(Q40569512)

English

Epstein-Barr virus transformation of human lymphoblastoid cells from patients with fragile X syndrome induces variable changes on CGG repeats size and promoter methylation

scientific article published on January 2003

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Epstein-Barr virus transformation of human lymphoblastoid cells from patients with fragile X syndrome induces variable changes on CGG repeats size and promoter methylation (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Epstein–Barr virus

0 references

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

Victoria Bonilla

1

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Francisco Sobrino

2

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Miguel Lucas

3

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Elizabeth Pintado

4

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

publication date

1 January 2003

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Molecular Diagnosis and Therapy

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

3-4

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

163-167

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

A decade of molecular studies of fragile X syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

A fragile balance: FMR1 expression levels

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Assessment of FMR1 expression by reverse transcriptase-polymerase chain reaction of KH domains.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Normal phenotype in two brothers with a full FMR1 mutation.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Signal transduction by the B cell antigen receptor and its coreceptors

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Binding of the Epstein-Barr virus major envelope glycoprotein gp350 results in the upregulation of the TNF-alpha gene expression in monocytic cells via NF-kappaB involving PKC, PI3-K and tyrosine kinases.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

In vitro reactivation of the FMR1 gene involved in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Synergistic effect of histone hyperacetylation and DNA demethylation in the reactivation of the FMR1 gene.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Induction of T-type calcium channel gene expression by chronic hypoxia

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Methylation-dependent gene silencing induced by interleukin 1beta via nitric oxide production

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Instability of CGG repeats in transgenic mice

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

DNA methylation and chromosome instability in lymphoblastoid cell lines.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Instability of the CGG repeat at the FRAXA locus and variable phenotypic expression in a large fragile X pedigree.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Transcription of the FMR1 gene in individuals with fragile X syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Reduced FMRP and increased FMR1 transcription is proportionally associated with CGG repeat number in intermediate-length and premutation carriers.

1 reference

https://api.crossref.org/works/10.1007%2FBF03260033

21 January 2018

Molecular analysis and test of linkage between the FMR-1 gene and infantile autism in multiplex families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15068386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15068386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CD4+, but not CD8+, T cells from mammary tumor-bearing mice have a down-regulated production of IFN-gamma: role of phosphatidyl serine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15068386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15068386

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF03260033

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 September 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q40569512&oldid=2203795082"