(Q34016335)

English

Testing the FMR1 promoter for mosaicism in DNA methylation among CpG sites, strands, and cells in FMR1-expressing males with fragile X syndrome

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Testing the FMR1 promoter for mosaicism in DNA methylation among CpG sites, strands, and cells in FMR1-expressing males with fragile X syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

DNA methylation

0 references

fragile X syndrome

1 reference

based on heuristic

inferred from title

Diane P Genereux

object named as

Diane P Genereux

2

0 references

Reinhard Stöger

object named as

Reinhard Stöger

1

0 references

Randi J. Hagerman

3

object named as

Randi J Hagerman

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

5

object named as

Flora Tassone

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Paul J Hagerman

4

object named as

Paul J Hagerman

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Charles D Laird

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

language of work or name

0 references

publication date

31 August 2011

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

e23648

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

copyright license

Creative Commons Attribution 4.0 International

31 August 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

The fragile X prevalence paradox

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Cyclical DNA methylation of a transcriptionally active promoter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Elevated FMR1 mRNA in premutation carriers is due to increased transcription.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Molecular barcodes detect redundancy and contamination in hairpin-bisulfite PCR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Phenotypic variation and FMRP levels in fragile X.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Hairpin-bisulfite PCR: assessing epigenetic methylation patterns on complementary strands of individual DNA molecules.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

DNA methylation patterns and epigenetic memory

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

A majority of fragile X males with methylated, full mutation alleles have significant levels of FMR1 messenger RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Interaction of the transcription factors USF1, USF2, and alpha -Pal/Nrf-1 with the FMR1 promoter. Implications for Fragile X mental retardation syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

DNA methylation directs a time-dependent repression of transcription initiation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166088

5 July 2018

Prevalence of the fragile X syndrome in African-Americans

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

Translational suppression by trinucleotide repeat expansion at FMR1.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

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/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

De novo methylation of an embryonic globin gene during normal development is strand specific and spreads from the proximal transcribed region

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

Hemimethylation and non-CpG methylation levels in a promoter region of human LINE-1 (L1) repeated elements

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0023648

21 January 2018

Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1

1 reference

https://pubmed.ncbi.nlm.nih.gov/21909353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MECP2 deletions and genotype-phenotype correlation in Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/21909353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Screening for fragile X syndrome in women of reproductive age

1 reference

https://pubmed.ncbi.nlm.nih.gov/21909353

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0023648

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2011PLoSO...623648S

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

0 references

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