Zi-Bing Jin

Publications

• Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4-Related Retinopathy: Deep Intronic Variants and Copy Number Variations
  Investigative Ophthalmology & Visual Science. 06, 2022  |   Pubmed ID: 35657619
• Therapeutic Effects of Human Pluripotent Stem Cell-Derived Mesenchymal Stem Cells on a Murine Model of Acute Type-2-Dominated Airway Inflammation
  Stem Cell Reviews and Reports. May, 2022  |   Pubmed ID: 35622293
• Identification of a New Mutation P.P88L in Connexin 50 Associated with Dominant Congenital Cataract
  Frontiers in Cell and Developmental Biology. 2022  |   Pubmed ID: 35531093
• Functional Microglia Derived from Human Pluripotent Stem Cells Empower Retinal Organ
  Science China. Life Sciences. Jun, 2022  |   Pubmed ID: 35451725
• Mutation of SLC7A14 Causes Auditory Neuropathy and Retinitis Pigmentosa Mediated by Lysosomal Dysfunction
  Science Advances. 04, 2022  |   Pubmed ID: 35394837
• MLL5 is Involved in Retinal Photoreceptor Maturation Through Facilitating CRX-mediated Photoreceptor Gene Transactivation
  IScience. Apr, 2022  |   Pubmed ID: 35359806
• CLEC3B is a Novel Causative Gene for Macular-retinal Dystrophy
  Genetics in Medicine : Official Journal of the American College of Medical Genetics. Jun, 2022  |   Pubmed ID: 35331648
• New Loci for Refractive Errors and Ocular Biometric Parameters in Young Chinese Han Adults
  Science China. Life Sciences. Mar, 2022  |   Pubmed ID: 35301706
• MiR-182 Targeting Reprograms Tumor-associated Macrophages and Limits Breast Cancer Progression
  Proceedings of the National Academy of Sciences of the United States of America. 02, 2022  |   Pubmed ID: 35105806
• Association Between Color Vision Deficiency and Myopia in Chinese Children Over a Five-Year Period
  Investigative Ophthalmology & Visual Science. 02, 2022  |   Pubmed ID: 35103751
• Requirements for Human-induced Pluripotent Stem Cells
  Cell Proliferation. Apr, 2022  |   Pubmed ID: 35083805
• The Association of Myopia Progression with the Morphological Changes of Optic Disc and β-peripapillary Atrophy in Primary School Students
  Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. Feb, 2022  |   Pubmed ID: 34357418
• The Impact of Study-at-Home During the COVID-19 Pandemic on Myopia Progression in Chinese Children
  Frontiers in Public Health. 2021  |   Pubmed ID: 35071149
• Implantable Collamer Lens Versus Small Incision Lenticule Extraction for High Myopia Correction: A Systematic Review and Meta-analysis
  BMC Ophthalmology. Dec, 2021  |   Pubmed ID: 34961514
• Clinical Features and Natural History in a Cohort of Chinese Patients with RPE65-Associated Inherited Retinal Dystrophy
  Journal of Clinical Medicine. Nov, 2021  |   Pubmed ID: 34830511
• Retinal Organoids As Models for Development and Diseases
  Cell Regeneration (London, England). Nov, 2021  |   Pubmed ID: 34719743
• Mitochondrial Mutations in Ethambutol-Induced Optic Neuropathy
  Frontiers in Cell and Developmental Biology. 2021  |   Pubmed ID: 34676220
• Retinal Degeneration Caused by Ago2 Disruption
  Investigative Ophthalmology & Visual Science. 09, 2021  |   Pubmed ID: 34529004
• MiR-183 and MiR-96 Orchestrate Both Glucose and Fat Utilization in Skeletal Muscle
  EMBO Reports. 09, 2021  |   Pubmed ID: 34358402
• Stem Cell-Based Regeneration and Restoration for Retinal Ganglion Cell: Recent Advancements and Current Challenges
  Biomolecules. 07, 2021  |   Pubmed ID: 34356611
• Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China
  Frontiers in Cell and Developmental Biology. 2021  |   Pubmed ID: 34222226
• Genotype Profile of Global EYS-Associated Inherited Retinal Dystrophy and Clinical Findings in a Large Chinese Cohort
  Frontiers in Cell and Developmental Biology. 2021  |   Pubmed ID: 34178978
• Polygenic Risk Scores Have High Diagnostic Capacity in Ankylosing Spondylitis
  Annals of the Rheumatic Diseases. Apr, 2021  |   Pubmed ID: 34161253
• Genetic Screening Revealed Latent Keratoconus in Asymptomatic Individuals
  Frontiers in Cell and Developmental Biology. 2021  |   Pubmed ID: 34136477
• Consanguinity-based Analysis of Exome Sequencing Yields Likely Genetic Causes in Patients with Inherited Retinal Dystrophy
  Orphanet Journal of Rare Diseases. 06, 2021  |   Pubmed ID: 34130719
• Conversion of Mouse Embryonic Fibroblasts into Neural Crest Cells and Functional Corneal Endothelia by Defined Small Molecules
  Science Advances. 06, 2021  |   Pubmed ID: 34088673
• Investigation of Macular Choroidal Thickness and Blood Flow Change by Optical Coherence Tomography Angiography After Posterior Scleral Reinforcement
  Frontiers in Medicine. 2021  |   Pubmed ID: 34017847
• Modeling Human Retinoblastoma Using Embryonic Stem Cell-derived Retinal Organoids
  STAR Protocols. 06, 2021  |   Pubmed ID: 33899024
• Modeling Retinitis Pigmentosa Through Patient-derived Retinal Organoids
  STAR Protocols. 06, 2021  |   Pubmed ID: 33899019
• Circular RNAs in the Central Nervous System
  Frontiers in Molecular Biosciences. 2021  |   Pubmed ID: 33816552
• Genotype-Phenotype Analysis and Mutation Spectrum in a Cohort of Chinese Patients With Congenital Nystagmus
  Frontiers in Cell and Developmental Biology. 2021  |   Pubmed ID: 33732697
• Transplantation of GMP-grade Human IPSC-derived Retinal Pigment Epithelial Cells in Rodent Model: the First Pre-clinical Study for Safety and Efficacy in China
  Annals of Translational Medicine. Feb, 2021  |   Pubmed ID: 33708872
• Eyes on Coronavirus
  Stem Cell Research. 03, 2021  |   Pubmed ID: 33535156
• Patient IPSC-derived Retinal Organoids: Observable Retinal Diseases In-a-dish
  Histology and Histopathology. Jan, 2021  |   Pubmed ID: 33491763
• The Road to Restore Vision with Photoreceptor Regeneration
  Experimental Eye Research. 01, 2021  |   Pubmed ID: 33010290
• Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa
  Frontiers in Cell and Developmental Biology. 2020  |   Pubmed ID: 33598457
• Human Embryonic Stem Cell-derived Organoid Retinoblastoma Reveals a Cancerous Origin
  Proceedings of the National Academy of Sciences of the United States of America. 12, 2020  |   Pubmed ID: 33318192
• Abundant Neural CircRNA Cdr1as Is Not Indispensable for Retina Maintenance
  Frontiers in Cell and Developmental Biology. 2020  |   Pubmed ID: 33240875
• Generation of Three Human IPSC Lines from a Retinitis Pigmentosa Family with SLC7A14 Mutation
  Stem Cell Research. 12, 2020  |   Pubmed ID: 33207307
• Towards Stem Cell-based Neuronal Regeneration for Glaucoma
  Progress in Brain Research. 2020  |   Pubmed ID: 32988476
• Generation of Nonhuman Primate Model of Cone Dysfunction Through AAV-Mediated Ablation
  Molecular Therapy. Methods & Clinical Development. Sep, 2020  |   Pubmed ID: 32953936
• COCO Enhances the Efficiency of Photoreceptor Precursor Differentiation in Early Human Embryonic Stem Cell-derived Retinal Organoids
  Stem Cell Research & Therapy. 08, 2020  |   Pubmed ID: 32831148
• Bioenergetic Crosstalk Between Mesenchymal Stem Cells and Various Ocular Cells Through the Intercellular Trafficking of Mitochondria
  Theranostics. 2020  |   Pubmed ID: 32641991
• Emerging Roles of Non-coding RNAs in Retinal Diseases: A Review
  Clinical & Experimental Ophthalmology. 11, 2020  |   Pubmed ID: 32519377
• ATP1A3 Mutation As a Candidate Cause Of autosomal Dominant Cone-rod Dystrophy
  Human Genetics. Nov, 2020  |   Pubmed ID: 32440726
• Molecular Genetic Analysis and Phenotypic Characteristics of a Consanguineous Family with Glycogen Storage Disease Type Ia
  Molecular Medicine Reports. Oct, 2016  |   Pubmed ID: 27511118
• The Association Between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing
  PloS One. 2015  |   Pubmed ID: 26421841
• A Recurrent Deletion Mutation in OPA1 Causes Autosomal Dominant Optic Atrophy in a Chinese Family
  Scientific Reports. Nov, 2014  |   Pubmed ID: 25374051
• Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing
  PloS One. 2014  |   Pubmed ID: 24763286