A series of Cre-ER drivers for manipulation of the skeletal muscle lineage
Genesis, ISSN: 1526-968X, Vol: 52, Issue: 8, Page: 759-770
2014
- 14Citations
- 38Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations14
- Citation Indexes14
- CrossRef14
- 11
- Captures38
- Readers38
- 38
Article Description
Summary: We report the generation of five mouse strains with the tamoxifen-inducible Cre (Cre-ER; CE) gene cassette knocked into the endogenous loci of Pax3, Myod1, Myog, Myf6, and Myl1, collectively as a resource for the skeletal muscle research community. We characterized these CE strains using the Cre reporter mice, R26R, during embryogenesis and show that they direct tightly controlled tamoxifen-inducible reporter expression within the expected cell lineage determined by each myogenic gene. We also examined a few selected adult skeletal muscle groups for tamoxifen-inducible reporter expression. None of these new CE alleles direct reporter expression in the cardiac muscle. All these alleles follow the same knock-in strategy by replacing the first exon of each gene with the CE cassette, rendering them null alleles of the endogenous gene. Advantages and disadvantages of this design are discussed. Although we describe potential immediate use of these strains, their utility likely extends beyond foreseeable questions in skeletal muscle biology. © 2014 Wiley Periodicals, Inc.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84904983731&origin=inward; http://dx.doi.org/10.1002/dvg.22792; http://www.ncbi.nlm.nih.gov/pubmed/24844572; https://onlinelibrary.wiley.com/doi/10.1002/dvg.22792; http://doi.wiley.com/10.1002/dvg.22792; http://onlinelibrary.wiley.com/doi/10.1002/dvg.22792/abstract
Wiley
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