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Circular RNAs in ferroptosis: regulation mechanism and potential clinical application in disease

Frontiers in pharmacology, 2023-06, Vol.14, p.1173040-1173040

2023

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Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis

Orphanet journal of rare diseases, 2020-08, Vol.15 (1), p.1-227, Article 227

2020

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Decreased Integrity, Content, and Increased Transcript Level of Mitochondrial DNA Are Associated with Keratoconus

PloS one, 2016-10, Vol.11 (10), p.e0165580-e0165580

2016

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De novo mutations of TUBA3D are associated with keratoconus

Scientific reports, 2017-10, Vol.7 (1), p.13570-10, Article 13570

2017

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Genetic mutation and aqueous humor metabolites alterations in a family with Marfan syndrome

Heliyon, 2024-01, Vol.10 (1), p.e23696-e23696, Article e23696

2024

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Cardiovascular toxicity and mechanism of bisphenol A and emerging risk of bisphenol S

The Science of the total environment, 2020-06, Vol.723, p.137952, Article 137952

2020

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Systematically Displaying the Pathogenesis of Keratoconus via Multi-Level Related Gene Enrichment-Based Review

Frontiers in medicine, 2022-01, Vol.8, p.770138-770138

2022

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Exome sequencing analysis identifies novel homozygous mutation in ABCA4 in a Chinese family with Stargardt disease

International journal of ophthalmology, 2020-04, Vol.13 (4), p.671-676

Hao, Xiao-Dan

2020

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Uncovering the profile of somatic mtDNA mutations in Chinese colorectal cancer patients

PloS one, 2011-06, Vol.6 (6), p.e21613-e21613

2011

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Circular RNA expression profile identifies potential circulating biomarkers for keratoconus

Experimental eye research, 2024-02, Vol.239, p.109759-109759, Article 109759

2024

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Targeting ferroptosis: a novel therapeutic strategy for the treatment of retinal diseases

Frontiers in pharmacology, 2024-10, Vol.15

2024

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The role of RNA modifications in hepatocellular carcinoma: functional mechanism and potential applications

Frontiers in immunology, 2024-08, Vol.15, p.1439485

2024

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Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts

Investigative ophthalmology & visual science, 2022-12, Vol.63 (13), p.1-1

2022

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Role of circular RNAs in retinoblastoma

Functional & integrative genomics, 2023-03, Vol.23 (1), p.13-13, Article 13

2023

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Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients

International journal of ophthalmology, 2016-02

2016

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Association of macular corneal dystrophy with excessive cell senescence and apoptosis induced by the novel mutant CHST6

Experimental eye research, 2022-01, Vol.214, p.108862-108862, Article 108862

2022

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Evidence for positive selection on the Osteogenin (BMP3) gene in human populations

PloS one, 2010-06, Vol.5 (6), p.e10959-e10959

2010

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Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population

Ophthalmic genetics, 2015-06, Vol.36 (2), p.132-136

2015

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Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population

Experimental eye research, 2015-03, Vol.132, p.59-63

2015

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Large-scale mtDNA screening reveals a surprising matrilineal complexity in east Asia and its implications to the peopling of the region

Molecular biology and evolution, 2011-01, Vol.28 (1), p.513-522

2011

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Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population

Gene, 2013-01, Vol.512 (2), p.460-463

2013

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Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer

Oncology reports, 2013-01, Vol.29 (1), p.226-236

2013

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Longevity factor FOXO3a: A potential therapeutic target for age-related ocular diseases

Life sciences (1973), 2024-08, Vol.350, p.122769, Article 122769

2024

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Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts

Investigative ophthalmology & visual science, 2022-12, Vol.63 (13)

2022

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Detection of dopamine using self-assembled diazoresin/single-walled carbon nanotube modified electrodes

Chinese chemical letters, 2014-04, Vol.25 (4), p.523-528

2014

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Circular RNAs in ferroptosis: regulation mechanism and potential clinical application in disease

Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis

Decreased Integrity, Content, and Increased Transcript Level of Mitochondrial DNA Are Associated with Keratoconus

De novo mutations of TUBA3D are associated with keratoconus

Genetic mutation and aqueous humor metabolites alterations in a family with Marfan syndrome

Cardiovascular toxicity and mechanism of bisphenol A and emerging risk of bisphenol S

Systematically Displaying the Pathogenesis of Keratoconus via Multi-Level Related Gene Enrichment-Based Review

Exome sequencing analysis identifies novel homozygous mutation in ABCA4 in a Chinese family with Stargardt disease

Uncovering the profile of somatic mtDNA mutations in Chinese colorectal cancer patients

Circular RNA expression profile identifies potential circulating biomarkers for keratoconus

Targeting ferroptosis: a novel therapeutic strategy for the treatment of retinal diseases

The role of RNA modifications in hepatocellular carcinoma: functional mechanism and potential applications

Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts

Role of circular RNAs in retinoblastoma

Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients

Association of macular corneal dystrophy with excessive cell senescence and apoptosis induced by the novel mutant CHST6

Evidence for positive selection on the Osteogenin (BMP3) gene in human populations

Evaluating the Association between Keratoconus and Reported Genetic Loci in a Han Chinese Population

Mitochondrial DNA copy number, but not haplogroup is associated with keratoconus in Han Chinese population

Large-scale mtDNA screening reveals a surprising matrilineal complexity in east Asia and its implications to the peopling of the region

Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population

Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer

Longevity factor FOXO3a: A potential therapeutic target for age-related ocular diseases

Insufficient Dose of ERCC8 Protein Caused by a Frameshift Mutation Is Associated With Keratoconus With Congenital Cataracts

Detection of dopamine using self-assembled diazoresin/single-walled carbon nanotube modified electrodes

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