Zobrazeno 1 - 10
of 228
pro vyhledávání: '"H.W. Kosterlitz"'
Autor:
Antoine Delfour, A.D. Corbett, Mohamed Amiche, H.W. Kosterlitz, Pierre Nicolas, Sandrine Sagan
1. To elucidate the structural features required for selective and potent action of dermenkephalin at the delta-opioid receptor, a series of analogues of dermenkephalin and dermorphin were tested for their effectiveness in depressing electrically-evo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9925a6a6e3232d3d0f4ec6cac301bf31
https://europepmc.org/articles/PMC1908574/
https://europepmc.org/articles/PMC1908574/
Publikováno v:
Neuroscience. 12:621-627
(-)-[3H]Bremazocine interacts almost equally well with the mu-, delta- and kappa-types of opioid binding sites. In homogenates of guinea-pig cerebellum, it was bound with high affinity (KD = 0.046 nM) and the maximum binding capacity was 7.04 pmol/g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b58fea6d5e4c8ceaedddeab3b1cd35
https://doi.org/10.1016/0306-4522(84)90077-0
https://doi.org/10.1016/0306-4522(84)90077-0
Autor:
A.T. McKnight, L.E. Robson, S J Paterson, Alistair D. Corbett, Maureen G. C. Gillan, H.W. Kosterlitz
Publikováno v:
Regulatory Peptides. 10:1-7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::160e9f31ce52cbb092fe3052d4dcea91
https://doi.org/10.1016/0167-0115(85)90209-5
https://doi.org/10.1016/0167-0115(85)90209-5
Autor:
A.B. Cairnie, H.W. Kosterlitz
Publikováno v:
International Journal of Neuropharmacology. 1:133-136
Summary Thresholds of excitability and conduction velocities were measured, before and after intravenous injection of morphine (1–5 mg/kg), in A and C groups of fibres of the rabbit vagus nerve and in α and C groups of fibres of the cat saphenous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::300234d6b175e3be44ee2191e4b187e0
https://doi.org/10.1016/0028-3908(62)90019-9
https://doi.org/10.1016/0028-3908(62)90019-9
Publikováno v:
FEBS Letters. (1):195-198
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d65d4f386c50e8c0b21303eecdea1a3
The three agonists, methionine-enkephalin, leucine-enkephalin and beta-endorphin have different pharmacological patterns. It may be of particular importance that they vary in their relative affinities to the enkephalin and naltrexone binding sites in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20d21fd7f626d4c65118397b3ccea836
https://doi.org/10.1016/b978-0-08-028021-9.50005-8
https://doi.org/10.1016/b978-0-08-028021-9.50005-8
Autor:
M.P. Blaustein, A.S. Clanachan, M. Fillenz, M. Göthert, W. Haefely, G. Häusler, G. Henderson, J. Hughes, I.J. Kopin, H.W. Kosterlitz, S.Z. Langer, K. Löffelholz, J.C. McGrath, E. Muscholl, D.M. Paton, A.D. Smith, K. Starke, L. Stjärne, U. Trendelenburg, D.J. Triggle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a2ab8766035e3aa454529ca7b467a65
https://doi.org/10.1016/b978-0-08-021536-5.50004-6
https://doi.org/10.1016/b978-0-08-021536-5.50004-6
In membrane suspensions from guinea pig brain or cerebellum, NaCl, LiCl, NH4Cl, and KCl inhibit the equilibrium binding at 25 degrees C of the selective mu-agonist [3H][2-D-alanine,4-methylphenylalanine,5-glycinol]enkephalin ([D-Ala2,MePhe4,Gly-ol5]E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b2c91d628a63aea7cabab8685a227ea
https://europepmc.org/articles/PMC386471/
https://europepmc.org/articles/PMC386471/