Biblio

Author Title Type [ Year(Asc)]
Filters: Author is Jin, Zi-Bing  [Clear All Filters]
2024
Xu J, Yu S-J, Sun S, Li Y-P, Zhang X, Jin K, Jin Z-B. Enhanced innate responses in microglia derived from retinoblastoma patient-specific iPSCs. Glia. 2024.
Lin X, Liu Z-L, Zhang X, Wang W, Huang Z-Q, Sun S-N, Jin Z-B. Modeling autosomal dominant retinitis pigmentosa by using patient-specific retinal organoids with a class-3 RHO mutation. Exp Eye Res. 2024:109856.
Wang W, Zhang X, Zhao N, Xu Z-H, Jin K, Jin Z-B. RNA Fusion in human retinal development. Elife. 2024;13.
2023
Pan D, Zhang X, Jin K, Jin Z-B. CRX haploinsufficiency compromises photoreceptor precursor translocation and differentiation in human retinal organoids. Stem Cell Res Ther. 2023;14(1):346.
Chen D, Wang L, Guo X, Zhang Z, Xu X, Jin Z-B, Liang Q. Evaluation of Limbal Stem Cells in Patients With Type 2 Diabetes: An In Vivo Confocal Microscopy Study. Cornea. 2023.
Li Y-P, Shen R-J, Cheng Y-M, Zhao Q, Jin K, Jin Z-B, Zhang S. Exome sequencing in retinal dystrophy patients reveals a novel candidate gene ER membrane protein complex subunit 3. Heliyon. 2023;9(9):e20146.
Wang L, Xu X, Chen Q, Wei Y, Wei Z, Jin Z-B, Liang Q. Extracellular Vesicle MicroRNAs From Corneal Stromal Stem Cell Enhance Stemness of Limbal Epithelial Stem Cells by Targeting the Notch Pathway. Invest Ophthalmol Vis Sci. 2023;64(12):42.
Qiu S, Zhang X, Zhang L, Liu Z, Wang L, Jin Z-B, Xiao P. Generation of the induced pluripotent stem cell line SFMUi001-A from a patient with usher syndrome type 2 caused by biallelic variants in the USH2A gene. Stem Cell Res. 2023;69:103101.
Cheng Y-M, Ma C, Jin K, Jin Z-B. Retinal organoid and gene editing for basic and translational research. Vision Res. 2023;210:108273.
2021
Li Y-P, Ma Y, Wang N, Jin Z-B. Eyes on coronavirus. Stem Cell Res. 2021;51:102200.
2020
Wu K-C, Lv J-N, Yang H, Yang F-M, Lin R, Lin Q, Shen R-J, Bin Wang J-, Duan W-H, Hu M, et al. Nonhuman Primate Model of Oculocutaneous Albinism with and Mutations. Research (Wash D C). 2020;2020:1658678.
Gao M-L, Lei X-L, Han F, He K-W, Jin S-Q, Zhang Y-Y, Jin Z-B. Patient-Specific Retinal Organoids Recapitulate Disease Features of Late-Onset Retinitis Pigmentosa. Front Cell Dev Biol. 2020;8:128.
Zhang C-J, Ma Y, Jin Z-B. The road to restore vision with photoreceptor regeneration. Exp Eye Res. 2020:108283.
Chow SH, Deo P, T Y Yeung A, Kostoulias XP, Jeon Y, Gao M-L, Seidi A, Olivier FAlwyn Bens, Sridhar S, Nethercott C, et al. Targeting NLRP3 and staphylococcal pore-forming toxin receptors in human-induced pluripotent stem cell-derived macrophages. J Leukoc Biol. 2020.
Chow SH, Deo P, T Y Yeung A, Kostoulias XP, Jeon Y, Gao M-L, Seidi A, Olivier FAlwyn Bens, Sridhar S, Nethercott C, et al. Targeting NLRP3 and staphylococcal pore-forming toxin receptors in human-induced pluripotent stem cell-derived macrophages. J Leukoc Biol. 2020.
2019
Sun L-F, Zhang B, Chen X-J, Wang X-Y, Zhang B-W, Ji Y-Y, Wu K-C, Wu J-Y, Jin Z-B. Circular RNAs in human and vertebrate neural retinas. RNA Biol. 2019.
Chen X-J, Zhang Z-C, Wang X-Y, Zhao H-Q, Li M-L, Ma Y, Ji Y-Y, Zhang C-J, Wu K-C, Xiang L, et al. The Circular RNome of Developmental Retina in Mice. Mol Ther Nucleic Acids. 2019;19:339-349.
Wu K-C, Chen X-J, Jin G-H, Wang X-Y, Yang D-D, Li Y-P, Xiang L, Zhang B-W, Zhou G-H, Zhang C-J, et al. Deletion of miR-182 Leads to Retinal Dysfunction in Mice. Invest Ophthalmol Vis Sci. 2019;60(4):1265-1274.
2018
Jin Z-B, Gao M-L, Deng W-L, Wu K-C, Sugita S, Mandai M, Takahashi M. Stemming retinal regeneration with pluripotent stem cells. Prog Retin Eye Res. 2018.
2016
Zhang L, Xiang L, Liu Y, Venkatraman P, Chong L, Cho J, Bonilla S, Jin Z-B, Pang CPui, Ko KMing, et al. A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration. PLoS One. 2016;11(3):e0149663.
2015
Huang X-F, Wu J, Lv J-N, Zhang X, Jin Z-B. Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing. Genet Med. 2015.
2013
Huang X-F, Xiang P, Chen J, Xing D-J, Huang N, Min Q, Gu F, Tong Y, Pang C-P, Qu J, et al. Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families. PLoS One. 2013;8(5):e63832.