PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
24505507-3	2013	In cell-based assays, whereas Sestd1 does not alter Dvl2 activation of the Wnt/beta-catenin signaling pathway, Dvl2 enhances activation of Rho family GTPases by Dact1 and Sestd1, consistent with a role in the PCP pathway.	pcp	209-212	dishevelled segment polarity protein 2	Homo sapiens	111-115	
24505507-5	2013	This genetic synergy stands in contrast to the epistasis we have previously reported between Sestd1 and Dact1 KO, and suggests independent or semi-independent functions for Dvl2 vs. Sestd1/Dact1 in the regulation of the PCP pathway during development.	pcp	220-223	dishevelled segment polarity protein 2	Homo sapiens	173-177	
24505507-6	2013	In conclusion, biochemical and genetic interactions between Dvl2, Sestd1, and Dact1, in addition to prior reported interactions between these same molecules and Vangl2, suggest that all these gene products can form complexes together and regulate the PCP pathway during mammalian development.	pcp	251-254	dishevelled segment polarity protein 2	Homo sapiens	60-64	
31340145-5	2019	We propose that a WWP1-USP9X axis regulates a ubiquitin rheostat on DVL2 that specifies its participation in either canonical WNT or WNT-PCP pathways.	pcp	137-140	dishevelled segment polarity protein 2	Homo sapiens	68-72	
29796181-6	2018	In RPGR, RPGRIP1 or RPGRIP1L KD cells, we observed increased levels of DVl2 and DVl3 proteins, the core components of the PCP pathway, due to impaired proteasomal activity.	pcp	122-125	dishevelled segment polarity protein 2	Homo sapiens	71-75