PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
8500547-14	1993	Induced SPARC expression was, in large part, dependent on autocrine transforming growth factor-beta (TGF-beta) production since incubation in the presence of NaB+neutralizing antibodies to TGF-beta inhibited both the expression of SPARC by 72% and development of mature CEs.	nab	158-161	transforming growth factor beta 1	Homo sapiens	68-99	
8500547-14	1993	Induced SPARC expression was, in large part, dependent on autocrine transforming growth factor-beta (TGF-beta) production since incubation in the presence of NaB+neutralizing antibodies to TGF-beta inhibited both the expression of SPARC by 72% and development of mature CEs.	nab	158-161	transforming growth factor beta 1	Homo sapiens	101-109	
27605008-7	2016	Furthermore, we demonstrated that blocking of TGF-beta by neutralizing Abs abrogated NaB-mediated protection of Tregs and experimental allergic encephalomyelitis.	nab	85-88	transforming growth factor beta 1	Homo sapiens	46-54	
1727055-3	1992	NaB also induces TGF-beta mRNA in the maturing suprabasal compartment, suggesting that TGF-beta may play a role in NaB-initiated NHEK differentiation.	nab	0-3	transforming growth factor beta 1	Homo sapiens	17-25	
1727055-3	1992	NaB also induces TGF-beta mRNA in the maturing suprabasal compartment, suggesting that TGF-beta may play a role in NaB-initiated NHEK differentiation.	nab	0-3	transforming growth factor beta 1	Homo sapiens	87-95	
1727055-3	1992	NaB also induces TGF-beta mRNA in the maturing suprabasal compartment, suggesting that TGF-beta may play a role in NaB-initiated NHEK differentiation.	nab	115-118	transforming growth factor beta 1	Homo sapiens	87-95	
1727055-5	1992	TGF-beta 1 was quite effective in inducing significant levels of CE expression when used simultaneously with suboptimal concentrations of NaB.	nab	138-141	transforming growth factor beta 1	Homo sapiens	0-10	
1727055-6	1992	The cooperative action of suboptimal NaB and TGF-beta 1 generated numbers of CEs which, in fact, exceeded the incidence of mature CEs formed in response to optimal levels of NaB alone.	nab	174-177	transforming growth factor beta 1	Homo sapiens	45-55	
1727055-7	1992	Neutralizing antibodies to TGF-beta, moreover, effectively reduced the incidence of CE formation in cultures treated with optimal NaB concentrations, further implicating endogenous TGF-beta activity in the NaB-initiated NHEK differentiation model.	nab	130-133	transforming growth factor beta 1	Homo sapiens	27-35	
1727055-7	1992	Neutralizing antibodies to TGF-beta, moreover, effectively reduced the incidence of CE formation in cultures treated with optimal NaB concentrations, further implicating endogenous TGF-beta activity in the NaB-initiated NHEK differentiation model.	nab	206-209	transforming growth factor beta 1	Homo sapiens	27-35	
1727055-7	1992	Neutralizing antibodies to TGF-beta, moreover, effectively reduced the incidence of CE formation in cultures treated with optimal NaB concentrations, further implicating endogenous TGF-beta activity in the NaB-initiated NHEK differentiation model.	nab	206-209	transforming growth factor beta 1	Homo sapiens	181-189	
1727055-8	1992	It is suggested, therefore, that within the NaB-induced pathway of NHEK differentiation, TGF-beta can positively modulate expression of the differentiated phenotype but alone is insufficient for generation of mature CEs.	nab	44-47	transforming growth factor beta 1	Homo sapiens	89-97	
27605008-4	2016	Because TGF-beta is an important inducer of Tregs, we examined the effect of NaB on the status of TGF-beta.	nab	77-80	transforming growth factor beta 1	Homo sapiens	98-106	
27605008-5	2016	In this study, we demonstrated that NaB induced the expression of TGF-beta mRNA and protein in normal as well as proteolipid protein-primed splenocytes.	nab	36-39	transforming growth factor beta 1	Homo sapiens	66-74	
1555205-1	1992	The effects of sodium butyrate (NaB) on the response of the RCA human colon carcinoma cell line to transforming growth factor-beta 1 (TGF-beta 1) were examined.	nab	32-35	transforming growth factor beta 1	Homo sapiens	99-132	
1555205-5	1992	Addition of TGF-beta 1 to cells grown in the presence of NaB resulted in a stimulation of growth.	nab	57-60	transforming growth factor beta 1	Homo sapiens	12-22	
1555205-6	1992	Cells pretreated with TGF-beta 1 remained sensitive to the growth inhibitory and differentiation inducing effects of NaB.	nab	117-120	transforming growth factor beta 1	Homo sapiens	22-32	
1555205-7	1992	These results suggest that NaB may alter the expression of proteins responsible for a stimulatory signal response to TGF-beta 1 in RCA cells.	nab	27-30	transforming growth factor beta 1	Homo sapiens	117-127	
2257881-3	1990	NaB induced a four-fold increase in TGF-beta mRNA transcript levels.	nab	0-3	transforming growth factor beta 1	Homo sapiens	36-44	
2257881-4	1990	This increase in TGF-beta mRNA abundance occurred only within the nonbasal keratinocyte subpopulation which maximally responds to NaB treatment by progression to cornified envelopes.	nab	130-133	transforming growth factor beta 1	Homo sapiens	17-25	
27605008-8	2016	These studies identify a new function of NaB in upregulating TGF-beta via activation of STAT6, which may be beneficial in MS patients.	nab	41-44	transforming growth factor beta 1	Homo sapiens	61-69