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Neuroligins determine synapse maturation and function
Neuron 51 (6), 741 (2006)
"his is a landmark paper showing that neuroligins are essential for synapse function in vivo. Although individual neuroligin knockout mice are viable, Nlgn1;Nlgn2;Nlgn3 triple knockout mice die at birth owing to respiratory failure. Their synapses seem to be morphologically normal, but transmission was dramatically reduced at GABAergic/glycinergic synapses, and also reduced at glutamatergic synapses, in the brainstem. This was accompanied by reduced clustering of GABAA receptors, reduced levels of synaptic vesicle proteins and a slight reduction in the ratio of VGAT puncta to VGlut puncta, but clustering of the scaffolding proteins PSD-95 and gephyrin was normal."
Current Opinion in Neurobiology 17 (1), 43 (2007)
Neurosci Lett, (09 Oct 2006)
4/203 (only in about 2% of cases) vs. 0/535, P=0.0056
Trends in neurosciences. 29 (1), 21-9 (Jan 2006)
The Journal of neuroscience : the official journal of the Society for Neuroscience. 26 (16), 4256-65 (19 Apr 2006)
Neuron. 48 (2), 229-36 (20 Oct 2005)
Cell 119 (7), 1013-26 (29 Dec 2004)
The Journal of biological chemistry. 280 (23), 22365-74 (10 Jun 2005)
Cell Mol Life Sci, (23 Jun 2006)
Nature neuroscience. 6 (7), 708-16 (Jul 2003)
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