Massachusetts Eye and Ear Infirmary
10 papers found
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
Optical genome mapping and revisiting short-read genome sequencing data reveal previously overlooked structural variants disrupting retinal disease−associated genes
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype.
Early audiological phenotype in patients with mutations in the USH2A gene
Potential Molecular Mechanisms of Rare Anti-Tumor Immune Response by SARS-CoV-2 in Isolated Cases of Lymphomas
The Spike of SARS-CoV-2: Uniqueness and Applications
Combinatorial Approaches for Cancer Treatment Using Oncolytic Viruses: Projecting the Perspectives through Clinical Trials Outcomes
Pathophysiological features of the visual cycle, cascade and metabolic pathways in retinitis pigmentosa
A novel multi-omics-based highly accurate prediction of symptoms, comorbid conditions, and possible long-term complications of COVID-19
Multi-omics-based identification of SARS-CoV-2 infection biology and candidate drugs against COVID-19
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