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ARVO Annual Meeting Abstract June 2024

Porcine model of chronic retinal neovascularization and vascular leakage induced by DL-2-aminoadipic acid

Sandeep Kumar; Xiaohui Zhang,; Sudan Puri; Jenny Walter; James Lee; Vivian Trenti; Vatsala Naageshwaran; Glenwood G Gum

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):286.

ARVO Annual Meeting Abstract June 2024

Retinal phenotypic differences between two dry age-related macular degeneration rat models

Xiaohui Zhang; James Lee; Jenny Walter; Cloe Moctezuma; Vivian Trenti; Ana Eguiza; Yessica Chaparro; Sujata Rijal; Vatsala Naageshwaran; Glenwood G Gum; Sandeep Kumar

Invest. Ophthalmol. Vis. Sci.. 2024; 65(7):3799.

ARVO Annual Meeting Abstract June 2023

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Autosomal Recessive Bestrophinopathy

Jie Shi; Yang Li; Xiaohui Zhang; Xin Zhang; tian lu; Yue Xie; Xu Ke

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):4524.

ARVO Annual Meeting Abstract June 2023

Pergolide is comparable to nerve growth factor in recovery after alkali trauma in mouse corneas

Xiaohui Zhang; Kieley Trempy; Kaitlyn Hunter; Baila Shakaib; Lintao Li; Cornelia Siegl; Bonnie Archer; Sandeep Kumar; Glenwood G Gum; Vatsala Naageshwaran; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):722.

Genetics September 2022

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings

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Xin Zhang; Yue Xie; Ke Xu; Haoyu Chang; Xiaohui Zhang; Yang Li
TAGS: chinese (other dialects), chinese people, cohort studies, genetic analysis, genetics, wolfram syndrome, genes, whole genome sequencing, eye, polymerase chain reaction
Invest. Ophthalmol. Vis. Sci.. 2022; 63(10):9. https://doi.org/10.1167/iovs.63.10.9

Includes: Supplemental Content

Genetics June 2022

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4 -Related Retinopathy: Deep Intronic Variants and Copy Number Variations

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Lu Tian; Chunjie Chen; Yuning Song; Xiaohui Zhang; Ke Xu; Yue Xie; Zi-Bing Jin; Yang Li
TAGS: abca4 gene, alleles, copy number polymorphism, genetic analysis, introns, phenotype, retinal diseases
Invest. Ophthalmol. Vis. Sci.. 2022; 63(6):5. https://doi.org/10.1167/iovs.63.6.5

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2022

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4 -Related Retinopathy: Deep Intronic Variants and Copy Number Variations

Tian Lu; Chunjie Chen; Yuning Song; Xiaohui Zhang; Ke Xu; Yue Xie; Zi-Bing Jin; Yang Li

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):2624.

ARVO Annual Meeting Abstract June 2022

Gene knockdown of Col8a2 in mouse corneal endothelium by non-homologous end joint repair using adenovirus-mediated Crispr/Cas9

Hironori Uehara; Xiaohui Zhang; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1899 – A0045.

ARVO Annual Meeting Abstract June 2020

Subretinal Injection of AAVBR1 Targets the RPE and Outer Retina

Lara Carroll; Hironori Uehara; Xiaohui Zhang; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2901.

Cornea January 2020

Topical Pergolide Enhance Corneal Nerve Regrowth Following Induced Corneal Abrasion

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Xiaohui Zhang; Santosh Muddana; Sangeetha Ravi Kumar; Joshua Nelson Burton; Pratima Labroo; Jill Shea; Parker Stocking; Cornelia Siegl; Bonnie Archer; Jayant Agarwal; Balamurali K. Ambati
TAGS: cornea, pergolide, corneal abrasions, neurons
Invest. Ophthalmol. Vis. Sci.. 2020; 61(1):4. https://doi.org/10.1167/iovs.61.1.4

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2019

Systemic Delivery Of Endothelial Colony Forming Cells Enables Vascular Integration Into Diabetic Mouse retinas, But Not Diabetic Mouse Retinas Treated With AAV2.COMP-Ang1

Lara Carroll; Xiaohui Zhang; Yufeng Huang; Yuanyuan Wu; Alan W Stitt; Tim M Curtis; Reinhold J. Medina; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2724.

ARVO Annual Meeting Abstract July 2019

Gene therapy targeting PDGF-B for neovascular AMD

Xiaohui Zhang; Hironori Uehara; Lara Carroll; Bonnie Archer; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):2981.

ARVO Annual Meeting Abstract July 2019

Mutation Screening of OPA1 in a cohort Chinese patients with Suspected Autosomal Dominant Optic Atrophy

YUE XIE; Ting Xiao; Ke Xu; Xiaohui Zhang; Yang Li

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):414.

ARVO Annual Meeting Abstract July 2019

TTR mutations and clinical characteristics of patients with vitreous amyloidosis

Xiaohui Zhang; Ke Xu; Xiaolin Xu; Yang Li

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):405.

Retina June 2019

Intravitreal AAV2.COMP-Ang1 Attenuates Deep Capillary Plexus Expansion in the Aged Diabetic Mouse Retina

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Lara S. Carroll; Hironori Uehara; Daniel Fang; Susie Choi; Xiaohui Zhang; Malkit Singh; Zoya Sandhu; Philip M. Cummins; Tim M. Curtis; Alan W. Stitt; Bonnie J. Archer; Balamurali K. Ambati
TAGS: angiotensin i, blood capillaries, diabetes mellitus, mice, retina
Invest. Ophthalmol. Vis. Sci.. 2019; 60(7):2494-2502. https://doi.org/10.1167/iovs.18-26182

Includes: Supplemental Content

ARVO Annual Meeting Abstract July 2018

Efficacy and Safety of AAV2.Flt23k Intraceptor Compared to AAV2.sFlt01

Xiaohui Zhang; Hironori Uehara; Lara S Carroll; Bonnie Archer; Balamurali K Ambati

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):1449.

ARVO Annual Meeting Abstract July 2018

Sector Retinitis Pigmentosa caused by mutations of the RHO gene

Yang Li; Ke Xu; Ting Xiao; Xiaohui Zhang; Yue Xie

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):5422.

ARVO Annual Meeting Abstract July 2018

Comprehensive Molecular Screening in a Large Chinese Cohort with Usher Syndrome

Tengyang Sun; Ke Xu; Xiaohui Zhang; Yang Li

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):2342.

Genetics March 2018

Comprehensive Molecular Screening in Chinese Usher Syndrome Patients

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Tengyang Sun; Ke Xu; Yanfan Ren; Yue Xie; Xiaohui Zhang; Lu Tian; Yang Li
TAGS: chinese (other dialects), chinese people, genes, mutation, screening, usher syndrome, hearing loss, transanal endoscopic surgery, family, polymerase chain reaction
Invest. Ophthalmol. Vis. Sci.. 2018; 59(3):1229-1237. https://doi.org/10.1167/iovs.17-23312

Includes: Supplemental Content

Genetics July 2017

Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy

PDF

Lu Tian; Tengyang Sun; Ke Xu; Xiaohui Zhang; Xiaoyan Peng; Yang Li
TAGS: autosomal recessive inheritance, chinese people, cohort studies, genes, mutation, screening, vitelliform dystrophy
Invest. Ophthalmol. Vis. Sci.. 2017; 58(9):3366-3375. https://doi.org/10.1167/iovs.17-21999

Includes: Supplemental Content

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Porcine model of chronic retinal neovascularization and vascular leakage induced by DL-2-aminoadipic acid

Retinal phenotypic differences between two dry age-related macular degeneration rat models

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Autosomal Recessive Bestrophinopathy

Pergolide is comparable to nerve growth factor in recovery after alkali trauma in mouse corneas

Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4 -Related Retinopathy: Deep Intronic Variants and Copy Number Variations

Phenotype-Based Genetic Analysis Reveals Missing Heritability of ABCA4 -Related Retinopathy: Deep Intronic Variants and Copy Number Variations

Gene knockdown of Col8a2 in mouse corneal endothelium by non-homologous end joint repair using adenovirus-mediated Crispr/Cas9

Subretinal Injection of AAVBR1 Targets the RPE and Outer Retina

Topical Pergolide Enhance Corneal Nerve Regrowth Following Induced Corneal Abrasion

Systemic Delivery Of Endothelial Colony Forming Cells Enables Vascular Integration Into Diabetic Mouse retinas, But Not Diabetic Mouse Retinas Treated With AAV2.COMP-Ang1

Gene therapy targeting PDGF-B for neovascular AMD

Mutation Screening of OPA1 in a cohort Chinese patients with Suspected Autosomal Dominant Optic Atrophy

TTR mutations and clinical characteristics of patients with vitreous amyloidosis

Intravitreal AAV2.COMP-Ang1 Attenuates Deep Capillary Plexus Expansion in the Aged Diabetic Mouse Retina

Efficacy and Safety of AAV2.Flt23k Intraceptor Compared to AAV2.sFlt01

Sector Retinitis Pigmentosa caused by mutations of the RHO gene

Comprehensive Molecular Screening in a Large Chinese Cohort with Usher Syndrome

Comprehensive Molecular Screening in Chinese Usher Syndrome Patients

Screening of BEST1 Gene in a Chinese Cohort With Best Vitelliform Macular Dystrophy or Autosomal Recessive Bestrophinopathy

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