Dave A - Search Results

1

Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform.

Sharma S, Burdon KP, Dave A, Jamieson RV, Yaron Y, Billson F, Van Maldergem L, Lorenz B, Gécz J, Craig JE. Sharma S, et al. Among authors: dave a. Mol Vis. 2008;14:1856-64. Epub 2008 Oct 20. Mol Vis. 2008. PMID: 18949062 Free PMC article.

2

NHS-A isoform of the NHS gene is a novel interactor of ZO-1.

Sharma S, Koh KS, Collin C, Dave A, McMellon A, Sugiyama Y, McAvoy JW, Voss AK, Gécz J, Craig JE. Sharma S, et al. Among authors: dave a. Exp Cell Res. 2009 Aug 15;315(14):2358-72. doi: 10.1016/j.yexcr.2009.05.008. Epub 2009 May 15. Exp Cell Res. 2009. PMID: 19447104

3

The status of intercellular junctions in established lens epithelial cell lines.

Dave A, Craig JE, Sharma S. Dave A, et al. Mol Vis. 2012;18:2937-46. Epub 2012 Dec 12. Mol Vis. 2012. PMID: 23288986 Free PMC article.

4

EPHA2 MUTATIONS CONTRIBUTE TO CONGENITAL CATARACT THROUGH DIVERSE MECHANISMS.

Dave A, Martin S, Kumar R, Craig JE, Burdon KP, Sharma S. Dave A, et al. Mol Vis. 2016 Jan 14;22:18-30. eCollection 2016. Mol Vis. 2016. PMID: 26900323 Free PMC article.

5

Novel protein constituents of pathological ocular pseudoexfoliation syndrome deposits identified with mass spectrometry.

Sharma S, Chataway T, Klebe S, Griggs K, Martin S, Chegeni N, Dave A, Zhou T, Ronci M, Voelcker NH, Mills RA, Craig JE. Sharma S, et al. Among authors: dave a. Mol Vis. 2018 Dec 28;24:801-817. eCollection 2018. Mol Vis. 2018. PMID: 30713420 Free PMC article.

6

Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia.

Dave A, Laurie K, Staffieri SE, Taranath D, Mackey DA, Mitchell P, Wang JJ, Craig JE, Burdon KP, Sharma S. Dave A, et al. PLoS One. 2013 Aug 27;8(8):e72518. doi: 10.1371/journal.pone.0072518. eCollection 2013. PLoS One. 2013. PMID: 24014202 Free PMC article. Clinical Trial.

7

Biological effect of LOXL1 coding variants associated with pseudoexfoliation syndrome.

Sharma S, Martin S, Sykes MJ, Dave A, Hewitt AW, Burdon KP, Ronci M, Voelcker NH, Craig JE. Sharma S, et al. Among authors: dave a. Exp Eye Res. 2016 May;146:212-223. doi: 10.1016/j.exer.2016.03.013. Epub 2016 Mar 18. Exp Eye Res. 2016. PMID: 26997634

8

Association of genetic variants in the TMCO1 gene with clinical parameters related to glaucoma and characterization of the protein in the eye.

Sharma S, Burdon KP, Chidlow G, Klebe S, Crawford A, Dimasi DP, Dave A, Martin S, Javadiyan S, Wood JP, Casson R, Danoy P, Griggs K, Hewitt AW, Landers J, Mitchell P, Mackey DA, Craig JE. Sharma S, et al. Among authors: dave a. Invest Ophthalmol Vis Sci. 2012 Jul 24;53(8):4917-25. doi: 10.1167/iovs.11-9047. Invest Ophthalmol Vis Sci. 2012. PMID: 22714896

9

Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian family.

Laurie KJ, Dave A, Straga T, Souzeau E, Chataway T, Sykes MJ, Casey T, Teo T, Pater J, Craig JE, Sharma S, Burdon KP. Laurie KJ, et al. Among authors: dave a. Hum Mutat. 2013 Mar;34(3):435-8. doi: 10.1002/humu.22260. Epub 2013 Jan 17. Hum Mutat. 2013. PMID: 23255486

10

Genotype, Age, Genetic Background, and Sex Influence Epha2-Related Cataract Development in Mice.

Dave A, Craig JE, Alamein M, Skrzypiec K, Beltz J, Pfaff A, Burdon KP, Ercal N, de Iongh RU, Sharma S. Dave A, et al. Invest Ophthalmol Vis Sci. 2021 Sep 2;62(12):3. doi: 10.1167/iovs.62.12.3. Invest Ophthalmol Vis Sci. 2021. PMID: 34495288 Free PMC article.

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