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1 opic tumors selectively using an activatable immunoconjugate.
2 in >95% of the (64)Cu being chelated by the immunoconjugate.
3 cted tumor, which synthesize and secrete the immunoconjugates.
4 cells and complement in the presence of the immunoconjugates.
5 ) to the activity of bivalent IgG-containing immunoconjugates.
6 und to the radiometal to create radiolabeled immunoconjugates.
7 ell death induced by the fusion peptides and immunoconjugates.
8 competitive binding assay demonstrates that immunoconjugate 2 binds to SKOV3 tumor cells comparably
10 Using fluorescence microendoscopy to monitor immunoconjugate activation and micrometastatic disease,
11 The results demonstrate that a mutated fVII immunoconjugate, administered separately or together wit
14 icited by active immunization with a cocaine immunoconjugate and binds free cocaine with excellent sp
15 lanoma protein was immunoprecipitated by the immunoconjugates and analyzed by mass spectrometry, usin
18 in vitro FcgammaRI binding of deglycosylated immunoconjugates and significant decreases in the in viv
19 ells were conducted with the photosensitizer immunoconjugates and, for comparison, with free PPa.
21 sine kinase inhibitors, synthetic retinoids, immunoconjugates, and immunosuppressive molecules with n
24 n prostate cancer, especially with anti-HER3 immunoconjugates, and targeting HER3 warrants clinical e
25 the development of a mouse B cell-depleting immunoconjugate (anti-CD22 monoclonal antibody [mAb] con
26 SMA(ext), thus targeting viable tumor, these immunoconjugates are better candidates for targeted radi
34 we synthesized an HER2-targeting trastuzumab immunoconjugate bearing a NIR-II aza-BODIPY fluorophore.
38 ature, presumably mediated by the factor VII immunoconjugate bound to tissue factor on neovasculature
39 n chemotherapy strategies, radiotherapy, the immunoconjugate brentuximab, checkpoint inhibitors nivol
41 second-generation TF-targeting antibody-like immunoconjugate (called L-ICON) for preclinical treatmen
44 4 days after treatment with a single dose of immunoconjugate carrying 2.5 ng of Dox, LoVo and SW-480
45 refractory CD33(+) AML were treated with an immunoconjugate (CMA-676) consisting of humanized anti-C
47 tion-incompetent adenoviral vectors encoding immunoconjugates composed of the Fc region of an IgG1 im
52 a crenulata (KLH) were prepared as effective immunoconjugates containing a sensitive fluorescent repo
53 othelial cells and tumor cells, a factor VII immunoconjugate could be used for immunotherapy against
54 tive vaccination of mature rats with ghrelin immunoconjugates decreases feed efficiency, relative adi
56 itro cytolysis assay was used to test for an immunoconjugate-dependent specific cytolytic response ag
58 N,N',N",N"'-tetraacetic acid) and the intact immunoconjugate DOTA-NR-LU-10 were labeled to high speci
59 experiments with 2IT-BAD-Lym-1 and a second immunoconjugate, DOTA-peptide-chimeric L6, with 248-492
60 that intratumoral delivery of the factor VII immunoconjugate, either alone or together with the singl
62 of acute myeloid leukemia and a doxorubicin immunoconjugate for treatment of carcinoma have recently
64 men described here could be applied to other immunoconjugates for targeted therapy of a broad spectru
65 of targeted amphipathic fusion peptides and immunoconjugates for the ablation of prostate cancer cel
66 per L) could receive an initial dose of the immunoconjugate gemtuzumab ozogamicin (6 mg/m(2) intrave
68 unization with the second-generation cocaine immunoconjugate GND-keyhole limpet hemocyanin (KLH) or w
75 reviously that an interferon (IFN)-MAb (1:1) immunoconjugate (IC) enhances tumor uptake by a factor o
77 ules and anti-LFA-1-Ricin and anti-Iak-Ricin immunoconjugates (IC) were prepared and administered in
80 ls and can be used as a target for cytotoxic immunoconjugates (ICs), in which cell-killing moieties,
87 Gemtuzumab ozogamicin (GO), a CD33-targeted immunoconjugate, is a re-emerging therapy for acute myel
88 nical studies using the (111)In radiolabeled immunoconjugate, MAb 7E11-C5.3-GYK-DTPA (capromab pendet
90 erapy with a HER50 and HER66 photosensitizer immunoconjugate mixture was significantly more effective
92 e treatment involves systemic delivery of an immunoconjugate molecule composed of a tumor-targeting d
97 describe the preclinical profile of another immunoconjugate of CalichDMH, CMC-544, targeted to CD22
98 tuzumab ozogamicin (CMA-676, a CD33-targeted immunoconjugate of N-acetyl-gamma-calicheamicin dimethyl
100 model of human colorectal carcinoma using an immunoconjugate of the huA33 antibody modified with TCO
104 ype-specific anti-Ia mAb, haplotype-specific immunoconjugates, or mAb directed against graft APC, adh
105 r-killing power of toxic effector molecules, immunoconjugates permit sensitive discrimination between
106 vent spurs antibody production against these immunoconjugates, possibly leading to drug sequestration
113 The specificity of antibodies have made immunoconjugates promising vectors for the delivery of r
114 rapy with a single anti-HER2 photosensitizer immunoconjugate, provided photosensitizer immunoconjugat
115 e of radiation-induced damage of 90Y-labeled immunoconjugate radiopharmaceuticals during preparation
116 ies (ENb) and imageable and proapoptotic ENb immunoconjugates released from stem cells (SC) to ultima
119 cination of GIX(+) mice with six unique METH immunoconjugates resulted in high antibody titers for th
120 r alone or together with the single-chain Fv immunoconjugate, resulted in growth inhibition and regre
121 g properties and rapid systemic clearance of immunoconjugates should lead to the design of effective
122 mor barrier and an (89)Zr-labeled pritumumab immunoconjugate showed the antibody specifically targete
130 eparately or together with a single-chain Fv immunoconjugate that binds to the tumor cells, can inhib
133 C242-DM1 represents a new generation of immunoconjugates that may yet fulfill the promise of eff
138 for the first time the use of micromagnetic immunoconjugates to establish a direct competitive assay
139 eloped fluorophore- and radioisotope-labeled immunoconjugates to target a DDR signaling protein, phos
141 tope HER2 targeting to boost photosensitizer immunoconjugate uptake as a way of enhancing photoimmuno
142 emtuzumab ozogamicin (GO; Mylotarg), a novel immunoconjugate used for treatment of acute myeloid leuk
146 cell adhesion molecule (EpCAM) targeting MMC-immunoconjugate was prepared and dual-labeled with (64)C
153 ulfanyl(alkanoyl) groups for taxoid-antibody immunoconjugates were designed, synthesized and their ac
158 hototoxic than free PPa, but photosensitizer immunoconjugates were selective for target cells whereas
161 thesized a series of desferrioxamine-bearing immunoconjugates with differing glycosylation states and
162 conjugates (ADCs) represent a novel class of immunoconjugates with growing therapeutic relevance, sin
165 riginally developed to label photosensitizer immunoconjugates with the photosensitizer, benzoporphyri