RESEARCH SUPPORT '; A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome View publications '; Genome-wide screening reveals the genetic basis of mammalian embryonic eye development View publications '; TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system View publications '; Investigating audible and ultrasonic noise in modern animal facilities View publications '; Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice View publications '; Mendelian gene identification through mouse embryo viability screening View publications '; TissUExM enables quantitative ultrastructural analysis in whole vertebrate embryos by expansion microscopy View publications '; Shift work-like patterns effect on female and male mouse behavior View publications '; Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities View publications '; A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning View publications
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