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Genome Wide Conditional Mouse Knockout Resources.
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The mammalian gene function resource: the International Knockout Mouse Consortium.
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The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium.
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The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data.
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CRISPR-Cas9 enables conditional mutagenesis of challenging loci.
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Accessing data from the International Mouse Phenotyping Consortium: state of the art and future plans.
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BioMart as an integration solution for the International Knockout Mouse Consortium.
Database (Oxford). 2011 Sep 18;2011:bar028. doi: 10.1093/database/bar028. Print 2011.
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Utilising the resources of the International Knockout Mouse Consortium: the Australian experience.
Mamm Genome. 2015 Apr;26(3-4):142-53. doi: 10.1007/s00335-015-9555-1. Epub 2015 Feb 3.

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Advances in mouse genetics for the study of human disease.
Hum Mol Genet. 2021 Oct 1;30(R2):R274-R284. doi: 10.1093/hmg/ddab153.

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Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium.
Nat Genet. 2017 Aug;49(8):1231-1238. doi: 10.1038/ng.3901. Epub 2017 Jun 26.
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Generation of a multipurpose mouse allele by targeted gene trapping.
Dis Model Mech. 2017 Jul 1;10(7):909-922. doi: 10.1242/dmm.029561. Epub 2017 Apr 19.
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High-throughput discovery of novel developmental phenotypes.
Nature. 2016 Sep 22;537(7621):508-514. doi: 10.1038/nature19356. Epub 2016 Sep 14.
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CRISPR-Cas9 enables conditional mutagenesis of challenging loci.
Sci Rep. 2016 Sep 1;6:32326. doi: 10.1038/srep32326.
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Animal Models Are Valid to Uncover Disease Mechanisms.
PLoS Genet. 2016 May 26;12(5):e1006013. doi: 10.1371/journal.pgen.1006013. eCollection 2016 May.
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Using the mouse to model human disease: increasing validity and reproducibility.
Dis Model Mech. 2016 Feb;9(2):101-3. doi: 10.1242/dmm.024547.
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Development and applications of CRISPR-Cas9 for genome engineering.
Cell. 2014 Jun 5;157(6):1262-1278. doi: 10.1016/j.cell.2014.05.010.

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