MLC

Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout';

Cleft palate and minor metabolic disturbances in a mouse global Arl15 gene knockout

View publications
Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations';

Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations

View publications
Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice';

Spi1 R235C point mutation confers hypersensitivity to radiation-induced acute myeloid leukemia in mice

View publications
Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice';

Comprehensive ECG reference intervals in C57BL/6N substrains provide a generalizable guide for cardiac electrophysiology studies in mice

View publications
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

View publications
Genotyping Genome-Edited Founders and Subsequent Generation';

Genotyping Genome-Edited Founders and Subsequent Generation

View publications
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

View publications
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

View publications
Genome-wide screening reveals the genetic basis of mammalian embryonic eye development';

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

View publications
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

View publications