Zobrazeno 1 - 8
of 8
pro vyhledávání: '"P. E. Persons"'
Publikováno v:
Heart and Mind, Vol 2, Iss 3, Pp 78-84 (2018)
Background: Previous research on bipolar disorder demonstrates greater-than-expected vascular dysfunction later in the course of illness, proportionate to the cumulative burden of mood symptoms. However, little is known about the effect of acute mood
Externí odkaz:
https://doaj.org/article/83b1832479f94c818d1f93484708de75
Publikováno v:
Heliyon, Vol 5, Iss 8, Pp e02267- (2019)
The inflammatory marker C-reactive protein has been linked to anxiety across a number of studies. This paper uses data for 1,439 participants of the National Health and Nutrition Examination Survey (NHANES) 1999–2004 to examine the association betw
Externí odkaz:
https://doaj.org/article/28bd63875031479da9b10ad7077e4451
Publikováno v:
ChemInform. 22
Publikováno v:
European Journal of Medicinal Chemistry. 26:473-475
Publikováno v:
The Journal of biological chemistry. 266(31)
Lavendustin-A was reported to be a potent tyrosine kinase inhibitor of the epidermal growth factor (EGF) receptor (Onoda, T., Iinuma, H., Sasaki, Y., Hamada, M., Isshibi, K., Naganawa, H., Takeuchi, T., Tatsuta, K., and Umezawa, K. (1989) J. Nat. Pro
Autor:
T, Yoneda, R M, Lyall, M M, Alsina, P E, Persons, A P, Spada, A, Levitzki, A, Zilberstein, G R, Mundy
Publikováno v:
Cancer research. 51(16)
Many human tumors of epithelial origin contain cells overexpressing the epidermal growth factor (EGF) receptor, and there is convincing evidence that cancer cell growth is correlated with the loss of the normal regulation of the EGF receptor signal t
Publikováno v:
ChemInform. 21
The dopaminergic activity of the indole (VII), the tetrahydrobenzindole (XIX), and of the related compounds (IX) and (XXI), synthesized as shown in the reaction scheme, is evaluated.
Autor:
E. Kelly, David E. Nichols, P. E. Persons, James A. Clemens, Lee A. Phebus, John M. Cassady, Ray W. Fuller, Martin D. Hynes, E.B. Smalstig
Publikováno v:
Life sciences. 34(11)
The dopaminergic activity of 4-(2-di-n-propylaminoethyl) indole (DPAI) was investigated. In animal models for postsynaptic dopaminergic activity DPAI showed only very weak or no effects. In rats with unilateral 6-hydroxydopamine lesions of the nigros