Stephen H. Tsang, MD, PhD
Affiliations: | Columbia University, New York, NY |
Area:
PhotoreceptorsWebsite:
http://sklad.cumc.columbia.edu/pharm/cumc/profile_new.php?id=295Google:
"Stephen Tsang"Mean distance: 17.25 (cluster 28) | S | N | B | C | P |
Parents
Sign in to add mentor| Victor A. McKusick | research assistant | Columbia | |
| Stephen Goff | grad student | Columbia |
Children
Sign in to add trainee| Lawrence Chan | research assistant | Columbia | |
| Huy Vu Nguyen | grad student | Columbia University Medical School | |
| Jack Chai Lin Chou | grad student | 2006-2009 | Columbia University Medical School |
| Katherine J. Wert | grad student | 2013 | Columbia |
| Susanne Koch | post-doc | Columbia | |
| Scott Smemo | post-doc | Columbia | |
| Nan-Kai Wang | post-doc | 2007-2009 | Columbia |
| Joaquin Tosi | post-doc | 2006-2010 | Columbia |
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Publications
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| Wang NK, Liu PK, Kong Y, et al. (2023) Spatiotemporal control of genome engineering in cone photoreceptors. Cell & Bioscience. 13: 119 |
| Jentzsch MC, Tsang SH, Koch SF. (2023) A New Preclinical Model of Retinitis Pigmentosa Due to Deficiency. Ophthalmology Science. 3: 100332 |
| Kong Y, Liu PK, Li Y, et al. (2023) HIF2α activation and mitochondrial deficit due to iron chelation cause retinal atrophy. Embo Molecular Medicine. e16525 |
| Kim AH, Liu PK, Chang YH, et al. (2022) Congenital Stationary Night Blindness: Clinical and Genetic Features. International Journal of Molecular Sciences. 23 |
| Tsai YT, da Costa BL, Nolan ND, et al. (2022) Prime Editing for the Installation and Correction of Mutations Causing Inherited Retinal Disease: A Brief Methodology. Methods in Molecular Biology (Clifton, N.J.). 2560: 313-331 |
| Kajtna J, Tsang SH, Koch SF. (2022) Late-stage rescue of visually guided behavior in the context of a significantly remodeled retinitis pigmentosa mouse model. Cellular and Molecular Life Sciences : Cmls. 79: 148 |
| Nolan ND, Jenny LA, Wang NK, et al. (2021) Retinal pigment epithelium lipid metabolic demands and therapeutic restoration. Taiwan Journal of Ophthalmology. 11: 216-220 |
| Wang NK, Liu PK, Kong Y, et al. (2021) Mouse Models of Achromatopsia in Addressing Temporal "Point of No Return" in Gene-Therapy. International Journal of Molecular Sciences. 22 |
| Liu PK, Ryu J, Yeh LK, et al. (2021) A novel KCNV2 mutation in a patient taking hydroxychloroquine associated with cone dystrophy with supernormal rod response. Ophthalmic Genetics. 1-6 |
| Nassisi M, Smirnov V, Hernandez CS, et al. (2021) CNGB1-related rod-cone dystrophy: a mutation review and update. Human Mutation |