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1 novel radiolabeled small molecules targeting prostate-specific membrane antigen.
2 specificity for the extracellular domain of prostate-specific membrane antigen.
3 investigated whether and how (68)Ga-labeled prostate-specific membrane antigen 11 ((68)Ga-PSMA-11) P
4 luate the feasibility of rechallenge (177)Lu-prostate-specific membrane antigen ((177)Lu-PSMA) radiol
5 e of early PSA changes after (177)Lu-labeled prostate-specific membrane antigen ((177)Lu-PSMA) radion
6 an serve as a response predictor for (177)Lu-prostate-specific membrane antigen 617 (PSMA) radioligan
7 in recipients of (177)Lu-DOTATOC or (177)Lu-prostate specific membrane antigen-617 (PSMA) radioligan
10 his study was to assess the impact of (68)Ga-prostate-specific membrane antigen ((68)Ga-PSMA) PET/CT
11 heses, or pedicle screws) and (68)Ga-labeled prostate-specific membrane antigen ((68)Ga-PSMA) PET/CT
13 investigate if the new tracer targeting the prostate-specific membrane antigen ((68)Ga-PSMA-11) coul
14 ents receiving (18)F-fluciclovine and (68)Ga-prostate-specific membrane antigen ((68)Ga-PSMA-11) for
15 onjugates with RNA aptamers that bind to the prostate-specific membrane antigen, a well-known prostat
17 cancer, antibodies to key antigens, such as prostate specific membrane antigen, along with metabolic
18 tate cancer (SyAM-Ps)-bind simultaneously to prostate-specific membrane antigen and Fc gamma receptor
19 )In-DOTAGA-(3-iodo-y)-f-k-Sub(KuE)) (PSMA is prostate-specific membrane antigen and I&T is imaging an
20 ing RLT with (177)Lu-DOTATATE, -DOTATOC, or -prostate-specific membrane antigen and showing laborator
21 acetic acid octreotate (or DOTATATE), (68)Ga prostate-specific membrane antigen, and (18)F-fluciclovi
22 es that target prostate-specific antigen and prostate-specific membrane antigen, and drugs that can b
23 against tumor-associated antigens, including prostate-specific membrane antigen, and elimination of p
24 vesicles displaying an aptamer that binds to prostate-specific membrane antigen, and loaded with surv
25 an spectroscopy, exogenous fluoroscopy using prostate-specific membrane antigen, and so on have led t
26 nal antibodies, antibody therapies targeting prostate-specific membrane antigen, and vaccines such as
27 PET and monoclonal antibody imaging with the prostate specific membrane antigen antibody (111)In-capr
31 ke therapeutics in which a derivative of the prostate-specific membrane antigen-binding small molecul
32 those directed to glucose, choline, acetate, prostate-specific membrane antigen, bombesin, and amino
33 KLK3 (prostate-specific antigen ) and FOLH1 (prostate-specific membrane antigen) but not in AR and KL
34 ion dependent upon T-cell recognition of the prostate-specific membrane antigen by a chimeric antigen
35 treatment of advanced prostate cancer using prostate-specific membrane antigen-directed radionuclide
36 d to assessment of (177)Lu-PSMA-617 therapy (Prostate-Specific Membrane Antigen) for metastatic prost
37 from the prostate-specific antigen (PSA) and prostate-specific membrane antigen gene regulatory regio
38 body that targets the external domain of the prostate-specific membrane antigen, has potential as an
39 Important PCa radiotracers include (68)Ga-prostate-specific membrane antigen HBED-CC ((68)Ga-PSMA)
41 state carcinoma tumors transduced with human prostate-specific membrane antigen (hPSMA) and a Renilla
42 dioimmunoscintigraphy (RIS) directed against prostate-specific membrane antigen in modifying postpros
43 3 lowered the kidney and liver uptake of the prostate-specific membrane antigen inhibitor each by a f
44 therapy (RLT) with (177)Lu-PSMA-617 (PSMA is prostate-specific membrane antigen) is a novel targeted
45 ode dissection (SLND) and pre/post procedure prostate-specific membrane antigen ligand positron emiss
46 a-linked acidic dipeptidase 2 (NAALAD2), and prostate-specific membrane antigen-like protein (PMSAL/G
47 esferrioxamine-IAB2M ((89)Zr-IAB2M), an anti-prostate-specific membrane antigen minibody, in patients
48 dose, 180 MBq; range, 126-189 MBq) targeting prostate-specific membrane antigen (n = 7) or human epid
51 ort (in the context of emerging evidence for prostate-specific membrane antigen PET in this setting)
54 DOTATOC PET/CT (GEP NET), and (68)Ga-labeled prostate-specific membrane antigen PET/CT (PCA) but is s
55 ancies in patients undergoing (68)Ga-labeled prostate-specific membrane antigen PET/CT for prostate c
60 68)Ga(HBED-CC)] ((68)Ga-PSMA ligand; PSMA is prostate-specific membrane antigen) PET/CT in patients w
62 for imaging metastases, whereas (68)Ga-PSMA (prostate-specific membrane antigen) PET/CT was introduce
65 eted RNAi agents that selectively sensitized prostate-specific membrane antigen-positive (PSMA-positi
66 te LNCaP epithelial cells, which express the prostate-specific membrane antigen protein (77-fold incr
68 PCR) for prostate-specific antigen (PSA) and prostate-specific membrane antigen (PSM) to predict path
69 r proteins, prostate specific antigen (PSA), prostate specific membrane antigen (PSMA) and platelet f
70 I) microfluidic device that combines an anti-prostate specific membrane antigen (PSMA) antibody with
71 SMA) is a radioligand with high affinity for prostate specific membrane antigen (PSMA) enabling targe
76 th small molecular entities, able to bind to prostate specific membrane antigen (PSMA), a transmembra
78 against prostate specific antigen (PSA) and prostate specific membrane antigen (PSMA), and then used
79 egy for the detection of a cancer biomarker, prostate specific membrane antigen (PSMA), at picomolar
80 which target the extracellular domain of the prostate specific membrane antigen (PSMA), for enhanced
81 roteins are prostate specific antigen (PSA), prostate specific membrane antigen (PSMA), platelet fact
82 to measure prostate specific antigen (PSA), prostate specific membrane antigen (PSMA), platelet fact
83 to aptamers that recognize the transmembrane prostate specific membrane antigen (PSMA), with cells se
86 -urea-Lys (Ahx)-HBED-CC ligand targeting the prostate-specific membrane antigen (PSMA) ((68)Ga-PSMA-1
87 -urea-Lys (Ahx)-HBED-CC ligand targeting the prostate-specific membrane antigen (PSMA) (hereafter cal
88 ent in prostate cancer patients using (68)Ga-prostate-specific membrane antigen (PSMA) 11 PET/CT.
89 Promising biochemical responses to (225)Ac-prostate-specific membrane antigen (PSMA) 617, even in p
90 partial-volume correction (PVC) on measured prostate-specific membrane antigen (PSMA) activity in sm
91 and accessibility of (68)Ga tracers for the prostate-specific membrane antigen (PSMA) and other targ
93 based low-molecular weight inhibitors of the prostate-specific membrane antigen (PSMA) are under inte
94 algorithms to predict peptide sequences from prostate-specific membrane antigen (PSMA) capable of sti
96 bivalent antibody fragments, including anti-prostate-specific membrane antigen (PSMA) diabody (Db) a
97 for targeted immunoPET and quantification of prostate-specific membrane antigen (PSMA) expression in
99 sferrioxamine B [DFO]-J591 for immuno-PET of prostate-specific membrane antigen (PSMA) expression was
100 ty of (68)Ga-labeled PET tracers against the prostate-specific membrane antigen (PSMA) for localizati
101 ed, (211)At-labeled small molecule targeting prostate-specific membrane antigen (PSMA) for the treatm
103 ecent years, a number of drugs targeting the prostate-specific membrane antigen (PSMA) have become im
104 recent years, several radioligands targeting prostate-specific membrane antigen (PSMA) have been clin
105 nt years, several radiotracers targeting the prostate-specific membrane antigen (PSMA) have been intr
108 range, 0.75-2.55 ng/mL) who underwent (68)Ga-prostate-specific membrane antigen (PSMA) HBED-CC PET/CT
109 sensitive immunoassay for quantitating serum prostate-specific membrane antigen (PSMA) hinders its cl
111 anced prostate cancer and positive uptake in prostate-specific membrane antigen (PSMA) imaging were t
113 dioimmunoscintigraphy (RIS) directed against prostate-specific membrane antigen (PSMA) in influencing
114 dioimmunoscintigraphy (RIS) directed against prostate-specific membrane antigen (PSMA) in influencing
115 ns of radioligand therapy (RLT) with (177)Lu-prostate-specific membrane antigen (PSMA) in metastasize
116 sis of the high and consistent expression of prostate-specific membrane antigen (PSMA) in metastatic
117 response to (177)Lu-labeled agents targeting prostate-specific membrane antigen (PSMA) in patients wi
119 ork aimed at the development of dual-labeled prostate-specific membrane antigen (PSMA) inhibitors der
153 on previous observations, we first show that prostate-specific membrane antigen (PSMA) is repressed b
156 efficacy of the (177)Lu-labeled DOTAGA-based prostate-specific membrane antigen (PSMA) ligand (177)Lu
158 (SLND) and pre-procedure and post-procedure prostate-specific membrane antigen (PSMA) ligand PET.
160 lar imaging using PET/CT with (68)Ga-labeled prostate-specific membrane antigen (PSMA) ligands and mo
165 zed with the A10 aptamer, which binds to the prostate-specific membrane antigen (PSMA) on prostate ca
166 nd the A10 aptamer (Apt), which binds to the prostate-specific membrane antigen (PSMA) on the surface
168 ced molecular imaging techniques, especially prostate-specific membrane antigen (PSMA) PET findings,
169 rrelation of PSA changes with the results of prostate-specific membrane antigen (PSMA) PET follow-up
170 aluated the diagnostic value and accuracy of prostate-specific membrane antigen (PSMA) PET for the in
175 mine the diagnostic capabilities of combined prostate-specific membrane antigen (PSMA) PET/CT and sen
185 ancer (PCa) cohort to date undergoing (68)Ga-prostate-specific membrane antigen (PSMA) PET/CT primary
187 Therefore, we evaluated consecutive (68)Ga-prostate-specific membrane antigen (PSMA) PET/CT, (11)C-
188 between fluciclovine and gallium 68 or (18)F prostate-specific membrane antigen (PSMA) PET/CT, a newe
193 er cells by constructing Pt(IV)-encapsulated prostate-specific membrane antigen (PSMA) targeted nanop
194 ion detection rate of (18)F-DCFPyL-PET/CT, a prostate-specific membrane antigen (PSMA) targeted PET a
195 rmaceuticals, we developed inhibitors of the prostate-specific membrane antigen (PSMA) that are label
196 e high-affinity urea-based inhibitors of the prostate-specific membrane antigen (PSMA) that were synt
197 highly specific small molecule targeting the prostate-specific membrane antigen (PSMA) to deliver (12
199 There is increasing interest in PET/CT with prostate-specific membrane antigen (PSMA) tracers for im
201 fect of androgen receptor (AR) inhibition on prostate-specific membrane antigen (PSMA) uptake imaged
202 compounds labeled with (86)Y for imaging the prostate-specific membrane antigen (PSMA) using PET.
203 which a bivalent aptamer specifically binds prostate-specific membrane antigen (PSMA) via an antibod
207 re that these materials are able to (1) bind prostate-specific membrane antigen (PSMA) with high affi
208 nt prostate cancer by radioligands targeting prostate-specific membrane antigen (PSMA), 30% of patien
209 cles selectively bound either an antibody or prostate-specific membrane antigen (PSMA), a biomarker f
212 was designed for label-free immunosensing of prostate-specific membrane antigen (PSMA), a prostate ca
213 o PEDOT films for electrochemical sensing of prostate-specific membrane antigen (PSMA), a prostate ca
214 body (mAb) construct for targeted imaging of prostate-specific membrane antigen (PSMA), a prototypica
217 at recognize the extracellular domain of the prostate-specific membrane antigen (PSMA), a well charac
218 n peripheral blood T lymphocytes targeted to prostate-specific membrane antigen (PSMA), an antigen ex
220 -617 is a radioligand with high affinity for prostate-specific membrane antigen (PSMA), enabling targ
222 Metastatic prostate carcinoma overexpresses prostate-specific membrane antigen (PSMA), making this a
223 radiofluorinated small-molecule inhibitor of prostate-specific membrane antigen (PSMA), N-[N-[(S)-1,3
224 tanis et al. report a new signaling role for prostate-specific membrane antigen (PSMA), providing a m
225 (68)Ga-labeled urea-based inhibitors of the prostate-specific membrane antigen (PSMA), such as (68)G
226 (68)Ga-labeled urea-based inhibitors of the prostate-specific membrane antigen (PSMA), such as (68)G
227 elopment of new imaging agents targeting the prostate-specific membrane antigen (PSMA), we have used
228 x 10(6)) (RM1), transduced to express human prostate-specific membrane antigen (PSMA), were injected
230 ad-to-head comparison between (68)Ga-labeled prostate-specific membrane antigen (PSMA)-11 and (18)F-f
231 was to estimate the effect of (68)Ga-labeled prostate-specific membrane antigen (PSMA)-11 PET on the
232 one metastases detected by total-body (68)Ga-prostate-specific membrane antigen (PSMA)-11 PET/CT and
233 eful lower limit of injected dose for (68)Ga-prostate-specific membrane antigen (PSMA)-11 PET/CT imag
235 A first analysis of simultaneous (68)Ga-prostate-specific membrane antigen (PSMA)-11 PET/MRI sho
236 tudy was to evaluate the efficacy of (177)Lu-prostate-specific membrane antigen (PSMA)-617 ((177)Lu-P
238 ted and applied to the assessment of (177)Lu-prostate-specific membrane antigen (PSMA)-617 therapy fo
239 Our objective was to introduce (90)Y-labeled prostate-specific membrane antigen (PSMA)-617 to clinica
243 rticle generator (225)Ac to selectively kill prostate-specific membrane antigen (PSMA)-expressing cel
244 tubule agent drug maytansinoid-1 directly to prostate-specific membrane antigen (PSMA)-expressing cel
245 stic pathway for prostate cancer management, prostate-specific membrane antigen (PSMA)-ligand PET has
249 tration as the first drug for PET imaging of prostate-specific membrane antigen (PSMA)-positive lesio
250 tion-resistant prostate cancer patients with prostate-specific membrane antigen (PSMA)-positive tumor
251 theranostic method that allows prediction of prostate-specific membrane antigen (PSMA)-positive tumor
254 ion detection rate of (18)F-DCFPyL PET/CT, a prostate-specific membrane antigen (PSMA)-targeted PET a
258 ic castration-resistant prostate cancer with prostate-specific membrane antigen (PSMA)-targeted radio
262 neuroendocrine biomarkers on the efficacy of prostate-specific membrane antigen (PSMA)-targeted radio
263 currently being revolutionized by the use of prostate-specific membrane antigen (PSMA)-targeted radio
267 function as well as therapeutic efficacy of prostate-specific membrane antigen (PSMA)-targeted radio
272 er has been shown to improve tumor uptake of prostate-specific membrane antigen (PSMA)-targeting radi
273 -HBED-CC-a (68)Ga-conjugated ligand of human prostate-specific membrane antigen (PSMA)-to localize ca
283 imaging and therapeutic agents targeting the prostate-specific membrane antigen (PSMA); these were am
289 oped tracer 2-methoxy-(18)F-DCFPyL ((18)F-JK-prostate-specific membrane antigen [PSMA]-7) has shown f
290 CT scans of 7 patients who underwent (177)Lu prostate-specific membrane antigen radioligand therapy w
293 simetry of a novel (18)F-labeled radiohybrid prostate-specific membrane antigen (rhPSMA) PET imaging
294 )Tc-MIP-1404), a small-molecule inhibitor of prostate-specific membrane antigen, shows high potential
295 he results of a prospective study evaluating prostate-specific membrane antigen-targeted (18)F-DCFPyL
296 clusion: In this prospective study using the prostate-specific membrane antigen-targeted PET agent (1
297 y recurrent prostate cancer were greater for prostate-specific membrane antigen-targeted radiotracers
298 conjugated to trastuzumab as well as to the prostate-specific membrane antigen-targeting compound RP
299 amino]-pentyl}-ureido)-pentanedioic acid), a prostate-specific membrane antigen-targeting radiotracer
300 phosphoramidate peptidomimetic inhibitors of prostate-specific membrane antigen was determined by inh