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Schick, J. ; Seisenberger, C. ; Beig, J. ; Bürger, A. ; Iyer, V.* ; Maier, V. ; Perera, S.* ; Rosen, B.* ; Skarnes, W.C.* ; Wurst, W.

CRISPR-Cas9 enables conditional mutagenesis of challenging loci.

Sci. Rep. 6:32326 (2016)
Publ. Version/Full Text Research data DOI PMC
Open Access Gold
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The International Knockout Mouse Consortium (IKMC) has produced a genome-wide collection of 15,000 isogenic targeting vectors for conditional mutagenesis in C57BL/6N mice. Although most of the vectors have been used successfully in murine embryonic stem (ES) cells, there remain a set of nearly two thousand genes that have failed to target even after several attempts. Recent attention has turned to the use of new genome editing technology for the generation of mutant alleles in mice. Here, we demonstrate how Cas9-assisted targeting can be combined with the IKMC targeting vector resource to generate conditional alleles in genes that have previously eluded targeting using conventional methods.
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Publication type Article: Journal article
Document type Scientific Article
Keywords One-step Generation; Homologous Recombination; Gene-function; Genome; Cas9; Consortium; Resource; System
Language english
Publication Year 2016
HGF-reported in Year 2016
ISSN (print) / ISBN 2045-2322
e-ISSN 2045-2322
Quellenangaben Volume: 6, Issue: , Pages: , Article Number: 32326 Supplement: ,
Publisher Nature Publishing Group
Publishing Place London
Reviewing status Peer reviewed
POF-Topic(s) 30204 - Cell Programming and Repair
30203 - Molecular Targets and Therapies
Research field(s) Genetics and Epidemiology
Enabling and Novel Technologies
PSP Element(s) G-500500-001
G-505200-001
PubMed ID 27580957
Scopus ID 84984868418
Erfassungsdatum 2016-09-05