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Eranga N Vithana

Showing results (1-10 of 86) with videos related to

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Investigative Ophthalmology & Visual Science|June 8, 2013
Ion transport function of SLC4A11 in corneal endotheliumSupriya S Jalimarada, Diego G Ogando, Eranga N Vithana, et al.
Molecular Vision|June 5, 2013
Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell cultureWilliam Shei, Jun Liu, Hla M Htoon, et al.
Current Opinion in Ophthalmology|January 3, 2020
Primary angle closure glaucoma genomic associations and disease mechanismChang Liu, Monisha E Nongpiur, Chiea-Chuen Khor, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulatorDiego G Ogando, Supriya S Jalimarada, Wenlin Zhang, et al.
Molecular Vision|September 1, 2010
Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese populationEranga N Vithana, Monisha E Nongpiur, Divya Venkataraman, 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.
Molecular Vision|April 26, 2006
A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of diseaseLeen Abu-Safieh, Eranga N Vithana, Irmela Mantel, et al.
Investigative Ophthalmology & Visual Science|May 3, 2008
Association of LOXL1 gene polymorphisms with pseudoexfoliation in the JapaneseMineo Ozaki, Kelvin Y C Lee, Eranga N Vithana, et al.
The Ocular Surface|January 6, 2015
Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutantsR Lakshminarayanan, Shyam S Chaurasia, Elavazhagan Murugan, et al.
Ophthalmology|November 2, 2010
The heritability and sibling risk of angle closure in AsiansNishani Amerasinghe, Jian Zhang, Anbupalam Thalamuthu, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Investigative Ophthalmology & Visual Science|June 8, 2013
Ion transport function of SLC4A11 in corneal endotheliumSupriya S Jalimarada, Diego G Ogando, Eranga N Vithana, et al.
Molecular Vision|June 5, 2013
Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell cultureWilliam Shei, Jun Liu, Hla M Htoon, et al.
Current Opinion in Ophthalmology|January 3, 2020
Primary angle closure glaucoma genomic associations and disease mechanismChang Liu, Monisha E Nongpiur, Chiea-Chuen Khor, et al.
American Journal of Physiology. Cell Physiology|July 19, 2013
SLC4A11 is an EIPA-sensitive Na(+) permeable pHi regulatorDiego G Ogando, Supriya S Jalimarada, Wenlin Zhang, et al.
Molecular Vision|September 1, 2010
Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese populationEranga N Vithana, Monisha E Nongpiur, Divya Venkataraman, 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.
Molecular Vision|April 26, 2006
A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of diseaseLeen Abu-Safieh, Eranga N Vithana, Irmela Mantel, et al.
Investigative Ophthalmology & Visual Science|May 3, 2008
Association of LOXL1 gene polymorphisms with pseudoexfoliation in the JapaneseMineo Ozaki, Kelvin Y C Lee, Eranga N Vithana, et al.
The Ocular Surface|January 6, 2015
Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutantsR Lakshminarayanan, Shyam S Chaurasia, Elavazhagan Murugan, et al.
Ophthalmology|November 2, 2010
The heritability and sibling risk of angle closure in AsiansNishani Amerasinghe, Jian Zhang, Anbupalam Thalamuthu, et al.
Pageof 9