Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Vicky Scripps"'
Autor:
Marisa Zallocchi, Katie Binley, Yatish Lad, Scott Ellis, Peter Widdowson, Sharifah Iqball, Vicky Scripps, Michelle Kelleher, Julie Loader, James Miskin, You-Wei Peng, Wei-Min Wang, Linda Cheung, Duane Delimont, Kyriacos A Mitrophanous, Dominic Cosgrove
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94272 (2014)
Usher syndrome type 1B is a combined deaf-blindness condition caused by mutations in the MYO7A gene. Loss of functional myosin VIIa in the retinal pigment epithelia (RPE) and/or photoreceptors leads to blindness. We evaluated the impact of subretinal
Externí odkaz:
https://doaj.org/article/15299d8f6d1046bd8a87be0928d96b1d
Autor:
Binoy Appukuttan, Tim Stout, Austen Yeager, Matt Hartzell, Trevor J. McFarland, Maria Parker, Vicky Scripps, Scott Ellis, Jessica Bellec, Kyriacos A. Mitrophanous, Thomas Hady
Publikováno v:
Human Gene Therapy. 25:408-418
Corneal transplantation is the oldest and one of the most successful transplant procedures with a success rate in many studies in excess of 90%. The high success rate is mainly attributable to the relatively immune-privileged status of the eye and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00f72c1a03824f35c0f6d181c774d137
https://doi.org/10.1089/hum.2013.079
https://doi.org/10.1089/hum.2013.079
Autor:
Kyriacos A. Mitrophanous, Michelle Kelleher, Yatish Lad, Linda Cheung, Weimin Wang, Vicky Scripps, Katie Binley, Marisa Zallocchi, You Wei Peng, Peter Widdowson, Dominic Cosgrove, S. Iqball, Scott Ellis, James Miskin, Julie Loader, Duane Delimont
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e94272 (2014)
PLoS ONE
PLoS ONE
Usher syndrome type 1B is a combined deaf-blindness condition caused by mutations in the MYO7A gene. Loss of functional myosin VIIa in the retinal pigment epithelia (RPE) and/or photoreceptors leads to blindness. We evaluated the impact of subretinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b35cef0a93aafbf19dddbcca17274d1
https://doi.org/10.1371/journal.pone.0094272
https://doi.org/10.1371/journal.pone.0094272