PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
28232486-5	2017	The disulfide bond cross-link caused a >=95% loss of cytochrome c reductase activity that was reversible with DTT treatment, whereas graded cross-link lengthening gradually increased activity, thus defining the conformational constraints in the catalytic process.	Dithiothreitol	113-116	cytochrome c, somatic	Homo sapiens	56-68	
16620791-9	2006	In agreement with the interplay between the mitochondrial and the endoplasmic reticulum pathways it was found that both staurosporine and DTT induced cytochrome c release.	Dithiothreitol	138-141	cytochrome c, somatic	Homo sapiens	150-162	
25224641-2	2014	We found that the mass of human cyt c increases by 16 Da in the Met80-Lys86 region by reaction with molecular oxygen in the presence of CL-containing liposomes and dithiothreitol (DTT).	Dithiothreitol	164-178	cytochrome c, somatic	Homo sapiens	32-37	
25224641-2	2014	We found that the mass of human cyt c increases by 16 Da in the Met80-Lys86 region by reaction with molecular oxygen in the presence of CL-containing liposomes and dithiothreitol (DTT).	Dithiothreitol	180-183	cytochrome c, somatic	Homo sapiens	32-37	
25224641-5	2014	A red-shift of the Soret band from 406 to 412 nm and absorption increase at ~536 and ~568 nm were observed for Delta8384 cyt c when it reacted with DTT and molecular oxygen, followed by a further red-shift of the Soret band to 416 nm and absorption increase at ~620 and ~650 nm.	Dithiothreitol	148-151	cytochrome c, somatic	Homo sapiens	121-126	
17122865-6	2007	Pre-treatment with the antioxidants vitamin C and dithiothreitol inhibited ROS generation, prevented HPR-induced ceramide accumulation, cell cycle arrest, cytochrome c release, caspase-activation and apoptosis.	Dithiothreitol	50-64	cytochrome c, somatic	Homo sapiens	155-167	
20655869-7	2010	On the other hand, a reducing agent, dithiothreitol (DTT), inhibited BAX insertion/oligomerization augmented by tBID or Ca(2+) and suppressed the BAX-mediated release of cytochrome c and Smac/DIABLO but failed to inhibit Ca(2+)-induced swelling.	Dithiothreitol	37-51	cytochrome c, somatic	Homo sapiens	170-182	
20655869-7	2010	On the other hand, a reducing agent, dithiothreitol (DTT), inhibited BAX insertion/oligomerization augmented by tBID or Ca(2+) and suppressed the BAX-mediated release of cytochrome c and Smac/DIABLO but failed to inhibit Ca(2+)-induced swelling.	Dithiothreitol	53-56	cytochrome c, somatic	Homo sapiens	170-182	
11368793-5	2001	Tributyltin-induced cytochrome c release is also prevented by dithiols such as dithiothreitol and 2,3-dimercaptopropanol but not by monothiols such as GSH, N-acetyl-L-cysteine, L-cysteine and 2-mercaptoethanol.	Dithiothreitol	79-93	cytochrome c, somatic	Homo sapiens	20-32	
15683237-9	2005	Surprisingly, cytochrome c is about a 100-fold better electron acceptor for ALR than oxygen when DTT is the reducing substrate.	Dithiothreitol	97-100	cytochrome c, somatic	Homo sapiens	14-26	
11710113-5	2000	The latter two were further reduced to SH-cytochrome c and SH-rGPIb alpha by dithiothreitol and conjugated with PD-AMS by a thiol-disulfide exchange reaction.	Dithiothreitol	77-91	cytochrome c, somatic	Homo sapiens	42-54