Kuot A - Search Results

1

Matrix metalloproteinase-9 genetic variation and primary angle closure glaucoma in a Caucasian population.

Awadalla MS, Burdon KP, Kuot A, Hewitt AW, Craig JE. Awadalla MS, et al. Among authors: kuot a. Mol Vis. 2011;17:1420-4. Epub 2011 May 27. Mol Vis. 2011. PMID: 21655354 Free PMC article.

2

Diabetic retinopathy is associated with elevated serum asymmetric and symmetric dimethylarginines.

Abhary S, Kasmeridis N, Burdon KP, Kuot A, Whiting MJ, Yew WP, Petrovsky N, Craig JE. Abhary S, et al. Among authors: kuot a. Diabetes Care. 2009 Nov;32(11):2084-6. doi: 10.2337/dc09-0816. Epub 2009 Aug 12. Diabetes Care. 2009. PMID: 19675197 Free PMC article.

3

Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes.

Abhary S, Burdon KP, Kuot A, Javadiyan S, Whiting MJ, Kasmeridis N, Petrovsky N, Craig JE. Abhary S, et al. Among authors: kuot a. PLoS One. 2010 Mar 1;5(3):e9462. doi: 10.1371/journal.pone.0009462. PLoS One. 2010. PMID: 20209122 Free PMC article.

4

Association of TCF4 and CLU polymorphisms with Fuchs' endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process.

Kuot A, Hewitt AW, Griggs K, Klebe S, Mills R, Jhanji V, Craig JE, Sharma S, Burdon KP. Kuot A, et al. Eur J Hum Genet. 2012 Jun;20(6):632-8. doi: 10.1038/ejhg.2011.248. Epub 2012 Jan 11. Eur J Hum Genet. 2012. PMID: 22234156 Free PMC article.

5

Screening of the COL8A2 gene in an Australian family with early-onset Fuchs' endothelial corneal dystrophy.

Kuot A, Mills R, Craig JE, Sharma S, Burdon KP. Kuot A, et al. Clin Exp Ophthalmol. 2014 Mar;42(2):198-200. doi: 10.1111/ceo.12122. Epub 2013 May 22. Clin Exp Ophthalmol. 2014. PMID: 23601356 No abstract available.

6

Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.

Afshari NA, Igo RP Jr, Morris NJ, Stambolian D, Sharma S, Pulagam VL, Dunn S, Stamler JF, Truitt BJ, Rimmler J, Kuot A, Croasdale CR, Qin X, Burdon KP, Riazuddin SA, Mills R, Klebe S, Minear MA, Zhao J, Balajonda E, Rosenwasser GO, Baratz KH, Mootha VV, Patel SV, Gregory SG, Bailey-Wilson JE, Price MO, Price FW Jr, Craig JE, Fingert JH, Gottsch JD, Aldave AJ, Klintworth GK, Lass JH, Li YJ, Iyengar SK. Afshari NA, et al. Among authors: kuot a. Nat Commun. 2017 Mar 30;8:14898. doi: 10.1038/ncomms14898. Nat Commun. 2017. PMID: 28358029 Free PMC article.

7

TGC repeat expansion in the TCF4 gene increases the risk of Fuchs' endothelial corneal dystrophy in Australian cases.

Kuot A, Hewitt AW, Snibson GR, Souzeau E, Mills R, Craig JE, Burdon KP, Sharma S. Kuot A, et al. PLoS One. 2017 Aug 23;12(8):e0183719. doi: 10.1371/journal.pone.0183719. eCollection 2017. PLoS One. 2017. PMID: 28832669 Free PMC article.

8

Reduced expression of apolipoprotein E and immunoglobulin heavy constant gamma 1 proteins in Fuchs endothelial corneal dystrophy.

Kuot A, Ronci M, Mills R, Klebe S, Snibson G, Wiffen S, Loh R, Corbett M, Zhou T, Chataway T, Burdon KP, Craig JE, Urbani A, Sharma S. Kuot A, et al. Clin Exp Ophthalmol. 2019 Nov;47(8):1028-1042. doi: 10.1111/ceo.13569. Epub 2019 Jul 5. Clin Exp Ophthalmol. 2019. PMID: 31206232

9

The genetic and clinical landscape of nanophthalmos and posterior microphthalmos in an Australian cohort.

Siggs OM, Awadalla MS, Souzeau E, Staffieri SE, Kearns LS, Laurie K, Kuot A, Qassim A, Edwards TL, Coote MA, Mancel E, Walland MJ, Dondey J, Galanopoulous A, Casson RJ, Mills RA, MacArthur DG, Ruddle JB, Burdon KP, Craig JE. Siggs OM, et al. Among authors: kuot a. Clin Genet. 2020 May;97(5):764-769. doi: 10.1111/cge.13722. Epub 2020 Mar 5. Clin Genet. 2020. PMID: 32052405 Free PMC article.

10

Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophy.

Kuot A, Corbett MA, Mills RA, Snibson G, Wiffen S, Loh R, Burdon KP, Craig JE, Sharma S. Kuot A, et al. Exp Eye Res. 2021 Sep;210:108692. doi: 10.1016/j.exer.2021.108692. Epub 2021 Jul 3. Exp Eye Res. 2021. PMID: 34228965

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