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Sampath K Loganathan

Showing results (1-10 of 14) with videos related to

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Human Mutation|June 12, 2014
Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapySampath K Loganathan, Joseph R Casey
American Journal of Physiology. Cell Physiology|November 20, 2015
The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11Sampath K Loganathan, Chris M Lukowski, Joseph R Casey
Investigative Ophthalmology & Visual Science|December 8, 2015
High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11Anthony M Chiu, Jake J Mandziuk, Sampath K Loganathan, et al.
Scientific Reports|July 6, 2019
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal DystrophiesDarpan Malhotra, Sampath K Loganathan, Anthony M Chiu, et al.
Biochemistry|February 4, 2011
A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophiesGonzalo L Vilas, Patricio E Morgan, Sampath K Loganathan, et al.
American Journal of Physiology. Cell Physiology|August 26, 2016
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophiesSampath K Loganathan, Hans-Peter Schneider, Patricio E Morgan, et al.
Human Mutation|November 11, 2011
Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutationsGonzalo L Vilas, Sampath K Loganathan, Anita Quon, et al.
Human Molecular Genetics|July 2, 2013
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseasesGonzalo L Vilas, Sampath K Loganathan, Jun Liu, et al.
Journal of Human Genetics|July 11, 2014
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophyNagasamy Soumittra, Sampath K Loganathan, Dharanija Madhavan, et al.
Science (New York, N.Y.)|March 14, 2020
Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signalingSampath K Loganathan, Krista Schleicher, Ahmad Malik, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Human Mutation|June 12, 2014
Corneal dystrophy-causing SLC4A11 mutants: suitability for folding-correction therapySampath K Loganathan, Joseph R Casey
American Journal of Physiology. Cell Physiology|November 20, 2015
The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11Sampath K Loganathan, Chris M Lukowski, Joseph R Casey
Investigative Ophthalmology & Visual Science|December 8, 2015
High Throughput Assay Identifies Glafenine as a Corrector for the Folding Defect in Corneal Dystrophy-Causing Mutants of SLC4A11Anthony M Chiu, Jake J Mandziuk, Sampath K Loganathan, et al.
Scientific Reports|July 6, 2019
Human Corneal Expression of SLC4A11, a Gene Mutated in Endothelial Corneal DystrophiesDarpan Malhotra, Sampath K Loganathan, Anthony M Chiu, et al.
Biochemistry|February 4, 2011
A biochemical framework for SLC4A11, the plasma membrane protein defective in corneal dystrophiesGonzalo L Vilas, Patricio E Morgan, Sampath K Loganathan, et al.
American Journal of Physiology. Cell Physiology|August 26, 2016
Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophiesSampath K Loganathan, Hans-Peter Schneider, Patricio E Morgan, et al.
Human Mutation|November 11, 2011
Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused by SLC4A11 mutationsGonzalo L Vilas, Sampath K Loganathan, Anita Quon, et al.
Human Molecular Genetics|July 2, 2013
Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseasesGonzalo L Vilas, Sampath K Loganathan, Jun Liu, et al.
Journal of Human Genetics|July 11, 2014
Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophyNagasamy Soumittra, Sampath K Loganathan, Dharanija Madhavan, et al.
Science (New York, N.Y.)|March 14, 2020
Rare driver mutations in head and neck squamous cell carcinomas converge on NOTCH signalingSampath K Loganathan, Krista Schleicher, Ahmad Malik, et al.
Pageof 2