RESEARCH SUPPORT

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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Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of down syndrome-related phenotypes';

Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of down syndrome-related phenotypes

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Linking the FTO obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo';

Linking the FTO obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo

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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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