Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 3 |
2009 | 1 |
2010 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
Page 1
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Nature. 2010 Nov 11;468(7321):263-9. doi: 10.1038/nature09582.
Nature. 2010.
PMID: 21068835
Free PMC article.
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.
Item in Clipboard
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.
Neuron. 2008 Sep 25;59(6):947-58. doi: 10.1016/j.neuron.2008.07.030.
Neuron. 2008.
PMID: 18817733
Free PMC article.
Item in Clipboard
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
Neul JL, Fang P, Barrish J, Lane J, Caeg EB, Smith EO, Zoghbi H, Percy A, Glaze DG.
Neul JL, et al.
Neurology. 2008 Apr 15;70(16):1313-21. doi: 10.1212/01.wnl.0000291011.54508.aa. Epub 2008 Mar 12.
Neurology. 2008.
PMID: 18337588
Free PMC article.
Item in Clipboard
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.
Item in Clipboard
Cite
Cite