DEAFNESS

Human and mouse essentiality screens as a resource for disease gene discovery';

Human and mouse essentiality screens as a resource for disease gene discovery

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

High-throughput mouse phenomics for characterizing mammalian gene function

View publications
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

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

Helios is a key transcriptional regulator of outer hair cell maturation

View publications
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

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

Gα11 mutation in mice causes hypocalcemia rectifiable by calcilytic therapy

View publications
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

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

Cinacalcet corrects hypercalcemia in mice with an inactivating Galpha11 mutation

View publications
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

View publications
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

View publications