Zobrazeno 1 - 4
of 4
pro vyhledávání: '"M W, Lutz"'
Autor:
D M, Lyall, S E, Harris, M E, Bastin, S, Muñoz Maniega, C, Murray, M W, Lutz, A M, Saunders, A D, Roses, M del C, Valdés Hernández, N A, Royle, J M, Starr, D J, Porteous, J M, Wardlaw, I J, Deary
Publikováno v:
Translational Psychiatry
Genetic polymorphisms in the APOE ɛ and TOMM40 '523' poly-T repeat gene loci have been associated with significantly increased risk of Alzheimer's disease. This study investigated the independent effects of these polymorphisms on human cognitive age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::14d722acc83ccfe6b42a33e4916fee30
https://pubmed.ncbi.nlm.nih.gov/25247594
https://pubmed.ncbi.nlm.nih.gov/25247594
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 278(1)
The activity of a series of busprione analogs at recombinant and rat thoracic aorta alpha-1 adrenoceptors was investigated. Compound affinity for recombinant alpha-1A, alpha-1B and alpha-1D adrenoceptors from human and animal sources was determined b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::619807996b271c043f918f3b5bb0271e
https://pubmed.ncbi.nlm.nih.gov/8764344
https://pubmed.ncbi.nlm.nih.gov/8764344
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 271(3)
Experiments were designed to characterize the predominant subtype of alpha-1 adrenoceptors in human and canine prostate tissue. The chemical (+/-)-beta-([125I]iodo-4-hydroxyphenyl)-ethyl- aminomethyl-tetralone bound in a specific, saturable manner to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::81c283c0ab1932cfb881306bf4b4dabf
https://pubmed.ncbi.nlm.nih.gov/7996431
https://pubmed.ncbi.nlm.nih.gov/7996431
Autor:
M W, Lutz, P H, Morgan, M K, James, P L, Feldman, M F, Brackeen, A P, Lahey, S V, James, J M, Bilotta, J C, Pressley
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 271(2)
A simple mathematical model of analgesia in the rat is developed and utilized to determine quantitative structure-activity relationships for a series of novel 4-anilidopiperidine opioids. The compounds tested (selected alkyl carboxyethyl esters attac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09162fc4202b30cfa9d52e5ca23f9a29
https://pubmed.ncbi.nlm.nih.gov/7965798
https://pubmed.ncbi.nlm.nih.gov/7965798