(Q37383682)

20 August 2017

A study of the treatment of Rett syndrome with folate and betaine (English)

1 reference

20 August 2017

0 references

1 reference

2

Alan K Percy

1 reference

20 August 2017

8

Jeffrey L Neul

1 reference

20 August 2017

1

Daniel G Glaze

1 reference

20 August 2017

Kathleen J Motil

3

1 reference

20 August 2017

Jane B Lane

4

1 reference

20 August 2017

Janet S Isaacs

5

1 reference

20 August 2017

Rebecca J Schultz

6

1 reference

20 August 2017

Judy O Barrish

7

1 reference

20 August 2017

William E O'Brien

9

1 reference

20 August 2017

E O'Brian Smith

10

1 reference

20 August 2017

18 February 2009

1 reference

Journal of Child Neurology

20 August 2017

1 reference

20 August 2017

24

1 reference

20 August 2017

5

1 reference

20 August 2017

551-556

1 reference

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

20 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

The biological functions of the methyl-CpG-binding protein MeCP2 and its implication in Rett syndrome.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Are somatic cells inherently deficient in methylation metabolism? A proposed mechanism for DNA methylation loss, senescence and aging.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Rett syndrome: controlled study of an oral opiate antagonist, naltrexone

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Folic acid--an innocuous means to reduce plasma homocysteine.

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Demyelination and decreased S-adenosylmethionine in 5,10-methylenetetrahydrofolate reductase deficiency

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2760386

An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001

2 September 2018

1 reference

12 December 2020

Extrapyramidal involvement in Rett's syndrome

1 reference

12 December 2020

Betaine dose and treatment intervals in therapy for homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency

1 reference

12 December 2020

Remethylation defects: guidelines for clinical diagnosis and treatment

1 reference

12 December 2020

Identifiers

DOI

10.1177/0883073808327827

1 reference

release_ntzb5pcxevgc5coppztxjah6ei

20 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ntzb5pcxevgc5coppztxjah6ei

24 November 2022

mapped directly with Wikidata item

1 reference

20 August 2017

PubMed publication ID

19225139

1 reference