Zebrafish, C. elegans and Human Polycystic Kidney Disease

dc.contributor.author	Lyman Gingerich, Jamie S.
dc.contributor.author	Meyer, Samantha
dc.date.accessioned	2017-12-08T18:23:27Z
dc.date.available	2017-12-08T18:23:27Z
dc.date.issued	2017-12-08T18:23:27Z
dc.identifier.uri	http://digital.library.wisc.edu/1793/77511
dc.description	Color poster with text, graphs, charts, and images.	en
dc.description.abstract	The focus of this project is to identify the downstream effects of mutations in the causative genes (PKD1 and PKD2) of polycystic kidney disease (ADPKD). ADPKD is responsible for 5% of all endstage renal disease and is characterized by large, fluid-filled cysts forming in kidney tubules and collecting ducts that disrupt the normal functioning of the kidneys. It is currently thought that primary cilia (1) and different signaling pathways may play a major role in the progression of ADPKD.	en
dc.description.sponsorship	University of Wisconsin--Eau Claire Office of Research and Sponsored Programs	en
dc.language.iso	en_US	en
dc.relation.ispartofseries	USGZE AS589;
dc.subject	C. elegans	en
dc.subject	Zebrafish	en
dc.subject	Polycystic kidney disease	en
dc.subject	Posters	en
dc.title	Zebrafish, C. elegans and Human Polycystic Kidney Disease	en
dc.type	Presentation	en