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1 ts and frequent thrombocytopenia complicates mucosal biopsy.
2 ittent diarrhea and can be diagnosed only by mucosal biopsy.
3 began yearly flexible gastroscopy and random mucosal biopsy.
4 stool, intestinal scrapings, and intestinal mucosal biopsies.
5 Lipidomics analyses were performed on mucosal biopsies.
6 ndirect immunofluorescence studies on buccal mucosal biopsies.
7 mplex medical procedures, such as intestinal mucosal biopsies.
8 ed the expression of VEGF-A in human colonic mucosal biopsies.
9 nd demonstrated its use on cryopreserved gut mucosal biopsies.
10 and histopathological evaluation of gastric mucosal biopsies.
11 tinguishable microscopically on the basis of mucosal biopsies.
12 ulfovibrio was enriched both in stool and in mucosal biopsies.
13 Rejection grades were consistently higher in mucosal biopsies.
14 high-powered field (eos/hpf) are detected in mucosal biopsies.
15 ides access to samples of ileal effluent and mucosal biopsies.
16 nty-two patients (54%) had a positive buccal mucosal biopsy; 64% of patients (14/22) demonstrated +DI
17 s found predominantly in CD vs UC intestinal mucosal biopsies; a second band of 24 kDa, consistent wi
18 eukocytes as well as local effects on rectal mucosal biopsies after adding a standardized inflammator
19 average gut mucosal microbiome composition, mucosal biopsies allowed detecting the subtle variations
22 f asthmatic subjects, we performed bronchial mucosal biopsies and airway lavage in seven atopic asthm
23 ls were incubated with supernatants from the mucosal biopsies and analyzed by morphometric and polyme
24 condary clinical measures, histopathology of mucosal biopsies and exploratory, patient reported outco
26 pidomic and functional analyses of MFSD2A in mucosal biopsies and primary human intestinal microvascu
28 ils per high-power field obtained from sinus mucosal biopsy and managed with neosinus cavity ESS and
29 es 20 to 49 yr, underwent videobronchoscopy, mucosal biopsy, and bronchial lavage to evaluate the air
31 In summary, we show that cryopreserved gut mucosal biopsies can be used to overcome the logistical
36 r studies establish the feasibility of using mucosal biopsies for NGS, which should enable the compar
37 ibility of using widely available endoscopic mucosal biopsies for successful NGS, using samples obtai
38 usually 3 to 5 mm in diameter, and an antral mucosal biopsy for subsequent urease testing should be p
39 ix patients with terminal ileum colonoscopic mucosal biopsies (four men, two women; mean age, 43 year
41 okine gene expression was also determined in mucosal biopsies from adenoma cases and controls by quan
42 n LP macrophages were identified commonly in mucosal biopsies from CD patients (25/35, 71 %), rarely
43 tion of CD27+ Vdelta2 T cells was present in mucosal biopsies from CD patients and produced elevated
44 entage of apoptosis induced by bile acids in mucosal biopsies from CRC patients with that of noncance
51 ate <0.05) in the exfoliome, but none in the mucosal biopsies, in response to 60 d of lignan suppleme
52 ation of the bronchial tree and histology of mucosal biopsies indicated no gross or microscopic adver
56 lyze the gut microbiota profile from colonic mucosal biopsy materials in CLD patients using a metagen
61 NA gene (V4 region) sequencing of 97 colonic mucosal biopsies obtained endoscopically from different
62 (CD) and ulcerative colitis (UC) we obtained mucosal biopsies of children with CD, UC and healthy con
63 sion profiles, and viral loads in intestinal mucosal biopsies of long-term nonprogressor (LTNP) patie
64 mina platform using libraries generated from mucosal biopsies of normal squamous epithelium (NSE), BE
65 lymerase chain reaction (qRT-PCR) in colonic mucosal biopsies of patients from three groups: controls
69 ven when using stool samples rather than the mucosal biopsies required for high discriminatory power
70 alysis of sequential blood samples and colon mucosal biopsies revealed increases in glutathione trans
71 fluorescence were performed on human gastric mucosal biopsy samples and showed that myeloid DCs in H.
74 various anatomical sites and 13 normal oral mucosal biopsy samples from healthy volunteers with micr
75 eration sequencing (NGS) method from colonic mucosal biopsy samples in CLD and healthy individuals.
76 healthy subjects); 232 fecal samples and 59 mucosal biopsy samples were collected and analyzed by 16
77 epithelial cell lines or cells isolated from mucosal biopsy samples were stimulated with H. pylori, C
82 suspected MMP and paired data on at least a mucosal biopsy specimen for direct immunofluorescence mi
83 equency of detection of H. pylori by gastric mucosal biopsy specimens after 7-30 days of NSAID ingest
86 e animals were then evaluated clinically and mucosal biopsy specimens assessed by histological and qu
87 ofluorescence analysis of IgG4 in esophageal mucosal biopsy specimens from 24 subjects with eosinophi
88 er in epithelial cells isolated from gastric mucosal biopsy specimens from H. pylori-infected subject
89 urthermore, incubation of P(HEMA-co-SS) with mucosal biopsy specimens from patients with celiac disea
90 ted mediators were secreted spontaneously in mucosal biopsy specimens from patients with EoE than con
99 ncrease in [(3)H]-thymidine incorporation in mucosal biopsy specimens, abolished by the addition of t
102 e acid-induced apoptosis assay to colorectal mucosal biopsies, the percentage of apoptosis was found
103 ssor were elevated at each of the three oral mucosal biopsy time points examined (day 2 to 4, 14 to 2
105 incubated with soluble mediators released by mucosal biopsies to highlight the mechanisms involved in
106 y shown that in vitro exposure of colorectal mucosal biopsies to low concentrations of bile acids pro
108 eration of the clinical features and colonic mucosal biopsies usually lead to the correct diagnosis a
109 to obtain reparative cells from an olfactory mucosal biopsy via intranasal endoscopy rather than requ
115 nd postintervention stool samples and rectal mucosal biopsies were collected and used to quantify cal
118 ving grapefruit juice, small bowel and colon mucosal biopsies were obtained endoscopically, oral felo
120 In the later period of the review, antral mucosal biopsies were performed through the juxtapyloric
122 Three months after randomization, gastric mucosal biopsies were taken for H. pylori culture and hi
126 duced damage and impaired closure of colonic mucosal biopsy wounds, which coincided with impaired neu