RESEARCH SUPPORT

Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities';

Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities

View publications
A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning';

A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning

View publications
ALS-related FUS mutations alter axon growth in motoneurons and affect HuD/ELAVL4 and FMRP activity';

ALS-related FUS mutations alter axon growth in motoneurons and affect HuD/ELAVL4 and FMRP activity

View publications
Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen';

Identifying genetic determinants of inflammatory pain in mice using a large-scale gene-targeted screen

View publications
Gadd45g is required for timely Sry expression independently of RSPO1 activity';

Gadd45g is required for timely Sry expression independently of RSPO1 activity

View publications
AKR1D1 knockout mice develop a sex dependent metabolic phenotype';

AKR1D1 knockout mice develop a sex dependent metabolic phenotype

View publications
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

View publications
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

View publications
Palmitoylated small GTPase ARL15 is translocated within Golgi network during adipogenesis';

Palmitoylated small GTPase ARL15 is translocated within Golgi network during adipogenesis

View publications
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

View publications