Results 31 to 40 of about 888,680 (335)

Editing DNA Methylation in Mammalian Embryos [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
DNA methylation in mammals is essential for numerous biological functions, such as ensuring chromosomal stability, genomic imprinting, and X-chromosome inactivation through transcriptional regulation. Gene knockout of DNA methyltransferases and demethylation enzymes has made significant contributions to analyzing the functions of DNA methylation in ...
Taiga Yamazaki   +4 more
openaire   +2 more sources

Enhancement of homology-directed repair with chromatin donor templates in cells. [PDF]

open access: yes, 2020
A key challenge in precise genome editing is the low efficiency of homology-directed repair (HDR). Here we describe a strategy for increasing the efficiency of HDR in cells by using a chromatin donor template instead of a naked DNA donor template.
Cruz-Becerra, Grisel, Kadonaga, James T
core   +1 more source

No evidence of genome editing activity from Natronobacterium gregoryi Argonaute (NgAgo) in human cells. [PDF]

open access: yesPLoS ONE, 2017
The argonaute protein from the thermophilic bacterium Thermus thermophilus shows DNA-guided DNA interfering activity at high temperatures, complicating its application in mammalian cells.
Parisa Javidi-Parsijani   +5 more
doaj   +1 more source

Tissue Specific DNA Repair Outcomes Shape the Landscape of Genome Editing

open access: yesFrontiers in Genetics, 2021
The use of Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-Cas9 has moved from bench to bedside in less than 10years, realising the vision of correcting disease through genome editing. The accuracy and safety of this approach relies on
Mathilde Meyenberg   +5 more
doaj   +1 more source

Translational potential of base-editing tools for gene therapy of monogenic diseases

open access: yesFrontiers in Bioengineering and Biotechnology, 2022
Millions of people worldwide have rare genetic diseases that are caused by various mutations in DNA sequence. Classic treatments of rare genetic diseases are often ineffective, and therefore great hopes are placed on gene-editing methods.
Vasiliy V. Reshetnikov   +7 more
doaj   +1 more source

DNA Damage, DNA Repair, and Cancer: Second Edition

open access: yesInternational Journal of Molecular Sciences, 2023
Following our first Special Issue, we are pleased to present this Special Issue in the International Journal of Molecular Sciences, titled ‘DNA Damage, DNA Repair, and Cancer: Second Edition’ [...]
openaire   +2 more sources

Two steps are better than one: improving gene editing to treat cancer

open access: yesFEBS Open Bio, 2022
Gene editing enables scientists to make precise changes to the genome of an organism using the cell’s own ability to repair damaged DNA using a supplied DNA template.
Francesca Minter
doaj   +1 more source

High-purity production and precise editing of DNA base editing ribonucleoproteins [PDF]

open access: yesScience Advances, 2021
Cytosine and adenine base editor ribonucleoproteins show precise base editing with reduced DNA and RNA off-target effects.
Hyeon-Ki Jang   +9 more
openaire   +2 more sources

Generation of AAVS1 integrated doxycycline-inducible CRISPR-Prime Editor human induced pluripotent stem cell line

open access: yesStem Cell Research, 2021
Prime editing uses the Cas9 nickase fused to a reverse transcriptase to copy a DNA sequence into a specific locus from a ‘prime editing’ guide RNA (pegRNA), eliminating the need for double-stranded DNA breaks and donor DNA templates.
Nike Bharucha   +3 more
doaj   +1 more source

Chimeric oligonucleotides combining guide RNA and single-stranded DNA repair template effectively induce precision gene editing

open access: yesRNA Biology, 2022
The ability to precisely alter the genome holds immense potential for molecular biology, medicine and biotechnology. The development of the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) into a genomic editing tool has vastly ...
Avantika Ghosh   +4 more
doaj   +1 more source

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