(Q35870262)

10 August 2017

Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridization (English)

1 reference

10 August 2017

1 reference

5

Eric P Hoffman

1 reference

10 August 2017

William A Thistlethwaite

1

1 reference

10 August 2017

Linda M Moses

2

1 reference

10 August 2017

Kristen C Hoffbuhr

3

1 reference

10 August 2017

Joseph M Devaney

4

1 reference

10 August 2017

1 May 2003

1 reference

The Journal of Molecular Diagnostics

10 August 2017

1 reference

10 August 2017

5

1 reference

10 August 2017

2

1 reference

10 August 2017

121-126

1 reference

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

10 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Mutation screening in Rett syndrome patients.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Rapid, high fidelity analysis of simple sequence repeats on an electronically active DNA microchip

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Methylation-induced repression--belts, braces, and chromatin

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Rett syndrome: clinical update and review of recent genetic advances.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Male Rett syndrome variant: application of diagnostic criteria

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Single nucleotide polymorphic discrimination by an electronic dot blot assay on semiconductor microchips

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Rett syndrome: a disorder affecting early brain growth

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Epidemiology of Rett syndrome: a population-based registry.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

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

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

A laminated, flex structure for electronic transport and hybridization of DNA.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

Electric manipulation of bioparticles and macromolecules on microfabricated electrodes

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

MECP2 mutations account for most cases of typical forms of Rett syndrome.

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1907318

MeCP2 mutations in children with and without the phenotype of Rett syndrome

24 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12707377

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/12707377

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S1525-1578(10)60461-8

1 reference

10 August 2017

1 reference

10 August 2017

PubMed publication ID

12707377

1 reference