Results 21 to 30 of about 4,242,968 (247)

Dynamic Genome Editing Using In Vivo Synthesized Donor ssDNA in Escherichia coli

open access: yesCells, 2020
As a key element of genome editing, donor DNA introduces the desired exogenous sequence while working with other crucial machinery such as CRISPR-Cas or recombinases.
Min Hao   +5 more
doaj   +1 more source

Undesignable RNA Structure Identification via Rival Structure Generation and Structure Decomposition [PDF]

open access: yesInternational Conference on Research in Computational Molecular Biology, pp. 270-287. Cham: Springer Nature Switzerland, 2024, 2023
RNA design is the search for a sequence or set of sequences that will fold into predefined structures, also known as the inverse problem of RNA folding. While numerous RNA design methods have been invented to find sequences capable of folding into a target structure, little attention has been given to the identification of undesignable structures ...
arxiv   +1 more source

Mechanistic Insights into Archaeal and Human Argonaute Substrate Binding and Cleavage Properties. [PDF]

open access: yesPLoS ONE, 2016
Argonaute (Ago) proteins from all three domains of life are key players in processes that specifically regulate cellular nucleic acid levels.
Sarah Willkomm   +3 more
doaj   +1 more source

Structural basis for sequence-specific recognition of guide and target strands by the Archaeoglobus fulgidus Argonaute protein

open access: yesScientific Reports, 2023
Argonaute (Ago) proteins are found in all three domains of life. The best-characterized group is eukaryotic Argonautes (eAgos). Being the structural core of RNA interference machinery, they use guide RNA molecules for RNA targeting.
Elena Manakova   +6 more
doaj   +1 more source

CRISPR guides induce gene silencing in plants in the absence of Cas

open access: yesGenome Biology, 2022
Background RNA-targeting CRISPR-Cas can provide potential advantages over DNA editing, such as avoiding pleiotropic effects of genome editing, providing precise spatiotemporal regulation, and expanded function including antiviral immunity.
Veerendra Kumar Sharma   +7 more
doaj   +1 more source

Evaluation of off-target and on-target scoring algorithms and integration into the guide RNA selection tool CRISPOR

open access: yesGenome Biology, 2016
BackgroundThe success of the CRISPR/Cas9 genome editing technique depends on the choice of the guide RNA sequence, which is facilitated by various websites.
M. Haeussler   +11 more
semanticscholar   +1 more source

Structural insights into RNA processing by the human RISC-loading complex. [PDF]

open access: yes, 2009
Targeted gene silencing by RNA interference (RNAi) requires loading of a short guide RNA (small interfering RNA (siRNA) or microRNA (miRNA)) onto an Argonaute protein to form the functional center of an RNA-induced silencing complex (RISC).
AD Haase   +41 more
core   +2 more sources

Massively parallel Cas13 screens reveal principles for guide RNA design

open access: yesNature Biotechnology, 2020
Type VI CRISPR enzymes are RNA-targeting proteins with nuclease activity that enable specific and robust target gene knockdown without altering the genome.
H. Wessels   +5 more
semanticscholar   +1 more source

CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites

open access: yesBioinform., 2014
Summary: CRISPRdirect is a simple and functional web server for selecting rational CRISPR/Cas targets from an input sequence. The CRISPR/Cas system is a promising technique for genome engineering which allows target-specific cleavage of genomic DNA ...
Y. Naito   +3 more
semanticscholar   +1 more source

High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity [PDF]

open access: yes, 2013
The RNA-programmable Cas9 endonuclease cleaves double-stranded DNA at sites complementary to a 20-base-pair guide RNA. The Cas9 system has been used to modify genomes in multiple cells and organisms, demonstrating its potential as a facile genome ...
D Hockemeyer   +26 more
core   +1 more source

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