Yu-Wai-Man P - Search Results

1

Human iPSC disease modelling reveals functional and structural defects in retinal pigment epithelial cells harbouring the m.3243A > G mitochondrial DNA mutation.

Chichagova V, Hallam D, Collin J, Buskin A, Saretzki G, Armstrong L, Yu-Wai-Man P, Lako M, Steel DH. Chichagova V, et al. Sci Rep. 2017 Sep 26;7(1):12320. doi: 10.1038/s41598-017-12396-2. Sci Rep. 2017. PMID: 28951556 Free PMC article.

2

Efficacy of intracameral and subconjunctival cefuroxime in preventing endophthalmitis after cataract surgery.

Yu-Wai-Man P, Morgan SJ, Hildreth AJ, Steel DH, Allen D. Yu-Wai-Man P, et al. J Cataract Refract Surg. 2008 Mar;34(3):447-51. doi: 10.1016/j.jcrs.2007.10.041. J Cataract Refract Surg. 2008. PMID: 18299070

3

Mitochondrial optic neuropathies - disease mechanisms and therapeutic strategies.

Yu-Wai-Man P, Griffiths PG, Chinnery PF. Yu-Wai-Man P, et al. Prog Retin Eye Res. 2011 Mar;30(2):81-114. doi: 10.1016/j.preteyeres.2010.11.002. Epub 2010 Nov 26. Prog Retin Eye Res. 2011. PMID: 21112411 Free PMC article. Review.

4

Inherited eye-related disorders due to mitochondrial dysfunction.

Yu-Wai-Man P, Newman NJ. Yu-Wai-Man P, et al. Hum Mol Genet. 2017 Aug 1;26(R1):R12-R20. doi: 10.1093/hmg/ddx182. Hum Mol Genet. 2017. PMID: 28481993 Free PMC article. Review.

5

Leber hereditary optic neuropathy: bridging the translational gap.

Jurkute N, Yu-Wai-Man P. Jurkute N, et al. Curr Opin Ophthalmol. 2017 Sep;28(5):403-409. doi: 10.1097/ICU.0000000000000410. Curr Opin Ophthalmol. 2017. PMID: 28650878 Free PMC article. Review.

6

Clonal expansion of mtDNA deletions: different disease models assessed by digital droplet PCR in single muscle cells.

Trifunov S, Pyle A, Valentino ML, Liguori R, Yu-Wai-Man P, Burté F, Duff J, Kleinle S, Diebold I, Rugolo M, Horvath R, Carelli V. Trifunov S, et al. Sci Rep. 2018 Aug 3;8(1):11682. doi: 10.1038/s41598-018-30143-z. Sci Rep. 2018. PMID: 30076399 Free PMC article.

7

A mutant wfs1 zebrafish model of Wolfram syndrome manifesting visual dysfunction and developmental delay.

Cairns G, Burté F, Price R, O'Connor E, Toms M, Mishra R, Moosajee M, Pyle A, Sayer JA, Yu-Wai-Man P. Cairns G, et al. Sci Rep. 2021 Oct 14;11(1):20491. doi: 10.1038/s41598-021-99781-0. Sci Rep. 2021. PMID: 34650143 Free PMC article.

8

Modelling autosomal dominant optic atrophy associated with OPA1 variants in iPSC-derived retinal ganglion cells.

Sladen PE, Jovanovic K, Guarascio R, Ottaviani D, Salsbury G, Novoselova T, Chapple JP, Yu-Wai-Man P, Cheetham ME. Sladen PE, et al. Hum Mol Genet. 2022 Oct 10;31(20):3478-3493. doi: 10.1093/hmg/ddac128. Hum Mol Genet. 2022. PMID: 35652445 Free PMC article.

9

Inherited mitochondrial optic neuropathies.

Yu-Wai-Man P, Griffiths PG, Hudson G, Chinnery PF. Yu-Wai-Man P, et al. J Med Genet. 2009 Mar;46(3):145-58. doi: 10.1136/jmg.2007.054270. Epub 2008 Nov 10. J Med Genet. 2009. PMID: 19001017 Free PMC article. Review.

10

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Greaves LC, Yu-Wai-Man P, Blakely EL, Krishnan KJ, Beadle NE, Kerin J, Barron MJ, Griffiths PG, Dickinson AJ, Turnbull DM, Taylor RW. Greaves LC, et al. Invest Ophthalmol Vis Sci. 2010 Jul;51(7):3340-6. doi: 10.1167/iovs.09-4659. Epub 2010 Feb 17. Invest Ophthalmol Vis Sci. 2010. PMID: 20164463 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

234 results

Search Page

Filters