HARWELL MICE

Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock';

Dynamic modulation of genomic enhancer elements in the suprachiasmatic nucleus, the site of the mammalian circadian clock

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A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome';

A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome

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Genotyping Genome-Edited Founders and Subsequent Generation';

Genotyping Genome-Edited Founders and Subsequent Generation

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Excess of guide RNA reduces knockin efficiency and drastically increases on-target large deletions';

Excess of guide RNA reduces knockin efficiency and drastically increases on-target large deletions

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Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington’s disease';

Longitudinal home-cage automated assessment of climbing behavior shows sexual dimorphism and aging-related decrease in C57BL/6J healthy mice and allows early detection of motor impairment in the N171-82Q mouse model of Huntington’s disease

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TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system';

TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system

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Investigating audible and ultrasonic noise in modern animal facilities';

Investigating audible and ultrasonic noise in modern animal facilities

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Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes';

Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes

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The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease';

The International Mouse Phenotyping Consortium: comprehensive knockout phenotyping underpinning the study of human disease

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Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice';

Early embryonic lethality in complex I associated p.L104P Nubpl mutant mice

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