Results 31 to 40 of about 12,345 (165)

A role for human homologous recombination factors in suppressing microhomology-mediated end joining. [PDF]

open access: yesNucleic Acids Res, 2016
DNA double-strand breaks (DSBs) are toxic lesions, which if improperly repaired can result in cell death or genomic instability. DSB repair is usually facilitated by the classical non-homologous end joining (C-NHEJ), or homologous recombination (HR ...
Ahrabi S   +6 more
europepmc   +7 more sources

DNA large fragment deleting by compact, sequence-motif-free and specific TaqTth-hpRNA assisted with the microhomology-mediated end joining pathway. [PDF]

open access: yesNucleic Acids Res
A DNA editing tool TaqTth-hpRNA was developed in this study, composed of a compact recombinant TaqTth nuclease (832 aa) and a simple hairpin-RNA guiding probe (hpRNA).
Liu Y   +10 more
europepmc   +2 more sources

Disruption of Microhomology-mediated End-joining in Ewing Sarcoma

open access: yesbioRxiv
Ewing sarcoma (EwS) is a group of bone and soft tissue cancers in children and young adults. Since EwS cells have pronounced sensitivity to radiation and chemotherapy-induced DNA damage, the role of the oncoprotein, EWS-FLI1, in DNA repair is likely ...
S. Asada   +18 more
semanticscholar   +3 more sources

In vivo and in vitro knockout system labelled using fluorescent protein via microhomology-mediated end joining [PDF]

open access: yesLife Science Alliance, 2020
This study provides a new method that enables the labelling of knockout cells with fluorescent protein through microhomology-mediated end joining (MMEJ)–based knock-in. Gene knockout is important for understanding gene function and genetic disorders. The
Shota Katayama, Kota Sato, Toru Nakazawa
doaj   +2 more sources

Microhomology-mediated end joining drives complex rearrangements and overexpression of MYC and PVT1 in multiple myeloma. [PDF]

open access: yesHaematologica, 2020
MYC is a widely acting transcription factor and its deregulation is a crucial event in many human cancers. MYC is important biologically and clinically in multiple myeloma, but the mechanisms underlying its dysregulation are poorly understood.
Mikulasova A   +21 more
europepmc   +6 more sources

Publisher Correction: Molecular basis of microhomology-mediated end-joining by purified full-length Polθ [PDF]

open access: yesNature Communications, 2020
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Samuel J. Black   +18 more
doaj   +2 more sources

Particulate hexavalent chromium inhibits global transcription of genes in DNA repair pathways, particularly targeting homologous recombination repair, base excision repair, mismatch repair and microhomology-mediated end-joining. [PDF]

open access: yesJ Hazard Mater
Hexavalent chromium [Cr(VI)] is a human lung carcinogen with widespread exposure. How Cr(VI) causes cancer is poorly understood, but chromosome instability plays a central role.
Meaza I   +4 more
europepmc   +2 more sources

The APE2 nuclease is essential for DNA double strand break repair by microhomology-mediated end-joining

open access: yesbioRxiv, 2022
Microhomology-mediated end-joining (MMEJ) is an intrinsically mutagenic pathway of DNA double strand break repair essential for proliferation of homologous recombination (HR) deficient tumors.
Fleury H   +12 more
europepmc   +2 more sources

Microhomology-mediated end joining is the predominant form of DNA repair in the mosquito Aedes aegypti with implications for gene editing, gene drive, and transgene removal. [PDF]

open access: yesNucleic Acids Res
Programmable site-specific nucleases have revolutionized the field of genetics, and in the field of mosquito vector control, gene editing by these tools has inspired a new wave of population control approaches that aim to prevent disease transmission ...
Romanowski JS, Myles KM, Adelman ZN.
europepmc   +2 more sources

ATM regulates Mre11-dependent DNA end-degradation and microhomology- mediated end joining [PDF]

open access: yesCell Cycle, 2010
The human disorder ataxia telangiectasia (AT), which is characterized by genetic instability and neurodegeneration, results from mutation of the ataxia telangiectasia mutated (ATM) kinase.
Dixon K.   +5 more
core   +3 more sources

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