MMG PUBLICATIONS

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Results: 4167  publications found.

Laurent, .  et al. 0

Jean-Christophe";Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain;BMC neuroscience;;1471-2202;10.1186/1471-2202-12-47;;BACKGROUND: Rett syndrome (RTT

revealed morphological and functional alterations of neurons. Several functions that are regulated by bioaminergic nuclei or peripheral ganglia are impaired in the absence of Mecp2. RESULTS: Using...
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at least in the tissue tested. Our data suggest that FER is not implicated in the mental retardation phenotype observed in the reported patient. Therefore the MR phenotype might not be caused by the translocation.", .  et al. 0

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PLoS One. 2014 Mar 25, .  et al. 0

El-Khoury R

10.1371/journal.pone.0092169
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bone malformations, .  et al. 0

and early death: a distinct MCA/MR syndrome;Mégarbané A

Jalkh N
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Nicolas, .  et al. 0

Violaine; Fontes

an X-linked progressive encephalopathy. We have collected the results of MECP2 analysis conducted in four laboratories in France. A total of 301 RTT alleles have been analyzed
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Am J Hum Genet. 2013 Sep 5, .  et al. 0

Cacciagli P

10.1016/j.ajhg.2013.07.023
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ATR-X/XNP/XH2 gene MIM #300032), .  et al. 0

Fontes M.;"Eur J Hum Genet. 2002 Apr;10(4):223-5. doi: 10.1038/sj.ejhg.5200800.";Villard L;Eur J Hum Genet;2002;29/05/2002;;;10.1038/sj.ejhg.5200800

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Ana, .  et al. 0

Adeline; Villard

by 5 w
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improved the lifespan and reduced motor defects, .  et al. 0

suggesting a new therapeutic strategy for Rett syndrome.;2012-02;04/08/2025 08:04;04/08/2025 08:04;;786-795;;2;45;;Neurobiol Dis;;;;;;;;eng;Copyright © 2011 Elsevier Inc. All rights reserved.;;;;;;Place: United States PMID: 22127389

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Eur J Hum Genet. 2014 Mar, .  et al. 0

Cacciagli P

10.1038/ejhg.2013.135
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Roux JC. "F1000Res. 2018 Mar 26, .  et al. 0

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Lossi AM, .  et al. 0

Chelly J

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we found that chronic L-Dopa treatment improved the motor deficits previously identified. Altogether, .  et al. 0

our findings demonstrate that Mecp2-deficiency induces nigrostriatal deficits

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Cécile, .  et al. 0

Bilal; Moncla

but it is highly expressed in the brai
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