Toggle navigation
About
Abstract
Editorial Board
Subscription & Newsletter
Contact
Issues
This issue
22-4
All issues
Download PDF
Download EPUB
Editor's Selection
This issue
22-4
Browse by topic
Browse by contributor
Dialogue & Opinion
Abstracts
Abstracts
Search
Classification List
Abstracted Journals
Index of Authors
News & Reports
Home
Abstracts
Index of Authors
Author #58474
advertisement
Tsang SH
31
Showing records 1 to 25 |
Display all abstracts from
Tsang SH
98430
Renormalization of metabolic coupling treats age-related degenerative disorders: an oxidative RPE niche fuels the more glycolytic photoreceptors
Nolan ND
Eye
2022; 36: 278-283
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Wu WH
Molecular Therapy
2022; 30: 1407-1420
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Oh JK
European Journal of Ophthalmology
2022; 32: NP235-NP239
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cui X; Kim HJ
Human Molecular Genetics
2022; 31: 2438-2451
98430
Renormalization of metabolic coupling treats age-related degenerative disorders: an oxidative RPE niche fuels the more glycolytic photoreceptors
Caruso SM
Eye
2022; 36: 278-283
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Nuzbrokh Y
European Journal of Ophthalmology
2022; 32: NP235-NP239
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Tsai YT
Molecular Therapy
2022; 30: 1407-1420
98430
Renormalization of metabolic coupling treats age-related degenerative disorders: an oxidative RPE niche fuels the more glycolytic photoreceptors
Cui X
Eye
2022; 36: 278-283
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cheng CH
Human Molecular Genetics
2022; 31: 2438-2451
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Lee W
European Journal of Ophthalmology
2022; 32: NP235-NP239
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Huang IW
Molecular Therapy
2022; 30: 1407-1420
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Lima de Carvalho JR
European Journal of Ophthalmology
2022; 32: NP235-NP239
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Jenny LA
Human Molecular Genetics
2022; 31: 2438-2451
98430
Renormalization of metabolic coupling treats age-related degenerative disorders: an oxidative RPE niche fuels the more glycolytic photoreceptors
Tsang SH
Eye
2022; 36: 278-283
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Cheng CH; Hsu CW
Molecular Therapy
2022; 30: 1407-1420
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Wang NK
European Journal of Ophthalmology
2022; 32: NP235-NP239
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
De Carvalho Junior JRL
Human Molecular Genetics
2022; 31: 2438-2451
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Sparrow JR
European Journal of Ophthalmology
2022; 32: NP235-NP239
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Chang YJ
Human Molecular Genetics
2022; 31: 2438-2451
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Cui X
Molecular Therapy
2022; 30: 1407-1420
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Kong Y
Human Molecular Genetics
2022; 31: 2438-2451
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Allikmets R
European Journal of Ophthalmology
2022; 32: NP235-NP239
98807
CRISPR genome surgery in a novel humanized model for autosomal dominant retinitis pigmentosa
Ryu J; Quinn PMJ
Molecular Therapy
2022; 30: 1407-1420
98900
Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Hsu CW
Human Molecular Genetics
2022; 31: 2438-2451
97975
A mutation in causing pigmented paravenous retinochoroidal atrophy
Tsang SH
European Journal of Ophthalmology
2022; 32: NP235-NP239
«
1
2
»
Issue
22-4
Table of Contents
Editor's Selection
PDF
EPUB
Change Issue
26-1
25-4
25-3
25-2
25-1
24-4
24-3
24-1/2
23-4
23-3
23-2
23-1
22-4
22-3
22-2
22-1
21-4
21-3
21-2
21-1
20-4
20-3
20-2
20-1
19-4
19-3
19-2
19-1
18-4
18-3
18-2
18-1
17-4
17-3
17-2
17-1
16-4
16-3
16-2
16-1
15-4
15-3
15-2
15-1
14-4
14-3
14-2
14-1
13-4
13-3
13-2
13-1
12-4
12-3
12-2
12-1
11-4
11-3
11-2
11-1
10-4
10-3
10-2
10-1
9-4
9-3
9-2
9-1
8-4
8-3
8-2
8-1
7-3
7-2
7-1
6-3
6-2
6-1
5-3
5-2
5-1
4-3
4-2
4-1
3-3
3-2
3-1
2-3
2-2
2-1
1-3
1-2
1-1
advertisement
We would like to use Google Analytics to see which parts of the review are read. It is only used to count visits, never for advertising.
Privacy statement
Decline
Accept