Joe Casey
Professor Emeritus - Retired
Ph.D, University of Toronto
Research:
Selected Publications:
Defective Cell Adhesion Function of Solute Transporter, SLC4A11, in Endothelial Corneal Dystrophies
Malhotra D, Jung M, Fecher-Trost C, Lovatt M, Peh GSL, Noskov S, Mehta JS, Zimmermann R, and Casey, J.R.
Hum Mol Genet. 2020 Jan 1;29(1):97-116.
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.
Malhotra D, Loganathan SK, Chiu AM, Lukowski CM, Casey JR.
Sci Rep. 2019 Jul 4;9(1):9681. doi: 10.1038/s41598-019-46094-y.
Ophthalmic Non-Steroidal Anti-inflammatory Drugs Correct Corneal Dystrophy-causing SLC4A11 Mutants
Alka, K. and Casey, J.R.
Invest. Ophthalmol. Visual Sci. (2018) 59: 4258-4267
A Ser725Arg mutation in Band 3 abolishes transport function and leads to anemia and renal tubular acidosis.
Yang E, Seo-Mayer P, Lezon-Geyda K, Badior KE, Li J, Casey JR, Reithmeier RAF, Gallagher PG.
Blood. 2018 Apr 12;131(15):1759-1763.
Molecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies.
Alka K, Casey JR.
Hum Mutat. 2018 May;39(5):676-690.Featured as cover for this issue of the journal.
SLC4A11 Three-Dimensional Homology Model Rationalizes Corneal Dystrophy-Causing Mutations.
Badior KE, Alka K, Casey JR.
Hum Mutat. 2017 Mar;38(3):279-288.
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies.
Loganathan SK, Schneider HP, Morgan PE, Deitmer JW, Casey JR.
Am J Physiol Cell Physiol. (2016) Nov 1;311(5):C735-C748.
The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11.
Loganathan SK, Lukowski CM, Casey JR.
Am J Physiol Cell Physiol. (2016) Jan 15;310(2):C161-74.
High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11.
Chiu AM, Mandziuk JJ, Loganathan SK, Alka K, Casey JR.
Invest Ophthalmol Vis Sci. (2015) Dec;56(13):7739-53.