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Repair of strand breaks by homologous recombination.

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TLDR
The enzymology of the process is discussed, followed by studies on DSB repair in living cells, and a historical context for the current view of HR is provided and how DSBs are processed during HR as well as interactions with other D SB repair pathways are described.
Abstract
In this review, we discuss the repair of DNA double-strand breaks (DSBs) using a homologous DNA sequence (i.e., homologous recombination [HR]), focusing mainly on yeast and mammals. We provide a historical context for the current view of HR and describe how DSBs are processed during HR as well as interactions with other DSB repair pathways. We discuss the enzymology of the process, followed by studies on DSB repair in living cells. Whenever possible, we cite both original articles and reviews to aid the reader for further studies.

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Transcriptional Regulation by DAX-1 in Pluripotent and Differentiated Cells

TL;DR: It is shown that in the years leading up to World War Two, the number of battles between the United States and Nazi Germany, known as the "Great Patriotic War", increased significantly, with the loss of fewer than 100 lives but the total number of conflicts more than doubled.
Journal ArticleDOI

DNA Damage Repair in Brain Tumor Immunotherapy

TL;DR: This review will focus on immunotherapy and analyze the mechanisms of DNA damage repair involved in the immune process, and review biomarkers that have been or may be used to evaluate immunotherapy for brain tumors, such as TAMs, RPA, and other molecules that may provide a precursor assessment for the rational implementation of immunotherapy in brain tumors.
Journal ArticleDOI

Understanding Rad51 function is a prerequisite for progress in cancer research

TL;DR: It is proposed that certain specific hydrophobic effects, recently discovered destabilizing stacking of nucleobases, may play a central role in this context for the function of Rad51.

Reducing the genetic complexity of glycolysis in Saccharomyces cerevisiae

TL;DR: Thesis.indb 36 16 2/2/2015 16:13:18 as discussed by the authors 16.2/15 16.13/2015 6:13.18].
Dissertation

Gene drive in Drosophila melanogaster and Aedes aegypti

TL;DR: Attempts at building different gene drive systems aiming for both population suppression or population replacement, as well as exploring the possibility of inserting exogenous sequences in the male locus of Aedes aegypti, marked the finding of a new female-specific recessive flightless target for use in future population suppression drive systems.
References
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Journal ArticleDOI

A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.

TL;DR: This study reveals a family of endonucleases that use dual-RNAs for site-specific DNA cleavage and highlights the potential to exploit the system for RNA-programmable genome editing.
Journal ArticleDOI

Multiplex Genome Engineering Using CRISPR/Cas Systems

TL;DR: The type II prokaryotic CRISPR (clustered regularly interspaced short palindromic repeats)/Cas adaptive immune system has been shown to facilitate RNA-guided site-specific DNA cleavage as discussed by the authors.

Multiplex Genome Engineering Using CRISPR/Cas Systems

TL;DR: Two different type II CRISPR/Cas systems are engineered and it is demonstrated that Cas9 nucleases can be directed by short RNAs to induce precise cleavage at endogenous genomic loci in human and mouse cells, demonstrating easy programmability and wide applicability of the RNA-guided nuclease technology.
Journal ArticleDOI

RNA-Guided Human Genome Engineering via Cas9

TL;DR: The type II bacterial CRISPR system is engineer to function with custom guide RNA (gRNA) in human cells to establish an RNA-guided editing tool for facile, robust, and multiplexable human genome engineering.
Journal ArticleDOI

Efficient genome editing in zebrafish using a CRISPR-Cas system

TL;DR: It is shown that the CRISPR-Cas system functions in vivo to induce targeted genetic modifications in zebrafish embryos with efficiencies similar to those obtained using zinc finger nucleases and transcription activator-like effector nucleases.
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