Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Li Wei Koh"'
Autor:
Anandalakshmi Venkatraman, Eranga N. Vithana, Tin Aung, Li-Fong Seet, Jun Liu, Li Wei Koh, Rajiv R. Mohan, Divya Venkataraman, Joseph A. Bonanno, Jeppe Praetorius
Publikováno v:
Liu, J, Seet, L-F, Koh, L W, Venkatraman, A, Venkataraman, D, Mohan, R R, Prætorius, J, Bonanno, J A, Aung, T & Vithana, E N 2012, ' Depletion of SLC4A11 causes cell death by apoptosis in an immortalized human corneal endothelial cell line ', Investigative Ophthalmology & Visual Science, vol. 53, no. 7, pp. 3270-9 . https://doi.org/10.1167/iovs.11-8724
To investigate the effects of SLC4A11 gene depletion in human corneal endothelial cells.To achieve stable downregulation of SLC4A11 gene expression in immortalized human corneal endothelial cells (HCECs), short-hairpin RNA (shRNA) targeted against SL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c91585f9b380e2731614626ac70569e2
https://pure.au.dk/portal/da/publications/depletion-of-slc4a11-causes-cell-death-by-apoptosis-in-an-immortalized-human-corneal-endothelial-cell-line(bf38ec9d-bb9d-4d7a-9052-0fd83b782fcd).html
https://pure.au.dk/portal/da/publications/depletion-of-slc4a11-causes-cell-death-by-apoptosis-in-an-immortalized-human-corneal-endothelial-cell-line(bf38ec9d-bb9d-4d7a-9052-0fd83b782fcd).html
Autor:
Li Wei Koh, S. Amer Riazuddin, Yee Meng Heng, Danielle N. Meadows, Yangjian Liu, Li-Fong Seet, Amr Al-Saif, Allen O. Eghrari, Nicholas Katsanis, Tin Aung, John D. Gottsch, Eranga N. Vithana
Publikováno v:
Human mutation. 31(11)
Homozygous mutations in the Borate Cotransporter SLC4A11 cause two early-onset corneal dystrophies: congenital hereditary endothelial dystrophy (CHED) and Harboyan syndrome. More recently, four sporadic patients with late-onset Fuchs corneal dystroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a234198e4eaf338893f84ecbefe22ca9
https://pubmed.ncbi.nlm.nih.gov/20848555
https://pubmed.ncbi.nlm.nih.gov/20848555
Autor:
Li Wei Koh, Eranga N. Vithana, Chiea Chuen Khor, Divya Venkataraman, Tin Aung, Anbupalam Thalamuthu, Jodhbir S. Mehta, Donald T.H. Tan
Publikováno v:
Investigative Opthalmology & Visual Science. 52:5573
To test the association between TCF4, a gene recently found to confer susceptibility to Fuchs' corneal dystrophy (FCD) in Caucasian populations, and Chinese patients with FCD.Fifty-seven Chinese subjects with clinically diagnosed FCD and 121 normal c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49e0c851a8abd4c1c927fe1a2d6232d3
https://doi.org/10.1167/iovs.11-7568
https://doi.org/10.1167/iovs.11-7568