Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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2018年學術文章

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

@en

Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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P1476

Transcriptome level analysis in Rett syndrome using human samples from different tissues.

@en

P2093

Stephen Shovlin

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Creative Commons Attribution 4.0 International

P2860

Apolipoprotein J (clusterin) activates rodent microglia in vivo and in vitro

MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin

Rett syndrome: revised diagnostic criteria and nomenclature

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

NF-kappa B functions in synaptic signaling and behavior

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution

Prevalence and onset of comorbidities in the CDKL5 disorder differ from Rett syndrome

Isogenic pairs of wild type and mutant induced pluripotent stem cell (iPSC) lines from Rett syndrome patients as in vitro disease model

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s13023-018-0857-8

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113

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scholarly article

review article

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10.1186/S13023-018-0857-8

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Daniela Tropea

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2018-07-11T00:00:00Z

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1105488939

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29996871

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P921

transcriptome

genetic variation

Rett syndrome

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6042368

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