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1 gate glucose utilization of BAT by (18)F-FDG PET imaging.
2 in healthy adult mice by dynamic and static PET imaging.
3 ikely to be achieved by the sole use of TSPO PET imaging.
4 p between fcMRI and both Tau-PET and amyloid-PET imaging.
5 vo radiography as well as static and dynamic PET imaging.
6 value was determined with the HEC method at PET imaging.
7 racer for investigating tumor perfusion with PET imaging.
8 Bs)-were studied with whole-body (11)C-ER176 PET imaging.
9 h(Hor)-dAph(Cbm)-Lys-Thr-Cys)-dTyr-NH2)) for PET imaging.
10 well with the behavior observed by standard PET imaging.
11 tracer uptake was assessed by (18)F-AH113804 PET imaging.
12 tivity MRI (fcMRI) in the context of amyloid-PET imaging.
13 s evaluated by (99m)Tc-MIBI SPECT /(18)F-FDG PET imaging.
14 ostic efficacy of beta-amyloid (Abeta) brain PET imaging.
15 8)F-FVIIai in the tumors measured in vivo by PET imaging.
16 2-deoxy-2-[F-18]fluoro-D-glucose ((18)F-FDG) PET imaging.
17 nt of NOD's elimination kinetics by means of PET imaging.
18 (41 women and 20 men) who underwent amyloid PET imaging.
19 s synthesized to incorporate fluorine-18 for PET imaging.
20 exposure to healthy tissues during repeated PET imaging.
21 asured in patients during [18F]FMISO and 15O PET imaging.
22 quence NLys-Lys-Pro-Tyr-Tle-Leu suitable for PET imaging.
23 fragments and have ideal characteristics for PET imaging.
24 51)Cr-GFR), using serial plasma sampling and PET imaging.
25 ed the feasible application of (64)Cu(I) for PET imaging.
26 ghrelin receptor expressing carcinomas using PET imaging.
27 (68)Ga-DOTATOC (an sst receptor agonist), in PET imaging.
28 ale, retired breeder Sprague-Dawley rats for PET imaging.
29 the in vivo status of DLL3 expression using PET imaging.
30 s-3 HABs, 3 MABs, and 2 LABs-underwent brain PET imaging.
31 all cerebral emboli were detected in vivo by PET imaging.
32 se model of bleomycin-induced fibrosis using PET imaging.
33 o underwent amyloid PET and MRI, but not tau PET imaging.
34 ets while significantly reducing the cost of PET imaging.
35 ng PDE4B-preferring radioligand for clinical PET imaging.
36 tic resonance imaging but not tau or amyloid PET imaging.
37 uclide with a half-life of 12.7 h, ideal for PET imaging.
38 d B (11C-PiB) positron emission tomographic (PET) imaging.
39 le for in vivo positron emission tomography (PET) imaging.
40 d non-invasive positron emission tomography (PET) imaging.
41 tory motion in positron emission tomography (PET) imaging.
42 8)F for use in positron-emission tomography (PET) imaging.
43 (18)F-FDS were determined by dynamic 35-min PET imaging (15 frames x 8 s, 26 frames x 30 s, 20 frame
44 , in the tracer concentration range used for PET imaging, [(18)F]CFA is primarily a substrate for dCK
45 y (1.) in-beam positron-emission tomography (PET) imaging; (2.) intracardiac voltage mapping with vis
47 post-myocardial infarction period, (18)F-FDG PET imaging after a single bolus administration may unde
48 Response-adapted therapy based on interim PET imaging after two cycles of ABVD seems promising wit
49 to determine the feasibility of the hypoxia PET imaging agent (64)Cu-ATSM to detect hypoxia in a rab
53 usion:(64)Cu-DOTA-alendronate is a promising PET imaging agent for the sensitive and specific detecti
54 nce that (64)Cu-NOTA-RamAb can function as a PET imaging agent for visualizing VEGFR-2 expression in
56 as modified for use as a (89)Zr-based immuno-PET imaging agent to noninvasively determine the local l
61 ose within the acceptable range for clinical PET imaging agents and the potential for translation int
69 ugh followed in 2011 with (68)Ga-PSMA-11 for PET imaging and (131)I-MIP-1095 for endoradiotherapy of
70 -18 is the most widely used radioisotope for PET imaging and a thorough overview of the available rad
71 tter (P < 0.05-0.001) than (18)F-FDG through PET imaging and biodistribution studies in MDA-MB-231 an
72 ynthesized to target CA125 and evaluated via PET imaging and biodistribution studies in mice bearing
78 ition and neuroinflammation, we used in vivo PET imaging and ex vivo autoradiography with Pittsburgh
82 s a promising bimodal ligand for noninvasive PET imaging and intraoperative optical imaging of GRPr-e
83 macokinetics in human subjects using dynamic PET imaging and metabolite-corrected arterial input func
85 te that our mouse model permits longitudinal PET imaging and quantification of T-cell homing during i
86 escent-labeled (68)Ga-tilmanocept allows for PET imaging and real-time intraoperative detection of SL
87 ecule cysteine cathepsin probes for clinical PET imaging and suggest that they have the potential to
88 n low-molecular-weight PSMA ligands for both PET imaging and therapeutic approaches, with a focus on
91 labeled version, (64)Cu-NOTA-PEG4-cRGD2, for PET imaging, and a fluorescent version, FITC-PEG4-cRGD2,
92 tau pathology, as measured with 18F-AV-1451-PET imaging, and cognitive deficits in Alzheimer's disea
93 eficient mice were used for biodistribution, PET imaging, and determination of in vivo metabolization
94 ND AND Amyloid-positron emission tomography (PET) imaging (API) detects amyloid-beta pathology early
96 eneic DLBCL mouse model, this PARP1-targeted PET imaging approach allowed us to discriminate between
98 [18F]AV-1451) positron emission tomographic (PET) imaging are linked with clinical phenotype and cort
99 w is to report on the value of (11)C-choline PET imaging as a diagnostic procedure for metastasis-dir
100 views the current evidence of ERalpha and PR PET imaging as predictive and early-response biomarkers
102 -hydroxyephedrin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16
103 -hydroxyephedrin ((11)C-HED) and (15)O-water PET imaging at rest and after exposure to mild cold (16
112 Overall, our results suggest granzyme B PET imaging can serve as a quantitatively useful predict
116 he quality of fluorine 18 fluorodeoxyglucose PET imaging conditions to ensure the comparability of PE
118 e uptake of (18)F-FVIIai measured in vivo by PET imaging correlated (r = 0.72, P < 0.02) with TF prot
120 plied mathematical modeling to Abeta in vivo PET imaging data to investigate competing theories of Ab
121 alpha-(11)C-methyl-l-tryptophan ((11)C-AMT) PET imaging demonstrated increased tryptophan uptake and
123 sonance imaging (MRI) experiments, Macroflor PET imaging detects changes in macrophage population siz
124 clinical trial was initiated to compare the PET imaging diagnostic potential of (18)F-4FMFES with th
125 Conclusion: Because of highly sensitive PET imaging even of tissues with low alphavbeta6 integri
128 ges in management resulting from PSMA ligand PET imaging for both biochemical recurrence and primary
130 spected Alzheimer disease) underwent dynamic PET imaging for up to 120 min after bolus injection of (
131 spected Alzheimer disease) underwent dynamic PET imaging for up to 120 min after bolus injection of (
133 451, T807) positron emission tomography (FTP-PET) imaging for tau and Pittsburgh compound B carbon 11
134 e number of publications about PSMA-targeted PET imaging from 2013 to 2016 (e.g., a search of the Web
138 ed that chelator-mediated nanoparticle-based PET imaging has its inherent drawbacks and can possibly
139 Hence, the increasing popularity of TSPO PET imaging has paradoxically introduced substantial unc
140 (68)Ga-labeled somatostatin receptor ligand PET imaging has recently been shown in preclinical and e
142 ose positron emission tomography ([(18)F]FDG-PET) imaging has an essential role in diagnosing DLBCL i
143 l and synthetic amino acids radiolabeled for PET imaging have been investigated in prostate cancer pa
144 uman myeloid sarcoma, we monitored by Immuno-PET imaging human central memory T cells (TCM), which we
147 ization before radiolabeling with (64)Cu for PET imaging in an apolipoprotein E-deficient (ApoE(-/-))
154 ed using ex vivo biodistribution and in vivo PET imaging in non-tumor-bearing animals as well as in K
155 Tissue metabolite analysis in rodents and PET imaging in nonhuman primates under baseline and bloc
156 ntal and neurodegenerative mouse models with PET imaging in patients with recent-onset schizophrenia
160 sed by (99m)Tc-duramycin SPECT and (18)F-FDG PET imaging in treatment-sensitive COLO205 and treatment
161 sed by (99m)Tc-duramycin SPECT and (18)F-FDG PET imaging in treatment-sensitive COLO205 and treatment
162 ory gating in positron emission tomographic (PET) imaging in a clinical trial comparing conventional
163 verview on the current status of PSMA ligand PET imaging, including imaging procedure and interpretat
166 he [18F]AV-1451 signal as seen on results of PET imaging is a valid marker of clinical symptoms and n
172 ocator-protein positron emission tomography (PET) imaging, is increased in unmedicated persons presen
173 We envision that SCN5A measurements using PET imaging may serve as a novel diagnostic tool to stra
175 e early symptomatic state and if [(18)F]MPPF PET imaging might be a promising biomarker of early dege
176 adiation dose from whole-body (11)C-nicotine PET imaging of 11 healthy (5 male and 6 female) subjects
182 e feasibility of a synthesis-free method for PET imaging of brown adipose tissue (BAT) and translocat
185 onal antibody that has shown promise for the PET imaging of cancers expressing carbohydrate antigen 1
186 s changes in neural circuitry (measured with PET imaging of cerebral glucose metabolism at baseline a
187 is suitable for noninvasive, highly specific PET imaging of CXCR4 expression in the atherosclerotic a
191 ising candidate for preclinical and clinical PET imaging of hNIS expression and thyroid-related disea
192 re, we sought to optimize noninvasive immuno-PET imaging of human programmed death-ligand 1 (PD-L1) e
193 ble of standardizing quantitative changes in PET imaging of patients with metastatic prostate cancer
197 )F-DPA-714 is a second-generation tracer for PET imaging of the 18-kDa translocator protein (TSPO), a
198 c 4T1luc tumors, allowing for the successful PET imaging of the tumors as early as 2 h after injectio
199 f this study was to explore the potential of PET imaging of the urokinase-type plasminogen activator
206 e studies used positron emission tomography (PET) imaging of the TSPO microglial marker and found inc
209 F-TFB, (18)F-BF4 (-)) has shown promise as a PET imaging probe for NIS, the current synthesis method
210 C-radiolabeled sarcosine was tested as a new PET imaging probe in comparison with (11)C-choline in 2
211 We successfully developed 4-(11)C-MBZA as a PET imaging probe, displaying properties advantageous ov
212 We successfully developed 4-(11)C-MBZA as a PET imaging probe, displaying properties advantageous ov
216 tate-specific membrane antigen (PSMA)-ligand PET imaging provides unprecedented accuracy for whole-bo
218 lective microglial markers are available for PET imaging, quantification of cytokines and other infla
221 nflammation using (18)F-FAZA and (18)F-FMISO PET imaging represents a promising new tool for uncoveri
222 f this technique in myelofibrosis, (18)F-FLT PET imaging results were compared with bone marrow histo
230 may be an attractive addition to the current PET imaging strategy to differentiate inflammation from
231 rotein expression levels in combination with PET imaging studies for functional characterization of G
232 ue of PF-367 was synthesized and preliminary PET imaging studies in non-human primates confirmed that
233 as well as in vivo biodistribution and brain PET imaging studies in wildtype and mGluR2 knockout rats
236 he past years, positron emission tomography (PET) imaging studies have investigated striatal molecula
237 F-Mefway) for positron emission tomography (PET) imaging studies of serotonin 5-HT1A receptors which
238 estigations indicated that the presence of a PET imaging study demonstrating abnormalities in individ
241 of the potential of combining a multitracer PET imaging technique and a longitudinal protocol applie
242 cterize a specific small-molecule tracer for PET imaging that binds with high affinity to GPIIb/IIIa
243 uthors have combined multiparametric MRI and PET imaging to address the important issue of intratumor
244 ents were examined using [(11) C]PBR28 brain PET imaging to assess brain immune cell activation.
245 view should be below 3.3 GBq at the time of PET imaging to avoid deadtime losses for this scanner.
246 monstrate the utility of noninvasive in vivo PET imaging to dynamically track T-cell checkpoint recep
248 nducted a first-in-human study of (18)F-MFBG PET imaging to evaluate the safety, feasibility, pharmac
249 11-labeled Pittsburgh Compound B ([11C]PiB) PET imaging to measure amyloid burden, and structural ma
252 oxyglucose positron emission tomography (FDG-PET) imaging to determine the utility of response-adapte
253 oxyglucose positron emission tomography (FDG-PET) imaging to understand the neural systems governing
255 linical profiles, structural MRI and amyloid PET imaging typical for svPPA, FTP signal was unexpected
259 c accumulation in TF-positive BXPC-3 tumors, PET imaging using (89)Zr-Df-ALT-836 promises to open new
263 coma, or cancer of unknown primary underwent PET imaging using the novel CXCR4 nuclear probe (68)Ga-p
265 ne ((18)F-FLT) is a proliferation tracer for PET imaging valuable in the monitoring of disease progre
267 TPM mouse model, suggesting that (64)Cu-GTSM PET imaging warrants clinical evaluation as a diagnostic
273 tly after administration of 3 MBq/kg of FCH, PET imaging was performed, followed by T1- and T2-weight
276 ntify a more suitable probe for clinical dCK PET imaging, we compared the selectivity of two candidat
279 In vivo biodistribution and small-animal PET imaging were performed in mice bearing B16F1 melanom
281 particle-based positron emission tomography (PET) imaging, whereas its accuracy remains questionable.
283 erphosphorylated tau in vivo, results of tau PET imaging will likely serve as a key biomarker that li
285 pathology were obtained through small-animal PET imaging with (18)F-FDG, (18)F-peripheral benzodiazep
287 ficking in a transgenic mouse model of AD by PET imaging with (64)Cu, to determine its potential as a
288 tly published biodistribution data of immuno-PET imaging with (64)Cu-cetuximab and of small-animal SP
291 disease; it is the first example of in vivo PET imaging with a tracer containing an S-(18)F bond.
294 a first look at the relationship between Tau-PET imaging with F(18)-AV1451 and functional connectivit
295 rther validation in large samples, (18)F-FDG PET imaging with network analysis may provide a viable b
297 c resonance-positron emission tomography (MR-PET) imaging with (11) C-PBR28, we quantified expression
298 re we describe positron emission tomography (PET) imaging with (18)F-Macroflor, a modified polyglucos
300 = 3), we used positron emission tomography (PET) imaging with the radioligand [(11)C]AZ10419369 admi
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