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Physico-chemical and antioxidant properties of four mango (Mangifera indica L.) cultivars in China

Food chemistry, 2013-05, Vol.138 (1), p.396-405

2013

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Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

British journal of ophthalmology, 2021-01, Vol.105 (1), p.87-92

2021

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Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

Acta ophthalmologica (Oxford, England), 2021-06, Vol.99 (4), p.e470-e479

2021

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Expanding the clinical and genetic spectrum of Heimler syndrome

Orphanet journal of rare diseases, 2019-12, Vol.14 (1), p.290-290, Article 290

2019

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Mutational spectrum in a Chinese cohort with congenital cataracts

Molecular genetics & genomic medicine, 2023-09, Vol.11 (9), p.e2196-n/a

2023

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Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy

British journal of ophthalmology, 2020-06, Vol.104 (6), p.846-851

2020

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Morphology-selective synthesis of Cu(NO3)2·2.5H2O micro/nanostructures achieved by rational manipulation of nucleation pathways and their morphology-preserved conversion to CuO porous micro/nanostructures

CrystEngComm, 2018-01, Vol.20 (12), p.1731-1738

2018

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Next‐generation sequencing‐aided precise diagnosis of Stickler syndrome type I

Acta ophthalmologica (Oxford, England), 2020-06, Vol.98 (4), p.e440-e446

2020

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Novel variants of ABCA4 in Han Chinese families with Stargardt disease

BMC medical genetics, 2020-10, Vol.21 (1), p.213-213, Article 213

2020

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Antidepressant effect of electroacupuncture on modulating the expression of c‐Fos/AP‐1 through the JNK signaling pathway

Anatomical record (Hoboken, N.J. : 2007), 2021-11, Vol.304 (11), p.2480-2493

2021

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Mutation spectrum in a cohort with familial exudative vitreoretinopathy

Molecular genetics & genomic medicine, 2022-09, Vol.10 (9), p.e2021-n/a

2022

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Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

Orphanet journal of rare diseases, 2021-04, Vol.16 (1), p.174-174, Article 174

2021

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Mutation Analysis of the RPGR Gene in a Chinese Cohort

Frontiers in genetics, 2022-03, Vol.13, p.850122-850122

2022

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Genetic Characteristics and Variation Spectrum of USH2A-Related Retinitis Pigmentosa and Usher Syndrome

Frontiers in genetics, 2022-08, Vol.13, p.900548-900548

2022

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Granulomatous Lobular Mastitis Associated with Mycobacterium abscessus in South China: A Case Report and Review of the Literature

Case reports in infectious diseases, 2017-01, Vol.2017 (2017), p.1-4

2017

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Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review

BMC medical genetics, 2020-02, Vol.21 (1), p.27-27, Article 27

2020

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ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

Frontiers in genetics, 2019-09, Vol.10, p.773-773

2019

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Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma

Neurobiology of disease, 2015-02, Vol.74, p.167-179

2015

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Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses

BMC ophthalmology, 2020-06, Vol.20 (1), p.212-212, Article 212

2020

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Expression and Distribution of Mesencephalic Astrocyte-Derived Neurotrophic Factor in the Retina and Optic Nerve

Frontiers in human neuroscience, 2017-01, Vol.10, p.686-686

2017

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Circular Noncoding RNA HIPK3 Mediates Retinal Vascular Dysfunction in Diabetes Mellitus

Circulation (New York, N.Y.), 2017-10, Vol.136 (17), p.1629-1642

2017

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The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing

Frontiers in genetics, 2019-11, Vol.10, p.1217-1217

2019

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High Pressure-Induced mtDNA Alterations in Retinal Ganglion Cells and Subsequent Apoptosis

Frontiers in cellular neuroscience, 2016-11, Vol.10, p.254-254

2016

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Quercetin Declines Apoptosis, Ameliorates Mitochondrial Function and Improves Retinal Ganglion Cell Survival and Function in In Vivo Model of Glaucoma in Rat and Retinal Ganglion Cell Culture In Vitro

Frontiers in molecular neuroscience, 2017-09, Vol.10, p.285-285

2017

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Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing

Frontiers in bioengineering and biotechnology, 2020-09, Vol.8, p.564057-564057

2020

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Physico-chemical and antioxidant properties of four mango (Mangifera indica L.) cultivars in China

Prevalence and genetic–phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease

Comprehensive analysis of genetic and clinical characteristics of 30 patients with X‐linked juvenile retinoschisis in China

Expanding the clinical and genetic spectrum of Heimler syndrome

Mutational spectrum in a Chinese cohort with congenital cataracts

Mutation spectrum of the bestrophin-1 gene in a large Chinese cohort with bestrophinopathy

Morphology-selective synthesis of Cu(NO3)2·2.5H2O micro/nanostructures achieved by rational manipulation of nucleation pathways and their morphology-preserved conversion to CuO porous micro/nanostructures

Next‐generation sequencing‐aided precise diagnosis of Stickler syndrome type I

Novel variants of ABCA4 in Han Chinese families with Stargardt disease

Antidepressant effect of electroacupuncture on modulating the expression of c‐Fos/AP‐1 through the JNK signaling pathway

Mutation spectrum in a cohort with familial exudative vitreoretinopathy

Frequency and phenotypic characteristics of RPE65 mutations in the Chinese population

Mutation Analysis of the RPGR Gene in a Chinese Cohort

Genetic Characteristics and Variation Spectrum of USH2A-Related Retinitis Pigmentosa and Usher Syndrome

Granulomatous Lobular Mastitis Associated with Mycobacterium abscessus in South China: A Case Report and Review of the Literature

Mutation Spectrum of Stickler Syndrome Type I and Genotype-phenotype Analysis in East Asian Population: a systematic review

ABCA4 Gene Screening in a Chinese Cohort With Stargardt Disease: Identification of 37 Novel Variants

Cumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucoma

Next-generation sequencing-based clinical diagnosis of choroideremia and comprehensive mutational and clinical analyses

Expression and Distribution of Mesencephalic Astrocyte-Derived Neurotrophic Factor in the Retina and Optic Nerve

Circular Noncoding RNA HIPK3 Mediates Retinal Vascular Dysfunction in Diabetes Mellitus

The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing

High Pressure-Induced mtDNA Alterations in Retinal Ganglion Cells and Subsequent Apoptosis

Quercetin Declines Apoptosis, Ameliorates Mitochondrial Function and Improves Retinal Ganglion Cell Survival and Function in In Vivo Model of Glaucoma in Rat and Retinal Ganglion Cell Culture In Vitro

Cell Development Deficiency and Gene Expression Dysregulation of Trisomy 21 Retina Revealed by Single-Nucleus RNA Sequencing

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