(Q34276943)

1 August 2017

title

A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome (English)

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1 August 2017

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Jan P Buschdorf

1

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1 August 2017

Wolf H Strätling

series ordinal

2

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1 August 2017

publication date

15 November 2003

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Journal of Molecular Medicine

1 August 2017

published in

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1 August 2017

volume

82

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1 August 2017

issue

2

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1 August 2017

page(s)

135-143

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De novo MECP2 frameshift mutation in a boy with moderate mental retardation, obesity and gynaecomastia.

1 August 2017

cites work

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Cross-intron bridging interactions in the yeast commitment complex are conserved in mammals

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Identification of Prp40, a novel essential yeast splicing factor associated with the U1 small nuclear ribonucleoprotein particle

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

The solution structure of the domain from MeCP2 that binds to methylated DNA

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Formin binding proteins bear WWP/WW domains that bind proline-rich peptides and functionally resemble SH3 domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

In-frame deletion inMECP2 causes mild nonspecific mental retardation

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

A matrix/scaffold attachment region binding protein: Identification, purification, and mode of binding

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Structure of the WW domain of a kinase-associated protein complexed with a proline-rich peptide.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

The methyl-CpG binding transcriptional repressor MeCP2 stably associates with nucleosomal DNA

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https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Chicken MAR-binding protein ARBP is homologous to rat methyl-CpG-binding protein MeCP2

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

The splicing factor, Prp40, binds the phosphorylated carboxyl-terminal domain of RNA polymerase II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Influence of mutation type and location on phenotype in 123 patients with Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

On a unusual brain atrophy syndrome in hyperammonemia in childhood

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

A novel pro-Arg motif recognized by WW domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

WW and SH3 domains, two different scaffolds to recognize proline-rich ligands

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Identification and characterization of a family of mammalian methyl-CpG binding proteins

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Microscopic Observations of the Brain in Rett Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

A single point mutation in a group I WW domain shifts its specificity to that of group II WW domains

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

WW domain-mediated interactions reveal a spliceosome-associated protein that binds a third class of proline-rich motif: the proline glycine and methionine-rich motif

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

MECP2 is highly mutated in X-linked mental retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Two-stage PCR protocol allowing introduction of multiple mutations, deletions and insertions using QuikChange Site-Directed Mutagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Rett syndrome: a surprising result of mutation in MECP2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Genetic evidence that formins function within the nucleus

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Histone deacetylase-independent transcriptional repression by methyl-CpG-binding protein 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

FBP WW domains and the Abl SH3 domain bind to a specific class of proline-rich ligands

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

Preserved speech variants of the Rett syndrome: molecular and clinical analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14618241

12 December 2020

10.1007/S00109-003-0497-9

Identifiers

DOI

1 reference

Dimensions Publication ID

1 August 2017

1032859841

0 references

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