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Albert S.B. Edge

Researcher at Massachusetts Eye and Ear Infirmary

Publications -  142
Citations -  9923

Albert S.B. Edge is an academic researcher from Massachusetts Eye and Ear Infirmary. The author has contributed to research in topics: Hair cell & Cochlea. The author has an hindex of 43, co-authored 140 publications receiving 8971 citations. Previous affiliations of Albert S.B. Edge include Albany Medical College & Harvard University.

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A promoter-level mammalian expression atlas

Alistair R. R. Forrest, +280 more
- 27 Mar 2014 - 
TL;DR: For example, the authors mapped transcription start sites (TSSs) and their usage in human and mouse primary cells, cell lines and tissues to produce a comprehensive overview of mammalian gene expression across the human body.
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Deglycosylation of glycoproteins by trifluoromethanesulfonic acid.

TL;DR: The procedure should prove useful not only for generation of deglycosylated proteins, but also for assessment of the number of asparagine-linked saccharide chains in a glycoprotein.
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Autologous skeletal myoblasts transplanted to ischemia-damaged myocardium in humans. Histological analysis of cell survival and differentiation.

TL;DR: In this article, autologous skeletal myoblast transplantation was investigated as a means to repair infarcted myocardium, and the transplanted skeletal myoblasts formed viable grafts in heavily scarred human myocardial tissue.
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Histological evidence of fetal pig neural cell survival after transplantation into a patient with Parkinson's disease

TL;DR: This is the first documentation of neural xenograft survival in the human brain and of appropriate growth of non-human dopaminergic neurons for a potential therapeutic response in Parkinson's disease.
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Improving the DNA specificity and applicability of base editing through protein engineering and protein delivery.

TL;DR: This work greatly reduces off-target base editing by installing mutations into the authors' third-generation base editor (BE3) to generate a high-fidelity baseeditor (HF-BE3), and applies these advances to deliver BE3 RNPs into both zebrafish embryos and the inner ear of live mice to achieve specific, DNA-free base editing in vivo.