Samaco RC - 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. Nat Genet. 2012 Jan 8;44(2):206-11. doi: 10.1038/ng.1066. Nat Genet. 2012. PMID: 22231481 Free PMC article.

2

MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

Balmer D, Arredondo J, Samaco RC, LaSalle JM. Balmer D, et al. Among authors: samaco rc. Hum Genet. 2002 Jun;110(6):545-52. doi: 10.1007/s00439-002-0724-4. Epub 2002 Apr 25. Hum Genet. 2002. PMID: 12107440

3

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders.

Samaco RC, Nagarajan RP, Braunschweig D, LaSalle JM. Samaco RC, et al. Hum Mol Genet. 2004 Mar 15;13(6):629-39. doi: 10.1093/hmg/ddh063. Epub 2004 Jan 20. Hum Mol Genet. 2004. PMID: 14734626

4

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

Braunschweig D, Simcox T, Samaco RC, LaSalle JM. Braunschweig D, et al. Among authors: samaco rc. Hum Mol Genet. 2004 Jun 15;13(12):1275-86. doi: 10.1093/hmg/ddh142. Epub 2004 Apr 28. Hum Mol Genet. 2004. PMID: 15115765

5

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

Samaco RC, Hogart A, LaSalle JM. Samaco RC, et al. Hum Mol Genet. 2005 Feb 15;14(4):483-92. doi: 10.1093/hmg/ddi045. Epub 2004 Dec 22. Hum Mol Genet. 2005. PMID: 15615769 Free PMC article.

6

Duplication of Atxn1l suppresses SCA1 neuropathology by decreasing incorporation of polyglutamine-expanded ataxin-1 into native complexes.

Bowman AB, Lam YC, Jafar-Nejad P, Chen HK, Richman R, Samaco RC, Fryer JD, Kahle JJ, Orr HT, Zoghbi HY. Bowman AB, et al. Among authors: samaco rc. Nat Genet. 2007 Mar;39(3):373-9. doi: 10.1038/ng1977. Epub 2007 Feb 18. Nat Genet. 2007. PMID: 17322884

7

A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome.

Samaco RC, Fryer JD, Ren J, Fyffe S, Chao HT, Sun Y, Greer JJ, Zoghbi HY, Neul JL. Samaco RC, et al. Hum Mol Genet. 2008 Jun 15;17(12):1718-27. doi: 10.1093/hmg/ddn062. Epub 2008 Mar 4. Hum Mol Genet. 2008. PMID: 18321864 Free PMC article.

8

miR-19, miR-101 and miR-130 co-regulate ATXN1 levels to potentially modulate SCA1 pathogenesis.

Lee Y, Samaco RC, Gatchel JR, Thaller C, Orr HT, Zoghbi HY. Lee Y, et al. Among authors: samaco rc. Nat Neurosci. 2008 Oct;11(10):1137-9. doi: 10.1038/nn.2183. Epub 2008 Aug 31. Nat Neurosci. 2008. PMID: 18758459 Free PMC article.

9

Deletion of Mecp2 in Sim1-expressing neurons reveals a critical role for MeCP2 in feeding behavior, aggression, and the response to stress.

Fyffe SL, Neul JL, Samaco RC, Chao HT, Ben-Shachar S, Moretti P, McGill BE, Goulding EH, Sullivan E, Tecott LH, Zoghbi HY. Fyffe SL, et al. Among authors: samaco rc. Neuron. 2008 Sep 25;59(6):947-58. doi: 10.1016/j.neuron.2008.07.030. Neuron. 2008. PMID: 18817733 Free PMC article.

10

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.

Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL. Samaco RC, et al. Proc Natl Acad Sci U S A. 2009 Dec 22;106(51):21966-71. doi: 10.1073/pnas.0912257106. Epub 2009 Dec 9. Proc Natl Acad Sci U S A. 2009. PMID: 20007372 Free PMC article.

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