A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome (Q34307505)

1 August 2017

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome (English)

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1 August 2017

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Stephen W Scherer

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1 August 2017

Gevork N Mnatzakanian

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Iulia Munteanu

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1 August 2017

Simon E Alfred

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1 August 2017

Takahiro Yamada

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1 August 2017

Patrick J M MacLeod

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1 August 2017

Julie R Jones

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N Carolyn Schanen

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1 August 2017

Michael J Friez

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John B Vincent

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Berge A Minassian

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1 August 2017

language of work or name

English

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publication date

21 March 2004

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36

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339-341

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4

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https://scigraph.springernature.com/pub.10.1038/ng1327

1 August 2017

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cites work

Clinical manifestations and stages of Rett syndrome

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7 January 2021

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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7 January 2021

Mutations and polymorphisms in the human methyl CpG-binding protein MECP2

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7 January 2021

Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions

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7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

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7 January 2021

Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2.

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7 January 2021

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression

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7 January 2021

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

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7 January 2021

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

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7 January 2021

A calcium microdomain near NMDA receptors: on switch for ERK-dependent synapse-to-nucleus communication

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7 January 2021

Methyl-CpG-binding protein 2 is localized in the postsynaptic compartment: an immunochemical study of subcellular fractions.

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7 January 2021

A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?

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7 January 2021

The phenotypic consequences of MECP2 mutations extend beyond Rett syndrome

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7 January 2021

Identifiers

DOI

10.1038/NG1327

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1 August 2017

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