MLC '; Fam151b, the mouse homologue of C.elegans menorin gene, is essential for retinal function View publications '; Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations View publications '; Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities View publications '; Male mice lacking ADAMTS-16 are fertile but exhibit testes of reduced weight View publications '; Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons View publications '; The development of a high throughput drug-responsive model of white adipose tissue comprising adipogenic 3T3-L1 cells in a 3D matrix View publications '; Mice With a Brd4 Mutation Represent a New Model of Nephrocalcinosis View publications '; Clarin-2 is essential for hearing by maintaining stereocilia integrity and function View publications '; Manipulation of dipeptidylpeptidase 10 in mouse and human in vivo and in vitro models indicates a protective role in asthma View publications '; Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration View publications
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