SMASH, a fragmentation and sequencing method for genomic copy number analysis.
Research Articles
A rapid chemical-genetic screen utilizing impaired movement phenotypes in C. elegans: Input into genetics of neurodevelopmental disorders.
The autism-linked UBE3AT485A mutant E3 ubiquitin ligase activates the Wnt/beta-catenin pathway by inhibiting the proteasome.
Developmental trajectories for young children with 16p11.2 copy number variation.
Hyperactivity and male-specific sleep deficits in the 16p11.2 deletion mouse model of autism.
Structures of neuroligin-1 and the neuroligin-1/neurexin-1 beta complex reveal specific protein-protein and protein-Ca2+ interactions.
Mice lacking the signaling molecule CalDAG-GEFI represent a model for leukocyte adhesion deficiency type III.
Correction of fragile X syndrome in mice.
Inhibition of p21-activated kinase rescues symptoms of fragile X syndrome in mice.
Ten_m3 regulates eye-specific patterning in the mammalian visual pathway and is required for binocular vision.
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