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http://purl.uniprot.org/citations/31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/31037730http://www.w3.org/2000/01/rdf-schema#comment"The CRISPR-Cas9 technology has been a powerful means to manipulate the genome in a wide range of organisms. A series of GFP knocked-in (GFPKI ) Drosophila strains have been generated through CRISPR-Cas9-induced double strand breaks coupled with homology-directed repairs in the presence of donor plasmids. They visualized specific cell types or intracellular structures in both fixed and live specimen. We provide a rapid and efficient strategy to identify KI lines. This method requires neither co-integration of a selection marker nor prior establishment of sgRNA-expressing transgenic lines. The injection of the mixture of a sgRNA/Cas9 expression plasmid and a donor plasmid into cleavage stage embryos efficiently generated multiple independent KI lines. A PCR-based selection allows to identify KI fly lines at the F1 generation (approximately 4 weeks after injection). These GFPKI strains have been deposited in the Kyoto Drosophila stock center, and made freely available to researchers at non-profit organizations. Thus, they will be useful resources for Drosophila research."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.org/dc/terms/identifier"doi:10.1111/dgd.12607"xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/author"Nakamura A."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/author"Hanyu-Nakamura K."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/author"Yoshitani T."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/author"Kina H."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/name"Dev Growth Differ"xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/pages"265-275"xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/title"Rapid and efficient generation of GFP-knocked-in Drosophila by the CRISPR-Cas9-mediated genome editing."xsd:string
http://purl.uniprot.org/citations/31037730http://purl.uniprot.org/core/volume"61"xsd:string
http://purl.uniprot.org/citations/31037730http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/31037730
http://purl.uniprot.org/citations/31037730http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/31037730
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http://purl.uniprot.org/uniprot/#_O18409-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730
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http://purl.uniprot.org/uniprot/#_M9PBB5-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730
http://purl.uniprot.org/uniprot/#_P25823-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730
http://purl.uniprot.org/uniprot/#_M9PDB0-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730
http://purl.uniprot.org/uniprot/#_O76922-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730
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http://purl.uniprot.org/uniprot/#_Q960Z4-mappedCitation-31037730http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/31037730