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Results by year

Year	Number of Results
1990	1
1992	3
1993	3
1994	1
1995	1
1996	4
1997	5
1998	6
1999	6
2000	17
2001	24
2002	32
2003	33
2004	26
2005	40
2006	51
2007	57
2008	60
2009	82
2010	78
2011	73
2012	92
2013	61
2014	6
2019	1
2020	1
2021	1
2024	0

671 results

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Page 1

Loss of MeCP2 from forebrain excitatory neurons leads to cortical hyperexcitation and seizures.

Zhang W, Peterson M, Beyer B, Frankel WN, Zhang ZW. Zhang W, et al. J Neurosci. 2014 Feb 12;34(7):2754-63. doi: 10.1523/JNEUROSCI.4900-12.2014. J Neurosci. 2014. PMID: 24523563 Free PMC article.

Adolescent onset cognitive regression and neuropsychiatric symptoms associated with the A140V MECP2 mutation.

Venkateswaran S, McMillan HJ, Doja A, Humphreys P. Venkateswaran S, et al. Dev Med Child Neurol. 2014 Jan;56(1):91-4. doi: 10.1111/dmcn.12334. Epub 2013 Nov 15. Dev Med Child Neurol. 2014. PMID: 24328834 Free article.

[Subchromosomal microdeletion identified by molecular karyotyping using DNA microarrays (array CGH) in Rett syndrome girls negative for MECP2 gene mutations].

Vorsanova SG, Iurov IIu, Voinova VIu, Kurinnaia OS, Zelenova MA, Demidova IA, Ulas EV, Iurov IuB. Vorsanova SG, et al. Zh Nevrol Psikhiatr Im S S Korsakova. 2013;113(10):63-8. Zh Nevrol Psikhiatr Im S S Korsakova. 2013. PMID: 24300809 Russian.

Oligodendrocyte lineage cells contribute unique features to Rett syndrome neuropathology.

Nguyen MV, Felice CA, Du F, Covey MV, Robinson JK, Mandel G, Ballas N. Nguyen MV, et al. J Neurosci. 2013 Nov 27;33(48):18764-74. doi: 10.1523/JNEUROSCI.2657-13.2013. J Neurosci. 2013. PMID: 24285883 Free PMC article.

De novo MECP2 duplication derived from paternal germ line result in dysmorphism and developmental delay.

Lin DS, Chuang TP, Chiang MF, Ho CS, Hsiao CD, Huang YW, Wu TY, Wu JY, Chen YT, Chen TC, Li LH. Lin DS, et al. Gene. 2014 Jan 1;533(1):78-85. doi: 10.1016/j.gene.2013.10.001. Epub 2013 Oct 12. Gene. 2014. PMID: 24129071

Leptin resistance and obesity in mice with deletion of methyl-CpG-binding protein 2 (MeCP2) in hypothalamic pro-opiomelanocortin (POMC) neurons.

Wang X, Lacza Z, Sun YE, Han W. Wang X, et al. Diabetologia. 2014 Jan;57(1):236-45. doi: 10.1007/s00125-013-3072-0. Diabetologia. 2014. PMID: 24078059

Time-dependent modulation of GABA(A)-ergic synaptic transmission by allopregnanolone in locus coeruleus neurons of Mecp2-null mice.

Jin X, Zhong W, Jiang C. Jin X, et al. Am J Physiol Cell Physiol. 2013 Dec 1;305(11):C1151-60. doi: 10.1152/ajpcell.00195.2013. Epub 2013 Sep 25. Am J Physiol Cell Physiol. 2013. PMID: 24067915 Free PMC article.

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.

Ran FA, Hsu PD, Lin CY, Gootenberg JS, Konermann S, Trevino AE, Scott DA, Inoue A, Matoba S, Zhang Y, Zhang F. Ran FA, et al. Cell. 2013 Sep 12;154(6):1380-9. doi: 10.1016/j.cell.2013.08.021. Epub 2013 Aug 29. Cell. 2013. PMID: 23992846 Free PMC article.

Pre- and postsynaptic modulations of hypoglossal motoneurons by α-adrenoceptor activation in wild-type and Mecp2(-/Y) mice.

Jin XT, Cui N, Zhong W, Jin X, Wu Z, Jiang C. Jin XT, et al. Am J Physiol Cell Physiol. 2013 Nov 15;305(10):C1080-90. doi: 10.1152/ajpcell.00109.2013. Epub 2013 Aug 28. Am J Physiol Cell Physiol. 2013. PMID: 23986203 Free PMC article.

A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient.

Sheikh TI, Mittal K, Willis MJ, Vincent JB. Sheikh TI, et al. Orphanet J Rare Dis. 2013 Jul 19;8:108. doi: 10.1186/1750-1172-8-108. Orphanet J Rare Dis. 2013. PMID: 23866855 Free PMC article.

671 results

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671 results

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