The discovery of the Warburg effect in the early twentieth century followed by the
development of the fluorinated glucose analogue 18 F-fluorodeoxyglucose (18 F-FDG) and …

OBJECTIVE. Recent advances in the fundamental understanding of the complex biology of
prostate cancer have provided an increasing number of potential targets for imaging and …

This trial was an initial assessment of the feasibility, in vivo targeting, and biokinetics of 16β-
18F-fluoro-5α-dihydrotestosterone (18F-FDHT) PET in patients with metastatic prostate …

Over the past several years, our group has provided considerable evidence that the
expression of sigma-2 (σ 2) receptors may serve as a biomarker of tumour cell proliferation …

Purpose The purpose of this study was to evaluate the feasibility of androgen receptor (AR)
imaging with 16β-[18 F] fluoro-5α-dihydrotestosterone (FDHT) by positron emission …

[18 F] fluoro-2-deoxy-d-glucose (FDG) is currently the only fluorinated tracer used in routine
clinical positron emission tomography (PET). Fluorine-18 is considered the ideal …

In addition to the well-known estrogen receptor (ER) and human epidermal growth factor
receptor 2, the androgen receptor (AR) is also a potential drug target in breast cancer …

Although 18 F-fluorodeoxyglucose (18 F-FDG) is still the most widely used positron emission
tomography (PET) radiotracer, there are a few well-known limitations to its use. The last …

Sex steroid hormones are major regulators of sexual characteristic among species. These
hormones, however, are also produced in the brain. Steroidal hormone‐mediated signalling …

The first organomediated asymmetric 18F fluorination has been accomplished using a chiral
imidazolidinone and [18F] N‐fluorobenzenesulfonimide. The method provides access to …