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Vitamin D and Ocular Diseases: A Systematic Review

International journal of molecular sciences, 2022-04, Vol.23 (8), p.4226

2022

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FBH1 Catalyzes Regression of Stalled Replication Forks

Cell reports (Cambridge), 2015-03, Vol.10 (10), p.1749-1757

2015

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Enhancers are activated by p300/CBP activity-dependent PIC assembly, RNAPII recruitment, and pause release

Molecular cell, 2021-05, Vol.81 (10), p.2166-2182.e6

2021

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Genetic Associations of Primary Angle-Closure Disease

Ophthalmology (Rochester, Minn.), 2016-06, Vol.123 (6), p.1211-1221

2016

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Poly ADP Ribose Polymerase Inhibitor Olaparib Targeting Microhomology End Joining in Retinoblastoma Protein Defective Cancer: Analysis of the Retinoblastoma Cell-Killing Effects by Olaparib after Inducing Double-Strand Breaks

International journal of molecular sciences, 2021-10, Vol.22 (19), p.10687

2021

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Reduced CD38 expression on CD34+ cells as a diagnostic test in myelodysplastic syndromes

Haematologica (Roma), 2009-08, Vol.94 (8), p.1160-1163

2009

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Growth hormone releasing hormone signaling promotes Th17 cell differentiation and autoimmune inflammation

Nature communications, 2023-06, Vol.14 (1), p.3298-3298, Article 3298

2023

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Post-translational modifications on the retinoblastoma protein

Journal of biomedical science, 2022-06, Vol.29 (1), p.33-16, Article 33

2022

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Novel epigenetic therapy for Th17 cell mediated autoimmune inflammatory diseases

EBioMedicine, 2022-12, Vol.86, p.104368-104368, Article 104368

2022

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RB Regulates DNA Double Strand Break Repair Pathway Choice by Mediating CtIP Dependent End Resection

International journal of molecular sciences, 2020-12, Vol.21 (23), p.9176

2020

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FBH1 influences DNA replication fork stability and homologous recombination through ubiquitylation of RAD51

Nature communications, 2015-01, Vol.6 (1), p.5931-5931, Article 5931

2015

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DNA replication stress and its impact on chromosome segregation and tumorigenesis

Seminars in cancer biology, 2019-04, Vol.55, p.61-69

2019

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DNA Methylation as a Noninvasive Epigenetic Biomarker for the Detection of Cancer

Disease markers, 2017-01, Vol.2017 (2017), p.1-13

2017

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Systemic and Ocular Anti-Inflammatory Mechanisms of Green Tea Extract on Endotoxin-Induced Ocular Inflammation

Frontiers in endocrinology (Lausanne), 2022-07, Vol.13

2022

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Green tea extract attenuates LPS-induced retinal inflammation in rats

Scientific reports, 2018-01, Vol.8 (1), p.429-429, Article 429

2018

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Genetic associations for keratoconus: a systematic review and meta-analysis

Scientific reports, 2017-07, Vol.7 (1), p.4620-11, Article 4620

2017

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Transcription-Replication Collisions and Chromosome Fragility

Frontiers in genetics, 2021-12, Vol.12, p.804547-804547

2021

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FBH1 Helicase Disrupts RAD51 Filaments in Vitro and Modulates Homologous Recombination in Mammalian Cells

The Journal of biological chemistry, 2013-11, Vol.288 (47), p.34168-34180

2013

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Correction: Post-translational modifications on the retinoblastoma protein

Journal of biomedical science, 2024-10, Vol.31 (1), p.98-1, Article 98

2024

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The Evolving Story of Pterygium

Cornea, 2018-11, Vol.37 (1), p.S55-S57

2018

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FBH1 co-operates with MUS81 in inducing DNA double-strand breaks and cell death following replication stress

Nature communications, 2013-01, Vol.4 (1), p.1423-1423, Article 1423

2013

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Growth hormone-releasing hormone receptor signaling in experimental ocular inflammation and neuroprotection

Neural regeneration research, 2022-12, Vol.17 (12), p.2643-2648

2022

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Epigallocatechin-3-gallate (EGCG) inhibits myofibroblast transformation of human Tenon's fibroblasts

Experimental eye research, 2020-08, Vol.197, p.108119-108119, Article 108119

2020

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Emerging Roles of cGAS-STING Signaling in Mediating Ocular Inflammation

Journal of innate immunity, 2023-01, Vol.15 (1), p.739-750

2023

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Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma

Genes, 2023-01, Vol.14 (2), p.310

2023

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Vitamin D and Ocular Diseases: A Systematic Review

FBH1 Catalyzes Regression of Stalled Replication Forks

Enhancers are activated by p300/CBP activity-dependent PIC assembly, RNAPII recruitment, and pause release

Genetic Associations of Primary Angle-Closure Disease

Poly ADP Ribose Polymerase Inhibitor Olaparib Targeting Microhomology End Joining in Retinoblastoma Protein Defective Cancer: Analysis of the Retinoblastoma Cell-Killing Effects by Olaparib after Inducing Double-Strand Breaks

Reduced CD38 expression on CD34+ cells as a diagnostic test in myelodysplastic syndromes

Growth hormone releasing hormone signaling promotes Th17 cell differentiation and autoimmune inflammation

Post-translational modifications on the retinoblastoma protein

Novel epigenetic therapy for Th17 cell mediated autoimmune inflammatory diseases

RB Regulates DNA Double Strand Break Repair Pathway Choice by Mediating CtIP Dependent End Resection

FBH1 influences DNA replication fork stability and homologous recombination through ubiquitylation of RAD51

DNA replication stress and its impact on chromosome segregation and tumorigenesis

DNA Methylation as a Noninvasive Epigenetic Biomarker for the Detection of Cancer

Systemic and Ocular Anti-Inflammatory Mechanisms of Green Tea Extract on Endotoxin-Induced Ocular Inflammation

Green tea extract attenuates LPS-induced retinal inflammation in rats

Genetic associations for keratoconus: a systematic review and meta-analysis

Transcription-Replication Collisions and Chromosome Fragility

FBH1 Helicase Disrupts RAD51 Filaments in Vitro and Modulates Homologous Recombination in Mammalian Cells

Correction: Post-translational modifications on the retinoblastoma protein

The Evolving Story of Pterygium

FBH1 co-operates with MUS81 in inducing DNA double-strand breaks and cell death following replication stress

Growth hormone-releasing hormone receptor signaling in experimental ocular inflammation and neuroprotection

Epigallocatechin-3-gallate (EGCG) inhibits myofibroblast transformation of human Tenon's fibroblasts

Emerging Roles of cGAS-STING Signaling in Mediating Ocular Inflammation

Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma

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