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1 nst human p53, have been used to construct a single-chain antibody.
2 otherapy for HIV-1 using novel CARs based on single-chain antibodies.
3 -binding regions of the microcystin-specific single-chain antibody, 3A8, with constant regions from t
5 These results indicate that such chimeric single-chain antibodies against IGF1R have future potent
6 es Edmonston-NSe vaccine strain displaying a single-chain antibody against EGFRvIII at the COOH termi
7 pendent methods, expression of intracellular single-chain antibody against HER-2 and treatment with a
9 using three carbohydrate-binding proteins, a single chain antibody, an antigen binding fragment, and
10 on solutions containing a target protein (a single chain antibody, an antigen binding fragment, or a
12 MegAnneal libraries based on three different single-chain antibodies and identified variants with enh
13 tely 100 million secreted and membrane-bound single-chain antibodies and identify antibodies that can
14 hile chimeric antigen receptors (CARs) using single-chain antibodies as binding domains are growing i
15 ould be useful in improving the stability of single-chain antibodies, as Ala/Met mutations at these c
16 een the antigen and a panel of small, 25 kDa single-chain antibodies at concentrations down to 1 nM.
19 ge, complex domains (either a 252-amino-acid single-chain antibody binding domain [scFv] or a 96-amin
20 also be achieved using a retroviral receptor-single-chain antibody bridge protein, the TVA-MR1 fusion
21 here the development of a novel, bispecific single-chain antibody (bscAb) referred to as bscEphA2xCD
22 roperties are comparable to those for stable single-chain antibodies, but are markedly improved over
23 orted earlier the delivery of antiangiogenic single chain antibodies by using oncolytic vaccinia viru
24 self-assembled nanorings (CSANs) displaying single chain antibodies can bind to both the CD3 epsilon
25 ed a membrane-tethered anti-Igkappa-reactive single chain antibody chimeric gene and expressed it as
27 mbinant proteins, and describe a new type of single chain antibody containing the entire heavy chain
29 of the FSTE with a growth factor ligand or a single-chain antibody, delivered a reporter gene selecti
31 ach requires development of a high-affinity, single chain antibody directed specifically against the
32 ticles of iron oxide (MPIOs) conjugated to a single-chain antibody directed against a ligand-induced
34 ately 5 nM) and specific localization to the single-chain antibody expressed in the endoplasmic retic
35 f chimeric antigen receptors (CARs) based on single-chain antibodies for gene immunotherapy of cancer
37 mor targeting of a novel internalizing human single chain antibody fragment (scFv) labeled with ((9)(
42 alian cell line that expresses a recombinant single-chain antibody fragment (scFv) derived from an NS
43 nes with an adenovirus (AV1Y28) expressing a single-chain antibody fragment (scFv) directed against R
44 f a hypothesis-driven mathematical model for single-chain antibody fragment (scFv) folding in Sacchar
45 h the corresponding conventional ER-targeted single-chain antibody fragment (scFv) intrabodies demons
46 cluster of differentiation 3 (CD3)-specific single-chain antibody fragment (scFv), effectively redir
48 body to its minimal functional unit (i.e., a single-chain antibody fragment [scFv]) is an effective s
49 of the AV1Y28 adenovirus, which expresses a single-chain antibody fragment directed against p21 Ras
50 sults demonstrate that the topically applied single-chain antibody fragment ESBA105 penetrated into t
52 ral vector was used to deliver a recombinant single-chain antibody fragment rabbit intrabody (pAd-2S0
53 ding and antigen-binding activity of a human single-chain antibody fragment were simultaneously impro
54 topic expression of an inhibitory anti-ATF-1 single-chain antibody fragment, ScFv, significantly inte
57 ant antivenom composed of a few neutralizing single chain antibody fragments (scFvs) that bind to two
58 is intermediate in size between peptides and single chain antibody fragments, both of which are super
62 arting from large phage display libraries of single-chain antibody fragments (scFvs), the three-stage
64 ariables by live-cell microscopic imaging of single-chain antibody fragments against carcinoembryonic
67 It has previously been reported that several single-chain antibody fragments of human origin (scFv) n
68 ity/specificity trade-offs, we have selected single-chain antibody fragments specific for the negativ
70 ells expressing tumor-associated antigens by single-chain antibodies fused to a receptor-binding-defi
73 odimer format was used to produce bispecific single chain antibody fusions and monovalent IgGs with m
75 f substantial levels of human monoclonal and single chain antibodies (>3 mg and >150 mg, respectively
76 unctional characterization of monoclonal and single-chain antibodies has become just as important as
78 es based on larger complex proteins, such as single chain antibodies, have stimulated interest in the
79 nscription are decorated specifically by the single-chain antibody HF1 and by the nuclear protein PAR
81 assessed using monoclonal antibody NV23 and single-chain antibody HJT-R3-A9 to identify both virus-l
82 inding kinetics of a recombinant mAb and its single-chain antibody homolog, single-chain variable fra
83 al growth factor]) or Hu-tagged anti-VEGFR-2 single-chain antibody (Hu-P4G7) and incubating on ice fo
84 ion X-ray structures of three high-affinity, single-chain antibodies in the 14B7 family; 14B7 and two
88 re identified by phage display from a biased single chain antibody library generated from the spleens
91 o different recombinant reporter proteins, a single-chain antibody (M18 scFv) that contains two disul
93 e second minireview describes application of single chain antibodies (nanobodies) for monitoring and
95 ignated ITEM4-rGel) and a humanized, dimeric single-chain antibody of ITEM-4 fused to rGel (designate
96 rating the Fc domain and either an anti-CD40 single-chain antibody or CD40L form stable complexes wit
100 nd expressed in high yields, relative to the single chain antibody (SCA) derivative (2 3-fold), in Es
101 essed a chimeric Sindbis gp which included a single-chain antibody (SCA) directed to the human Her2/n
103 omplementarity determining regions (CDRs) of single-chain antibody (scAb) fragments is demonstrated.
104 e displayed on the viral hemagglutinin (H) a single-chain antibody (scAb) specific for the tumor-asso
105 ed a new receptor by fusing a virus-binding, single-chain antibody (scAb) to intracellular adhesion m
106 t express (1) an intracellular, neutralizing single-chain antibody (scAb) to p21 ras (Ad.K-ras scAb),
108 iral vectors derived from SNV that displayed single-chain antibodies (scAs) directed against a carcin
110 ific antibodies by fusing the DNA encoding a single chain antibody (ScFv) after the C terminus (CH3-S
111 ing mesothelin-targeted TR3 variants using a single chain antibody (scFv) delivery format (SS-TR3), w
114 d rapid production and recovery of idiotypic single-chain antibodies (scFv) derived from each patient
116 marker CD38 was constructed in the form of a single-chain antibody (scFv) and (2) display of that scF
117 ification, we constructed an anti-annexin IV single-chain antibody (scFv) and an scFv linked to Crry,
118 l binding interface consisting of a anti-Myc single-chain antibody (ScFv) and its peptide epitope.
119 of immunotoxins containing either the human single-chain antibody (scFv) C6.5 or the murine scFv e23
120 A uniform immunoreagent was prepared from a single-chain antibody (scFv) gene specific for digoxin.
121 o biopanning strategy in which a human phage single-chain antibody (scFv) library was injected into h
124 ced by genetic fusion of a T84.66 (anti-CEA) single-chain antibody (scFv) to the human IgG1 CH3 domai
128 ding epitopes of a panel of eight agonistic, single-chain antibody (scFv-Fc) constructs were determin
129 n order to fulfill this goal, we generated a single-chain antibody (scFv47) from our parental IL13Ral
130 as characterized by stable transfection of a single chain antibody (ScFv5R) against ErbB2 containing
132 m for the comparative functional analysis of single-chain antibodies (scFvs) expressed on the plasma
133 ns of rapidly selecting tailored linkers for single-chain antibodies (scFvs) from protein linker libr
134 i mosquitoes expressing m1C3, m4B7, or m2A10 single-chain antibodies (scFvs) have significantly lower
135 een isolated by screening a library of human single-chain antibodies (scFvs) using derivatives of thi
137 venient 1E12 immunoreagent, we constructed a single chain antibody (sFv) using recombinant protein te
139 superfamily, was fused to a gene encoding a single-chain antibody (sFv) against the human transferri
141 these synthetic receptors was derived from a single-chain antibody (sFv) with specificity for Ad5 kno
142 r, coexpression of an intracellular anti-Rev single-chain antibody (SFv), which has been shown to int
143 roach based upon intracellular expression of single-chain antibodies (sFvs) to achieve modulation of
144 A recombinant PfCHT1/PgCHT2-neutralizing single-chain antibody significantly reduced P. falciparu
145 tilizing Herceptin and its derived humanized single-chain antibody (single-chain fragment variable, d
146 d gas-filled MBs were conjugated to either a single-chain antibody specific for activated glycoprotei
149 show that custom superantigens generated by single chain antibody technology permit the study of tol
150 n, we generated a CSPG4-specific fully human single-chain antibody termed scFv-FcC21 and characterize
151 orm for the selection of very high affinity, single-chain antibodies that have tremendous potential a
152 achment of sporozoites to salivary glands; a single-chain antibody that agglutinates sporozoites; or
153 n leukosis viruses (ALV-A), fused to the MR1 single-chain antibody that binds specifically to EGFRvII
155 is-regulatory elements to express an encoded single-chain antibody that prevents the P3A2 protein fro
156 mpetitive selection techniques to generate a single-chain antibody that shows >1000-fold discriminati
157 s approach we have developed a CCR5-specific single-chain antibody that was expressed intracellularly
158 e enhanced by inclusion of sequences such as single-chain antibodies to target the antigen to DCs.
161 F) was expressed, consisting of a His tag, a single-chain antibody to the myeloid antigen CD33, and t
164 and experimental validation of two different single-chain antibody variable fragment libraries that e
166 using two different binding scaffold types (single-chain antibody variable fragments and fibronectin
167 we have generated immune-challenged chicken single-chain antibody variable-region fragment (scFv) li
168 rapeutic applications.The therapeutic use of single-chain antibodies (VHHs) is limited by their short
170 al vector (33E67) containing a CD33-specific single-chain antibody was generated in an attempt to tar
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