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

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

8 hospholipid composition compared with normal glandular and stromal tissue.

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

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

11 (NBI) enhances the visualization of mucosal glandular and vascular structures.

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

13 Disruption of glandular architecture associates with poor clinical out

14 growth-arrested, acini-like structures with glandular architecture.

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

16 Glandular atrophy and a positive CagA status are determi

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

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

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

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

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

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

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

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

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

26 These proteins reflected the damage of glandular cells and inflammation of the oral cavity syst

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

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

29 compared with morphologically normal breast glandular cells.

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

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

32 modalities for breasts of varying sizes and glandular compositions.

33 f the antrum and in mucous neck cells of the glandular corpus.

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

35 Three-dimensional (3D) glandular culture showed that KLF8 expression disrupted

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

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

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

39 defects in cardiovascular, craniofacial and glandular development.

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

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

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

43 ecular processes that can promote epithelial glandular disruption.

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

45 Mean glandular dose for DR photon counting was significantly

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

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

48 cated breast CT scan relative to the average glandular dose to the imaged breast (relative organ dose

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 For constant glandular dose, mass and microcalcification conspicuity

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

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

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

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

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

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

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

60 d enzymes act on proteins emanating from the glandular ducts.

61 leading to inflammation and dilation of the glandular ducts.

62 2(b).C-Stat6(-/-) sera were unable to induce glandular dysfunction when injected into naive recipient

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

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

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

66 Moreover, glandular epithelia from DAB2IP(-/-) animal exhibited hy

67 d with canonical Wnt activity throughout the glandular epithelia regardless of androgen status.

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

69 s have unequivocally identified TMEM16A as a glandular epithelial CaCC.

70 monstrated previously that the protein GEC1 (glandular epithelial cell 1) bound to the human kappa op

71 o its expression in proliferating ductal and glandular epithelial cells during pregnancy.

72 opin receptor, PROK1, PROKR1, and LIF to the glandular epithelial cells of the first trimester decidu

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

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

75 herpesvirus that persistently replicates in glandular epithelial tissue.

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

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

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

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

80 re systems recreate the cardinal features of glandular epithelium in vivo and represent a valuable to

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

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

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

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

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

86 gulation of cellular polarity of endometrial glandular epithelium.

87 lls in an organotypic culture of the mammary glandular epithelium.

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

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

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

91 hesis, we conducted chemical analyses on the glandular fluid from snakes collected in toad-free and t

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

93 3R) plays a pivotal role in the induction of glandular fluid secretions.

94 processes including tissue morphogenesis and glandular formation.

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

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

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

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

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

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

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

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

103 atinized, squamous esophagus/forestomach and glandular hindstomach.

104 1.2 microM, representing 59, 27, and 11% of glandular histatins 1, 3, and 5 levels, respectively.

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

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

107 cell transplants showed rare development of glandular hyperplasia, prostatic intraepithelial neoplas

108 /+)Ctnnb1(f(ex3)/+), resulted in endometrial glandular hyperplasia, whereas ablation of beta-catenin,

109 artments, which alters turnover kinetics and glandular hyperplasia.

110 lls due to enhanced apoptotic cell death and glandular hypertrophy associated with cellular transform

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

116 Although glandular inversion in epithelial tumors is thought to b

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

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

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

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

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

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

123 Glandular mast cells and the diverse subsets of mast cel

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

125 fluid (HSF) is a complex mixture of reacting glandular metabolite and protein secretions that provide

126 tion of mutualism between meerkats and their glandular microbiota.

127 rexpression in aggressive cell lines induced glandular morphogenesis and inhibited invasiveness, tumo

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

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

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

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

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

133 y CRCs from which they were derived, such as glandular organization, cell polarity, gap junctions, an

134 ible for the characteristic architectures of glandular organs such as kidney, lung, prostate and sali

135 In glandular organs, tubulogenesis is a multistep process r

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

137 This inversion of glandular orientation is accompanied by Rac1 inactivatio

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

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

140 toantibody responses can be dissociated from glandular pathology.

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

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

143 epithelial cysts, reminiscent of tumorigenic glandular phenotypes.

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

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

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

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

148 The glandular proliferative niche was disrupted in pPDX-FGF1

149 While keeping the glandular radiation dose constant with respective standa

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

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

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

153 bine to suppress the cancer phenotype during glandular regeneration.

154 controlling epithelial morphogenesis during glandular repair or regeneration.

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

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

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

158 Plant glandular secreting trichomes are epidermal protuberance

159 Glandular secreting trichomes of cultivated tomato (Sola

160 Glandular secreting trichomes of cultivated tomato (Sola

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 Once glandular secretions enter the non-sterile oral environm

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

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

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

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

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

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

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

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

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

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

177 effect of epithelial TGF-beta production on glandular stability was tested in vivo.

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

179 ic expression of genes normally expressed in glandular stomach and intestine.

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

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

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

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

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

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

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

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

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

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

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

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

192 at CSCs admixed with CAFs produced prostatic glandular structures with more numerous lesions, high pr

193 ivation induces the formation of cell-filled glandular structures with multiple lumens and disassembl

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

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

196 e and -promoting functions within individual glandular structures.

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

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

199 neural network designed for segmentation of glandular structures.

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

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

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

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

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

205 DW imaging with glandular tissue-normalized ADC assessment improves the

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

207 awn on ADC maps of breast lesions and normal glandular tissue.

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

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

210 Tumor development in glandular tissues is associated with structural alterati

211 cally, the degree of (18)F-FDG uptake in the glandular tissues of the normal breast can affect the de

212 TSPO is highly expressed in secretory and glandular tissues, especially in steroidogenic cells, an

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

214 It is widely found in secretory and glandular tissues, with a possible involvement in transf

215 ithelial polarity and formation of lumens in glandular tissues.

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

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

218 were selected to approximate the dynamics of glandular trichome distribution/density and enzyme conce

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

220 The glandular trichome is an excellent model system for inve

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

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

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

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

225 Several glandular trichome types express genes associated with p

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

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

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

229 7-fold, respectively, harboring 5-fold more glandular trichomes (as determined by rhodamine B staini

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

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

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

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

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

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

236 (Solanum lycopersicum) cultivar M82 type VI glandular trichomes and encodes an enzyme that catalyzes

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

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

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

240 Glandular trichomes are currently known only to store mo

241 Multicellular glandular trichomes are epidermal outgrowths characteriz

242 Glandular trichomes are metabolic cell factories with th

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

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

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

246 Finally, Solanum type 7 glandular trichomes do not appear to be involved in the

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

248 Glandular trichomes from tomato (Solanum lycopersicum) a

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

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

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

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

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

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

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

256 Glandular trichomes of cultivated tomato (Solanum lycope

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

258 and all accumulate at high concentrations in glandular trichomes of hop cones.

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

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

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

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

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

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

265 opanoid versus terpenoid constituents in the glandular trichomes of the different basil lines.

266 onstrated that although the proteomes of the glandular trichomes of the four basil lines shared many

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

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

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

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

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

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

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

274 Glandular trichomes play important roles in protecting p

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

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

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

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

279 s demonstrated that the final mature size of glandular trichomes was the same across all experiments.

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

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

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

283 Some types, commonly called glandular trichomes, produce large amounts of specialize

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

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

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

287 mented the defect in terpenoid production in glandular trichomes.

288 ic productivity for secondary metabolites in glandular trichomes.

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

290 yl diphosphate synthase is expressed only in glandular trichomes.

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

292 hology, density, and chemical composition of glandular trichomes.

293 ay, and not the mevalonate pathway, in basil glandular trichomes.

294 oids, which accumulate predominantly in leaf glandular trichomes.

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

296 uch as sesquiterpenes is feasible in complex glandular trichomes.

297 monocots, many of which are known to possess 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.