DEAFNESS

High-throughput mouse phenomics for characterizing mammalian gene function';

High-throughput mouse phenomics for characterizing mammalian gene function

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An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice';

An N-ethyl-N-nitrosourea (ENU)-induced Tyr265Stop mutation of the DNA polymerase accessory subunit gamma 2 (Polg2) is associated with renal calcification in mice

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Helios is a key transcriptional regulator of outer hair cell maturation';

Helios is a key transcriptional regulator of outer hair cell maturation

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A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways';

A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways

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Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy';

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy

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N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice';

N-ethyl-N-nitrosourea-Induced Adaptor Protein 2 Sigma Subunit 1 (Ap2s1) Mutations Establish Ap2s1 Loss-of-Function Mice

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Cinacalcet corrects hypercalcemia in mice with an inactivating Galpha11 mutation';

Cinacalcet corrects hypercalcemia in mice with an inactivating Galpha11 mutation

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A mutation in Nischarin causes otitis media via LIMK1 and NF-kappaB pathways';

A mutation in Nischarin causes otitis media via LIMK1 and NF-kappaB pathways

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Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair';

Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair

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Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing';

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing

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