Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes

Six genes in the 1.5 Mb region of chromosome 22 deleted in DiGeorge/22q11 deletion syndrome– Mrpl40, Prodh, Slc25a1, Txnrd2, T10, and Zdhhc8–encode mitochondrial proteins. All six genes are expressed in the brain, and maximal expression coincides with peak forebrain synaptogenesis shortly after birt...

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Veröffentlicht in:	Molecular and cellular neuroscience 2008-10, Vol.39 (3), p.439-451
Hauptverfasser:	Maynard, T.M., Meechan, D.W., Dudevoir, M.L., Gopalakrishna, D., Peters, A.Z., Heindel, C.C., Sugimoto, T.J., Wu, Y., Lieberman, J.A., LaMantia, A.-S.
Format:	Artikel
Sprache:	eng
Schlagworte:	Acyltransferases - genetics Acyltransferases - metabolism Animals Brain - cytology Brain - metabolism Cells, Cultured Chromosome Deletion Chromosomes, Human, Pair 22 - genetics Computational Biology DiGeorge Syndrome - genetics Fibroblasts - cytology Fibroblasts - physiology Humans Membrane Proteins - genetics Membrane Proteins - metabolism Mice Mitochondria - genetics Mitochondria - metabolism Mitochondrial Proteins - genetics Mitochondrial Proteins - metabolism Recombinant Fusion Proteins - genetics Recombinant Fusion Proteins - metabolism Synapses - metabolism Two-Hybrid System Techniques
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