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1 CML28 was used to generate a CML28-specific murine monoclonal antibody.
2 cytometry using FITC-conjugated anti-rat IgM murine monoclonal antibody.
3 y after single administration was lower than murine monoclonal antibodies.
4 ified enzyme was used to generate a panel of murine monoclonal antibodies.
5 ked immunosorbent assay using group-specific murine monoclonal antibodies.
6 es have been defined and characterized using murine monoclonal antibodies.
7 ine pancreas was used to generate a panel of murine monoclonal antibodies.
8 ) and light (L) chains were determined for a murine monoclonal antibody, 12/231/93, which is specific
11 in an orthotopic murine xenograft using the murine monoclonal antibody 17.1A conjugated to the photo
14 c efficacy of astatine-211 ((211)At)-labeled murine monoclonal antibody 7G7/B6 alone and in combinati
15 that reduced binding and neutralization by a murine monoclonal antibody (A20) were localized, while m
17 al growth factor receptor chimeric human and murine monoclonal antibody, administered with cisplatin
18 celiac-toxic epitopes was measured by using murine monoclonal antibodies against gliadin and high-mo
21 ecular rationale for the inability to obtain murine monoclonal antibodies against the receptor bindin
22 chemotaxis of human VSMCs that is blocked by murine monoclonal antibody against CCR8 and by the G-pro
23 nal anti-CCR8 antibody and a newly developed murine monoclonal antibody against CCR8 inhibited this a
24 man macrophages using virions opsonized by a murine monoclonal antibody against the MV hemagglutinin
25 the immune response, which develops against murine monoclonal antibodies, allowing for multiple dose
28 finity-purified immunoglobulin fractions and murine monoclonal antibodies and show that antibodies to
30 Fv antibody fragments from the CD20-specific murine monoclonal antibody B9E9 were genetically enginee
32 the present study we have identified a novel murine monoclonal antibody, BOB93, which bound to the su
33 (90)Y-ibritumomab tiuxetan consists of a murine monoclonal antibody covalently attached to a meta
35 e further characterized the targeting of the murine monoclonal antibody DAB4 specifically to dead tum
39 assigned to receive 2 doses of either E5, a murine monoclonal antibody directed against endotoxin (n
40 been most widely used clinically is OKT3, a murine monoclonal antibody directed against the CD3 rece
41 uzumab (HuM195) is an unconjugated humanized murine monoclonal antibody directed against the cell sur
43 ignificant limitation to the repeated use of murine monoclonal antibodies for treatment of transplant
46 e characterization of a broadly neutralizing murine monoclonal antibody, H5M9, to most H5N1 clades an
49 e number of isolates that did not react with murine monoclonal antibodies indicates that DNA sequence
50 neutralizing epitopes on gD2 are targeted by murine monoclonal antibodies, it is not known whether th
51 man platelet factor 4 (PF4)/heparin-specific murine monoclonal antibody (KKO) binds to peripheral blo
54 ation of each of the 3 human FcgammaR, using murine monoclonal antibodies (mAb) to each receptor as a
56 rmined the affinities of two cocaine-binding murine monoclonal antibodies (mAb: clones 3P1A6 and MM02
60 (1), IgG(2a), and IgG(2b) switch variants of murine monoclonal antibody (mAb) 3E5 IgG(3) with identic
61 ducreyi 35000 defective in expression of the murine monoclonal antibody (MAb) 3F11 epitope on H. ducr
64 y, the use of a radiolabeled fibril-reactive murine monoclonal antibody (mAb) as an amyloid-specific
65 imicrotubule agent, covalently linked to the murine monoclonal antibody (mAb) B-B4 targeting syndecan
66 We investigated the functional activity of murine monoclonal antibody (MAb) B5 that recognizes a hi
67 igated the antigenic targets of a protective murine monoclonal antibody (MAb) prepared against a N-Pr
69 III coat protein of fd phage using C355.1, a murine monoclonal antibody (mAb) that recognizes a confo
71 To circumvent this problem, we developed a murine monoclonal antibody (mAb) to human (h) PF4/hepari
74 study tested the hypothesis that a humanized murine monoclonal antibody (MAb) would protect against R
80 d evaluated for the effects of GPVI-specific murine monoclonal antibodies (mAbs) on platelet survival
82 apeutic doses of 131I-labeled NP-4 and MN-14 murine monoclonal antibodies (MAbs) reactive with carcin
87 ) to determine the reactivity patterns of 21 murine monoclonal antibodies (MAbs) with structurally de
89 e generated and subsequently characterized 7 murine monoclonal antibodies (MAbs), which fell into 4 d
90 ressed this question using quinine-dependent murine monoclonal antibodies (mAbs), which, in vitro and
95 s evaluated with a group of affinity-diverse murine monoclonal antibodies (MoAbs) specific for human
97 sted the hypothesis that the CA-125-specific murine monoclonal antibody, oregovomab, administered as
99 [Chemical reaction: See text] 29G12 is a murine monoclonal antibody programmed to catalyze the re
102 ts with adenocarcinomas reactive to NR-LU-10 murine monoclonal antibody received the 3 components.
105 ue immunoassays with human IgE antibodies or murine monoclonal antibodies showed that these allergens
106 Here we report the development of novel murine monoclonal antibodies specific for different G4 D
111 avy- and light-chain variable regions from a murine monoclonal antibody that recognize Pseudomonas ae
113 ilized Fv fragment (dsFv) was derived from a murine monoclonal antibody that recognizes the alpha sub
114 ensitive), each conjugated with mAb H18/7, a murine monoclonal antibody that recognizes the extracell
117 adult bone marrow mononuclear cells using a murine monoclonal antibody to human platelet glycoprotei
119 (Id)-bearing antibodies sharing an Id with a murine monoclonal antibody to myelin basic protein pepti
122 fragments of CB2, an immunoglobulin G1kappa murine monoclonal antibody, to an epitope in the carboxy
124 sis, we treated human endothelial cells with murine monoclonal antibody W6/32 to HLA class I and then
129 22 different serovar-specific or bispecific murine monoclonal antibodies were localized with synthet
132 thymectomized and treated with Ox8 and Ox38 murine monoclonal antibodies, which deplete CD8+ and CD4
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