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Keratin 12 missense mutation induces the unfolded protein response and apoptosis in Meesmann epithelial corneal dystrophy.Human Molecular GeneticsDate: (2016) CRISPR/Cas9 DNA cleavage at SNP-derived PAM enables both in vitro and in vivo KRT12 mutation-specific targetingGene TherapyDate: (2015) In vivo gene silencing by siRNA delivery to the corneal epithelium in a keratin-12- bioluminescence mouse modelDate: (2015) Protein Composition of TGFBI-R124C- and TGFBI-R555W- Associated Aggregates Suggests Multiple Mechanisms Leading to Lattice and Granular Corneal Dystrophy.Investigative ophthalmology & visual scienceDate: (2015) Development of allele specific gene silencing siRNAs for TGFBI Arg124Cys in Lattice Corneal Dystrophy Type IInvest. Ophthalmol. Vis. SciDate: (2014) siRNA Silencing of the Mutant Keratin 12 Allele in Corneal Limbal Epithelial Cells Grown from Patients with Meesmann’s Epithelial Corneal DystrophyInvest Ophthalmol Vis SciDate: (2014) A Comparison of the Clinical and Molecular Diagnosis of Herpes Simplex KeratitisOpen Journal of Ophthalmology.Date: (2014) Identifying the role of matrix metalloproteinases in the pathomechanism of TGFBI Arg124Cys related Lattice Corneal Dystrophy Type IDate: (2014) Development of allele specific gene silencing siRNAs for TGFBI Arg124Cys in Lattice Corneal Dystrophy Type I.Date: (2014) Protection of corneal epithelial stem cells prevents UV-A damage during corneal collagen cross-linking treatment for keratoconusBr J OphthalmolDate: (2013)