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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 1, 1997
p53, proliferating cell nuclear antigen, and Ki-67 expression in extrauterine leiomyosarcomasP E O'Reilly, S S Raab, T H Niemann, et al.
The Journal of Experimental Medicine|January 1, 1994
Availability of endogenous peptides limits expression of an M3a-Ld major histocompatibility complex class I chimeraJ M Vyas, R R Rich, D D Howell, et al.
Human Pathology|April 1, 1995
p53 protein overexpression in smooth muscle tumors of the uterusT H Niemann, S S Raab, J C Lenel, et al.
The Journal of Pharmacy and Pharmacology|January 1, 1991
Orally active carbamate prodrugs of the selective dopamine agonist N-0437: in-vivo activities in the 6-OHDA turning model and in-vitro activitiesI den Daas, P de Boer, P G Tepper, et al.
Fundamental & Clinical Pharmacology|January 1, 1988
Pharmacokinetics and pharmacodynamics of 2,4-diaminopyridine in the catP T Biessels, M C Houwertjes, A H Scaf, et al.
Life Sciences|March 21, 1983
In vivo dopamine receptor binding studies with a non-radioactively labeled agonist, dipropyl-5,6-ADTNM G Feenstra, H Rollema, T B Mulder, et al.
European Journal of Pharmacology|February 26, 1985
N-methyl,N-propargyl-2-aminotetralins:novel dopamine agonists with monoamine oxidase inhibiting propertiesB Hazelhoff, J B De Vries, D Dijkstra, et al.
European Journal of Pharmacology|June 17, 1986
Pharmacological profiles of three new, potent and selective dopamine receptor agonists: N-0434, N-0437 and N-0734J Van der Weide, J B De Vries, P G Tepper, et al.
Journal of Medicinal Chemistry|October 1, 1993
2-Amido-8-methoxytetralins: a series of nonindolic melatonin-like agentsS Copinga, P G Tepper, C J Grol, et al.
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