Search Results - "Jia, Danna"
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Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration
Published in PLoS genetics (04-03-2022)“…Neural retina leucine zipper (NRL) is an essential gene for the fate determination and differentiation of the precursor cells into rod photoreceptors in…”
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Differentially Expressed Genes in Atopic Dermatitis: Bioinformatics analysis of pooled microarray gene expression datasets in Gene Expression Omnibus
Published in Journal of education, health and sport (08-03-2024)“…Introduction: Atopic dermatitis (AD) is a chronic and refractory inflammatory skin disease characterized by relapsing eczematous and pruritic skin lesions…”
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Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration
Published in The Journal of biological chemistry (20-09-2019)“…Mutations in human prominin 1 (PROM1), encoding a transmembrane glycoprotein localized mainly to plasma membrane protrusions, have been reported to cause…”
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Tulp1 deficiency causes early-onset retinal degeneration through affecting ciliogenesis and activating ferroptosis in zebrafish
Published in Cell death & disease (17-11-2022)“…Mutations in TUB-like protein 1 ( TULP1 ) are associated with severe early-onset retinal degeneration in humans. However, the pathogenesis remains largely…”
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Cross-species single-cell landscapes identify the pathogenic gene characteristics of inherited retinal diseases
Published in Frontiers in genetics (11-07-2024)“…Inherited retinal diseases (IRDs) affect ∼4.5 million people worldwide. Elusive pathogenic variants in over 280 genes are associated with one or more clinical…”
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Retinal degeneration in rpgra mutant zebrafish
Published in Frontiers in cell and developmental biology (07-06-2023)“…Pathogenic mutations in , one of two major human isoforms, were responsible for most X-linked retinitis pigmentosa cases. Previous studies have shown that…”
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The splicing factor DHX38 enables retinal development through safeguarding genome integrity
Published in iScience (17-11-2023)“…DEAH-Box Helicase 38 (DHX38) is a pre-mRNA splicing factor and also a disease-causing gene of autosomal recessive retinitis pigmentosa (arRP). The role of…”
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Knockout of mafba Causes Inner-Ear Developmental Defects in Zebrafish via the Impairment of Proliferation and Differentiation of Ionocyte Progenitor Cells
Published in Biomedicines (16-11-2021)“…Zebrafish is an excellent model for exploring the development of the inner ear. Its inner ear has similar functions to that of humans, specifically in the…”
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IFT27 regulates the long-term maintenance of photoreceptor outer segments in zebrafish
Published in Gene (05-05-2024)“…•Ablation of ift27 in zebrafish leads to progressive late-onset photoreceptor degeneration.•Rods degenerate before cones in ift27-/- zebrafish.•IFT27 is…”
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Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing
Published in Nucleic acids research (26-02-2021)“…Abstract Dysfunction of splicing factors often result in abnormal cell differentiation and apoptosis, especially in neural tissues. Mutations in pre-mRNAs…”
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CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1
Published in Autophagy (04-03-2019)“…Macroautophagy/autophagy is an important intracellular mechanism for the maintenance of cellular homeostasis. Here we show that the CERKL (ceramide kinase…”
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Accumulation of Lipid Droplets in a Novel Bietti Crystalline Dystrophy Zebrafish Model With Impaired PPARα Pathway
Published in Investigative ophthalmology & visual science (26-05-2022)“…Bietti crystalline dystrophy (BCD) is a progressive retinal degenerative disease primarily characterized by numerous crystal-like deposits and degeneration of…”
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The splicing factor Prpf31 is required for hematopoietic stem and progenitor cell expansion during zebrafish embryogenesis
Published in The Journal of biological chemistry (01-03-2024)“…Pre-mRNA splicing is a precise regulated process and is crucial for system development and homeostasis maintenance. Mutations in spliceosomal components have…”
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A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome
Published in Molecular vision (2020)“…To identify the genetic cause in a four-generation Chinese family with Axenfeld-Rieger syndrome (ARS). The family members received clinical examinations of the…”
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BCAS2 is essential for hematopoietic stem and progenitor cell maintenance during zebrafish embryogenesis
Published in Blood (21-02-2019)“…Hematopoietic stem and progenitor cells (HSPCs) originate from the hemogenic endothelium via the endothelial-to-hematopoietic transition, are self-renewing,…”
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