This decommissioned ERA site remains active temporarily to support our final migration steps to https://ualberta.scholaris.ca, ERA's new home. All new collections and items, including Spring 2025 theses, are at that site. For assistance, please contact erahelp@ualberta.ca.
Search
Skip to Search Results- 2Water transport
- 1Aquaporins
- 1Corneal dystrophies CHED FECD
- 1ER retention and protein misfolding
- 1Membrane protein
- 1Plant physiology
-
Spring 2023
Although many aspects of salinity tolerance in plants have been thoroughly researched, some of the fundamental aspects of plant water relations remain unclear. The main objective of my thesis research was to examine the role of aquaporin-mediated water transport in salinity tolerance of three...
-
Fall 2015
Congenital hereditary endothelial corneal dystrophy type 2 (CHED2), Harboyan Syndrome (HS) and Fuchs endothelial corneal dystrophy (FECD) are caused by SLC4A11 mutations. The majority of SLC4A11 point mutations cause SLC4A11 misfolding and retention in the endoplasmic reticulum (ER). This impairs...