity and glandular inflammation.

115 e-tracing experiments with a model of severe glandular injury in the mouse submandibular gland, we sh

116 ized defect in the production and release of glandular innate defense molecules.

117 Although glandular inversion in epithelial tumors is thought to b

118 n (HSA) and 8-fold increase versus the human glandular kallikrein 2 (hK2).

119 cantly more highly-expressed in EAC, SCC and glandular lesions than in SE and more in EAC than in BE

120 of its association with difficult-to-detect glandular lesions.

121 esolution of modern imaging may characterize glandular level differences between malignant and benign

122 e discovered additional changes in aging, as glandular-like epithelial invaginations (GLEIs) derived

123 , highly branched, and poorly differentiated glandular-like structures in Matrigel.

124 in vitro model system to study UDH biology, glandular lumen formation, and stem cell biology of the

125 revealed by correlations with levels of the glandular marker lactoferrin.

126 displayed high expression of epithelial and glandular markers and a unique fingerprint of open chrom

127 Glandular mast cells and the diverse subsets of mast cel

128 nds, in situ, PKC-alpha redistributed across glandular membrane compartments and underwent a rapid an

129 tion of mutualism between meerkats and their glandular microbiota.

130 PTEN controls three-dimensional (3D) glandular morphogenesis by coupling juxtamembrane signal

131 f lumen formation in a 3D model of human CRC glandular morphogenesis.

132 tivation, mitotic spindle orientation and 3D glandular morphogenesis.

133 The tumor cells had a glandular morphology, similar to human intestinal-type g

134 high expression occurred more frequently in glandular mucosa with or without dysplasia than in squam

135 jects and demonstrate MUC19 glycoproteins in glandular mucous cells and saliva.

136 In three patients with glandular necrosis, the density of iodine was 1.53mg/ml.

137 In glandular organs, tubulogenesis is a multistep process r

138 ortance of ARF6 as a critical determinant of glandular orientation and the matrix environment in dict

139 This inversion of glandular orientation is accompanied by Rac1 inactivatio

140 t with cholesterol-lowering statins switches glandular pancreatic carcinomas to a basal (mesenchymal)

141 pler study of the spermatic cord vessels and glandular parenchyma.

142 alivary glands, as well as new insights into glandular pathobiology.

143 toantibody responses can be dissociated from glandular pathology.

144 uency ultrasound was used to facilitate deep glandular penetration of the nanoshells.

145 s, reticular basement membrane thickness, or glandular percentage area was observed between PAR and h

146 the natural compound isolated from perianal glandular pheromone secretion of the African civet cat.

147 In the first synthesis of relationships with glandular plants for any insect family, we review mirid

148 enic cues and signaling pathways that govern glandular polarity and organization.

149 n rats that resects approximately 80% of the glandular portion, leaving the forestomach almost intact

150 yosis, and between normal and mixed squamous/glandular pre-invasive and adenocarcinoma cervical lesio

151 screen-film mammography involve average mean glandular radiation doses of 3.7 and 4.7 mGy, respective

152 eleased in the vicinity of the gland, act on glandular receptors, and influence the production, secre

153 e cancer, cabazitaxel treatment induced MET, glandular redifferentiation, and AR nuclear localization

154 Glandular regeneration following a near complete loss of

155 bine to suppress the cancer phenotype during glandular regeneration.

156 controlling epithelial morphogenesis during glandular repair or regeneration.

157 n a multicenter prospective study, whole and glandular saliva were collected both before and 5 mo aft

158 hiolar SCPC niches, we hypothesized that the glandular SCPC niche may be dysfunctional in CF.

159 esis, CFTR-deficient mice failed to maintain glandular SCPCs following airway injury.

160 Plant glandular secreting trichomes are epidermal protuberance

161 Glandular secreting trichomes on the surface of tomato p

162 Increased cholesterol in the glandular secretion has been postulated to be necessary

163 nance imaging, we monitored stimulus-coupled glandular secretion into the flytrap.

164 needed to store sperm, while a non-canonical glandular secretion stimulates ovulation.

165 Royal jelly and other glandular secretions are the primary food of growing lar

166 viparity (maternal nourishment of progeny by glandular secretions followed by live birth).

167 eproductive tract signals to the ovary using glandular secretions, and that this pathway has been con

168 and stromal tissue growth as well as reduced glandular secretory activity of the lesions.

169 This was mainly because of an increased glandular secretory activity, whereas cell proliferation

170 GUS expression was exclusively localized to glandular secretory trichomes (GSTs) of leaf primordia a

171 est that the specialized subapical cavity of glandular secretory trichomes functions as a location fo

172 iterpene lactone produced by Artemisia annua glandular secretory trichomes, is the active ingredient

173 uction of the two compounds is restricted to glandular sepal tips; thus, differential expression anal

174 trong correlation between a novel measure of glandular shape and grade of the tumour.

175 terizing four adult stem cell populations of glandular skin, we show that they display distinct regen

176 Our findings provide insight into glandular stem cells and a framework for the further stu

177 Gene expression profiles in glandular stomach of the mice were investigated by oligo

178 These data suggest that at least in rat, the glandular stomach plays a central role in the improvemen

179 ivation in epithelial precursor cells of the glandular stomach, providing a new conditional model of

180 Ptf1a(EDD) converted essentially the entire glandular stomach, rostral duodenum and extrahepatic bil

181 al salivary gland homeostasis and during the glandular stress responses of therapeutic radiation, duc

182 ermination of apical polarity in live breast glandular structures (acini) produced in three-dimension

183 sease with autoantibodies against most solid glandular structures and evidence of glandular atrophy a

184 jones and other monoterpenoids accumulate in glandular structures in the foliage of WRC.

185 initial step in this process is the loss of glandular structures in the gastric mucosa, presumably a

186 vel, whereas that of 6 glands and 7 putative glandular structures is completely unknown.

187 ally indistinguishable from colorectal tumor glandular structures used by pathologists to grade tumor

188 ot only stall tumor growth, but also induces glandular structures with marked expression of CDX2, a t

189 letely unknown for 6 glands, for 10 putative glandular structures, and for the exocrine component of

190 n multipotency to produce de novo ductal and glandular structures, but that these can retain their id

191 e and -promoting functions within individual glandular structures.

192 ithelium of NPs but were not found in normal glandular structures.

193 ned by morphology and degree of formation of glandular structures.

194 neural network designed for segmentation of glandular structures.

195 e epithelial cells separate into luminal and glandular subtypes.

196 of fibrous connective tissue (CT) and fatty/glandular tissue (FGT) is currently unknown and is histo

197 Prominent preneoplastic changes in glandular tissue adjacent to these tumors occurred only

198 ) were calculated and correlated for healthy glandular tissue and benign and malignant lesions.

199 y do not address the regeneration of mammary glandular tissue and have been associated to the increme

200 re able to distinguish adipose, stromal, and glandular tissue based on their metabolomic fingerprint.

201 method of imaging mammary glands with higher glandular tissue content.

202 tive kinetic curve data), absolute ADCs, and glandular tissue-normalized ADCs were included in multiv

203 lial polarity and the formation of lumens in glandular tissues during morphogenesis.

204 Glandular tissues form ducts (tubes) and acini (spheres)

205 Tumor development in glandular tissues is associated with structural alterati

206 ons and is highly expressed in secretory and glandular tissues, especially in steroidogenic cells.

207 ithelial polarity and formation of lumens in glandular tissues.

208 This problem is mainly caused by the glandular trichome (GT)-specific biosynthesis of artemis

209 ults are consistent with the hypothesis that glandular trichome acylsugar acetylation is under select

210 ximum biomass correspondingly, while a large glandular trichome density was recorded for J1.

211 detailed knowledge on, the biology of plant glandular trichome development and metabolism will gener

212 erstanding of the transcriptional control of glandular trichome initiation and development is still i

213 es are preferentially expressed in secreting glandular trichome types 1 and 4 and to a lesser degree

214 wild Solanum species: Solanum lycopersicum (glandular trichome types 1, 6, and 7), Solanum habrochai

215 fferences in and between Solanum species and glandular trichome types are likely determined by the re

216 ce, leading to the conclusion that these two glandular trichome types are the same and differ perhaps

217 Several glandular trichome types express genes associated with p

218 aracterize the differences between different glandular trichome types in several domesticated and wil

219 cultivar, and demonstrating the utility of a glandular trichome-specific promoter to increase express

220 brid screens with this fragment identified a glandular trichome-specific transcription factor, design

221 7-fold, respectively, harboring 5-fold more glandular trichomes (as determined by rhodamine B staini

222 Here, we show that secreting glandular trichomes (designated types 1 and 4) and stora

223 in specialized anatomical structures called glandular trichomes (GTs).

224 Sticky plants-those having glandular trichomes (hairs) that produce adhesive, visco

225 homes (designated types 1 and 4) and storage glandular trichomes (type 6) on the leaf surface of wild

226 A model is proposed on how glandular trichomes achieve high metabolic productivity.

227 etone biosynthesis occurs in the plastids of glandular trichomes and begins with intermediates of de

228 s, proteomics, and (13)C-labeling of type VI glandular trichomes and leaves from a cultivated (Solanu

229 ed transcripts of two genes expressed in the glandular trichomes and showed that they encode enzymes

230 monstrating high-flux plasticity in A. annua glandular trichomes and their potential as factories for

231 which display preferential expression in the glandular trichomes and thereby seem to be potential can

232 Glandular trichomes are currently known only to store mo

233 Multicellular glandular trichomes are epidermal outgrowths characteriz

234 Glandular trichomes are metabolic cell factories with th

235 Glandular trichomes are specialized anatomical structure

236 The findings demonstrate that plant glandular trichomes can selectively secrete in a basipet

237 y may be involved in recycling metabolic CO2 Glandular trichomes cope with oxidative stress by produc

238 aporation of the liquid content of the small glandular trichomes covering fruits and leaves surfaces

239 We analyzed the transcriptome of glandular trichomes from female cannabis flowers, which

240 Glandular trichomes from tomato (Solanum lycopersicum) a

241 Terpene biosynthesis in tomato glandular trichomes has been well studied, with most if

242 o saliva with increased densities of Type VI glandular trichomes in newly emerged leaves.

243 to tap the largely unexploited potential of glandular trichomes in plant resistance to pests and lea

244 A key and unique feature of glandular trichomes is their ability to synthesize and s

245 Type VI glandular trichomes isolated from od-2 leaves accumulate

246 enes and proteins expressed in leaf and stem glandular trichomes of 3-week-old plants.

247 screen of volatile terpene production in the glandular trichomes of 79 accessions of Solanum habrocha

248 The capitate-stalked glandular trichomes of Cannabis sativa (cannabis), situa

249 Glandular trichomes of cultivated tomato (Solanum lycope

250 ssion of the ShZIS and zFPP synthases in the glandular trichomes of cultivated tomato resulted in the

251 We isolated over 8,000 ESTs from the glandular trichomes of L. x intermedia flowers (where bu

252 ose backbones that are produced in secretory glandular trichomes of many solanaceous plants, includin

253 nd gene regulatory networks operating in the glandular trichomes of N. tabacum are of pivotal signifi

254 ation of metabolism and/other aspects in the glandular trichomes of N. tabacum The glandular trichome

255 with the primary metabolism are modulated in glandular trichomes of N. tabacum, providing a plausible

256 specially regulatory genes expressing in the glandular trichomes of N. tabacum.

257 ondary metabolism and gene expression in the glandular trichomes of N. tabacum.

258 in the regulation of gene expression in the glandular trichomes of N. tabacum.

259 s expressing at a cutoff of FPKM >= 1 in the glandular trichomes of N. tabacum.

260 ve carried out next-generation sequencing of glandular trichomes of N. tabcaum and investigated diffe

261 in the glandular trichomes of N. tabacum The glandular trichomes of Nicotiana tabacum are highly prod

262 owards secondary metabolism operating in the glandular trichomes of Nicotiana tabacum.

263 e class of protective compounds, are made in glandular trichomes of plants across the Solanaceae fami

264 idal specialized metabolites produced in the glandular trichomes of plants in the Solanaceae family.

265 c variation of volatile terpene synthesis in glandular trichomes of S. habrochaites is due at least i

266 cal evolution of terpene biosynthesis in the glandular trichomes of Solanum species.

267 Here, we show that glandular trichomes of the anthocyanin free (af) mutant

268 as seen in the lateral roots and in the long glandular trichomes of the leaves, stem, and flowers.

269 Acylsugars are synthesized in the glandular trichomes of the Solanaceae family and are imp

270 The formation of multicellular glandular trichomes of the xerophytic shrub Cistus creti

271 However, terpene biosynthesis in glandular trichomes of tomato (Solanum lycopersicum) and

272 strated by labeling acylsugar metabolites in glandular trichomes of tomato (Solanum lycopersicum) usi

273 hylated flavonoids are detected in secreting glandular trichomes of various Solanum species, includin

274 otective acylated sugars in the tip cells of glandular trichomes on stems and leaves.

275 Solanaceae glandular trichomes produce defensive acylsugars, with s

276 Comparison of S. habrochaites type 1 and 4 glandular trichomes revealed few differences in chemical

277 he size distribution and the total number of glandular trichomes strongly correlated with differences

278 Specific features of glandular trichomes that drive the formation of secondar

279 Finally, distinct mechanisms are present in glandular trichomes to increase the supply of precursors

280 Glandular trichomes were isolated from each of these str

281 OAC transcript is present at high levels in glandular trichomes, an expression profile that parallel

282 anthocyanin accumulation, a lower density of glandular trichomes, and an associated reduction in tric

283 izes large amounts of 2-methylketones in its glandular trichomes, but cultivated tomato trichomes con

284 genes, expressing in trichome free leaf and glandular trichomes, respectively, at a cutoff of FPKM >

285 e to the density and/or distribution of leaf glandular trichomes, the specialized anatomical structur

286 se (SlMTS1, recently renamed SlTPS5) gene in glandular trichomes, we functionally dissected its promo

287 s also takes place in the secretory cells of glandular trichomes, which are epidermal outgrowths (hai

288 uch as sesquiterpenes is feasible in complex glandular trichomes.

289 mented the defect in terpenoid production in glandular trichomes.

290 flower achenes, which are densely covered by glandular trichomes.

291 yl diphosphate synthase is expressed only in glandular trichomes.

292 nt properties that is produced and stored in glandular trichomes.

293 biosynthesis of secondary metabolism in the glandular trichomes.

294 monocots, many of which are known to possess glandular trichomes.

295 ic productivity for secondary metabolites in glandular trichomes.

296 oids, which accumulate predominantly in leaf glandular trichomes.

297 ed schweinfurthins, is only located in these glandular trichomes.

298 Glandular tumors arising in epithelial cells comprise th

299 and a parameter used in pathology grading of glandular tumors.

300 The secretions of 13 glandular types have been analyzed chemically.