MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively
about
Rett syndrome - biological pathways leading from MECP2 to disorder phenotypesInvestigating mechanisms underlying neurodevelopmental phenotypes of autistic and intellectual disability disorders: a perspective.Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardationMeCP2 is required for activity-dependent refinement of olfactory circuits.Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.The role of MeCP2 in CNS development and function.Normal mitral cell dendritic development in the setting of Mecp2 mutationMeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.Brain metabolism in Rett syndrome: age, clinical, and genotype correlations.Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.Synaptic plasticity and signaling in Rett syndrome.Acquired microcephaly, regression of milestones, mitochondrial dysfunction, and episodic rigidity in a 46,XY male with a de novo MECP2 gene mutation.MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neuronsMeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett SyndromeGene therapy for Rett syndrome: prospects and challenges
P2860
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P2860
MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively
description
2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի ապրիլին հրատարակված գիտական հոդված
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artículu científicu espublizáu en 2008
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im April 2008 veröffentlichter wissenschaftlicher Artikel
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scientific journal article
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vedecký článok (publikovaný 2008/04/01)
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vědecký článek publikovaný v roce 2008
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wetenschappelijk artikel (gepubliceerd op 2008/04/01)
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наукова стаття, опублікована у квітні 2008
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مقالة علمية (نشرت في أبريل 2008)
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name
MeCP2 mutation causes distingu ...... and maintenance, respectively
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MeCP2 mutation causes distingu ...... and maintenance, respectively
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MeCP2 mutation causes distingu ...... and maintenance, respectively
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type
label
MeCP2 mutation causes distingu ...... and maintenance, respectively
@ast
MeCP2 mutation causes distingu ...... and maintenance, respectively
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MeCP2 mutation causes distingu ...... and maintenance, respectively
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prefLabel
MeCP2 mutation causes distingu ...... and maintenance, respectively
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MeCP2 mutation causes distingu ...... and maintenance, respectively
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MeCP2 mutation causes distingu ...... and maintenance, respectively
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P2093
P1476
MeCP2 mutation causes distingu ...... and maintenance, respectively
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P2093
Amy Palmer
Gabriele Ronnett
Jibran Qayumi
P304
P356
10.1016/J.MCN.2008.01.005
P577
2008-04-01T00:00:00Z