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Current Biology : CB|July 5, 2003
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouseJohn A Curtin, Elizabeth Quint, Vicky Tsipouri, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 14, 2011
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imagingAngelo Karunaratne, Christopher R Esapa, Jennifer Hiller, et al.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.Pageof 48