HARWELL MICE

Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout';

Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout

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Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations';

Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations

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A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice';

A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice

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Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice';

Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice

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Cysteine-lowering treatment with mesna against obesity: Proof of concept and results from a human phase I, dose-finding study';

Cysteine-lowering treatment with mesna against obesity: Proof of concept and results from a human phase I, dose-finding study

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Tissue specific differences in the assembly of mitochondrial complex I is revealed by a novel ENU mutation in ECSIT';

Tissue specific differences in the assembly of mitochondrial complex I is revealed by a novel ENU mutation in ECSIT

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Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice';

Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice

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Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock';

Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock

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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';

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';

Genotyping Genome-Edited Founders and Subsequent Generation

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