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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2006 | 1 |
2007 | 2 |
2008 | 2 |
2009 | 2 |
2024 | 0 |
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5 results
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Page 1
The Odyssey of MeCP2 and parental imprinting.
Epigenetics. 2007 Jan-Mar;2(1):5-10. doi: 10.4161/epi.2.1.3697. Epub 2006 Dec 12.
Epigenetics. 2007.
PMID: 17965611
Free PMC article.
Review.
Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions.
Maezawa I, Swanberg S, Harvey D, LaSalle JM, Jin LW.
Maezawa I, et al.
J Neurosci. 2009 Apr 22;29(16):5051-61. doi: 10.1523/JNEUROSCI.0324-09.2009.
J Neurosci. 2009.
PMID: 19386901
Free PMC article.
Item in Clipboard
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.
Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.
Swanberg SE, et al.
Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10.
Hum Mol Genet. 2009.
PMID: 19000991
Free PMC article.
Item in Clipboard
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.
Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM.
Yasui DH, et al.
Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19416-21. doi: 10.1073/pnas.0707442104. Epub 2007 Nov 27.
Proc Natl Acad Sci U S A. 2007.
PMID: 18042715
Free PMC article.
Item in Clipboard
MECP2 promoter methylation and X chromosome inactivation in autism.
Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM.
Nagarajan RP, et al.
Autism Res. 2008 Jun;1(3):169-78. doi: 10.1002/aur.24.
Autism Res. 2008.
PMID: 19132145
Free PMC article.
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