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pro vyhledávání: '"Richard A. Keith"'
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Autor:
Brenda S. Keith, Amanda S. Andrijević, Ryanne Sullivan, Sara R. Morris, H. David Sheets, Richard S. Keith
Publikováno v:
The Wilson Journal of Ornithology. 125:70-78
Nearctic-neotropical passerines may spend up to one-third of the year in migration. Stopover sites have a critical role in providing migrant passerines with areas to rest and replenish fat stores. We characterized the stopover ecology of the Tennesse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e44a347334686fa08985620e134a03c
https://doi.org/10.1676/08-131.1
https://doi.org/10.1676/08-131.1
Autor:
Richard, K. Keith
Publikováno v:
Oregon Historical Quarterly, 1989 Dec 01. 90(4), 385-393.
Externí odkaz:
https://www.jstor.org/stable/20614270
Autor:
Richard, K. Keith
Publikováno v:
Oregon Historical Quarterly, 1983 Apr 01. 84(1), 29-55.
Externí odkaz:
https://www.jstor.org/stable/20613888
Autor:
Taylor, Hugh A., Richard, K. Keith
Publikováno v:
The American Archivist, 1979 Apr 01. 42(2), 259-266.
Externí odkaz:
https://www.jstor.org/stable/40292857
Autor:
Edward P. Vacek, Thomas Michael Bare, Martin C. Dyroff, Kathy L. Neilson, Rebecca Urbanek, J. Empfield, Alan S. Kirschner, Christine Barlaam, Joseph Lewis, Chi-Ming C. Lee, Wenhua Xiao, Megan Murphy, Vernon Alford, Janet Marie Forst, Gary Steelman, Shephali Trivedi, Richard A. Keith, Frances M. Mclaren, Dean G. Brown, Keith John Herzog, Horchler Carey
Publikováno v:
Journal of Medicinal Chemistry. 50:3113-3131
A series of 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5H)-triones were synthesized and found to have potent activity at the glycine site of the NMDA receptor. In some cases, these compounds possessed poor aqueous s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52e6df439ce03cdca255c44c5222f7a4
https://doi.org/10.1021/jm060212s
https://doi.org/10.1021/jm060212s
Autor:
Dean G. Brown, Kathy L. Neilson, Horchler Carey, Thomas Michael Bare, Frances M. Mclaren, Gary Steelman, James Empfield, Richard A. Keith, Martin C. Dyroff, Wenhua Xiao, Rebecca Urbanek, Janet Marie Forst, Chi-Ming C. Lee, Shephali Trivedi, Keith John Herzog, Megan Murphy
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 13:3553-3556
Several members of the 7-chloro-2,3-dihydro-2-[1-(pyridinyl)alkyl]-pyridazino[4,5-b]quinoline-1,4,10(5H)-triones (2) have been identified as being potent and selective NMDA glycine-site antagonists. Increasing size of the alkyl substituent on the alp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5c094ed082aa4e657e79b5ec88d0a5
https://doi.org/10.1016/s0960-894x(03)00750-9
https://doi.org/10.1016/s0960-894x(03)00750-9
Autor:
Allen L. Dennis, W. David Nes, Stephen T. Furlong, Timothy Piser, Haoxia Li, Wenxu Zhou, Zhonghua Jia, Richard A. Keith
Publikováno v:
Biochemical Journal. 367:587-599
CHO 2, encoding human sterol 8-isomerase (hSI), was introduced into plasmids pYX213 or pET23a. The resulting native protein was overexpressed in erg 2 yeast cells and purified to apparent homogeneity. The enzyme exhibited a K (m) of 50 microM and a t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df97385def92449bc09e63cfc44aff2a
https://doi.org/10.1042/bj20020551
https://doi.org/10.1042/bj20020551
Autor:
William E. Fieles, Ratan Bhat, Maryann P. Correll, Chi-Ming Lee, Clay W Scott, Jason Shanley, Richard A. Keith
Publikováno v:
Proceedings of the National Academy of Sciences. 97:11074-11079
Inactivation of glycogen synthase kinase-3β (GSK3β) by S 9 phosphorylation is implicated in mechanisms of neuronal survival. Phosphorylation of a distinct site, Y 216 , on GSK3β is necessary for its activity; however, whether this site can be regu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d918b2d0827c1443a7f6db88131fc69
https://doi.org/10.1073/pnas.190297597
https://doi.org/10.1073/pnas.190297597
Publikováno v:
Molecular Pharmacology. 52:1095-1104
We studied the mechanism by which the peptide omega-grammotoxin-SIA inhibits voltage-dependent calcium channels. Grammotoxin at concentrations of50 nM completely inhibited inward current carried by 2 mM barium through P-type channels in rat cerebella
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36d61b9fa7b450673d77bda9daae7f7c
https://doi.org/10.1124/mol.52.6.1095
https://doi.org/10.1124/mol.52.6.1095