Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D E Murphy"'
Autor:
C McAteer, R Sullivan, C McRory, O O’Domhnaill, D E Murphy, M A Rehman, T Muller, M Gallagher, J Miranda, V Parihar, K Mulpeter
Publikováno v:
Age and Ageing. 50:ii9-ii41
Background Approximately 25% of inpatients have urinary catheters at some point during their hospital stay; over half are deemed inappropriate. This is significant as catheter-associated urinary tract infections (CAUTI) increase morbidity, mortality
Autor:
D E, Murphy
Publikováno v:
The New York times on the Web.
Publikováno v:
Geographical Society of Ireland. Bulletin. 1:8-15
Autor:
R. E. Sparks, D. E. Murphy
Publikováno v:
Industrial & Engineering Chemistry Fundamentals. 7:642-645
Autor:
C. A. Boast, D. E. Murphy
Publikováno v:
Annals of the New York Academy of Sciences. 444:450-452
Autor:
D. E. MURPHY, P. C. JUN. LANE
Publikováno v:
Chemischer Informationsdienst. 6
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 240(3)
3-(2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP), a rigid analog of 2-amino-7-phosphonoheptanoic acid, has been reported as a selective N-methyl-D-aspartate (NMDA) antagonist. [3H]CPP bound with relatively high affinity (Kd = 201 nM) to Trit
Autor:
J, Lehmann, J, Schneider, S, McPherson, D E, Murphy, P, Bernard, C, Tsai, D A, Bennett, G, Pastor, D J, Steel, C, Boehm
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 240(3)
3-(2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP) was synthesized as a rigid analog of 2-amino-7-phosphonoheptanoate, a previously known antagonist at the N-methyl-D-aspartate (NMDA) preferring, or NMDA-type, of excitatory amino acid receptor
Autor:
J, Lehmann, A J, Hutchison, S E, McPherson, C, Mondadori, M, Schmutz, C M, Sinton, C, Tsai, D E, Murphy, D J, Steel, M, Williams
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 246(1)
CGS 19755 (cis-4-phosphonomethyl-2-piperidine carboxylic acid) was found to be a potent, stereospecific inhibitor of N-methyl-D-aspartate (NMDA)-evoked, but not KCl-evoked, [3H] acetylcholine release from slices of the rat striatum. The concentration