Stephen H. Tsang
Stephen H. Tsang
Geverifieerd e-mailadres voor columbia.edu
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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
7161998
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
4052013
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
3662017
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
2862014
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
2121998
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
2021996
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
1742012
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), 1-6, 2016
1602016
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
1582015
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
1392011
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
1372014
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
1332009
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
1212008
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
1152014
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
1042011
Outer retinal tubulation in degenerative retinal disorders
NR Goldberg, JP Greenberg, K Laud, S Tsang, KB Freund
Retina (Philadelphia, Pa.) 33 (9), 1871, 2013
1032013
Structural assessment of hyperautofluorescent ring in patients with retinitis pigmentosa
LH Lima, W Cella, VC Greenstein, NK Wang, M Busuioc, RT Smith, ...
Retina (Philadelphia, Pa.) 29 (7), 1025, 2009
972009
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
942017
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
942015
Allelic and phenotypic heterogeneity in ABCA4 mutations
TR Burke, SH Tsang
Ophthalmic genetics 32 (3), 165-174, 2011
922011
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Artikelen 1–20