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1  as PTPsigma and CD45 (also called leukocyte common antigen).
2 d did not contain cells expressing leukocyte common antigen.
3 t the Ly5 locus, which encodes the leukocyte common antigen.
4 ce antigens, and HSP60 was identified as one common antigen.
5 is of lipopolysaccharide and enterobacterial common antigen.
6 ighly improbable and suggests selection by a common antigen.
7 nal selection in T-LGL, possibly driven by a common antigen.
8 s detected with immunostaining for leukocyte common antigen.
9  of multiple Candida species opsonized via a common antigen.
10 ecE was unable to synthesize enterobacterial common antigen.
11 cts, suggesting clonal expansion driven by a common antigen.
12 ollicular zones, suggesting recognition of a common antigen.
13 nds serving bacterial colonization belong to common antigens.
14 clusters based on autoantibody expression to common antigens.
15 in 40 of 61 cases including many of the less common antigens.
16 noncapsulated strain, which expose many such common antigens.
17 protein and prothrombin are considered to be common antigens.
18 ma and glioma cells, respectively, may share common antigens.
19  two different sugar chains, the homopolymer common antigen (A band) and the heteropolymer O antigen
20 g an enzyme that polymerizes enterobacterial common antigen, a surface polysaccharide different from
21 geneic canine and human meningiomas, showing common antigens across breed and species.
22 bile only in the presence of enterobacterial common antigen, an outer-membrane glycolipid that contri
23 ed with comparable frequencies as with other common antigens and were sustained over time.
24 al staining for cytokeratin, CD45 (leukocyte common antigen), and a hepatocyte-specific antigen.
25              CD45 is also known as leukocyte common antigen, and it is expressed in virtually all whi
26 ratory dysfunction, asthma, sensitization to common antigens, and more.
27  gliomas, have been shown in humans to share common antigens at the RNA level.
28 ccharide, peptidoglycan, and enterobacterial common antigen biosynthesis in Proteobacteria.
29                  Although innocuous to some, common antigens can cause serious allergic reactions in
30 njugates in which cell wall teichoic acid (a common antigen capable of T cell activation) is coupled
31 y MSCs, nor were expression of the leukocyte common antigen CD45 and the cytokine transcriptional act
32 MV UL11 protein interacts with the leukocyte common antigen CD45, a cellular receptor tyrosine phosph
33 his glycoprotein was identified as leukocyte common antigen (CD45) by immunoprecipitation with a spec
34 antified by immunofluorescence for leukocyte common antigen (CD45).
35 pha SMA), vimentin, fibulin-2, and leukocyte common antigen (CD45).
36               Cells expressing the leukocyte common antigen, CD45(+), entered the area of infection f
37 pecific membrane molecule, and the leukocyte common antigen, CD45.
38 by both the C. difficile toxin A (Tox A) and common antigen components of the Triage Panel had cytoto
39 ty of samples positive only for C. difficile common antigen contained nontoxigenic bacteria.
40 water-soluble cyclic form of enterobacterial common antigen (ECA(CYC)) from Escherichia coli K-12 as
41      Phosphoglyceride-linked enterobacterial common antigen (ECA(PG)) is a cell surface glycolipid th
42 sphoglyceride-linked form of enterobacterial common antigen (ECA(PG)) occurs by a mechanism that invo
43 two surface polysaccharides: enterobacterial common antigen (ECA) and a high-molecular-weight O-chain
44 The polysaccharide chains of enterobacterial common antigen (ECA) are comprised of the trisaccharide
45 hat rffH, a gene involved in enterobacterial common antigen (ECA) biosynthesis, is partly deleted in
46                              Enterobacterial common antigen (ECA) is expressed by Gram-negative bacte
47 onsible for synthesis of the enterobacterial common antigen (ECA), a glycolipid situated on the outer
48 olved in the biosynthesis of enterobacterial common antigen (ECA), a non-essential outer membrane gly
49 characterize the role of the enterobacterial common antigen (ECA), a surface glycolipid ubiquitous am
50 equired for the synthesis of enterobacterial common antigen (ECA), suggesting that H. ducreyi may exp
51 ss a polysaccharide known as enterobacterial common antigen (ECA), which is an attractive target for
52 ivatives, used to synthesize enterobacterial common antigen (ECA).
53  unit in the biosynthesis of enterobacterial common antigen (ECA).
54 water-soluble cyclic form of enterobacterial common antigen, ECA(CYC), purified from Escherichia coli
55 e biosynthetic locus restore enterobacterial common-antigen expression to Escherichia coli mutants de
56                   Microarray analysis of 123 common antigens failed to reveal a specific target for t
57 at TCR chain usage is non-random, suggesting common antigens for Vdelta1 and Vdelta2 lymphomas respec
58  patients implicate chronic stimulation by a common antigen, for example, persistent infection.
59 of MAB-T88 in the bacteremic enterobacterial common antigen group (p <.05).
60 in BM cells occurs within CD45(+) (leukocyte common antigen) hematopoietic cells and that the majorit
61 apsule, group II capsule and enterobacterial common antigen; (iii) genes involved in metabolic pathwa
62 atory molecule CD45 (also known as leukocyte common antigen) in Alzheimer's disease (AD).
63 n those patients with proven enterobacterial common antigen infections.
64                              CD45 (leukocyte common) antigen is a hemopoietic cell-specific tyrosine
65                          CD45, the leucocyte common antigen, is a haemopoietic cell-specific tyrosine
66  (PS), E-Selectin (ES), platelets, leukocyte common antigen, macrophages, T cells, and neutrophils in
67 tigen inclusion has been challenged and new, common antigens may have to be defined to achieve the go
68                            Additionally, the common antigens may serve as potential feline vaccine ca
69 erleukin 2 (IL-2) secretion in response to a common antigen (mumps), N-IgG, Cl-IgG, and heat-aggregat
70 nd P[8] genotypes shared reactivity with the common antigens of Lewis b (Le(b)) and H type 1, while s
71  production is cumbersome; thus, targeting a common antigen on malignant B cells using an off-the-she
72                                  From the 25 common antigens, only 36% (n = 9) have a moderate correl
73 samples were Triage Panel Tox A negative but common antigen positive.
74                   However, with Triage Panel common antigen-positive patients, a sensitive cytotoxin
75                               A Triage Panel common antigen-positive result indicated a sensitivity,
76 ll differentiation programmes, rather than a common antigen-presenting cell that they endow with appr
77 ared lineages might be driven by exposure to common antigens, previous exposure to foreign antigens w
78 es positive for at least 1 antigen, the most common antigen profiles were PfHRP2+/pAldo+/pLDH+ (167,
79  have also shown that CWPS and other species-common antigens protect against colonization by a simila
80 -existing Th(mem) cells specific for 2 other common antigens: purified protein derivative of tubercul
81 teractions, but two members of the leukocyte common antigen related (LAR) phosphatase subfamily, prot
82                                    Leukocyte-common antigen related (LAR)-like phosphatase receptors
83  tyrosine phosphatase, called LAR (leukocyte common antigen related gene), whose expression is often
84  which interact with LAR-type (for leukocyte common antigen related) receptor proteins with tyrosine
85 eptor protein tyrosine phosphatase leukocyte common antigen-related (LAR) and other synaptic proteins
86  along with its sister phosphatase leukocyte common antigen-related (LAR) and the nogo receptors 1 an
87                                    Leukocyte common antigen-related (LAR) family receptor protein tyr
88 nd genomic clones encoding the rat leukocyte common antigen-related (LAR) PTP receptor predicted a sm
89 er of receptor PTPs, including the leukocyte common antigen-related (LAR) receptor and PTPmu, contain
90                                The leukocyte common antigen-related (LAR) receptor is known to be pre
91 enetically and physically with the leukocyte common antigen-related (Lar) receptor protein tyrosine p
92                                    Leukocyte-common antigen-related (LAR) receptor tyrosine phosphata
93 ophila and vertebrate rPTPs of the Leukocyte common antigen-related (LAR) subfamily.
94 omain-containing PTPase-2 (SHP-2), leukocyte common antigen-related (LAR), and leukocyte antigen-rela
95 rosine phosphatase (PTP)-alpha and leukocyte common antigen-related (LAR), were detected predominantl
96 e phosphatase sigma (PTPsigma) and leukocyte common antigen-related phosphatase (LAR), have been iden
97 ctions with neuronal transmembrane leukocyte common antigen-related phosphatase (LAR).
98               We also identify the leukocyte common antigen-related phosphatase receptor (PTPRF) as a
99  the receptor tyrosine phosphatase leukocyte common antigen-related protein (LAR) negatively regulate
100 s very similar to that observed in leukocyte common antigen-related protein with both active sites in
101     It has long been proposed that leukocyte common antigen-related receptor protein tyrosine phospha
102                                The leucocyte common antigen-related receptor tyrosine phosphatase int
103 s caused by down-regulation of the leukocyte common antigen-related tyrosine phosphatase receptor tha
104 tein-tyrosine phosphatase LAR (for leukocyte common antigen-related) has been implicated as a physiol
105 of presynaptic SAMs, Neurexins and leukocyte common antigen-related-type receptor phospho-tyrosine ph
106 e (PTP)-delta, PTP-sigma, and LAR (leukocyte common-antigen-related)] and the type III RPTP, PTP rece
107 tting suggested that EtpA is one of the most common antigens secreted by these pathogens.
108                           We speculated that common antigens shared by these viruses explain this fin
109 array of 24 vaccine-, endemic pathogen-, and common antigen-specific antibodies were assessed across
110 tal ion coordination and the generation of a common antigen specificity in CBD.
111                                     The most common antigen target for ANCAs is myeloperoxidase (MPO)
112  by the host of a limited immune response to common antigens that are likely not involved in adherenc
113 Evidence suggests that these tissues share a common antigen: the thyroid-stimulating hormone receptor
114             The high NPV of the Triage Panel common antigen, together with rapid reporting of results
115 rotein (VP)-4 and VP7, and group A rotavirus common antigen VP6 were analyzed by an immunocytochemist
116  LOS core (galU), as well as enterobacterial common antigen (wecB and wecC), is important for surviva
117    Although leukemia cells undoubtedly share common antigens with other tissues of the recipient resu

 
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