Samaco RC - Search Results

1

Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.

Samaco RC, McGraw CM, Ward CS, Sun Y, Neul JL, Zoghbi HY. Samaco RC, et al. Hum Mol Genet. 2013 Jan 1;22(1):96-109. doi: 10.1093/hmg/dds406. Epub 2012 Oct 1. Hum Mol Genet. 2013. PMID: 23026749 Free PMC article.

2

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

3

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

4

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.

5

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.

6

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.

7

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.

8

Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.

Chao HT, Chen H, Samaco RC, Xue M, Chahrour M, Yoo J, Neul JL, Gong S, Lu HC, Heintz N, Ekker M, Rubenstein JL, Noebels JL, Rosenmund C, Zoghbi HY. Chao HT, et al. Among authors: samaco rc. Nature. 2010 Nov 11;468(7321):263-9. doi: 10.1038/nature09582. Nature. 2010. PMID: 21068835 Free PMC article.

9

Complexities of Rett syndrome and MeCP2.

Samaco RC, Neul JL. Samaco RC, et al. J Neurosci. 2011 Jun 1;31(22):7951-9. doi: 10.1523/JNEUROSCI.0169-11.2011. J Neurosci. 2011. PMID: 21632916 Free PMC article. Review. No abstract available.

10

Adult neural function requires MeCP2.

McGraw CM, Samaco RC, Zoghbi HY. McGraw CM, et al. Among authors: samaco rc. Science. 2011 Jul 8;333(6039):186. doi: 10.1126/science.1206593. Epub 2011 Jun 2. Science. 2011. PMID: 21636743 Free PMC article.

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