RESEARCH SUPPORT

Loss of O-GlcNAcase catalytic activity leads to defects in mouse embryogenesis';

Loss of O-GlcNAcase catalytic activity leads to defects in mouse embryogenesis

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Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2';

Ap2s1 mutation causes hypercalcaemia in mice and impairs interaction between calcium-sensing receptor and adaptor protein-2

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Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring';

Maternal and offspring high-fat diet leads to platelet hyperactivation in male mice offspring

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A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits';

A novel knockout mouse for the small EDRK-rich factor 2 (Serf2) showing developmental and other deficits

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Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not';

Mylk3 null C57BL/6N mice develop cardiomyopathy, whereas Nnt null C57BL/6J mice do not

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Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13';

Protection Against XY Gonadal Sex Reversal by a Variant Region on Mouse Chromosome 13

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Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells';

Age-related changes in the biophysical and morphological characteristics of mouse cochlear outer hair cells

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Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism';

Studies of mice deleted for Sox3 and uc482: relevance to X-linked hypoparathyroidism

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Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function';

Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function

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Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations';

Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations

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