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Plos Genetics|August 15, 2017
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathwaysMichael Crompton, Tom Purnell, Hayley E Tyrer, et al.
Cell Reports|December 20, 2018
A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response PathwaysThomas Agnew, Michelle Goldsworthy, Carlos Aguilar, et al.
Nucleic Acids Research|November 26, 2009
EuroPhenome: a repository for high-throughput mouse phenotyping dataHugh Morgan, Tim Beck, Andrew Blake, et al.
Scientific Reports|June 29, 2016
Mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M) and serine biosynthetic pathway genes are co-ordinately increased during anabolic agent-induced skeletal muscle growthD M Brown, H Williams, K J P Ryan, et al.
Plos Genetics|October 13, 2006
Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis mediaNicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, et al.
Endocrinology|December 5, 2013
An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excessLiz Bentley, Christopher T Esapa, M Andrew Nesbit, et al.
Cell Death Discovery|August 2, 2022
Human-specific gene CT47 blocks PRMT5 degradation to lead to meiosis arrestChao Li, Yuming Feng, Zhenxin Fu, et al.
Plos Genetics|February 6, 2013
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutationsKatherine R Bull, Andrew J Rimmer, Owen M Siggs, et al.
Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.
Genome Research|September 15, 2004
Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouseAnn-Marie Mallon, Laurens Wilming, Joseph Weekes, et al.
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