Shaw CA - Search Results

1

Crh and Oprm1 mediate anxiety-related behavior and social approach in a mouse model of MECP2 duplication syndrome.

Samaco RC, Mandel-Brehm C, McGraw CM, Shaw CA, McGill BE, Zoghbi HY. Samaco RC, et al. Among authors: shaw ca. Nat Genet. 2012 Jan 8;44(2):206-11. doi: 10.1038/ng.1066. Nat Genet. 2012. PMID: 22231481 Free PMC article.

2

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.

Lim J, Hao T, Shaw C, Patel AJ, Szabó G, Rual JF, Fisk CJ, Li N, Smolyar A, Hill DE, Barabási AL, Vidal M, Zoghbi HY. Lim J, et al. Cell. 2006 May 19;125(4):801-14. doi: 10.1016/j.cell.2006.03.032. Cell. 2006. PMID: 16713569 Free article.

3

Lithium therapy improves neurological function and hippocampal dendritic arborization in a spinocerebellar ataxia type 1 mouse model.

Watase K, Gatchel JR, Sun Y, Emamian E, Atkinson R, Richman R, Mizusawa H, Orr HT, Shaw C, Zoghbi HY. Watase K, et al. PLoS Med. 2007 May;4(5):e182. doi: 10.1371/journal.pmed.0040182. PLoS Med. 2007. PMID: 17535104 Free PMC article.

4

The insulin-like growth factor pathway is altered in spinocerebellar ataxia type 1 and type 7.

Gatchel JR, Watase K, Thaller C, Carson JP, Jafar-Nejad P, Shaw C, Zu T, Orr HT, Zoghbi HY. Gatchel JR, et al. Proc Natl Acad Sci U S A. 2008 Jan 29;105(4):1291-6. doi: 10.1073/pnas.0711257105. Epub 2008 Jan 23. Proc Natl Acad Sci U S A. 2008. PMID: 18216249 Free PMC article.

5

MeCP2, a key contributor to neurological disease, activates and represses transcription.

Chahrour M, Jung SY, Shaw C, Zhou X, Wong ST, Qin J, Zoghbi HY. Chahrour M, et al. Science. 2008 May 30;320(5880):1224-9. doi: 10.1126/science.1153252. Science. 2008. PMID: 18511691 Free PMC article.

6

Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching.

Carvalho CM, Zhang F, Liu P, Patel A, Sahoo T, Bacino CA, Shaw C, Peacock S, Pursley A, Tavyev YJ, Ramocki MB, Nawara M, Obersztyn E, Vianna-Morgante AM, Stankiewicz P, Zoghbi HY, Cheung SW, Lupski JR. Carvalho CM, et al. Among authors: shaw c. Hum Mol Genet. 2009 Jun 15;18(12):2188-203. doi: 10.1093/hmg/ddp151. Epub 2009 Mar 26. Hum Mol Genet. 2009. PMID: 19324899 Free PMC article.

7

Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.

Ben-Shachar S, Chahrour M, Thaller C, Shaw CA, Zoghbi HY. Ben-Shachar S, et al. Among authors: shaw ca. Hum Mol Genet. 2009 Jul 1;18(13):2431-42. doi: 10.1093/hmg/ddp181. Epub 2009 Apr 15. Hum Mol Genet. 2009. PMID: 19369296 Free PMC article.

8

Partial loss of ataxin-1 function contributes to transcriptional dysregulation in spinocerebellar ataxia type 1 pathogenesis.

Crespo-Barreto J, Fryer JD, Shaw CA, Orr HT, Zoghbi HY. Crespo-Barreto J, et al. Among authors: shaw ca. PLoS Genet. 2010 Jul 8;6(7):e1001021. doi: 10.1371/journal.pgen.1001021. PLoS Genet. 2010. PMID: 20628574 Free PMC article.

9

Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia.

Kahle JJ, Gulbahce N, Shaw CA, Lim J, Hill DE, Barabási AL, Zoghbi HY. Kahle JJ, et al. Among authors: shaw ca. Hum Mol Genet. 2011 Feb 1;20(3):510-27. doi: 10.1093/hmg/ddq496. Epub 2010 Nov 15. Hum Mol Genet. 2011. PMID: 21078624 Free PMC article.

10

Protein interactome reveals converging molecular pathways among autism disorders.

Sakai Y, Shaw CA, Dawson BC, Dugas DV, Al-Mohtaseb Z, Hill DE, Zoghbi HY. Sakai Y, et al. Among authors: shaw ca. Sci Transl Med. 2011 Jun 8;3(86):86ra49. doi: 10.1126/scitranslmed.3002166. Sci Transl Med. 2011. PMID: 21653829 Free PMC article.

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