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1 . Academic Journal
Targeting miR-181a/b in retinitis pigmentosa: implications for disease progression and therapy
저자
by
Bruna Lopes da Costa
;
Peter M. J. Quinn
;
Wen-Hsuan Wu
;
Siyuan Liu
;
Nicholas D. Nolan
, et al.
소스
Cell & Bioscience, Vol 14, Iss 1, Pp 1-20 (2024)
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7 . Academic Journal
Genetic underpinnings explored: OPA1 deletion and complex phenotypes on chromosome 3q29
저자
by
Ethan Hung-Hsi Wang
;
Pei-Hsuan Lin
;
Pei-Liang Wu
;
Eugene Yu-Chuan Kang
;
Laura Liu
, et al.
소스
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-7 (2024)
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7 . Academic Journal
A GUCY2D variant associated cone-rod dystrophy with electronegative ERG: A case report and review
저자
by
Pei-Liang Wu
;
Pei-Hsuan Lin
;
Winston Lee
;
Ethan Hung-Hsi Wang
;
Eugene Yu-Chuan Kang
, et al.
소스
American Journal of Ophthalmology Case Reports, Vol 36, Iss , Pp 102094- (2024)
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7 . Academic Journal
Mitochondria in Retinal Ganglion Cells: Unraveling the Metabolic Nexus and Oxidative Stress
저자
by
Tsai-Hsuan Yang
;
Eugene Yu-Chuan Kang
;
Pei-Hsuan Lin
;
Benjamin Ben-Chi Yu
;
Jason Hung-Hsuan Wang
, et al.
소스
International Journal of Molecular Sciences, Vol 25, Iss 16, p 8626 (2024)
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7 . Academic Journal
Spatiotemporal control of genome engineering in cone photoreceptors
저자
by
Nan-Kai Wang
;
Pei-Kang Liu
;
Yang Kong
;
Yun-Ju Tseng
;
Laura A. Jenny
, et al.
소스
Cell & Bioscience, Vol 13, Iss 1, Pp 1-19 (2023)
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7 . Academic Journal
Maternal mosaicism in SSBP1 causing optic atrophy with retinal degeneration: implications for genetic counseling
저자
by
Yin-Hsi Chang
;
Eugene Yu-Chuan Kang
;
Laura Liu
;
Laura A. Jenny
;
Rin Khang
, et al.
소스
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-5 (2023)
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7 . Academic Journal
Case report: novel PCDH15 variant causes usher syndrome type 1F with congenital hearing loss and syndromic retinitis pigmentosa
저자
by
Nelson Chen
;
Hane Lee
;
Angela H. Kim
;
Pei-Kang Liu
;
Eugene Yu-Chuan Kang
, et al.
소스
BMC Ophthalmology, Vol 22, Iss 1, Pp 1-5 (2022)
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7 . Academic Journal
Foveal hypoplasia and characteristics of optical components in patients with familial exudative vitreoretinopathy and retinopathy of prematurity
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by
Pei-Ying Chen
;
Eugene Yu-Chuan Kang
;
Kuan-Jen Chen
;
Xiao Chun Ling
;
Yin-Hsi Chang
, et al.
소스
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
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7 . Academic Journal
HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy
저자
by
Yang Kong
;
Pei‐Kang Liu
;
Yao Li
;
Nicholas D Nolan
;
Peter M J Quinn
, et al.
소스
EMBO Molecular Medicine, Vol 15, Iss 2, Pp n/a-n/a (2023)
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7 . Academic Journal
The Value of Electroretinography in Identifying Candidate Genes for Inherited Retinal Dystrophies: A Diagnostic Guide
저자
by
Tsai-Hsuan Yang
;
Eugene Yu-Chuan Kang
;
Pei-Hsuan Lin
;
Pei-Liang Wu
;
Jacob Aaron Sachs
, et al.
소스
Diagnostics, Vol 13, Iss 19, p 3041 (2023)
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