PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19741202-1	2009	The extent to which the acute phase response (APR) influences iron status indicators in chronic infections is not well documented.	Iron	62-66	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	46-49	
25714024-0	2015	Dihydroartemisinin and its derivative induce apoptosis in acute myeloid leukemia through Noxa-mediated pathway requiring iron and endoperoxide moiety.	Iron	121-125	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	89-93	
29343315-1	2018	OBJECTIVE: To assess the impact of the acute-phase response (APR) during inflammation on Fe, Zn and vitamin A biomarkers to allow accurate evaluation of micronutrient status in populations.	Iron	89-91	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	61-64	
25714024-6	2015	Interfering with the integrity of the endoperoxide moiety of DHA and X-11, as well as chelating intracellular iron with deferoxamine, diminish apoptosis and Noxa induction.	Iron	110-114	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	157-161	
25714024-8	2015	DHA and X-11 represent a new group of AML cells-apoptosis inducing compounds which work through Noxa up-regulation utilizing the specific endoperoxide moiety and intracellular iron.	Iron	176-180	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	96-100	
25398733-8	2014	Traditional indicators of iron, zinc, and vitamin A status are altered during the APR, leading to inaccurate estimations of deficiency in populations with a high or unknown prevalence of infection.	Iron	26-30	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	82-85	
23770082-5	2013	When lysosomal membranes were stabilized by the iron-chelating agent desferrioxamine, H2O2-induced increase in DNA damage, Noxa expression, and subsequent apoptosis were abolished by the inhibition of LMP.	Iron	48-52	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	123-127	
18506200-1	2009	OBJECTIVES: The acute phase response (APR) influences indicators of iron status.	Iron	68-72	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	38-41	
19175946-12	2009	It may be possible to develop algorithms, based on the markers of the APR and Fe status, to assess the Fe status among the patients with tuberculosis or other infections eliciting an APR.	Iron	78-80	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	183-186	
19175946-12	2009	It may be possible to develop algorithms, based on the markers of the APR and Fe status, to assess the Fe status among the patients with tuberculosis or other infections eliciting an APR.	Iron	103-105	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	70-73	
19175946-12	2009	It may be possible to develop algorithms, based on the markers of the APR and Fe status, to assess the Fe status among the patients with tuberculosis or other infections eliciting an APR.	Iron	103-105	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	183-186	
18506200-4	2009	We examined whether the APR (measured by AGP) influences the expected relationships between iron status indicators in an HIV-infected population.	Iron	92-96	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	24-27	
18506200-10	2009	CONCLUSIONS: AGP captured the influence of the APR on iron indicators and their relationships with each other.	Iron	54-58	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	47-50	
18506200-15	2009	We support the WHO/CDC recommendation that AGP is a useful indicator to assess the influence of the APR on iron status indicators.	Iron	107-111	phorbol-12-myristate-13-acetate-induced protein 1	Homo sapiens	100-103