Stephen H. Tsang
Stephen H. Tsang
Geverifieerd e-mailadres voor columbia.edu
Geciteerd door
Geciteerd door
Neuronal defects and delayed wound healing in mice lacking fibroblast growth factor 2
S Ortega, M Ittmann, SH Tsang, M Ehrlich, C Basilico
Proceedings of the National Academy of Sciences 95 (10), 5672-5677, 1998
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes
JK White, AK Gerdin, NA Karp, E Ryder, M Buljan, JN Bussell, J Salisbury, ...
Cell 154 (2), 452-464, 2013
Unexpected mutations after CRISPR–Cas9 editing in vivo
KA Schaefer, WH Wu, DF Colgan, SH Tsang, AG Bassuk, VB Mahajan
Nature methods 14 (6), 547-548, 2017
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases
S Yamamoto, M Jaiswal, WL Charng, T Gambin, E Karaca, G Mirzaa, ...
Cell 159 (1), 200-214, 2014
Role for the target enzyme in deactivation of photoreceptor G protein in vivo
SH Tsang, ME Burns, PD Calvert, P Gouras, DA Baylor, SP Goff, ...
Science 282 (5386), 117-121, 1998
Retinal degeneration in mice lacking the γ subunit of the rod cGMP phosphodiesterase
SH Tsang, P Gouras, CK Yamashita, H Kjeldbye, J Fisher, DB Farber, ...
Science 272 (5264), 1026-1029, 1996
Long-term safety and efficacy of human-induced pluripotent stem cell (iPS) grafts in a preclinical model of retinitis pigmentosa
Y Li, YT Tsai, CW Hsu, D Erol, J Yang, WH Wu, RJ Davis, D Egli, ...
Molecular medicine 18 (9), 1312-1319, 2012
Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia
S Kohl, D Zobor, WC Chiang, N Weisschuh, J Staller, IG Menendez, ...
Nature genetics 47 (7), 757-765, 2015
Precision medicine: genetic repair of retinitis pigmentosa in patient-derived stem cells
AG Bassuk, A Zheng, Y Li, SH Tsang, VB Mahajan
Scientific reports 6 (1), 19969, 2016
Allele-specific chromosome removal after Cas9 cleavage in human embryos
MV Zuccaro, J Xu, C Mitchell, D Marin, R Zimmerman, B Rana, ...
Cell 183 (6), 1650-1664. e15, 2020
Quantitative fundus autofluorescence in recessive Stargardt disease
TR Burke, T Duncker, RL Woods, JP Greenberg, J Zernant, SH Tsang, ...
Investigative ophthalmology & visual science 55 (5), 2841-2852, 2014
Analysis of the ABCA4 gene by next-generation sequencing
J Zernant, C Schubert, KM Im, T Burke, CM Brown, GA Fishman, ...
Investigative ophthalmology & visual science 52 (11), 8479-8487, 2011
Viral delivery systems for CRISPR
CL Xu, MZC Ruan, VB Mahajan, SH Tsang
Viruses 11 (1), 28, 2019
Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degeneration
J Zernant, W Lee, FT Collison, GA Fishman, YV Sergeev, K Schuerch, ...
Journal of medical genetics 54 (6), 404-412, 2017
A comparison of fundus autofluorescence and retinal structure in patients with Stargardt disease
NL Gomes, VC Greenstein, JN Carlson, SH Tsang, RT Smith, RE Carr, ...
Investigative ophthalmology & visual science 50 (8), 3953-3959, 2009
Analysis of the ABCA4 genomic locus in Stargardt disease
J Zernant, Y Xie, C Ayuso, R Riveiro-Alvarez, MA Lopez-Martinez, ...
Human molecular genetics 23 (25), 6797-6806, 2014
Effects of extracellular matrix and neighboring cells on induction of human embryonic stem cells into retinal or retinal pigment epithelial progenitors
J Gong, O Sagiv, H Cai, SH Tsang, LV Del Priore
Experimental eye research 86 (6), 957-965, 2008
Differentiation of hypothalamic-like neurons from human pluripotent stem cells
L Wang, K Meece, DJ Williams, KA Lo, M Zimmer, G Heinrich, JM Carli, ...
The Journal of clinical investigation 125 (2), 796-808, 2015
Gene therapy and genome surgery in the retina
JE DiCarlo, VB Mahajan, SH Tsang
The Journal of clinical investigation 128 (6), 2177-2188, 2018
The inner segment/outer segment border seen on optical coherence tomography is less intense in patients with diminished cone function
DC Hood, X Zhang, R Ramachandran, CL Talamini, A Raza, ...
Investigative ophthalmology & visual science 52 (13), 9703-9709, 2011
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