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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
19 geneic canine and human meningiomas, showing common antigens across breed and species.
20 bile only in the presence of enterobacterial common antigen, an outer-membrane glycolipid that contri
21 al staining for cytokeratin, CD45 (leukocyte common antigen), and a hepatocyte-specific antigen.
22              CD45 is also known as leukocyte common antigen, and it is expressed in virtually all whi
23 ratory dysfunction, asthma, sensitization to common antigens, and more.
24  gliomas, have been shown in humans to share common antigens at the RNA level.
25                  Although innocuous to some, common antigens can cause serious allergic reactions in
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
30 pha SMA), vimentin, fibulin-2, and leukocyte common antigen (CD45).
31 antified by immunofluorescence for leukocyte common antigen (CD45).
32               Cells expressing the leukocyte common antigen, CD45(+), entered the area of infection f
33 pecific membrane molecule, and the leukocyte common antigen, CD45.
34 by both the C. difficile toxin A (Tox A) and common antigen components of the Triage Panel had cytoto
35 ty of samples positive only for C. difficile common antigen contained nontoxigenic bacteria.
36 water-soluble cyclic form of enterobacterial common antigen (ECA(CYC)) from Escherichia coli K-12 as
37      Phosphoglyceride-linked enterobacterial common antigen (ECA(PG)) is a cell surface glycolipid th
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
41                              Enterobacterial common antigen (ECA) is expressed by Gram-negative bacte
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
47  unit in the biosynthesis of enterobacterial common antigen (ECA).
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
50  patients implicate chronic stimulation by a common antigen, for example, persistent infection.
51 of MAB-T88 in the bacteremic enterobacterial common antigen group (p <.05).
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
54 atory molecule CD45 (also known as leukocyte common antigen) in Alzheimer's disease (AD).
55 n those patients with proven enterobacterial common antigen infections.
56                              CD45 (leukocyte common) antigen is a hemopoietic cell-specific tyrosine
57                          CD45, the leucocyte common antigen, is a haemopoietic cell-specific tyrosine
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
60                            Additionally, the common antigens may serve as potential feline vaccine ca
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
64 samples were Triage Panel Tox A negative but common antigen positive.
65                   However, with Triage Panel common antigen-positive patients, a sensitive cytotoxin
66                               A Triage Panel common antigen-positive result indicated a sensitivity,
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
70                                    Leukocyte-common antigen related (LAR)-like phosphatase receptors
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
75                                    Leukocyte common antigen-related (LAR) family receptor protein tyr
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
78                                The leukocyte common antigen-related (LAR) receptor is known to be pre
79 enetically and physically with the leukocyte common antigen-related (Lar) receptor protein tyrosine p
80                                    Leukocyte-common antigen-related (LAR) receptor tyrosine phosphata
81 ophila and vertebrate rPTPs of the Leukocyte common antigen-related (LAR) subfamily.
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
85 ctions with neuronal transmembrane leukocyte common antigen-related phosphatase (LAR).
86               We also identify the leukocyte common antigen-related phosphatase receptor (PTPRF) as a
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
89                                The leucocyte common antigen-related receptor tyrosine phosphatase int
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
93 tting suggested that EtpA is one of the most common antigens secreted by these pathogens.
94                           We speculated that common antigens shared by these viruses explain this fin
95 tal ion coordination and the generation of a common antigen specificity in CBD.
96                                     The most common antigen target for ANCAs is myeloperoxidase (MPO)
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
99             The high NPV of the Triage Panel common antigen, together with rapid reporting of results
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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