(Q34565370)

3 August 2017

title

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus (English)

1 reference

3 August 2017

1 reference

4

Jeannie Visootsak

1 reference

3 August 2017

Reid S Alisch

1

1 reference

3 August 2017

Tao Wang

2

1 reference

3 August 2017

Pankaj Chopra

3

1 reference

3 August 2017

Karen N Conneely

5

1 reference

3 August 2017

Stephen T Warren

6

1 reference

3 August 2017

language of work or name

1 reference

29 January 2013

1 reference

3 August 2017

1 reference

3 August 2017

volume

14

1 reference

3 August 2017

page(s)

18

1 reference

New perspectives on the biology of fragile X syndrome

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Age-associated DNA methylation in pediatric populations

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Specific age-associated DNA methylation changes in human dermal fibroblasts

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Hotspots of aberrant epigenomic reprogramming in human induced pluripotent stem cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Differential modeling of fragile X syndrome by human embryonic stem cells and induced pluripotent stem cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

DNA methylation pattern changes upon long-term culture and aging of human mesenchymal stromal cells

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Developmental study of fragile X syndrome using human embryonic stem cells derived from preimplantation genetically diagnosed embryos

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Gene body-specific methylation on the active X chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

RNA and microRNAs in fragile X mental retardation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

RNAi-mediated targeting of heterochromatin by the RITS complex

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

A point mutation in the FMR-1 gene associated with fragile X mental retardation

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3599197

Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat

7 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-14-18

Timing of the absence of FMR1 expression in full mutation chorionic villi.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-14-18

Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2350-14-18

Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23356558

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2350-14-18

1 reference

Dimensions Publication ID

3 August 2017

0 references

1 reference

3 August 2017

1 reference