Titlebook: Advances in Vision Research, Volume IV; From Basic to Transl Gyan Prakash,Takeshi Iwata Book 2024 This is a U.S. government work and not un

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1612-3212 tificial retina/cornea.Describes application of AI in transl.This fourth volume in the series .Advances in Vision Research. describes importance advancements in?basics to?translational research, including new therapeutics for genetic eye diseases. Recent US FDA approval of the first gene therapy for

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Establishment of the Clinical Genome Resource (ClinGen) X-Linked Inherited Retinal Disease Variant c heterogeneity of IRD, targeted gene therapy is emerging as the main effective approach for treating the disease with many clinical trials currently underway. To maximize the benefit of these emerging therapies to patients, molecular diagnosis is the first critical step. In coordination with the Cl

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Genotype and Phenotype Characteristics of Major Genes Causing Inherited Retinal Diseases in Difference of IRD in Israel is estimated between 1:1000 and 1:2000 individuals. IRDs are divided into subgroups according to the mutated genes causing the disorder and/or according to the main cell type, which is damaged and does not function properly, i.e., rod-cone dystrophies, the most common example in

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Ocular Genetics and Genetic Eye Research in the Philippines,ng with a lack of healthcare professionals. Due to these compounding factors, emphasis in healthcare has been directed to the leading causes of morbidity and mortality, which are infectious, cardiovascular, and pulmonary diseases. Genetics, which is widely viewed as new and costly, has been given li

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Custom Ampliseq Targeted Sequencing Panel for Orphan Pediatric Retinal Diseases, that impact the retinal vasculature and retinal layer adhesion are very rare. Familial Exudative Vitreo-Retinopathy (FEVR), Norrie Disease (ND), and Persistent Fetal Vascular Syndrome (PFVS) are caused by variants in several genes required for the normal function of retinal vascular endothelial cel

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RPE Senescence and Its Implication in Age-Related Macular Degeneration,d persistent DNA damage response, and is associated with metabolic reprogramming, chromatin rearrangement, and autophagy modulation. Senescent cells produce and secrete a combination of factors to exert non-cell-autonomous effects, referred to as senescence-associated secretory phenotype (SASP). Acc

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