Results 71 to 80 of about 4,580,472 (190)

Effective in vivo RNA base editing via engineered cytidine deaminase APOBECs fused with PUF proteins

open access: yesNature Communications
Base editing stands at the forefront of genetic engineering, heralding precise genetic modifications with broad implications. While CRISPR-based DNA and RNA base editing systems capitalize on sgRNA-guided specificity and diverse deaminase functionalities,
Wenjian Han   +10 more
doaj   +1 more source

Seamlessly Editing the Web [PDF]

open access: yes, 2010
The typical process of editing content on the web is strongly moded. Authors are forced to switch between editing and previewing and publishing modes before, during, and after the editing process. This thesis explores a new paradigm of editing content on
Novak, Brook Jesse
core  

Precise correction of Duchenne muscular dystrophy exon deletion mutations by base and prime editing

open access: yes, 2023
openLa distrofia muscolare di Duchenne (DMD) è una malattia genetica rara e mortale, causata dalla mancanza di distrofina. Le mutazioni nel gene DMD, localizzato nel cromosoma X, sono trasmesse in modo recessivo legato al sesso; in particolare, una ...
DE ANTONI, NOEMI
core  

Programmable DNA pyrimidine base editing via engineered uracil-DNA glycosylase

open access: yesNature Communications
DNA base editing technologies predominantly utilize engineered deaminases, limiting their ability to edit thymine and guanine directly. In this study, we successfully achieve base editing of both cytidine and thymine by leveraging the translesion DNA ...
Zongyi Yi   +10 more
doaj   +1 more source

In the business of base editors: Evolution from bench to bedside

open access: yesPLoS Biology, 2023
With the advent of recombinant DNA technology in the 1970s, the idea of using gene therapies to treat human genetic diseases captured the interest and imagination of scientists around the world.
Elizabeth M. Porto, Alexis C. Komor
doaj  

DNA and RNA base editors can correct the majority of pathogenic single nucleotide variants

open access: yesnpj Genomic Medicine
The majority of human genetic diseases are caused by single nucleotide variants (SNVs) in the genome sequence. Excitingly, new genomic techniques known as base editing have opened efficient pathways to correct erroneous nucleotides.
Ariel Dadush   +8 more
doaj   +1 more source

Base-pairing probability in the microRNA stem region affects the binding and editing specificity of human A-to-I editing enzymes ADAR1-p110 and ADAR2

open access: yes, 2019
Adenosine deaminases acting on RNA (ADARs) catalyze the deamination of adenosine (A) to inosine (I). A-to-I RNA editing targets double-stranded RNA (dsRNA), and increases the complexity of gene regulation by modulating base pairing-dependent processes ...
Rintaro Ishii (5462111)   +7 more
core   +1 more source

An improved SNAP-ADAR tool enables efficient RNA base editing to interfere with post-translational protein modification

open access: yesNature Communications
RNA base editing relies on the introduction of adenosine-to-inosine changes into target RNAs in a highly programmable manner in order to repair disease-causing mutations.
Karthika Devi Kiran Kumar   +14 more
doaj   +1 more source

An optimized toolkit for precision base editing

open access: yes, 2018
CRISPR base editing is a potentially powerful technology that enables the creation of genetic mutations with single base pair resolution. By re-engineering both DNA and protein sequences, we developed a collection of constitutive and inducible base ...
Lukas E Dow   +16 more
core   +1 more source

Predicting adenine base editing efficiencies in different cellular contexts by deep learning

open access: yesGenome Biology
Background Adenine base editors (ABEs) enable the conversion of A•T to G•C base pairs. Since the sequence of the target locus influences base editing efficiency, efforts have been made to develop computational models that can predict base editing ...
Lucas Kissling   +15 more
doaj   +1 more source

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