Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
about
A Combination of CRISPR/Cas9 and Standardized RNAi as a Versatile Platform for the Characterization of Gene Function.Advances and perspectives in the application of CRISPR/Cas9 in insectsHeritable CRISPR/Cas9-mediated genome editing in the yellow fever mosquito, Aedes aegypti.Gene-specific cell labeling using MiMIC transposons.Systematic Evaluation of Drosophila CRISPR Tools Reveals Safe and Robust Alternatives to Autonomous Gene Drives in Basic Research.piRNA-guided slicing of transposon transcripts enforces their transcriptional silencing via specifying the nuclear piRNA repertoire.High-throughput genotyping of CRISPR/Cas9-mediated mutants using fluorescent PCR-capillary gel electrophoresis.Silencio/CG9754 connects the Piwi-piRNA complex to the cellular heterochromatin machinery.Genome engineering: Drosophila melanogaster and beyondRab8 directs furrow ingression and membrane addition during epithelial formation in Drosophila melanogaster.Rapid Screening for CRISPR-Directed Editing of the Drosophila Genome Using white Coconversion.Linear ubiquitination by LUBEL has a role in Drosophila heat stress response.Genetic and mechanistic diversity of piRNA 3'-end formation.Recent Advances in CRISPR-Cas9 Genome Editing Technology for Biological and Biomedical Investigations.Genome editing in Drosophila melanogaster: from basic genome engineering to the multipurpose CRISPR-Cas9 system.CRISPR/Cas9 Targets Chicken Embryonic Somatic Cells In Vitro and In Vivo and generates Phenotypic Abnormalities.Progress and Prospects of CRISPR/Cas Systems in Insects and Other Arthropods.Planar polarized Rab35 functions as an oscillatory ratchet during cell intercalation in the Drosophila epithelium.A versatile two-step CRISPR- and RMCE-based strategy for efficient genome engineering in Drosophila.Gene Tagging Strategies To Assess Protein Expression, Localization, and Function in Drosophila.A heterochromatin-dependent transcription machinery drives piRNA expression.The postsynaptic t-SNARE Syntaxin 4 controls traffic of Neuroligin 1 and Synaptotagmin 4 to regulate retrograde signaling.Highly Efficient Site-Specific Mutagenesis in Malaria Mosquitoes Using CRISPR.The tumor suppressor Brat controls neuronal stem cell lineages by inhibiting Deadpan and Zelda.The splicing co-factor Barricade/Tat-SF1 is required for cell cycle and lineage progression in Drosophila neural stem cells.Notum coordinates synapse development via extracellular regulation of Wingless trans-synaptic signaling.An alternatively spliced form affecting the Marked Box domain of Drosophila E2F1 is required for proper cell cycle regulation.Cell-type specific sequencing of microRNAs from complex animal tissues.The contribution of mutant GBA to the development of Parkinson disease in Drosophila.The asymmetrically segregating lncRNA cherub is required for transforming stem cells into malignant cells.CRISPR/Cas9 mediated high efficiency knockout of the eye color gene Vermillion in Helicoverpa zea (Boddie).
P2860
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P2860
Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
description
2014 nî lūn-bûn
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2014年の論文
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2014年論文
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2014年論文
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2014年論文
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name
Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
@en
type
label
Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
@en
prefLabel
Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
@en
P2093
P2860
P356
P1433
P1476
Efficient CRISPR/Cas9 plasmids for rapid and versatile genome editing in Drosophila
@en
P2093
Grzegorz Sienski
Joseph Gokcezade
Peter Duchek
P2860
P304
P356
10.1534/G3.114.014126
P577
2014-09-17T00:00:00Z