Fei Yi

Affiliations: 
Stanford University, Palo Alto, CA 
Area:
Stem cell, Disease modeling, Human neuron differentiation
Google:
"Fei Yi"
Mean distance: 14.79 (cluster 11)
 
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Publications

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Wang L, Yi F, Fu L, et al. (2017) CRISPR/Cas9-mediated targeted gene correction in amyotrophic lateral sclerosis patient iPSCs. Protein & Cell
Yi F, Danko T, Botelho SC, et al. (2016) Autism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neurons. Science (New York, N.Y.). 352: aaf2669
Duan S, Yuan G, Liu X, et al. (2015) PTEN deficiency reprogrammes human neural stem cells towards a glioblastoma stem cell-like phenotype. Nature Communications. 6: 10068
Patzke C, Han Y, Covy J, et al. (2015) Analysis of conditional heterozygous STXBP1 mutations in human neurons. The Journal of Clinical Investigation. 125: 3560-71
Pak C, Danko T, Zhang Y, et al. (2015) Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1. Cell Stem Cell. 17: 316-28
Wang S, Yi F, Qu J. (2015) Eliminate mitochondrial diseases by gene editing in germ-line cells and embryos. Protein & Cell. 6: 472-5
Zhang W, Li J, Suzuki K, et al. (2015) Aging stem cells. A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging. Science (New York, N.Y.). 348: 1160-3
Ding Z, Sui L, Ren R, et al. (2015) A widely adaptable approach to generate integration-free iPSCs from non-invasively acquired human somatic cells. Protein & Cell. 6: 386-9
Zhu X, Fu L, Yi F, et al. (2014) Regeneration: making muscle from hPSCs. Cell Research. 24: 1159-61
Liu GH, Suzuki K, Li M, et al. (2014) Modelling Fanconi anemia pathogenesis and therapeutics using integration-free patient-derived iPSCs. Nature Communications. 5: 4330
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