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Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 7, 2002
Novel phenotypes identified by plasma biochemical screening in the mouseTertius A Hough, Patrick M Nolan, Vicky Tsipouri, et al.Nature|November 23, 2018
Helios is a key transcriptional regulator of outer hair cell maturationLauren Chessum, Maggie S Matern, Michael C Kelly, et al.Genome Research|July 13, 1999
A high-density integrated genetic linkage and radiation hybrid map of the laboratory ratR G Steen, A E Kwitek-Black, C Glenn, et al.Current Biology : CB|March 11, 2008
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsMatthias Groszer, David A Keays, Robert M J Deacon, et al.Nature Communications|January 22, 2025
Myosin-based nucleation of actin filaments contributes to stereocilia development critical for hearingZane G Moreland, Fangfang Jiang, Carlos Aguilar, et al.The American Journal of Psychiatry|June 10, 1998
Genome scan of schizophreniaD F Levinson, M M Mahtani, D J Nancarrow, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 2004
A gene-driven ENU-based approach to generating an allelic series in any geneMohamed Mohideen Quwailid, Alison Hugill, Neil Dear, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 27, 2011
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutationChristopher T Esapa, Tertius A Hough, Sarah Testori, et al.Brain : a Journal of Neurology|October 29, 2014
Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysisSilvia Corrochano, Roope Männikkö, Peter I Joyce, et al.JBMR Plus|June 7, 2023
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith SyndromeKreepa G Kooblall, Mark Stevenson, Michelle Stewart, et al.Pageof 48