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Items: 3

1.
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
E Maestrini, A T Pagnamenta, J A Lamb, E Bacchelli, N H Sykes, I Sousa, C Toma, G Barnby, H Butler, L Winchester, T S Scerri, F Minopoli, J Reichert, G Cai, J D Buxbaum, O Korvatska, G D Schellenberg, G Dawson, A de Bildt, R B Minderaa, E J Mulder, A P Morris, A J Bailey, A P Monaco, IMGSAC
Mol Psychiatry. 2010 Sep; 15(9): 954–968. Published online 2009 Apr 28. doi: 10.1038/mp.2009.34
PMCID:
PMC2934739
AbstractArticlePDF–376K
2.
Disruption of a Novel Gene (IMMP2L) by a Breakpoint in 7q31 Associated with Tourette Syndrome
Erwin Petek, Christian Windpassinger, John B. Vincent, Joseph Cheung, Andrew P. Boright, Stephen W. Scherer, Peter M. Kroisel, Klaus Wagner
Am J Hum Genet. 2001 Apr; 68(4): 848–858. Published online 2001 Mar 9. doi: 10.1086/319523
PMCID:
PMC1275638
AbstractArticlePDF–4.9M
3.
Mature DIABLO/Smac Is Produced by the IMP Protease Complex on the Mitochondrial Inner Membrane
Lena Burri, Yvan Strahm, Christine J. Hawkins, Ian E. Gentle, Michelle A. Puryer, Anne Verhagen, Bernard Callus, David Vaux, Trevor Lithgow
Mol Biol Cell. 2005 Jun; 16(6): 2926–2933. doi: 10.1091/mbc.E04-12-1086
PMCID:
PMC1142436
AbstractArticlePDF–473K

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