Search Results - "Jiao, Kangwei"
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Inhibition of the MAPK/c-Jun-EGR1 Pathway Decreases Photoreceptor Cell Death in the rd1 Mouse Model for Inherited Retinal Degeneration
Published in International journal of molecular sciences (23-11-2022)“…Retinitis pigmentosa (RP) is a group of inherited retinal dystrophies that typically results in photoreceptor cell death and vision loss. Here, we explored the…”
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Single-Cell Transcriptomic Profiling in Inherited Retinal Degeneration Reveals Distinct Metabolic Pathways in Rod and Cone Photoreceptors
Published in International journal of molecular sciences (12-10-2022)“…The cellular mechanisms underlying hereditary photoreceptor degeneration are still poorly understood. The aim of this study was to systematically map the…”
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3
T-type voltage-gated channels, Na+/Ca2+-exchanger, and calpain-2 promote photoreceptor cell death in inherited retinal degeneration
Published in Cell communication and signaling (01-02-2024)“…Inherited retinal degenerations (IRDs) are a group of untreatable and commonly blinding diseases characterized by progressive photoreceptor loss. IRD pathology…”
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4
RNA Biological Characteristics at the Peak of Cell Death in Different Hereditary Retinal Degeneration Mutants
Published in Frontiers in genetics (29-10-2021)“…Purpose: The present work investigated changes in the gene expression, molecular mechanisms, and pathogenesis of inherited retinal degeneration (RD) in three…”
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Inherited Retinal Degeneration: Towards the Development of a Combination Therapy Targeting Histone Deacetylase, Poly (ADP-Ribose) Polymerase, and Calpain
Published in Biomolecules (Basel, Switzerland) (23-03-2023)“…Inherited retinal degeneration (IRD) represents a diverse group of gene mutation-induced blinding diseases. In IRD, the loss of photoreceptors is often…”
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Inherited Retinal Degeneration: PARP-Dependent Activation of Calpain Requires CNG Channel Activity
Published in Biomolecules (Basel, Switzerland) (15-03-2022)“…Inherited retinal degenerations (IRDs) are a group of blinding diseases, typically involving a progressive loss of photoreceptors. The IRD pathology is often…”
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Tracking astrocyte polarization in the retina in retinopathy of prematurity
Published in Experimental eye research (01-01-2025)“…Astrocyte patterns affect the normal development of the retinal vascular network in retinopathy of prematurity (ROP), which is associated with VEGF secretion…”
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miR-200-3p suppresses cell proliferation and reduces apoptosis in diabetic retinopathy via blocking the TGF-β2/Smad pathway
Published in Bioscience reports (27-11-2020)“…Increasing evidence has shown that microRNAs (miRNAs) play an important role in the pathogenesis of diabetic retinopathy (DR). However, the role and mechanism…”
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HDAC inhibition delays photoreceptor loss in Pde6b mutant mice of retinitis pigmentosa: insights from scRNA-seq and CUT&Tag
Published in PeerJ (San Francisco, CA) (12-07-2023)“…This research aimed to ascertain the neuroprotective effect of histone deacetylase (HDAC) inhibition on retinal photoreceptors in mice, a model of retinitis…”
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10
Expression of glucose transporter‐2 in murine retina: Evidence for glucose transport from horizontal cells to photoreceptor synapses
Published in Journal of neurochemistry (01-01-2022)“…The retina has the highest relative energy consumption of any tissue, depending on a steady supply of glucose from the bloodstream. Glucose uptake is mediated…”
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Integrative RNA-seq and ATAC-seq analyses of phosphodiesterase 6 mutation-induced retinitis pigmentosa
Published in International ophthalmology (01-08-2022)“…Purpose Inhibition of poly-ADP-ribose polymerase 1 (PARP1) could relieve phosphodiesterase 6 mutation-induced retinitis pigmentosa (RP). However, the mechanism…”
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HDAC inhibition delays photoreceptor loss in Pde6b mutant mice of retinitis pigmentosa: insights from scRNA-seq and CUT Tag
Published in PeerJ (San Francisco, CA) (01-07-2023)“…Purpose This research aimed to ascertain the neuroprotective effect of histone deacetylase (HDAC) inhibition on retinal photoreceptors in Pde6brd1 mice, a…”
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13
Retinitis pigmentosa: impact of different Pde6a point mutations on the disease phenotype
Published in Human molecular genetics (01-10-2015)“…Mutations in the PDE6A gene can cause rod photoreceptors degeneration and the blinding disease retinitis pigmentosa (RP). While a number of pathogenic PDE6A…”
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14
T-type voltage-gated channels, Na + /Ca 2+ -exchanger, and calpain-2 promote photoreceptor cell death in inherited retinal degeneration
Published in Cell communication and signaling (01-02-2024)“…Inherited retinal degenerations (IRDs) are a group of untreatable and commonly blinding diseases characterized by progressive photoreceptor loss. IRD pathology…”
Get full text
Journal Article