PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 25774718-1 2015 To test the hypothesis that a fall in cellular ATP following stimulation of endothelial cells with thrombin is secondary to a decrease in NAD levels caused by poly(ADP-Ribose)polymerase (PARP), we measured the levels of NAD and ATP in endothelial cells after treatment with thrombin, the Ca(++)-ionophore A23187, or hydrogen peroxide (H2O2), and compared the effects of inhibitors of PARP, NAD synthesis, and ADP-ribose breakdown on these responses. NAD 138-141 coagulation factor II, thrombin Homo sapiens 99-107 29537672-9 2018 Interestingly, the NADH-stimulated oxygen consumption and ATP synthesis increased in the presence of the physiological platelets agonists, thrombin or collagen. NAD 19-23 coagulation factor II, thrombin Homo sapiens 139-147 25774718-1 2015 To test the hypothesis that a fall in cellular ATP following stimulation of endothelial cells with thrombin is secondary to a decrease in NAD levels caused by poly(ADP-Ribose)polymerase (PARP), we measured the levels of NAD and ATP in endothelial cells after treatment with thrombin, the Ca(++)-ionophore A23187, or hydrogen peroxide (H2O2), and compared the effects of inhibitors of PARP, NAD synthesis, and ADP-ribose breakdown on these responses. NAD 220-223 coagulation factor II, thrombin Homo sapiens 99-107 25774718-1 2015 To test the hypothesis that a fall in cellular ATP following stimulation of endothelial cells with thrombin is secondary to a decrease in NAD levels caused by poly(ADP-Ribose)polymerase (PARP), we measured the levels of NAD and ATP in endothelial cells after treatment with thrombin, the Ca(++)-ionophore A23187, or hydrogen peroxide (H2O2), and compared the effects of inhibitors of PARP, NAD synthesis, and ADP-ribose breakdown on these responses. NAD 220-223 coagulation factor II, thrombin Homo sapiens 99-107 23850783-2 2013 Herein, the AuNCs prepared by using polyamidoamine dendrimer as template were constructed not only as nanocarriers for anchoring the large amounts of secondary thrombin aptamers but also as nanocatalysts to catalyze the oxidation of NADH efficiently. NAD 233-237 coagulation factor II, thrombin Homo sapiens 160-168 23146393-2 2012 The hemin/G-quadruplex formed by intercalating hemin into thrombin binding aptamer (TBA), firstly acted as a NADH oxidase, assisting the oxidation of NADH to NAD(+) accompanying with the generation of H(2)O(2) in the presence of dissolved O(2). NAD 109-113 coagulation factor II, thrombin Homo sapiens 58-66 23146393-2 2012 The hemin/G-quadruplex formed by intercalating hemin into thrombin binding aptamer (TBA), firstly acted as a NADH oxidase, assisting the oxidation of NADH to NAD(+) accompanying with the generation of H(2)O(2) in the presence of dissolved O(2). NAD 158-164 coagulation factor II, thrombin Homo sapiens 58-66 20054824-6 2010 Importantly, beta-NAD significantly attenuated thrombin-induced EC permeability as well as the barrier-compromising effects of Gram-negative and Gram-positive bacterial toxins representing the barrier-protective function of beta-NAD. NAD 13-21 coagulation factor II, thrombin Homo sapiens 47-55 10391925-5 1999 This effect of thrombin was accompanied by increased O-2 and H2O2 generation and NADH/NADPH consumption. NAD 81-85 coagulation factor II, thrombin Homo sapiens 15-23