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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
22 bile only in the presence of enterobacterial common antigen, an outer-membrane glycolipid that contri
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
38 by both the C. difficile toxin A (Tox A) and common antigen components of the Triage Panel had cytoto
40 water-soluble cyclic form of enterobacterial common antigen (ECA(CYC)) from Escherichia coli K-12 as
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
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
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
57 at TCR chain usage is non-random, suggesting common antigens for Vdelta1 and Vdelta2 lymphomas respec
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
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
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
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
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
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
91 enetically and physically with the leukocyte common antigen-related (Lar) receptor protein tyrosine p
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
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
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
109 array of 24 vaccine-, endemic pathogen-, and common antigen-specific antibodies were assessed across
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
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