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1 ) layer and dissipated in deeper layers (ie, submucosa).
2 vated mucosal crypts, myenteric ganglia, and submucosa.
3 in the intestinal epithelium but not in the submucosa.
4 ere largely absent around gland acini in the submucosa.
5 cells compared with 47% of mast cells in the submucosa.
6 d to smooth muscle and isolated cells in the submucosa.
7 Y1 R, P2Y2 R, P2Y4 R, P2Y6 R, and P2Y12 R in submucosa.
8 of serovar Typhi invasion of the intestinal submucosa.
9 ocation of this microorganism to the gastric submucosa.
10 as injected in a tangential fashion into the submucosa.
11 onella enterica serovar Typhi to the gastric submucosa.
12 administration localized exclusively in the submucosa.
13 ll types (nerves, inflammatory cells) in the submucosa.
14 tubuloacinar glands, and occasionally in the submucosa.
15 rated a few eosinophils within the bronchial submucosa.
16 t affecting the number of eosinophils in the submucosa.
17 from the tips of the villus back toward the submucosa.
18 these cells and subsequent invasion into the submucosa.
19 monolayer by an intracellular pathway to the submucosa.
20 ntly in the epithelial cells but also in the submucosa.
21 lergic inflammation of the airway mucosa and submucosa.
22 e lamina propria, muscularis mucosae, and/or submucosa.
23 projected into the alveoli) and the trachea submucosa.
24 nd MGP genes in CD subserosa compared to the submucosa.
25 lamina propria, whereas Mf4 was enriched in submucosa.
26 s in circular muscle, myenteric ganglia, and submucosa.
27 lity to recruit mast cells in the intestinal submucosa.
28 ajority of cells expressing RELM-beta in the submucosa.
29 is distributed primarily within the vaginal submucosa.
30 l tumor cells were seen in the mucosa and/or submucosa.
31 of pericardium, dermis, and small intestine submucosa.
32 of the submucosa, or the final third of the submucosa.
33 ficantly more likely to be invasive into the submucosa.
34 here is no "safe" level of invasion into the submucosa.
35 epth of tumor infiltration of the mucosa and submucosa.
36 in 4 expression in the intestinal mucosa and submucosa.
37 that extended into the deeper layers of the submucosa.
38 c mucosal resection in gastric cancer to the submucosa.
39 sed in colonic muscularis externa and mucosa/submucosa.
40 of wound repair in a model of the intestinal submucosa.
41 etter represents the normal human mucosa and submucosa.
42 ction with macrophages within the intestinal submucosa.
44 infected cells were detected in the cervical submucosa 3-4 days after exposure to a primary HIV isola
46 ircumferential doughnut of rectal mucosa and submucosa above the dentate line excised and closed with
47 actic gradient to guide neutrophils from the submucosa across epithelia to the luminal site of an inf
48 ronal cultures generated from the intestinal submucosa, after exclusion of the mucosa, muscle layers,
49 .4-9.6 years), 17 (65.4%) porcine intestinal submucosa and 22 (44.9%) AP patients underwent at least
51 r patient's resected tumor invaded only into submucosa and all lymph nodes were negative; in that sen
52 tivity within the gastric mucosa and gastric submucosa and also within the tuberomamillary nucleus of
55 responsiveness by infiltrating the bronchial submucosa and disrupting airway smooth muscle (ASM) cell
56 ric gp41; 2) produced by plasma cells in the submucosa and ectopic tertiary lymphoid follicles in the
57 onuclear cell inflammation of the mucosa and submucosa and epithelial cell proliferation and dediffer
58 ificantly more IL-17RA-positive cells in the submucosa and epithelium in children with STRA compared
59 cells develop after birth in the intestinal submucosa and expand around the crypts during the third
60 nfected mice, most jejunal MCs reside in the submucosa and express mMCP-6 and mMCP-7, but not mMCP-9
61 l intestines were processed as whole mounts (submucosa and mucosa removed) to examine CSMG efferent t
62 a conspicuous eosinophilic infiltrate in the submucosa and muscle layers, but the villi were unaffect
65 9, essentially all of the MCs in the jejunal submucosa and spleen of T. spiralis-infected mice expres
66 b reduced eosinophil counts in airway mucosa/submucosa and sputum and suppressed eosinophil counts in
67 the carcinoid tumors of the gastrointestinal submucosa and the islet cell endocrine tumors of the pan
68 es mean+/-SD, lumen-negative with respect to submucosa) and was significantly more lumen-negative tha
69 around smooth muscle cells of the asthmatic submucosa, and (iii) around reserve cells of the asthmat
70 umors were confined to the mucosa, 16 to the submucosa, and 13 to the muscularis propria, and 55 were
72 ies inhibited neutrophil infiltration in the submucosa, and cyclosporine A inhibited the tissue expre
75 ocal or diffuse hemorrhages in mucosa and/or submucosa, and infiltration by eosinophil and by lymphoc
76 enetrate the mucosa, accurately localize the submucosa, and safely deploy this device to directly int
78 ollagen deposition in the lamina propria and submucosa, as well as extensive inflammatory infiltrates
79 lic inflammation was enumerated in bronchial submucosa, blood, and sputum and related to their body m
81 e flow of nonself antigens in the intestinal submucosa can cause both intestinal and extraintestinal
82 umbers of chymase-positive mast cells in the submucosa compared to patients with nonpersistent obstru
83 nd TGF-beta3 in normal tongue and esophageal submucosa compared with gut mucosal tissues, as well as
85 mRNA profiles of mouse and human intestinal submucosa, coupled with fine-resolution microscopy and g
86 anscriptase polymerase chain reaction of the submucosa demonstrated mRNA for P2Y1R, P2Y2, P2Y4, P2Y6,
89 ellularized porcine-derived small intestinal submucosa ECM into monocellular spheroids, resulting in
91 quantities of decellularized small intestine submucosa ECM, which proteomically mimicked colorectal c
92 ularized porcine small intestine (SI) mucosa/submucosa enable formation and growth of endoderm-derive
93 of cells within the bronchial epithelium and submucosa expressing mRNA for TSLP, TARC/CCL17, MDC/CCL2
94 s in the mucosa and 100% of the cells in the submucosa expressing TNF-alpha mRNA were identified as m
95 binatory transplantation of small intestinal submucosa-extracellular matrix (SIS-ECM) with gingival m
99 ts without involvement of the mucosa and the submucosa had isolated remnants in the muscle layer (5/1
100 ), defined as tumor invasion confined to the submucosa, has traditionally been managed by surgery.
102 atients with asthma and are increased in the submucosa in a subgroup of obese patients with asthma (O
103 ion of this organism to the gastrointestinal submucosa in transgenic mice that are heterozygous carri
107 Aortic valvuloplasty with porcine intestinal submucosa is associated with earlier time to reintervent
109 iral infection and chronic inflammation, the submucosa is susceptible to bacterial invasion by lung m
110 P-1 as the cells progressively appear in the submucosa, lamina propria, and epithelium, respectively.
111 The mucosa showed high signal intensity, the submucosa low signal intensity, and the muscularis propr
112 2 cm in diameter, localized to the mucosa or submucosa, may be safely and effectively removed via min
113 associated gastrinomas, which develop in the submucosa, might arise from enteric glial cells through
114 r morphologies and neural projections in the submucosa-mucosa context, finding connections among all
115 slides, visual differentiation among mucosa, submucosa, muscle, dysplastic, and benign tissue was pos
116 es and eight with gastric wall infiltration (submucosa, n = 4; muscularis propria, n = 3; serosa, n =
117 studies demonstrate that, in contrast to the submucosa, nerve fibers innervating the epithelium of th
120 aled that more CFTR bound to S. typhi in the submucosa of Cftr wild-type mice than in deltaF508 heter
121 ells were frequently observed in the gastric submucosa of Gal3-deficient mice.In vitro, peritoneal ma
122 ers within the smooth muscle, epithelium and submucosa of healthy subjects (n = 10) and well-characte
123 was significantly increased in the bronchial submucosa of human asthmatics compared with controls, an
124 Examination of the intestinal epithelial submucosa of mice after primary and secondary infections
125 t lead to excessive fibrin deposition in the submucosa of NP, which might contribute to the tissue re
126 te to the excessive fibrin deposition in the submucosa of NP, which might contribute to the tissue re
127 al vascular architecture was observed in the submucosa of the jejunum of human patients, cows, and sh
129 l-associated lymphoid organs embedded in the submucosa of the nasal passage, in the initial priming a
131 ctrodes in the submucosa of the stomach, the submucosa of the small bowel, and the abdominal wall mus
132 from a collagen biomaterial derived from the submucosa of the small intestine and type I bovine colla
135 ipt and protein were observed in the jejunal submucosa of Trichinella spiralis-infected BALB/c mice.
136 framework of dual involvement of mucosa and submucosa on the one hand, and of the muscularis propria
143 h stroking-evoked Isc response in mucosa and submucosa preparations (M-SMP) of rat colon was reduced
144 infiltration of eosinophils into the airway submucosa; proliferation of goblet cells in the airway e
145 , cytokines are released into the mucosa and submucosa propagating and sustaining the inflammatory re
146 iated with tumors confined to the mucosa and submucosa provides justification for more limited and le
150 btained by lavage or scraping, and the nasal submucosa, sampled by biopsy, are two distinct compartme
151 de metastases once the tumor infiltrates the submucosa seems to necessitate surgery in these cases.
152 rejection primarily involves vessels of the submucosa, serosa, and mesentery, some mucosal alteratio
153 r esophageal cancer, both the mucosa and the submucosa show frequent residual malignant involvement.
155 ssels (A-TEVs) comprised of small intestinal submucosa (SIS) immobilized with heparin and vascular en
158 octamethylene citrate)] or small intestinal submucosa (SIS) scaffolds and their contribution to blad
159 omaterials, such as porcine small-intestinal submucosa (SIS), have been successfully used clinically
161 irds of pT1a = mucosa (m1, m2, m3) or pT1b = submucosa (sm1, sm2, sm3) and number and infiltration of
163 low-risk features (<500-mum invasion in the submucosa [sm1], good to moderate differentiation, and n
164 63(+)CD206(+) DP macrophages remained in the submucosa, supporting their potential role as an SIV/HIV
165 86% fewer S. typhi into the gastrointestinal submucosa than wild-type Cftr mice; no translocation occ
166 C populations were transitional forms in the submucosa that expressed mMCP-2 and mMCP-5 without mMCP-
167 e day 3 with lymphocytic infiltration of the submucosa that progressed to the epithelial surface-thes
169 nfined to the mucosa, the first third of the submucosa, the middle third of the submucosa, or the fin
170 we identified a shift in mast cells from the submucosa to the airway epithelium specifically associat
172 ammation, when the jejunal MCs move from the submucosa to the tips of the villus, the MCs briefly exp
173 a biological scaffold (SIS; small intestinal submucosa) to regenerate bladder tissue in our baboon bl
175 sion showed that 5 of 22 "first third of the submucosa" tumors had LNM (23%), 1 of 24 "middle third o
176 had LNM (23%), 1 of 24 "middle third of the submucosa" tumors had LNM (4%), and 2 of 19 "final third
177 n multivariable analysis, porcine intestinal submucosa use was significantly associated with unplanne
179 expression for RANTES in the epithelium and submucosa was 26 +/- 9% and 26 +/- 10% in the asthmatic
180 elastic fibres and total collagen within the submucosa was also measured, and the morphology of the e
182 neutrophilic infiltration of the mucosa and submucosa was observed from day 1 until day 14 and was a
189 are key structural cells that reside in the submucosa where they are in contact with large numbers o
190 sed inflammation and bacterial access to the submucosa, which are fundamental aspects of S. flexneri
192 d CRHR1 expression was mainly located in the submucosa while CRHR2 expression was mainly in uroepithe
193 broader cellular invasion capacity into the submucosa, while Omicron displayed enhanced nasal respir
196 7.3% was in the mucosa (ypT1a), 16.5% in the submucosa (ypT1b) and 6.4% only in lymph nodes (ypT0N+).