JOURN

Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy';

Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

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An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation';

An animal model for Pierpont syndrome: a mouse bearing the Tbl1xr1Y446C/Y446C mutation

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An Improved Method for Growing Primary Neurons on Electron Microscopy Grids Co-Cultured with Astrocytes';

An Improved Method for Growing Primary Neurons on Electron Microscopy Grids Co-Cultured with Astrocytes

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A method for TAT-Cre recombinase-mediated floxed allele modification in ex vivo tissue slices';

A method for TAT-Cre recombinase-mediated floxed allele modification in ex vivo tissue slices

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The parenting hub of the hypothalamus is a focus of imprinted gene action';

The parenting hub of the hypothalamus is a focus of imprinted gene action

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Absence of Embigin accelerates hearing loss and causes sub-viability, brain and heart defects in C57BL/6N mice due to interaction with Cdh23(ahl)';

Absence of Embigin accelerates hearing loss and causes sub-viability, brain and heart defects in C57BL/6N mice due to interaction with Cdh23(ahl)

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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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