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3 osition of Charcot-Leyden-like crystals, and subepithelial airway fibrosis were also prominently note
6 modality is capable of in vivo diagnosis of subepithelial airway wall pathology as signs of intubati
9 ute rejection and lymphocytic bronchitis, to subepithelial and intraluminal fibrotic lesions of bronc
10 tase and dipeptidyl peptidase 4) and visible subepithelial and smooth muscle layers when compared wit
14 the GBM that became most prominent along the subepithelial aspect at maturity; labeling was greatly r
15 rity; labeling was greatly reduced along the subepithelial aspect in agrin-deficient and conditional
18 % [25th-75th IQR], 3.5% to 10.1%, P < .001), subepithelial basement membrane thickening (4.4 mum [25t
19 ssessed for airway smooth muscle (ASM) area, subepithelial basement membrane thickness, nerve fibers,
21 correlated with severity, thickening of the subepithelial basement membrane, and pulmonary function.
24 noreactivities (IRs) in supporting cells and subepithelial Bowman's gland acinar cells, two OE non-ne
27 ative central corneal thicknesses when these subepithelial cells were and were not visible were 652 (
28 sity and number and the presence of abnormal subepithelial cells were determined from confocal images
35 including intraluminal mucus production and subepithelial collagen deposition, but did not alter eos
38 re respectively characterized by a thickened subepithelial collagen plate and increased intraepitheli
40 as compared in three distinct epithelial and subepithelial compartments isolated from biopsies of nor
41 s in the portal tracts and in epithelial and subepithelial compartments of extrahepatic bile ducts, w
44 epithelialized free soft tissue autografts, subepithelial connective tissue autografts, coronally po
45 eive either a coronally advanced flap with a subepithelial connective tissue graft (control) or a cor
46 ing and a coronally advanced flap (CAF) to a subepithelial connective tissue graft (CTG) in combinati
49 e similarities between collagen membrane and subepithelial connective tissue graft (SCTG) have made c
52 Most clinicians adopt two versions of the subepithelial connective tissue graft (SCTG) procedure,
54 perative morbidity, and esthetic outcomes of subepithelial connective tissue graft (SCTG) technique w
55 The first paper in this series evaluated the subepithelial connective tissue graft and the coronally
56 lap resulted in root coverage similar to the subepithelial connective tissue graft but without the mo
57 ng excision of the lesion, by placement of a subepithelial connective tissue graft concurrently with
58 and patient-reported discomfort, whereas the subepithelial connective tissue graft demonstrated great
60 Most of the literature suggests that the subepithelial connective tissue graft has the highest pe
64 eth that were randomized to receive either a subepithelial connective tissue graft or a coronally adv
67 ed to eliminate the lesion, beginning with a subepithelial connective tissue graft to increase tissue
68 and submitted for histologic examination; a subepithelial connective tissue graft was harvested and
69 y advanced flap with EMD was superior to the subepithelial connective tissue graft with regard to ear
70 coverage of 73% (collagen membrane) and 84% (subepithelial connective tissue graft) was achieved.
71 re, including a laterally positioned flap, a subepithelial connective tissue graft, and a coronally p
73 ce after free soft tissue grafting (FSTG) or subepithelial connective tissue grafting (SCTG) procedur
78 acid root demineralization in the outcome of subepithelial connective tissue grafts performed to cove
79 oethylene (ePTFE) membranes and conventional subepithelial connective tissue grafts, respectively.
81 ve placed under a coronally advanced flap to subepithelial connective tissue placed under a coronally
88 [91%]), elevated circumferential peripheral subepithelial corneal opacities and adjacent abnormal li
91 hans' cells did not express DC-SIGN, whereas subepithelial DCs in the lamina propria expressed modera
92 rix metalloproteinase-dependent migration of subepithelial DCs into the FAE, but not into villus epit
93 rix metalloproteinase-dependent migration of subepithelial dendritic cells (DCs) into the FAE, better
94 us, MV infection of alveolar macrophages and subepithelial dendritic cells in the airways precedes in
97 ptors did not ameliorate injury, implicating subepithelial deposition of immune complexes and consequ
99 omplex deposition, and absence of glomerular subepithelial deposits compared with MRL/lpr mice of any
100 buminuria and nephrotic syndrome, because of subepithelial deposits of mouse IgG and C3 with correspo
102 sease involving the eye and characterized by subepithelial detachment resulting from an immunologic r
103 sigma1, but not sigmaNS, was detected in the subepithelial dome (SED) in association with CD11c(+)/CD
105 molecules, particles, and pathogens into the subepithelial dome (SED) region of Peyer's patch mucosa,
106 oid DCs were determined to be present in the subepithelial dome (SED) region, whereas CD8alpha(+) lym
107 orted from the mucosal surface of PPs to the subepithelial dome (SED), through the specialized epithe
109 al bacteria targeting dendritic cells in the subepithelial dome region of PPs represents a mechanism
110 )CD8(-) dendritic cell subset located in the subepithelial dome region of PPs, confirming that the ho
111 t reduction of the CD11b(+) DC number in the subepithelial dome regions of Peyer's patches of both wi
112 (+) dendritic cells (DCs) distributed in the subepithelial dome regions of the Peyer's patches, and m
114 8alpha(-) (myeloid) DCs are localized in the subepithelial dome, CD11b(-)/CD8alpha(+) (lymphoid) DCs
118 on molecules on EC nearest the airway lumen (subepithelial EC) were different from those on the oppos
120 ts without any sputum eosinophils had normal subepithelial eosinophil numbers (< 1.2%; NPV, 89%).
122 his condition from other conditions in which subepithelial, eosinophilic, amorphous materials are dep
124 antigen-specific CD8+ T cells were intra- or subepithelial, expressed alphaE-integrin CD103, produced
127 get gene Gli1 is preferentially expressed in subepithelial fibroblast-like cells, one of four prostat
128 gically, interstitial monocytes/macrophages, subepithelial fibroblast-like interstitial cells, and ad
129 in the mesenchyme caused progressive loss of subepithelial fibroblasts and abbreviated gut length, re
130 induction of cyclooxygenase 2 expression in subepithelial fibroblasts and in villous, but not crypt,
132 ecovery, induced IL-1 receptor expression in subepithelial fibroblasts, and activated de novo inflamm
135 aplasia, B and T cell-rich inflammation, and subepithelial fibrosis and augmented the levels of mRNA
137 ucus hypersecretion, goblet cell metaplasia, subepithelial fibrosis and enhanced airway hyperreactivi
140 n, dye staining, and the presence of corneal subepithelial fibrosis and meibomian gland (MG) orifice
141 ployed in cases wherein visually significant subepithelial fibrosis and scarring become evident after
142 l remodeling of the airways characterized by subepithelial fibrosis and smooth muscle hyperplasia.
143 ammation and significantly reduced levels of subepithelial fibrosis as assessed by either trichrome s
145 x protein, has been localized to deposits of subepithelial fibrosis in asthmatic patients, and perios
147 anisms underlying esophageal remodeling with subepithelial fibrosis in subjects with eosinophilic eso
148 cus plugging, smooth muscle hyperplasia, and subepithelial fibrosis in the OVA-sensitized/challenged
149 whether the secretin/SR axis plays a role in subepithelial fibrosis observed during cholestasis.
150 corneas were vascularized or had pronounced subepithelial fibrosis on results of slitlamp examinatio
151 -mesenchymal signaling, leading to increased subepithelial fibrosis or hyperplasia of smooth muscle.
152 ia, smooth muscle cell layer thickening, and subepithelial fibrosis present on Day 73 persisted at Da
153 ith subsequent epithelial transformation and subepithelial fibrosis that could not be reversed with i
154 yperreactivity, goblet cell hyperplasia, and subepithelial fibrosis that is initiated by the intratra
155 e, significantly fewer goblet cells and less subepithelial fibrosis were observed around large airway
156 ion, hyper-responsiveness to spasmogens, and subepithelial fibrosis were significantly enhanced in CC
157 cytokine that induces tissue remodeling with subepithelial fibrosis when expressed in the airway.
158 e of chronic asthma that often culminates in subepithelial fibrosis with variable airway obstruction.
159 l hyperplasia, basement membrane thickening, subepithelial fibrosis, airway smooth muscle hyperplasia
160 ypersecretion leading to airway obstruction, subepithelial fibrosis, airway smooth muscle hyperplasia
161 ed pulmonary inflammation, mucus metaplasia, subepithelial fibrosis, and airway remodeling are signif
163 osinophilic inflammation, mucin composition, subepithelial fibrosis, and corticosteroid responsivenes
164 plasia, smooth muscle cell layer thickening, subepithelial fibrosis, and levels of T helper type 2 ce
167 athophysiologic aspects of human asthma (ie, subepithelial fibrosis, angiogenesis, neural biology, an
168 features of airway remodeling, in particular subepithelial fibrosis, by reducing the production of eo
169 tion did not affect epithelial thickening or subepithelial fibrosis, despite significantly inhibiting
170 diagnosis, eosinophil counts, and indices of subepithelial fibrosis, eosinophil peroxidase, and TGF-b
171 eactivity, and remodeling of the airway (eg, subepithelial fibrosis, goblet cell metaplasia, and smoo
172 elial mosaic, cystic epithelial changes, and subepithelial fibrosis, in the eyes affected by partial
173 rway smooth muscle cell layer thickening and subepithelial fibrosis, key allergen-induced airway stru
174 tion, eosinophil infiltration of the airway, subepithelial fibrosis, mucus metaplasia, and airway-hyp
175 with significantly reduced mucus secretion, subepithelial fibrosis, smooth muscle thickness, and per
184 tural analysis revealed occasional knob-like subepithelial GBM thickening but intact podocyte foot pr
185 pithelium in the chilled saline group and to subepithelial glands in both the room-temperature and ch
186 e degree of injury to biliary epithelium and subepithelial glands was assessed on a scale of 0%-100%.
188 characterized by (1) the formation of large, subepithelial glomerular immune deposits, which stain fo
191 atal connective tissue (CT) were compared as subepithelial grafts for the treatment of gingival reces
192 uble immunofluorescence staining showed that subepithelial granular deposits contained rhASB colocali
193 with BCVA (r = 0.59; P<0.001; n = 27), with subepithelial haze (r = 0.41; P = 0.01; n = 25), and wit
194 .001 and r = 0.46, P = 0.003), postoperative subepithelial haze (r = 0.43, P = 0.004 and r = 0.39, P
195 e correlations between BCVA and preoperative subepithelial haze (r = 0.61, P < 0.001 and r = 0.46, P
198 thelial, stromal, and corneal thickness, and subepithelial haze following photorefractive keratectomy
199 of Diabetic Retinopathy Study protocol, and subepithelial haze was measured from the brightness of c
201 g best corrected visual acuity (BCVA), IVCM (subepithelial haze, interface haze, graft thickness) and
203 lts show that FcRn promotes the formation of subepithelial immune complexes and subsequent glomerular
204 astructurally, there were subendothelial and subepithelial immune deposits and extensive podocyte foo
205 nvestigators induced formation of glomerular subepithelial immune deposits and tubular lesions in pig
206 pathy (MN) have shown that IgG antibodies in subepithelial immune deposits initiate complement activa
207 icroscopy were present in subendothelial and subepithelial immune deposits, whereas WT kidneys in WT
208 visual acuity (BCVA), evaluation of corneal subepithelial infiltrate scores (CSIS), intraocular pres
209 ical analyses of the oral lesions revealed a subepithelial infiltrate that was primarily composed of
211 adenovirus replication and the formation of subepithelial infiltrates in the Ad5/New Zealand White r
217 the gut and contribute substantially to the subepithelial intestinal myofibroblast population in the
218 We recently demonstrated that normal human subepithelial intestinal myofibroblasts (IMFs) express M
220 This study reviews current concepts in laser subepithelial keratectomy (LASEK), variations in LASEK t
225 dividual cells or small cell clusters in the subepithelial lamina propria of monkeys infected with ei
226 ) DCs proliferate in both the epithelial and subepithelial layers of the airway mucosa as well as in
229 s of remodeling that included epithelial and subepithelial layers, as well as mucus production, were
230 line the recommended course of action when a subepithelial lesion is encountered during upper endosco
232 of the esophageal epithelium with a striking subepithelial lichenoid lymphocytic infiltrate extending
233 led granular antigen-antibody complexes in a subepithelial location along the glomerular filtration b
234 has been shown to be useful in evaluation of subepithelial masses of the colon and rectum and evaluat
239 Hedgehog (Hh) signals promote aggregation of subepithelial mesenchymal clusters that drive villus eme
241 helped to determine the HSV-1 distribution: subepithelial myeloid cells provided a route of spread f
242 show that PGE(2) activated human intestinal subepithelial myofibroblasts (18Co) through Gs protein-c
243 racrine, from epithelium to Ptch1-expressing subepithelial myofibroblasts (ISEMFs) and smooth muscle
244 ate that alpha-smooth muscle actin(+), CD90+ subepithelial myofibroblasts (stromal cells) constitutiv
245 1RL1 associated with two stromal cell types, subepithelial myofibroblasts and mast cells, in Apc(Min/
246 Whereas GREM1 is expressed in intestinal subepithelial myofibroblasts in controls, GREM1 is predo
248 The association between COX-2 expression and subepithelial myofibroblasts was also noted in tumors de
250 ignal leads to mislocalization of intestinal subepithelial myofibroblasts, loss of smooth muscle in v
254 mal tumors (GIST) are stromal or mesenchymal subepithelial neoplasms affecting the gastrointestinal t
256 x adult patients developed bilateral diffuse subepithelial opacifications in the central and paracent
257 A distinctive feature is the appearance of subepithelial opacities in adult life, accompanied by a
258 bullosa hemorrhagica (ABH) describes benign subepithelial oral blood blisters not attributable to a
259 tea mediterranea generates porphyrins in its subepithelial pigment cells under physiological conditio
260 propria thickness (defined as the extent of subepithelial portion of the biopsy containing </=25% or
262 scripts with the cells expressing KGF in the subepithelial, rather than the deeper, connective tissue
264 gastritis, COX-2 expression localizes to the subepithelial region, with variable levels in the epithe
266 periostin are hypothesized to be involved in subepithelial remodeling and are overexpressed in adult
268 epithelial and smooth muscle thickening, and subepithelial reticular fiber deposition in the distal a
270 type of afferent, the crypt afferent, forms subepithelial rings of varicose processes encircling the
272 immune blistering disorders characterized by subepithelial separation and the deposition of immunoglo
273 nty patients with histologic confirmation of subepithelial separation with or without direct immunofl
274 numbers and thickness of the epithelium and subepithelial smooth muscle layer, which was accompanied
277 n, indicating that cell types inhabiting the subepithelial space can provide such an activity to the
280 important to process immune complexes in the subepithelial space, where it also limits complement act
283 onjunctival and oral/pharyngeal lesions with subepithelial splitting were found in 80% and 100% of mi
284 roblasts were present at high density in the subepithelial stroma of rabbit eyes that had -9.0D PRK,
288 ype XVIII collagen immunolocalization to the subepithelial stromal wound region peaked at 1 week afte
291 nd blood eosinophils, higher serum IgE, more subepithelial thickening, and higher expression of Th2 s
292 s in rat trachea, whereas basal cells in the subepithelial tissue displayed heavy, non-polarized stai
295 therapies for achalasia and gastrointestinal subepithelial tumors originating from the muscularis pro
296 SD with enucleation for treatment of gastric subepithelial tumors originating from the muscularis pro
297 ique with enucleation for removal of gastric subepithelial tumors originating from the muscularis pro
299 subepithelial, so this colonization implies subepithelial viral spread, where myeloid cells provide
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