GEN

Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice';

Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in ‘FUSDelta14’ knockin mice

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Mutant mice with calcium-sensing receptor (CaSR) activation have hyperglycemia, that is rectified by calcilytic therapy';

Mutant mice with calcium-sensing receptor (CaSR) activation have hyperglycemia, that is rectified by calcilytic therapy

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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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Genetic Analyses Reveal Functions for MAP2K3 and MAP2K6 in Mouse Testis Determination';

Genetic Analyses Reveal Functions for MAP2K3 and MAP2K6 in Mouse Testis Determination

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Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration';

Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration

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Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy';

Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy

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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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Exploring the Lean Phenotype of Glutathione-Depleted Mice: Thiol, Amino Acid and Fatty Acid Profiles';

Exploring the Lean Phenotype of Glutathione-Depleted Mice: Thiol, Amino Acid and Fatty Acid Profiles

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Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway';

Mice with an N-Ethyl-N-Nitrosourea (ENU) Induced Tyr209Asn Mutation in Natriuretic Peptide Receptor 3 (NPR3) Provide a Model for Kyphosis Associated with Activation of the MAPK Signaling Pathway

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