Zobrazeno 1 - 10
of 53
pro vyhledávání: '"G A, Boyle"'
Autor:
S. M. Mewes, G. J. Boyle, A. Ferran Pousa, R. J. Shalloo, J. Osterhoff, C. Arran, L. Corner, R. Walczak, S. M. Hooker, M. Thévenet
Publikováno v:
Physical Review Research, Vol 5, Iss 3, p 033112 (2023)
In recent years, hydrodynamic optical-field-ionized (HOFI) channels have emerged as a promising technique to create laser waveguides suitable for guiding tightly focused laser pulses in a plasma, as needed for laser-plasma accelerators. While experim
Externí odkaz:
https://doaj.org/article/13240ad65ded4dab8d8fa3682b0e649d
Publikováno v:
Behaviour Research and Therapy. 144:103906
Autor:
T. G. McCarthy, G. E. Boyle
Publikováno v:
Oxford Bulletin of Economics and Statistics. 59:257-264
We propose a simple measure of β-convergence which is not subject to Galton's fallacy. We illustrate our measure with OECD data for the period 1950–1988. We find evidence of β-convergence but only in the presence of σ-convergence.
Autor:
S. R. Steindl, G. J. Boyle
Publikováno v:
Archives of Clinical Neuropsychology. 10:205-210
Publikováno v:
Xenobiotica. 23:1241-1253
1. Five healthy male volunteers received a single oral dose (50 mg; 42 microCi) of 14C-Casodex, a racemic compound, which has its antiandrogen activity predominantly in R-Casodex, the (-)-enantiomer, with little activity in S-Casodex, the (+)-enantio
Publikováno v:
Xenobiotica. 23:781-798
1. Casodex, a non-steroidal antiandrogen, was eliminated primarily in faeces by rat, mouse, rabbit and dog. Rat, mouse and rabbit eliminated 20-30% of a single oral dose (8-25 mg/kg) in urine; only 3-4% was excreted in urine by dog (2.5 mg/kg). Oral
Publikováno v:
Neoplasma. 55(1)
The development of colorectal cancer in former Czechoslovakia and its successor states is illustrated using recorded mortality and from 1968 incidence rates retrieved from National Cancer Registry of Slovakia. The relatively high mortality rates in C
Publikováno v:
Current topics in medicinal chemistry. 7(14)
This manuscript describes a comparison of the physicochemical properties of marketed oral drugs with those of 45 structurally confirmed orally bioavailable anti-cancer protein kinase inhibitors currently in different phases of clinical development. I
Publikováno v:
Journal of bioenergetics and biomembranes. 32(6)
We have sought to elucidate how the oligomycin sensitivity-conferring protein (OSCP) of the mitochondrial F(1)F(0)-ATP synthase (mtATPase) can influence proton channel function. Variants of OSCP, from the yeast Saccharomyces cerevisiae, having amino
Publikováno v:
Journal of bioenergetics and biomembranes. 32(5)
Oligomycin has long been known as an inhibitor of mitochondrial ATP synthase, putatively binding the F(o) subunits 9 and 6 that contribute to proton channel function of the complex. As its name implies, OSCP is the oligomycin sensitivity-conferring p