Zobrazeno 1 - 7
of 7
pro vyhledávání: '"R. C. Garrad"'
Autor:
L I, Santiago-Pérez, R V, Flores, C, Santos-Berríos, N E, Chorna, B, Krugh, R C, Garrad, L, Erb, G A, Weisman, F A, González
Publikováno v:
Journal of cellular physiology. 187(2)
Activation of P2Y(2) receptors by extracellular nucleotides has been shown to induce phenotypic differentiation of human promonocytic U937 cells that is associated with the inflammatory response. The P2Y(2) receptor agonist, UTP, induced the phosphor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::24310083a75fd1d6dcc4b39aba8cb069
https://pubmed.ncbi.nlm.nih.gov/11267999
https://pubmed.ncbi.nlm.nih.gov/11267999
Publikováno v:
Molecular and cellular biochemistry. 206(1-2)
The equal potency and efficacy of the agonists, ATP and UTP, pharmacologically distinguish the P2Y2 receptor from other nucleotide receptors. Investigation of the desensitization of the P2Y2 receptors is complicated by the simultaneous expression of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ae13dc798e8000fb104633a432fe2e1
https://pubmed.ncbi.nlm.nih.gov/10839197
https://pubmed.ncbi.nlm.nih.gov/10839197
Autor:
M, Otero, R C, Garrad, B, Velázquez, M G, Hernández-Pérez, J M, Camden, L, Erb, L L, Clarke, J T, Turner, G A, Weisman, F A, González
Publikováno v:
Molecular and cellular biochemistry. 205(1-2)
UTP activates P2Y, receptors in both 1321N1 cell transfectants expressing the P2Y2 receptor and human HT-29 epithelial cells expressing endogenous P2Y, receptors with an EC50 of 0.2-1.0 microM. Pretreatment of these cells with UTP diminished the effe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c1876eeef8739146b090ae880720ae5
https://pubmed.ncbi.nlm.nih.gov/10821429
https://pubmed.ncbi.nlm.nih.gov/10821429
Publikováno v:
Progress in brain research. 120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::13fcbcf9d120a6e1627e444e21a8cc8d
https://pubmed.ncbi.nlm.nih.gov/10550986
https://pubmed.ncbi.nlm.nih.gov/10550986
Autor:
R C, Garrad, M A, Otero, L, Erb, P M, Theiss, L L, Clarke, F A, Gonzalez, J T, Turner, G A, Weisman
Publikováno v:
The Journal of biological chemistry. 273(45)
Molecular determinants of P2Y2 receptor desensitization and sequestration have been investigated. Wild-type P2Y2 receptors and a series of five C-terminal truncation mutants of the receptor were epitope-tagged and stably expressed in 1321N1 cells. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::462c90b525c938248b22aa7dfbfd60ca
https://pubmed.ncbi.nlm.nih.gov/9792648
https://pubmed.ncbi.nlm.nih.gov/9792648
Publikováno v:
Advances in experimental medicine and biology. 431
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5bfe14a48c8515f5be7629407bce30a6
https://pubmed.ncbi.nlm.nih.gov/9598102
https://pubmed.ncbi.nlm.nih.gov/9598102
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461374565
Cystic fibrosis (CF) is caused by mutations in the gene encoding the cystic fibrosis transmembrane-conductance regulator (CFTR), a cAMP-dependent chloride transporter expressed in epithelial tissue. A novel treatment being developed for CF utilizes i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd93ff7c6e96fbf8bd3c84ec84b75fd3
https://doi.org/10.1007/978-1-4615-5381-6_82
https://doi.org/10.1007/978-1-4615-5381-6_82
