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Physiological Genomics|November 8, 2007
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant YodaIvana Barbaric, Mark J Perry, T Neil Dear, et al.
Plos One|April 11, 2015
N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse modelsChristopher T Esapa, Fadil M Hannan, Valerie N Babinsky, et al.
Plos One|December 14, 2016
Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling PathwayChristopher T Esapa, Sian E Piret, M Andrew Nesbit, et al.
Scientific Reports|January 2, 2020
Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic backgroundSara Falcone, Laura Wisby, Thomas Nicol, et al.
Genome Medicine|February 16, 2016
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repairJoffrey Mianné, Lauren Chessum, Saumya Kumar, et al.
Laboratory Animals|May 12, 2010
Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cagesMichael J Stechman, Bushra N Ahmad, Nellie Y Loh, et al.
The Journal of Pathology|November 20, 2008
An impending crisis in the provision of histopathology expertise for mouse functional genomicsM V Warren, M L Studley, P Dubus, et al.
Plos One|October 2, 2012
A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutationSian E Piret, Christopher T Esapa, Caroline M Gorvin, et al.
Human Molecular Genetics|April 4, 2002
Novel ENU-induced eye mutations in the mouse: models for human eye diseaseCaroline Thaung, Katrine West, Brian J Clark, et al.
The Journal of Physiology|November 5, 2020
Loss of Baiap2l2 destabilizes the transducing stereocilia of cochlear hair cells and leads to deafnessAdam J Carlton, Julia Halford, Anna Underhill, et al.
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