Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Lars O. Hansson"'
Autor:
Townsend, Patricia K.
Publikováno v:
Health Transition Review, 1996 Oct 01. 6(2), 233-234.
Externí odkaz:
https://www.jstor.org/stable/40652223
Autor:
Atosa Nejatian, Therese Djärv, Jonas Höijer, Kai M. Eggers, Lars O. Hansson, Per Svensson, Åsa Omstedt
Publikováno v:
Journal of the American College of Cardiology. 69(21)
Background Most patients with chest pain are discharged from the emergency department (ED) with the diagnosis “unspecified chest pain.” It is unknown if evaluation with a high-sensitivity troponin T (hsTnT) assay affects prognosis in this large p
Publikováno v:
Scopus-Elsevier
Two human Mu class glutathione transferases, hGST M1-1 and hGST M2-2, with high sequence identity (84%) exhibit a 100-fold difference in activities with the substrates aminochrome, 2-cyano-1,3-dimethyl-1-nitrosoguanidine (cyanoDMNG), and 1,2-dichloro
Publikováno v:
Journal of Biological Chemistry. 278:24108-24112
Kinetic instability of p53 core domain mutants. Implications for rescue by small molecules.
Autor:
Mark R. Proctor, Thomas M Rippin, Lars O. Hansson, Penka V. Nikolova, Assaf Friedler, Alan R. Fersht, Dmitry B. Veprintsev, Stefan M.V. Freund, Stefan G.D. Rüdiger
Publikováno v:
Proceedings of the National Academy of Sciences. 99:937-942
Conformationally compromised oncogenic mutants of the tumor suppressor protein p53 can, in principle, be rescued by small molecules that bind the native, but not the denatured state. We describe a strategy for the rational search for such molecules.
Publikováno v:
Journal of Molecular Biology. 287:265-276
A library of variant enzymes was created by combined shuffling of the DNA encoding the human Mu class glutathione transferases GST M1-1 and GST M2-2. The parental GSTs are 84% sequence identical at the protein level, but their specific activities wit
Publikováno v:
Journal of Medicinal Chemistry. 38:3121-3131
The quantitative structure-activity relationship between physicochemical properties and effects on dopamine (DA) synthesis and release in the rat brain, in a series of meta-substituted (S)-phenylpiperidines, has been investigated by means of partial
Autor:
Robert Louis Hoffman, Stjernlöf P, Lars O. Hansson, Håkan Wikström, Arvid Carlsson, Ennis, Kjell A. Svensson, Nabil B. Ghazal, M. W. Smith, S. Sundell
Publikováno v:
Journal of Medicinal Chemistry. 38:2202-2216
A series of 1-, 3-, and 4-substituted analogs to the potent 5-HT1A against 8-(dipropylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1-carbaldehyde (5) were prepared and tested in vitro at 5-HT1A, 5-HT1D alpha, 5-HT1D beta, D2, and D3 receptors and in vi
Autor:
Arvid Carlsson, M. W. Smith, Kjell A. Svensson, Chiu-Hong Lin, Nicholas Waters, Håkan Wikström, Lars O. Hansson, Clas Sonesson
Publikováno v:
Journal of Medicinal Chemistry. 37:2735-2753
A series of (S)-phenylpiperidines in which the substituents on the aromatic ring and nitrogen have been varied has been prepared. They have been evaluated pharmacologically to explore the importance of these substituents for the interaction with cent
Autor:
Lars O. Hansson, Michael D. Ennis, P. Stjernloef, Arvid Carlsson, N. B. Ghazal, M. W. Smith, S. Sundell, Kjell A. Svensson, H. Wikstroem, Robert Louis Hoffman
Publikováno v:
ChemInform. 26