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1 receptor gamma rearrangement present in the gastric biopsies.
2 ith symptoms of gastritis, routinely undergo gastric biopsies.
3 to accurately diagnose H. pylori presence on gastric biopsies.
4 red formalin-fixed, paraffin-embedded (FFPE) gastric biopsies.
5 t esophagogastroduodenoscopy procedures with gastric biopsies.
6 plications, potentially reducing unnecessary gastric biopsies.
7 be applied on regular whole slide images of gastric biopsies.
8 pathologic analysis of random post-treatment gastric biopsies.
9 cytoplasm of all bacteria examined in human gastric biopsies.
10 se and HspB within bacteria present in human gastric biopsies.
12 ence of mucosal dysplasia is noted on random gastric biopsy and may serve as a histologic marker in t
15 ssue samples were obtained during sequential gastric biopsies beginning at 3 weeks postinoculation an
20 ls of NOD1, CXCL8, IRF1, and CXCL10 in human gastric biopsies displaying severe gastritis, when compa
21 es, high-magnification endoscopy with random gastric biopsies, endoscopic ultrasonography, CT, and PE
23 ired formalin-fixed paraffin-embedded (FFPE) gastric biopsies from 100 H. pylori-positive patients wi
26 D74 expression was increased dramatically on gastric biopsies from H. pylori-positive patients and ga
27 rDNA PCR fragment was amplified from 90% of gastric biopsies from histological H. pylori positive pa
30 upper gastrointestinal endoscopy with random gastric biopsies, high-magnification endoscopy with rand
35 otype using a molecular approach directly on gastric biopsies of dyspeptic patients attending consecu
36 tions using a molecular approach directly on gastric biopsies of dyspeptic patients consecutively att
37 with clinical isolates and in vivo by using gastric biopsies of infected and noninfected individuals
43 shed by detection of CMV inclusion bodies in gastric biopsy samples and by hybridization with a CMV p
44 ed mucin oligosaccharides were released from gastric biopsy samples by beta-elimination and profiled
51 ctive gastritis and intestinal metaplasia in gastric biopsy samples were inversely associated with Ba
54 rophy with or without intestinal metaplasia, gastric biopsies should be obtained according to a syste
63 tative culture and histologic examination of gastric biopsy specimens from 29 H. pylori-infected dysp
65 ogen Helicobacter pylori, was quantitated in gastric biopsy specimens from 41 H. pylori-infected pati
66 dy, formalin-fixed, paraffin-embedded (FFPE) gastric biopsy specimens from a cohort of individuals fr
67 is study, 28 H. pylori strains isolated from gastric biopsy specimens from a high-gastric-cancer-risk
68 of disease, from gastritis to carcinoma, and gastric biopsy specimens from Colombian and Honduran coh
69 e in epithelial cell p27(kip1) expression in gastric biopsy specimens from H. pylori-infected patient
72 iption polymerase chain reaction analysis of gastric biopsy specimens from patients with and without
77 cross- sectional study was performed on 800 gastric biopsy specimens of cows, sheep, goats and human
78 immunohistochemistry on mononuclear cells in gastric biopsy specimens of infected but not uninfected
80 oarray screening of H. pylori-infected human gastric biopsy specimens to identify candidate genes inv
82 cter pylori using DNA isolated from infected gastric biopsy specimens was approximately equal to geno
83 that IL-17C expression in H. pylori-infected gastric biopsy specimens was predominantly localized to
90 2016 to January 2017, 133 H. pylori-infected gastric biopsy specimens were identified histologically
91 -1), KATO III cells, and cells isolated from gastric biopsy specimens were infected with H pylori.
92 med before, during, and after treatment, and gastric biopsy specimens were obtained for quantitative
94 distinguish H. pylori strains directly from gastric biopsy specimens without culture of the organism
95 icobacter species present in urease-negative gastric biopsy specimens, 16S rDNA amplicons were cloned
96 anscript profiles and histologic features of gastric biopsy specimens, as well as blood eosinophil co
108 in our practice, a judicious performance of gastric biopsies to detect gastric PCCs should be adopte
110 sceptibility test results from pre-treatment gastric biopsies was a pre-condition for matching 52 aiH
111 usceptibility test results from pretreatment gastric biopsies was a precondition for matching 52 aiHp
112 H. pylori isolates obtained from endoscopic gastric biopsy was determined by using agar dilution.
120 In the MALT lymphoma group, time-matched gastric biopsies were used as reference standard and sho
125 d of their H pylori infection as assessed by gastric biopsy, with elimination of gastritis; median an