Casey JR - Search Results

1

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases.

Vilas GL, Loganathan SK, Liu J, Riau AK, Young JD, Mehta JS, Vithana EN, Casey JR. Vilas GL, et al. Among authors: casey jr. Hum Mol Genet. 2013 Nov 15;22(22):4579-90. doi: 10.1093/hmg/ddt307. Epub 2013 Jun 27. Hum Mol Genet. 2013. PMID: 23813972 Free PMC article.

2

Increased water flux induced by an aquaporin-1/carbonic anhydrase II interaction.

Vilas G, Krishnan D, Loganathan SK, Malhotra D, Liu L, Beggs MR, Gena P, Calamita G, Jung M, Zimmermann R, Tamma G, Casey JR, Alexander RT. Vilas G, et al. Among authors: casey jr. Mol Biol Cell. 2015 Mar 15;26(6):1106-18. doi: 10.1091/mbc.E14-03-0812. Epub 2015 Jan 21. Mol Biol Cell. 2015. PMID: 25609088 Free PMC article.

3

Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutations.

Vilas GL, Loganathan SK, Quon A, Sundaresan P, Vithana EN, Casey J. Vilas GL, et al. Hum Mutat. 2012 Feb;33(2):419-28. doi: 10.1002/humu.21655. Epub 2011 Dec 20. Hum Mutat. 2012. PMID: 22072594

4

A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophies.

Vilas GL, Morgan PE, Loganathan SK, Quon A, Casey JR. Vilas GL, et al. Among authors: casey jr. Biochemistry. 2011 Mar 29;50(12):2157-69. doi: 10.1021/bi101887z. Epub 2011 Feb 14. Biochemistry. 2011. PMID: 21288032

5

Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapy.

Loganathan SK, Casey JR. Loganathan SK, et al. Among authors: casey jr. Hum Mutat. 2014 Sep;35(9):1082-91. doi: 10.1002/humu.22601. Epub 2014 Jun 28. Hum Mutat. 2014. PMID: 24916015

6

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy.

Soumittra N, Loganathan SK, Madhavan D, Ramprasad VL, Arokiasamy T, Sumathi S, Karthiyayini T, Rachapalli SR, Kumaramanickavel G, Casey JR, Rajagopal R. Soumittra N, et al. Among authors: casey jr. J Hum Genet. 2014 Aug;59(8):444-53. doi: 10.1038/jhg.2014.55. Epub 2014 Jul 10. J Hum Genet. 2014. PMID: 25007886

7

Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies.

Loganathan SK, Schneider HP, Morgan PE, Deitmer JW, Casey JR. Loganathan SK, et al. Among authors: casey jr. Am J Physiol Cell Physiol. 2016 Nov 1;311(5):C735-C748. doi: 10.1152/ajpcell.00078.2016. Epub 2016 Aug 24. Am J Physiol Cell Physiol. 2016. PMID: 27558157 Free PMC article.

8

Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal Dystrophies.

Malhotra D, Loganathan SK, Chiu AM, Lukowski CM, Casey JR. Malhotra D, et al. Among authors: casey jr. Sci Rep. 2019 Jul 4;9(1):9681. doi: 10.1038/s41598-019-46094-y. Sci Rep. 2019. PMID: 31273259 Free PMC article.

9

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. Chiu AM, et al. Among authors: casey jr. Invest Ophthalmol Vis Sci. 2015 Dec;56(13):7739-53. doi: 10.1167/iovs.15-17802. Invest Ophthalmol Vis Sci. 2015. PMID: 26641551

10

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, Casey JR. Malhotra D, et al. Among authors: casey jr. Hum Mol Genet. 2020 Jan 1;29(1):97-116. doi: 10.1093/hmg/ddz259. Hum Mol Genet. 2020. PMID: 31691803

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