HARWELL MICE

Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation';

Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation

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Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing';

Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearing

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A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background';

A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background

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Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C';

Broad-spectrum XX and XY gonadal dysgenesis in patients with a homozygous L193S variant in PPP2R3C

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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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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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