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Browsing by Author Sharma, Shiwani

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PreviewIssue DateTitleAuthor(s)
2008Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Hewitt, Alex W; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; McMellon, Amy E
2007Heme carrier protein 1 (HCP1) expression and functional analysis in the retina and retinal pigment epitheliumBroer, Stefan; Sharma, Shiwani; Dimasi, David Paul; Kumar, Raman; Della, N G
Mar-2013Identification of a novel oligomerization disrupting mutation in CRYAA associated with congenital cataract in a South Australian familyLaurie, Kate; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy Kennion; Sykes, Matthew James; Casey, Theresa; Teo, Theodosia; Pater, John Brian; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
1-Apr-2013MALDI MS imaging analysis of apolipoprotein E and lysyl oxidase-like 1 in human lens capsules affected by pseudoexfoliation syndromeRonci, M; Sharma, Shiwani; Martin, Sarah; Craig, Jamie E; Voelcker, Nicolas Hans
2003Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan Syndrome including severe congenital cataract, dental anomalies and mental retardationThomas, P; Thomas, T; Voss, A K; Sharma, Shiwani; Russell-Eggit, Isabelle M; Craig, Jamie E; Sale, Michele M; Mackey, David A; Wirth, M Gabriela; Gajovic, S; Clarke, M P; Gecz, Jozef; Elder, James E; Gruss, P; Fitzgerald, Liesel M; McKay, James D; Shaw, Marie A; Nicholl, A; Ross, S; Stankich, J M; Burdon, Kathryn Penelope
2006Nance-Horan syndrome protein, NHS, associates with epithelial cell junctionsSharma, Shiwani; Ang, Sharyn; Shaw, Marie A; Mackey, David A; Gecz, Jozef; McAvoy, J; Craig, Jamie E
2008Novel causative mutations in patients with Nance-Horan Syndrome and altered localization of the mutant NHS-A protein isoformSharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Dave, Alpana; Jamieson, Robyn; Yaron, Yuval; Billson, Frank; Maldergem, Lionel; Lorenz, Birgit; Gecz, Jozef
2007A novel deletion in the FTL gene causes hereditary hyperferritinemia cataract syndrome (HHCS) by alteration of the transcription start siteBurdon, Kathryn Penelope; Sharma, Shiwani; Mackey, David A; Dimasi, David Paul; Craig, Jamie E; Chen, Celia S
Sep-2013Ocular Expression and Distribution of Products of the POAG-Associated Chromosome 9p21 Gene RegionChidlow, Glyn; Wood, John P M; Sharma, Shiwani; Dimasi, David Paul; Burdon, Kathryn P; Casson, Robert J; Craig, Jamie E
2004RZF, a zinc-finger protein in the photoreceptors of human retinaHigginson, K A; Sharma, Shiwani; Della, N G; Dimasi, David Paul
Mar-2014Screening of the COL8A2 gene in an Australian family with early-onset Fuchs’ endothelial corneal dystrophyKuot, Abraham; Mills, Richard Arthur; Craig, Jamie E; Sharma, Shiwani; Burdon, Kathryn Penelope
12-Dec-2012The status of intercellular junctions in established lens epithelial cell linesDave, Alpana; Craig, Jamie E; Sharma, Shiwani
2003Virus-mediated secretion gene therapy - a potential treatment for ocular neovascularisationSharma, Shiwani; Lai, Y-C; Brankov, M; Constable, I J; Lai, C M; Rakoczy, P E
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