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Publications: Zaw, Khine

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Number of items: 7.

Journal Article

Zaw, K.ORCID: 0000-0002-4121-1985, Carvalho, L.S., Aung-Htut, M.T., Fletcher, S., Wilton, S.D., Chen, F.K. and McLenachan, S. (2022) Pathogenesis and Treatment of Usher Syndrome Type IIA. Asia-Pacific Journal of Ophthalmology, 11 (4). pp. 369-379.

McLenachan, S., Zhang, D., Grainok, J., Zhang, X., Huang, Z., Chen, S-C, Zaw, K.ORCID: 0000-0002-4121-1985, Lima, A., Jennings, L., Roshandel, D., Moon, S.Y., Heath Jeffery, R.C., Attia, M.S., Thompson, J.A., Lamey, T.M., McLaren, T.L., De Roach, J., Fletcher, S. and Chen, F.K. (2021) Determinants of disease penetrance in PRPF31-associated retinopathy. Genes, 12 (10). Article 1542.

Zaw, K.ORCID: 0000-0002-4121-1985, Wong, E.Y.M., Zhang, X., Zhang, D., Chen, S-C, Thompson, J.A., Lamey, T., McLaren, T., De Roach, J.N., Wilton, S.D., Fletcher, S., Mitrpant, C., Atlas, M.D., Chen, F.K. and McLenachan, S. (2021) Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene. Stem Cell Research, 50 . Article 102129.

Zhang, D., McLenachan, S., Chen, S.-C., Zaw, K.ORCID: 0000-0002-4121-1985, Alziyadat, Y., Zhang, X., Lamey, T.M., Thompson, J.A., McLaren, T.L., Mellough, C., De Roach, J.N. and Chen, F.K. (2021) Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200. Stem Cell Research, 51 . Article 102154.

Ham, K.A.ORCID: 0000-0002-7036-5334, Keegan, N.P., McIntosh, C.S., Aung-Htut, M.T., Zaw, K.ORCID: 0000-0002-4121-1985, Greer, K., Fletcher, S. and Wilton, S.D. (2021) Induction of cryptic pre-mRNA splice-switching by antisense oligonucleotides. Scientific Reports, 11 (1). Article 15137.

Zaw, K.ORCID: 0000-0002-4121-1985, Greer, K., Aung-Htut, M.T., Mitrpant, C., Veedu, R.N., Fletcher, S. and Wilton, S.D. (2019) Consequences of making the inactive active through changes in antisense oligonucleotide chemistries. Frontiers in Genetics, 10 . Article 1249.

Non-refereed Article

Ham, K.ORCID: 0000-0002-7036-5334, Keegan, N., McIntosh, C., Aung-Htut, M., Zaw, K.ORCID: 0000-0002-4121-1985, Greer, K., Fletcher, S. and Wilton, S. (2021) Cryptic U2-dependent pre-mRNASplice site usage induced by splice switching antisense oligonucleotides. Research Square . In Review.

This list was generated on Sun Mar 26 02:01:42 2023 UTC.