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The American Journal of Pathology|November 17, 2011
TLR9 ligand CpG-ODN applied to the injured mouse cornea elicits retinal inflammationHolly R Chinnery, Samuel McLenachan, Nicolette Binz, et al.Transgenic Research|August 19, 2008
Transgenic mice expressing the Peripherin-EGFP genomic reporter display intrinsic peripheral nervous system fluorescenceSamuel McLenachan, Yona Goldshmit, Kerry J Fowler, et al.Stem Cells and Development|November 21, 2013
Plant hormones increase efficiency of reprogramming mouse somatic cells to induced pluripotent stem cells and reduce tumorigenicityAna Belén Alvarez Palomo, Samuel McLenachan, Jordi Requena Osete, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 21, 2005
Evaluation of an FRDA-EGFP genomic reporter assay in transgenic miceJoseph P Sarsero, Timothy P Holloway, Lingli Li, et al.The CRISPR Journal|April 5, 2024
Rapid Variant Pathogenicity Analysis by CRISPR Activation of CRB1 Gene Expression in Patient-Derived FibroblastsSang Yoon Moon, Dan Zhang, Shang-Chih Chen, et al.Stem Cell Research|May 13, 2018
Generation of an induced pluripotent stem cell line from a patient with non-syndromic CLN3-associated retinal degeneration and a coisogenic control lineXiao Zhang, Dan Zhang, Shang-Chih Chen, et al.Journal of Drug Targeting|January 3, 2025
Nanoparticle-Based gene therapy strategies in retinal deliveryThomas Foster, Patrick Lim, Susbin Raj Wagle, et al.Stem Cell Research|September 9, 2019
Generation of three induced pluripotent stem cell lines from an isolated inherited retinal dystrophy patient with RCBTB1 frameshifting mutationsZhiqin Huang, Dan Zhang, Shang-Chih Chen, et al.Stem Cell Research|April 12, 2025
Generation of the induced pluripotent stem cell line LEIi023-A from a rod-cone dystrophy patient carrying the dominant PRPF31 c.267del variantDan Zhang, Di Huang, Shang-Chih Chen, et al.Stem Cell Research|June 9, 2024
Establishment of an induced pluripotent stem cell line LEIi019-A from an early-onset retinal dystrophy patient with the autosomal dominant OTX2 c.259G>A variantDan Zhang, Luke Jennings, Shang-Chih Chen, et al.Pageof 9