(Q24680140)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

title

CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1. (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Frank Kooy

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

author name string

Birgitta Winnepenninckx

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Kim Debacker

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Jacqueline Ramsay

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Dominique Smeets

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Arie Smits

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

language of work or name

English

0 references

publication date

12 December 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

24 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

volume

80

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

page(s)

221-231

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

24 December 2019

cites work

1 reference

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7 April 2017

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DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci

7 April 2017

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7 April 2017

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

7 April 2017

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Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

7 April 2017

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7 April 2017

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7 April 2017

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Worms gang up on bacteria

7 April 2017

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A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

7 April 2017

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Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

7 April 2017

1 reference

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Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells. The carboxyl-terminal domain of the mammalian enzymes is related to bacterial restriction methyltransferases

7 April 2017

1 reference

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

7 April 2017

1 reference

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Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

7 April 2017

1 reference

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DNA methylation and human disease

7 April 2017

1 reference

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

7 April 2017

1 reference

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Methyl-CpG binding proteins in the nervous system

7 April 2017

1 reference

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Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein

28 September 2017

1 reference

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Fragile X-associated tremor/ataxia syndrome (FXTAS).

28 September 2017

1 reference

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Cloning, genomic organization and expression pattern of a novel Drosophila gene, the disco-interacting protein 2 (dip2), and its murine homolog

28 September 2017

1 reference

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Molecular-clinical spectrum of the ATR-X syndrome

28 September 2017

1 reference

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Methylated cytosine and the brain: a new base for neuroscience

28 September 2017

1 reference

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DNA methylation in health and disease

28 September 2017

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Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A.

28 September 2017

1 reference

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Maintenance-type DNA methyltransferase is highly expressed in post-mitotic neurons and localized in the cytoplasmic compartment

28 September 2017

1 reference

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FMR2 expression in families with FRAXE mental retardation.

28 September 2017

1 reference

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Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cells

28 September 2017

1 reference

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A general method for the detection of large CAG repeat expansions by fluorescent PCR

28 September 2017

1 reference

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Establishment of neuronal connectivity during development of the Drosophila larval visual system.

30 May 2018

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Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

30 May 2018

1 reference

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Fragile site at 12q13 associated with phenotypic abnormalities

30 May 2018

1 reference

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Heritable fragility at 11q13 and 12q13.

30 May 2018

1 reference

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Disconnected: a locus required for neuronal pathway formation in the visual system of Drosophila.

30 May 2018

1 reference

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30 May 2018

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The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(qh?,RHG,GAG,CBG)

30 May 2018

1 reference

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Dynamic expression of de novo DNA methyltransferases Dnmt3a and Dnmt3b in the central nervous system

30 May 2018

1 reference

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A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replication

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

DNA hypomethylation perturbs the function and survival of CNS neurons in postnatal animals.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

DNA mismatch repair and DNA methylation in adult brain neurons.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

Expression of DNA methyltransferase gene in mature and immature neurons as well as proliferating cells in mice.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

A family with craniofrontonasal dysplasia, and fragile site 12q13 segregating independently

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

A cytogenetic survey of a mentally retarded school-age population with special reference to fragile sites.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1785358

Genomic imprinting of IGF2 and H19 in human meningiomas

28 November 2018

1 reference

12 December 2020

Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13

1 reference

12 December 2020

[Genetic aspects of autosomal fragile sites. Apropos of 40 Cases]

1 reference

12 December 2020

Two different structural abnormalities of chromosome 13 in offspring of chromo-somally normal parents with two fragile sites

1 reference

12 December 2020

Fragile site in chromosome 12 in a patient with two miscarriages

1 reference

12 December 2020

Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites

1 reference

12 December 2020

12q13 fragility in a family with recurrent spontaneous abortions: expression of the fragile site under different culture conditions

1 reference

12 December 2020

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE

1 reference

12 December 2020

The fundamental role of epigenetic events in cancer

1 reference

12 December 2020

Growing Y-junction carbon nanotubes

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F510800

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/510800

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17236128%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

1 reference