Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations
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Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice
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Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice
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A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome
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Genotyping Genome-Edited Founders and Subsequent Generation
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Excess of guide RNA reduces knockin efficiency and drastically increases on-target large deletions
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Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington’s disease
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Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
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TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
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