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1 ococcus gallolyticus and Limosilactobabillus mucosae).
2 entry (i.e. the gastrointestinal and vaginal mucosae).
3 thymic alphabeta T cells in gastrointestinal mucosae.
4 gh normally B cell-enriched gastrointestinal mucosae.
5 nd, later, to the villus core and muscularis mucosae.
6 s administered ex vivo to rat distal colonic mucosae.
7 e signal proteins and are present in several mucosae.
8 ssues and distinguishes them from intestinal mucosae.
9 1 infection, or redistribution from blood to mucosae.
10 d in epithelial cells of the glands and oral mucosae.
11 -laden droplets that reach the nasal or oral mucosae.
12 irmed SARS-CoV-2 infection in the glands and mucosae.
13 temic immunity or re-target responses to the mucosae.
14 tic infiltrate extending into the muscularis mucosae.
15 ring colonization of human respiratory tract mucosae.
16 ning vaccination strategies targeting distal mucosae.
17 V is usually acquired via the oral and nasal mucosae.
18 S) is the most common disease affecting oral mucosae.
19 MV) enters its host via the oral and genital mucosae.
20 c the environment in the oral and esophageal mucosae.
21 to bolster the innate defenses of vulnerable mucosae.
22 homing to the intestinal and female genital mucosae.
23 n and effector function are generated in the mucosae.
24 e, a bacterial pathogen of the human genital mucosae.
25 asias, and 3 of the 5 (60%) nonneoplastic UC mucosae.
26 ular bacterium that infects the oculogenital mucosae.
27 ted in normal gastric, duodenal, and colonic mucosae.
28 ch are present in the skin and surface-close mucosae.
29 nce differing between enteric and nonenteric mucosae.
30 included 4 L. jensenii, 2 L. crispatus, 1 L. mucosae, 1 L. vaginalis and the L. acidophilus probiotic
31 bserved in 4 of 59 and 0 of 64 nondysplastic mucosae, 20 of 38 and 1 of 25 dysplasias, and 28 of 61 a
32 d esophageal tissue specimens from 16 normal mucosae, 30 dysplastic lesions, and 157 esophageal tumor
33 equence: 17p loss occurred in 14% of Barrett mucosae, 42% of low-grade dysplasias, 79% of high-grade
36 ation in the suprabasilar layers of skin and mucosae and anti-desmoglein-3 (Dsg3) autoantibodies boun
40 is normally a commensal fungus of the human mucosae and skin, but it causes life-threatening systemi
42 s infects the murine respiratory and genital mucosae and that T cells, but not Abs, elicited through
48 any mucosal route colonized multiple murine mucosae and, in most cases, the spleen, liver, and kidne
49 rated that DC-T cell mixtures from the skin, mucosae, and blood of healthy macaques similarly support
50 ll subsets in blood, liver, oral, and rectal mucosae, and lymph nodes (LN) that persisted through the
52 stem cells, smooth muscle of the muscularis mucosae, and smooth muscle surrounding the lymphatic lac
58 During acute infection, intestinal and other mucosae are preferential sites of virus replication and
61 ne (C-C motif) ligand 28 (CCL28; also called mucosae-associated epithelial chemokine), is secreted by
64 K cells away from the lymph nodes to the gut mucosae but alters NK cell function independent of traff
65 nanomaterials that interact intimately with mucosae by different mechanisms in the nanomedicine fiel
67 eclude cancer invasion beyond the muscularis mucosae, cautioning against the use of mucosal ablative
68 ization within the mouse female reproductive mucosae, CD8(+) T(RM) cells secrete cytokines that trigg
71 ture, demonstrated by loss of the muscularis mucosae, deterioration of the extracellular matrix, and
73 allisepticum populations present on tracheal mucosae during a 7-day experimental infection in the nat
74 and chemokine receptor expression in genital mucosae during genital chlamydial infection in a murine
75 occus aureus adhesion to the host's skin and mucosae enables asymptomatic colonization and the establ
77 cells to the spleen, vaginal and intestinal mucosae, for example CCL25 enhanced splenic and vaginal
78 intraepithelial CD8+ T lymphocytes in ileal mucosae from acutely infected calves compared with those
80 g experiments were performed with intestinal mucosae from GC-C knockout (KO) and wild type (WT) mice.
81 Here we report development of engineered VF mucosae from hiPSC, transfected via TALEN constructs for
82 Ex-vivo bioluminescence recordings of ileum mucosae from transgenic mice revealed endogenous circadi
83 Although the accumulated pDCs in the gut mucosae had robust cytokine responses to TLR7/8 stimulat
84 mmary, comprehensive analysis of the colonic mucosae has uncovered common pathogenesis and therapeuti
87 elative virus transmissibility across intact mucosae in macaques using a single stock of SHIV-1157ipd
89 opulations residing on healthy and ulcerated mucosae in patients with RAS (recruited using highly str
90 ctions between ETEC and the gastrointestinal mucosae in which host glycoproteins promote bacterial at
91 ic immunoglobulin G (IgG) in sera and IgA in mucosae, including saliva, vaginal-wash samples, lung, a
92 they are expressed at high levels in several mucosae, including the mouth, where the concentration of
93 iptomic perturbations in avian host tracheal mucosae infected with virulent, immunopathologic Mycopla
94 ade, lymphocytic infiltration, or muscularis mucosae invasion, was associated with cancer progression
96 into three major domains: skin (S), visible mucosae (M), and organs (O), with gradation of severity
98 an, 245 vs 64 mum; P = .019), and muscularis mucosae (median, 451 vs 80 mum; P = .031) were wider tha
101 were required for protection of the vaginal mucosae of HSV-immune mice and could be detected by 24 h
102 ction perturbs the oral and gastrointestinal mucosae of infant macaques through alterations of reside
103 ta suggest that T lymphocytes in the vaginal mucosae of mice are phenotypically distinct from those i
105 gondii or S typhimurium were present within mucosae of mice with migration-defective occludin KO gam
107 --namely, increased Bacteroidales species in mucosae of RAS patients not affected by active ulceratio
108 organisms in both the rectal and the genital mucosae of women may require local immunization at both
109 osis (LP), also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease (OMIM 247100) is a rare
110 Our study revealed that similar to the GI mucosae, oral CD4 + T cells were rapidly depleted, and a
111 volving the oral, ocular, nasal, and genital mucosae, respectively, and 35 (22.7%) presented with cut
112 t role of the TLR signaling pathway in nasal mucosae-respiratory tracts-neuroepithelium environment i
113 ed IFN-gamma, whereas NKp44(+) NK cells were mucosae-restricted, noncytotoxic, and produced IL-22 and
117 red cells in the superficial portions of the mucosae spread laterally and downward to form new crypts
118 n of the conjunctival, pulmonary, or genital mucosae stimulated significant changes in tissue archite
120 ler (NK) cells are found throughout the oral mucosae, the effects of HIV/simian-human immunodeficienc
121 eceptor agonism in the rat tunica muscularis mucosae (TMM) assay, and for 5-HT(3) receptor-mediated f
124 airways, upper gastrointestinal and squamous mucosae unifies the non-intestinal mucosal tissues and d
125 to home to the gastrointestinal and vaginal mucosae using genetic chemokine adjuvants and assessed t
126 Colons were evaluated for ACF, and colonic mucosae were assayed for COX and NOS isoform enzyme acti
127 of internal muscularis propria and mucularis mucosae were associated with RTE-assessed strain (P = .0
131 le layer of the colon, the tunica muscularis mucosae, were examined using the patch clamp technique.
132 ls found in the outermost layers of the oral mucosae, where they not only provide a first line of def
133 conjugate was applied topically to the nasal mucosae whereas gp140 alone was poorly immunogenic.
134 plastic and approximately half of dysplastic mucosae, whereas RAB32 methylation occurs at the transit
135 e composition of microbiota residing on oral mucosae, which in turn modulates immunity and thereby af