PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
25854767-0	2014	Ratjadone C-mediated nuclear accumulation of HDAC4: implications on Runx2-induced osteoblast differentiation of C3H10T1/2 mesenchymal stem cells.	ratjadone c	0-11	histone deacetylase 4	Mus musculus	45-50
25854767-0	2014	Ratjadone C-mediated nuclear accumulation of HDAC4: implications on Runx2-induced osteoblast differentiation of C3H10T1/2 mesenchymal stem cells.	ratjadone c	0-11	runt related transcription factor 2	Mus musculus	68-73
25854767-7	2014	Under the influence of ratjadone C, HDAC4 is retained in the nucleus and co-localizes with Runx2.	ratjadone c	23-34	histone deacetylase 4	Mus musculus	36-41
25854767-7	2014	Under the influence of ratjadone C, HDAC4 is retained in the nucleus and co-localizes with Runx2.	ratjadone c	23-34	runt related transcription factor 2	Mus musculus	91-96
25854767-8	2014	However, forced nuclear accumulation of HDAC4 by ratjadone C or overexpression of the nuclear resident form of HDAC4 does not inhibit osteoblast differentiation, suggesting that the Runx2- induced osteogenic program of C3H10T1/2 cells is not affected by HDAC4.	ratjadone c	49-60	histone deacetylase 4	Mus musculus	40-45
25854767-11	2014	Additionally, the ratjadone C-mediated nuclear retention assay can potentially be used as a screening tool to identify novel regulatory mechanisms of HDAC4 and its functional partners in various pathophysiological conditions.	ratjadone c	18-29	histone deacetylase 4	Mus musculus	150-155
12749860-6	2003	Finally, the binding of ratjadone C to CRM1 was demonstrated.	ratjadone c	24-35	exportin 1	Homo sapiens	39-43