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A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal DegenerationModeling retinal degeneration using patient-specific induced pluripotent stem cellsMolecular diagnosis of putative Stargardt disease by capture next generation sequencingCorrection: A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal DegenerationA recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese familyTrio-based exome sequencing arrests de novo mutations in early-onset high myopiaGenetic signatures of high-altitude adaptation in TibetansMutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients.'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degenerationComparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells.miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance.Whole exome sequencing reveals genetic predisposition in a large family with retinitis pigmentosaTargeted exome sequencing identified novel USH2A mutations in Usher syndrome families.VEGF-mediated proliferation of human adipose tissue-derived stem cells.Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.The Association between Maternal Reproductive Age and Progression of Refractive Error in Urban Students in Beijing.Identification of novel mutations by targeted exome sequencing and the genotype-phenotype assessment of patients with achromatopsia.Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmusClinical and genetic analyses reveal novel pathogenic ABCA4 mutations in Stargardt disease families.Novel CHM mutations identified in Chinese families with Choroideremia.Identification of three novel mutations in the FRMD7 gene for X-linked idiopathic congenital nystagmus.Identification of a novel GJA8 (Cx50) point mutation causes human dominant congenital cataracts.R102W mutation in the RS1 gene responsible for retinoschisis and recurrent glaucoma.SLC7A14 linked to autosomal recessive retinitis pigmentosa.Toll-Like Receptor 3 Activation Initiates Photoreceptor Cell Death In Vivo and In Vitro.Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.Molecular genetic analysis and phenotypic characteristics of a consanguineous family with glycogen storage disease type Ia.Use of lectins to enrich mouse ES-derived retinal progenitor cells for the purpose of transplantation therapy.Loss of miR-182 affects B-cell extrafollicular antibody response.Identification and population history of CYP4V2 mutations in patients with Bietti crystalline corneoretinal dystrophy.Association of CD59 and CFH polymorphisms with acute anterior uveitis in Chinese population.miR-182 Regulates Metabolic Homeostasis by Modulating Glucose Utilization in Muscle.Unraveling the genetic cause of a consanguineous family with unilateral coloboma and retinoschisis: expanding the phenotypic variability of RAX mutations.Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis.A novel Bruch's membrane-mimetic electrospun substrate scaffold for human retinal pigment epithelium cells.Macular hole formation in patients with retinitis pigmentosa and prognosis of pars plana vitrectomy.CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients.Detection of localized retinal malfunction in retinal degeneration model using a multielectrode array system.Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs.
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description
onderzoeker
@nl
researcher
@en
հետազոտող
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name
Zi-Bing Jin
@ast
Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
@nl
Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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Zi-Bing Jin
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P106
P31
P496
0000-0003-0515-698X