Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout
Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations
A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice
Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice
Cysteine-lowering treatment with mesna against obesity: Proof of concept and results from a human phase I, dose-finding study
Tissue specific differences in the assembly of mitochondrial complex I is revealed by a novel ENU mutation in ECSIT
Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock
A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
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