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1 y (P < .001 for each variable, compared with secretors).
2 ting and therefore filamented bacteria (high secretors).
3 ic E. coli isolates compared with cells from secretors.
4 l P[8]/P[4] rotavirus infected children were secretors.
5 R that prepares cells to become professional secretors.
6 pectrum to saliva samples of all A, B, and O secretors.
7 GII.4 norovirus exclusively infected secretors.
8 effector programs, but remained stable IL-17 secretors.
9 competent cytotoxic effectors and IFN-gamma secretors.
10 frequencies of cross-reactive IL-4 and IL-2 secretors.
13 The presence of histo-blood group antigens (secretor, ABO, and Lewis type) was determined in saliva.
16 ells are capable of acting as both IFN-gamma secretors and cytotoxic T lymphocyte (CTL) effectors; ho
17 ive status, including those with A, B, and O secretors and Lewis positive blood types, were sensitive
19 HMO concentrations from women classified as secretors and nonsecretors, a phenotype that can be iden
20 , were sensitive to the virus, while the non-secretors and the Lewis negative individual were not.
22 he GI.7 strain bound to H- and A-type, Lewis secretor, and Lewis nonsecretor families of HBGAs, allow
23 arious types 1 and 2 HBGAs, including Lewis, secretor, and nonsecretor antigens, distributing on the
24 ree patterns (VA387, NV, and MOH) recognized secretors, and 1 pattern (VA207) recognized Lewis-positi
28 s that do not secrete IL-9, as purified IL-9 secretors demonstrate the same loss of IL-9 in subsequen
30 ions is determined by genetically controlled secretor-dependent expression of histo-blood group antig
33 uals with a functional FUT2 gene are termed "secretors." FUT2 polymorphisms may influence viral bindi
34 viduals have a functional copy of the FUT2 ("secretor") gene required for gut HBGA expression; these
36 (n=843) expressing the combined MBL2 5' LYQA secretor haplotype (CGTCGG) and 3' haplotype (CGGGT) was
41 ntraoperative variables to determine if MBL2 secretor haplotypes are independent predictors of PMI in
45 exchanger 2 (AE2), the principal bicarbonate secretor in the human biliary tree, is down-regulated in
46 certain Mm non-producing mutants to act as 'secretors' in cosynthesis with other 'convertor' mutants
47 enhanced functionality (i.e., multicytokine secretors, including IL-2; enhanced CD137 and CD107a exp
49 ain structure of a 2004 variant with ABH and secretor Lewis HBGAs and compared it with the previously
52 rates of non-GII.4 infections were found in secretor-negative children (relative risk, 0.56; P = .02
56 tzii A2-165 and Clostridium hathewayi, a low secretor of IL-10, on the Th1-driven inflammatory respon
57 thcare-acquired infections and is a prolific secretor of proteins, including three chitinases (ChiA,
58 ells (pDCs) have been identified as a potent secretor of the type I interferons (IFNs) in response to
60 only as a permeability barrier but also as a secretor of urinary proteins that can play physiological
61 only 2 (5%) of 44 consistent or intermittent secretors of acid had ratios in this range (P<.001).
62 ing tumour was a prolactinoma; three ectopic secretors of ACTH (two bronchial and one thymic carcinoi
64 0 aa not linked to a signal peptide are poor secretors of IL-16 and show little if any resistance to
66 tional CD4(+) effector T cells identified as secretors of prototypical cytokines IFNgamma, IL4, IL9,
67 transplant recipients studied who were high secretors of S-HLA-I postoperatively carried HLA-A24 or
71 ikely than norovirus-negative controls to be secretors (P < .001) in a logistic regression model adju
74 ltransferase gene (FUT2) responsible for the secretor phenotype is required for susceptibility to Nor
75 um P[8]/P[4]-specific IgG and host Lewis and secretor phenotypes has been found among 206 studied ser
76 atic patients showed that individuals with a secretor positive status, including those with A, B, and
77 ximately 1320 genomic equivalents [gEq]) for secretor-positive blood group O or A persons and 7.0 (ap
78 RV strains (n = 27) infected only Lewis- and secretor-positive children (27/27; P < .0001), but no Le
79 II, genotype 4 (GII.4) infections were among secretor-positive children (P < .001), but higher rates
80 GII.4 infections were uniquely detected in secretor-positive children, while non-GII.4 infections w
91 EC and determined that nonsecretors (but not secretors) selectively express two extended globoseries
92 lyses assessed the preventive association of secretor status against severe rotavirus gastroenteritis
94 d whether an association exists between FUT2 secretor status and laboratory-confirmed rotavirus infec
97 A24 or HLA-A29 resulted in the observed high secretor status in liver transplant recipients after tra
98 tibility to some noroviruses depends on FUT2 secretor status, but the population impact of this assoc
106 nvironment, however, our model predicts that secretor strains of any one species will be surrounded b
107 expression; these individuals are known as "secretors." Susceptibility to some noroviruses depends o
108 igh proportion of nonsecreting bacteria (low secretors) than from populations with a high proportion
109 CA11 gene appears to be located between the secretor type alpha(1,2)-fucosyltransferase gene cluster
114 Strain VA387 binds to HBGAs of A, B, and O secretors, whereas strain MOH binds to HBGAs of A and B
116 s Pseudomonas aeruginosa, a prolific protein secretor with the potential to produce seven different s
117 d by FUT2), an intermediate rate (30%) among secretors with non-blood group O, and the highest rate (
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