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Akademický článek
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Publikováno v:
American Journal of Physiology-Cell Physiology
American Journal of Physiology-Cell Physiology, American Physiological Society, 1992, 262 (1), pp.C156-C163. ⟨10.1152/ajpcell.1992.262.1.C156⟩
American Journal of Physiology-Cell Physiology, American Physiological Society, 1992, 262 (1), pp.C156-C163. ⟨10.1152/ajpcell.1992.262.1.C156⟩
B7 is a cell clone derived from rat brain microvessels. Expression of an amiloride-sensitive cationic channel has been recently established in these cells. In this study, the polymerase chain reaction (PCR) was used to amplify definite segments of mi
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 10(7)
Autor:
J, Simon, P, Vigne, K M, Eklund, A D, Michel, A M, Carruthers, P P, Humphrey, C, Frelin, E A, Barnard
Publikováno v:
British journal of pharmacology. 132(1)
1. A P2Y (nucleotide) receptor activity in a clonal population (B10) of rat brain capillary endothelial cells is coupled to inhibition of adenylyl cyclase and has functional similarities to the P2Y(T) (previously designated 'P2T') receptor for ADP of
Publikováno v:
British journal of pharmacology. 125(4)
1. ADP is a potent agonist of rat and human P2Y1 purinoceptors. ATP is a weak competitive antagonist. This study analyses the situation in which P2Y1 receptors are exposed to ATP in the presence of exogenous ecto-nucleotidases (apyrases) that have hi
Publikováno v:
Blood. 92(1)
The human P2Y1 receptor heterologously expressed in Jurkat cells behaves as a specific adenosine 5'-diphosphate (ADP) receptor at which purified adenosine triphosphate (ATP) is an ineffective agonist, but competitively antagonizes the action of ADP.
Publikováno v:
Molecular pharmacology. 53(4)
Pharmacological properties of the human P2Y1 receptor transfected in Jurkat cells and of the endogenous receptor in rat brain capillary endothelial cells were analyzed under conditions in which the purity of adenine triphosphate nucleotides was contr
Publikováno v:
The American journal of physiology. 265(5 Pt 1)
The effects of ATP and UTP on intracellular Ca2+ levels and on the secretion of the bronchial inhibitor and high-molecular-weight glycoproteins were studied in cultures of human bronchotracheal gland cells. ATP, adenosine 5'-O-(3-thiotriphosphate) (A
Publikováno v:
Annals of oncology : official journal of the European Society for Medical Oncology. 3(1)