Browsing Research Flagships, Centres and Institutes by Author "Kuot, Abraham"
Screening of the COL8A2 gene in an Australian family with early-onset Fuchs’ endothelial corneal dystrophy Kuot, Abraham; Mills, Richard Arthur; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope (John Wiley & Sons, Ltd, 2014-03)
Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes Kuot, Abraham; Javadiyan, Shahrbanou; Abhary, Sotoodeh; Burdon, Kathryn Penelope; Whiting, Malcolm John; Kasmeridis, Nicholas; Petrovsky, Nikolai; Craig, Jamie E (2010)Asymmetric dimethylarginine (ADMA), present in human serum, is an endogenous inhibitor of nitric oxide synthase and contributes to vascular disease. Dimethylarginine dimethylaminohydrolase (DDAH) is an ADMA degrading enzyme ...
TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases Kuot, Abraham; Hewitt, Alex W; Snibson, Grant R; Souzeau, Emmanuelle; Mills, Richard Arthur; Craig, Jamie E; Burdon, Kathryn Penelope; Sharma, Shiwani (Public Library of Science, 2017-08-23)Fuchs’ endothelial corneal dystrophy (FECD) is a progressive, vision impairing disease. Common single nucleotide polymorphisms (SNPs) and a trinucleotide repeat polymorphism, thymine-guanine-cytosine (TGC), in the TCF4 ...