Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gerald Stankus"'
Autor:
Henry M. Sarau, Valeria Camarda, Stephen A. Douglas, Girolamo Calo, David G. Lambert, Nambi Aiyar, Robert N. Willette, Dulcie B. Schmidt, Parvathi Nuthulaganti, Gerald Stankus, Christopher P. Doe, David J. Behm, James J. Foley, James A. Fornwald, Robert S. Ames
Publikováno v:
British Journal of Pharmacology. 148:173-190
Several peptidic urotensin-II (UT) receptor antagonists exert 'paradoxical' agonist activity in recombinant cell- and tissue-based bioassay systems, likely the result of differential urotensin-II receptor (UT receptor) signal transduction/coupling ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4be855e96b51b4b74e5c2a722847fd95
https://doi.org/10.1038/sj.bjp.0706716
https://doi.org/10.1038/sj.bjp.0706716
Autor:
David J. Behm, Alexandra Wibberley, Stephen A. Douglas, Douglas G. Johns, Christopher P. Doe, Gerald Stankus, Robert N. Willette, Kristeen Maniscalco
Publikováno v:
Naunyn-Schmiedeberg's Archives of Pharmacology. 369:274-280
Urotensin-II, a potent mammalian vasoconstrictor, may play a role in the etiology of essential hypertension. However, a species suitable for assessing such a role, one where a "classical" systemic hypertensive response (increase in mean blood pressur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87315121103101a1736881e474f7902
https://doi.org/10.1007/s00210-004-0873-1
https://doi.org/10.1007/s00210-004-0873-1
Autor:
Robert N. Willette, Sandhya S. Nerurkar, Cindy E. Fishman, Gregory H. Turner, Kevin S. Thorneloe, Weike Bao, Gerald Stankus, Robert W. Marquis, Tian-Li Yue, David J. Figueroa, David J. Behm, Robert E. Lee Trout, Bartholomew J. Votta, Xiaoping Xu, Anthony Sulpizio, Erin S. R. Lashinger, Heath Thomas, Chris P. Doe, Linda N. Casillas, Zuojun Lin, Irina M. Lozinskaya, Sandra J. Hoffman, Haisong Ju, Min Lin
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 326(2)
The transient receptor potential (TRP) vanilloid subtype 4 (V4) is a nonselective cation channel that exhibits polymodal activation and is expressed in the endothelium, where it contributes to intracellular Ca2+ homeostasis and regulation of cell vol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7e1487a0206ac966ebc38fbb142f50e
https://pubmed.ncbi.nlm.nih.gov/18499744
https://pubmed.ncbi.nlm.nih.gov/18499744
Autor:
Robert N Willette, Weike Bao, Sandhya Nerurkar, Tian-li Yue, Chris P Doe, Gerald Stankus, Haisong Ju, Ross Bentley, Anthony Sulpizio, David Behm, Hoffman Sandra, Kristeen Maniscalco, Zuojun Lin, Casillas N Linda, Min Lin, Robert E Trout, Bartholomew J Votta, Robert W Marquis, Xu Xiaoping
Publikováno v:
Circulation. 116
Transient receptor potential V4 (TRPV4), is an osmo/mechano-sensitive ligand-gated non-selective cationic channel that contributes to intracellular Ca 2+ homeostasis and regulation of cell volume. TRPV4 is highly expressed in endothelial and various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7d7eaae0afe9a0a4c388a9bbcf5858f
https://doi.org/10.1161/circ.116.suppl_16.ii_263-b
https://doi.org/10.1161/circ.116.suppl_16.ii_263-b
Autor:
David J, Behm, Gerald, Stankus, Christopher P A, Doe, Robert N, Willette, Henry M, Sarau, James J, Foley, Dulcie B, Schmidt, Parvathi, Nuthulaganti, James A, Fornwald, Robert S, Ames, David G, Lambert, Girolamo, Calo', Valeria, Camarda, Nambi V, Aiyar, Stephen A, Douglas
Publikováno v:
British journal of pharmacology. 148(2)
Several peptidic urotensin-II (UT) receptor antagonists exert 'paradoxical' agonist activity in recombinant cell- and tissue-based bioassay systems, likely the result of differential urotensin-II receptor (UT receptor) signal transduction/coupling ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::249ae4975412a0f449f9355a3b0fb05b
https://pubmed.ncbi.nlm.nih.gov/16547525
https://pubmed.ncbi.nlm.nih.gov/16547525
Autor:
Chris P. Doe, S Graham, Yi Cui, Gerald Stankus, Bronagh M. Heath, Elisa Ballini, Nick McMahon
Publikováno v:
Journal of Pharmacological and Toxicological Methods. 60:221
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d943741be9d9f15e31bf12c028ee6dff
https://doi.org/10.1016/j.vascn.2009.04.060
https://doi.org/10.1016/j.vascn.2009.04.060