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1 as PTPsigma and CD45 (also called leukocyte common antigen).
2 ce antigens, and HSP60 was identified as one common antigen.
3 cts, suggesting clonal expansion driven by a common antigen.
4 is of lipopolysaccharide and enterobacterial common antigen.
5 ighly improbable and suggests selection by a common antigen.
6 nal selection in T-LGL, possibly driven by a common antigen.
7 s detected with immunostaining for leukocyte common antigen.
8 of multiple Candida species opsonized via a common antigen.
9 ecE was unable to synthesize enterobacterial common antigen.
10 ollicular zones, suggesting recognition of a common antigen.
11 d did not contain cells expressing leukocyte common antigen.
12 t the Ly5 locus, which encodes the leukocyte common antigen.
13 noncapsulated strain, which expose many such common antigens.
14 protein and prothrombin are considered to be common antigens.
15 ma and glioma cells, respectively, may share common antigens.
16 nds serving bacterial colonization belong to common antigens.
17 two different sugar chains, the homopolymer common antigen (A band) and the heteropolymer O antigen
18 g an enzyme that polymerizes enterobacterial common antigen, a surface polysaccharide different from
20 bile only in the presence of enterobacterial common antigen, an outer-membrane glycolipid that contri
26 njugates in which cell wall teichoic acid (a common antigen capable of T cell activation) is coupled
27 y MSCs, nor were expression of the leukocyte common antigen CD45 and the cytokine transcriptional act
28 MV UL11 protein interacts with the leukocyte common antigen CD45, a cellular receptor tyrosine phosph
29 his glycoprotein was identified as leukocyte common antigen (CD45) by immunoprecipitation with a spec
34 by both the C. difficile toxin A (Tox A) and common antigen components of the Triage Panel had cytoto
36 water-soluble cyclic form of enterobacterial common antigen (ECA(CYC)) from Escherichia coli K-12 as
38 sphoglyceride-linked form of enterobacterial common antigen (ECA(PG)) occurs by a mechanism that invo
39 The polysaccharide chains of enterobacterial common antigen (ECA) are comprised of the trisaccharide
40 hat rffH, a gene involved in enterobacterial common antigen (ECA) biosynthesis, is partly deleted in
42 onsible for synthesis of the enterobacterial common antigen (ECA), a glycolipid situated on the outer
43 olved in the biosynthesis of enterobacterial common antigen (ECA), a non-essential outer membrane gly
44 characterize the role of the enterobacterial common antigen (ECA), a surface glycolipid ubiquitous am
45 equired for the synthesis of enterobacterial common antigen (ECA), suggesting that H. ducreyi may exp
46 ss a polysaccharide known as enterobacterial common antigen (ECA), which is an attractive target for
48 water-soluble cyclic form of enterobacterial common antigen, ECA(CYC), purified from Escherichia coli
49 e biosynthetic locus restore enterobacterial common-antigen expression to Escherichia coli mutants de
52 in BM cells occurs within CD45(+) (leukocyte common antigen) hematopoietic cells and that the majorit
53 apsule, group II capsule and enterobacterial common antigen; (iii) genes involved in metabolic pathwa
58 (PS), E-Selectin (ES), platelets, leukocyte common antigen, macrophages, T cells, and neutrophils in
59 tigen inclusion has been challenged and new, common antigens may have to be defined to achieve the go
61 erleukin 2 (IL-2) secretion in response to a common antigen (mumps), N-IgG, Cl-IgG, and heat-aggregat
62 nd P[8] genotypes shared reactivity with the common antigens of Lewis b (Le(b)) and H type 1, while s
63 production is cumbersome; thus, targeting a common antigen on malignant B cells using an off-the-she
67 have also shown that CWPS and other species-common antigens protect against colonization by a simila
68 -existing Th(mem) cells specific for 2 other common antigens: purified protein derivative of tubercul
69 teractions, but two members of the leukocyte common antigen related (LAR) phosphatase subfamily, prot
71 tyrosine phosphatase, called LAR (leukocyte common antigen related gene), whose expression is often
72 which interact with LAR-type (for leukocyte common antigen related) receptor proteins with tyrosine
73 eptor protein tyrosine phosphatase leukocyte common antigen-related (LAR) and other synaptic proteins
74 along with its sister phosphatase leukocyte common antigen-related (LAR) and the nogo receptors 1 an
76 nd genomic clones encoding the rat leukocyte common antigen-related (LAR) PTP receptor predicted a sm
77 er of receptor PTPs, including the leukocyte common antigen-related (LAR) receptor and PTPmu, contain
79 enetically and physically with the leukocyte common antigen-related (Lar) receptor protein tyrosine p
82 omain-containing PTPase-2 (SHP-2), leukocyte common antigen-related (LAR), and leukocyte antigen-rela
83 rosine phosphatase (PTP)-alpha and leukocyte common antigen-related (LAR), were detected predominantl
84 e phosphatase sigma (PTPsigma) and leukocyte common antigen-related phosphatase (LAR), have been iden
87 the receptor tyrosine phosphatase leukocyte common antigen-related protein (LAR) negatively regulate
88 s very similar to that observed in leukocyte common antigen-related protein with both active sites in
90 s caused by down-regulation of the leukocyte common antigen-related tyrosine phosphatase receptor tha
91 tein-tyrosine phosphatase LAR (for leukocyte common antigen-related) has been implicated as a physiol
92 e (PTP)-delta, PTP-sigma, and LAR (leukocyte common-antigen-related)] and the type III RPTP, PTP rece
97 by the host of a limited immune response to common antigens that are likely not involved in adherenc
98 Evidence suggests that these tissues share a common antigen: the thyroid-stimulating hormone receptor
100 rotein (VP)-4 and VP7, and group A rotavirus common antigen VP6 were analyzed by an immunocytochemist
101 LOS core (galU), as well as enterobacterial common antigen (wecB and wecC), is important for surviva
102 Although leukemia cells undoubtedly share common antigens with other tissues of the recipient resu
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