Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Hung-Hsi Wang"'
Autor:
Nan-Kai Wang, Pei-Kang Liu, Yang Kong, Yun-Ju Tseng, Laura A. Jenny, Nicholas D. Nolan, Nelson Chen, Hung-Hsi Wang, Chun Wei Hsu, Wan-Chun Huang, Janet R. Sparrow, Chyuan-Sheng Lin, Stephen H. Tsang
Publikováno v:
Cell & Bioscience, Vol 13, Iss 1, Pp 1-19 (2023)
Abstract Background Cones are essential for color recognition, high resolution, and central vision; therefore cone death causes blindness. Understanding the pathophysiology of each cell type in the retina is key to developing therapies for retinal di
Externí odkaz:
https://doaj.org/article/f06c541ff511434ab196ba88974fd001
Autor:
Ethan Hung-Hsi Wang1,2 (AUTHOR), Pei-Hsuan Lin1,3 (AUTHOR), Pei-Liang Wu1,4 (AUTHOR), Eugene Yu-Chuan Kang1,5,6,7 (AUTHOR), Liu, Laura6,8 (AUTHOR), Lung-Kun Yeh5,6 (AUTHOR), Kuan-Jen Chen5,6 (AUTHOR), Meng-Chang Hsiao9 (AUTHOR), Nan-Kai Wang1,5,6,10 (AUTHOR) wang.nankai@gmail.com
Publikováno v:
BMC Medical Genomics. 4/19/2024, Vol. 17 Issue 1, p1-7. 7p. 1 Color Photograph, 1 Black and White Photograph, 2 Graphs.
Autor:
Ning Chiu, Winston Lee, Pei-Kang Liu, Sarah R Levi, Hung-Hsi Wang, Nelson Chen, Eugene Yu-Chuan Kang, Go Hun Seo, Hane Lee, Laura Liu, Wei-Chi Wu, Shawn H. Tsai, Nan-Kai Wang
Publikováno v:
Ophthalmic Genetics. 43:378-384
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e44dc346174d5ab2a0f6e3e66bdcf1
https://doi.org/10.1080/13816810.2021.2010773
https://doi.org/10.1080/13816810.2021.2010773
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 2560
Retinitis pigmentosa (RP) is the most common inherited retinal dystrophy. There are three main characteristics of RP: night blindness, retinal pigmentation, and visual field constriction. Among these three features, night blindness was the first to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1dceef2a86f30ab139470b848116ec0
https://pubmed.ncbi.nlm.nih.gov/36481879
https://pubmed.ncbi.nlm.nih.gov/36481879
Publikováno v:
Methods in Molecular Biology ISBN: 9781071626504
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca54cb793d3c5d13daa2a503a13a613d
https://doi.org/10.1007/978-1-0716-2651-1_1
https://doi.org/10.1007/978-1-0716-2651-1_1
Autor:
Nan-Kai Wang, Wan-Chun Huang, Yun-Ju Tseng, Yang Kong, Ming-Hong Tai, Chyuan-Sheng Lin, Hung-Hsi Wang, Stephen H. Tsang, Chun-Wei Hsu, Sarah R. Levi, Pei-Kang Liu, Nelson Chen, Peter M Quinn
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8069, p 8069 (2021)
Volume 22
Issue 15
International Journal of Molecular Sciences, Vol 22, Iss 8069, p 8069 (2021)
Achromatopsia is characterized by amblyopia, photophobia, nystagmus, and color blindness. Previous animal models of achromatopsia have shown promising results using gene augmentation to restore cone function. However, the optimal therapeutic window t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbbc663b9c3b4112eb0b8b8e98dc0c13
https://doi.org/10.3390/ijms22158069
https://doi.org/10.3390/ijms22158069
Autor:
Pei-Liang Wu, Pei-Hsuan Lin, Winston Lee, Ethan Hung-Hsi Wang, Eugene Yu-Chuan Kang, Laura Liu, Nan-Kai Wang
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 36, Iss , Pp 102094- (2024)
Purpose: Cone-rod dystrophies (CORD) are inherited retinal dystrophies characterized by primary cone degeneration with secondary rod involvement. We report two patients from the same family with a dominant variant in the guanylate cyclase 2D (GUCY2D)
Externí odkaz:
https://doaj.org/article/43287b412b3d44e28a593f7169965e8b