Scholars@Duke
Search form
Search
Advanced Search
Support
Index
Subscribe to Announcements
Menu
Search
Home
People
Schools / Institutes
Research
About
Home
People
Schools / Institutes
Research
Polycystic Kidney, Autosomal Recessive
Subject Areas on Research
Another cystic mystery solved.
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.
Nephronophthisis-associated ciliopathies.
Sec63 and Xbp1 regulate IRE1α activity and polycystic disease severity.
Transplantation and autosomal recessive polycystic kidney disease.
