(Q33932429)

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Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

inferred from title

13

object named as

Janusz Limon

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

12

object named as

Izabela Brozek

1 reference

Europe PubMed Central

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30 July 2017

author name string

Dirk Prawitt

1

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Europe PubMed Central

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30 July 2017

Thorsten Enklaar

2

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Europe PubMed Central

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30 July 2017

Barbara Gärtner-Rupprecht

3

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Europe PubMed Central

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30 July 2017

Christian Spangenberg

4

1 reference

Europe PubMed Central

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30 July 2017

Monika Oswald

5

1 reference

Europe PubMed Central

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30 July 2017

Ekkehart Lausch

6

1 reference

Europe PubMed Central

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30 July 2017

Peter Schmidtke

7

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Europe PubMed Central

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30 July 2017

Dirk Reutzel

8

1 reference

Europe PubMed Central

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30 July 2017

Stephan Fees

9

1 reference

Europe PubMed Central

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30 July 2017

Rob Lucito

10

1 reference

Europe PubMed Central

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30 July 2017

Maria Korzon

11

1 reference

Europe PubMed Central

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30 July 2017

David E Housman

14

1 reference

Europe PubMed Central

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30 July 2017

Jerry Pelletier

15

1 reference

Europe PubMed Central

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30 July 2017

Bernhard Zabel

16

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30 July 2017

language of work or name

0 references

publication date

2 March 2005

1 reference

Europe PubMed Central

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30 July 2017

Proceedings of the National Academy of Sciences of the United States of America

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Europe PubMed Central

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30 July 2017

102

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Europe PubMed Central

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30 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

4085-4090

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Transgenic RNAi reveals essential function for CTCF in H19 gene imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Nucleosome positioning signals in the DNA sequence of the human and mouse H19 imprinting control regions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

ETV6-NTRK3 transformation requires insulin-like growth factor 1 receptor signaling and is associated with constitutive IRS-1 tyrosine phosphorylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

A dyad oct-binding sequence functions as a maintenance sequence for the unmethylated state within the H19/Igf2-imprinted control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Multiple nucleosome positioning sites regulate the CTCF-mediated insulator function of the H19 imprinting control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Large scale mapping of methylcytosines in CTCF-binding sites in the human H19 promoter and aberrant hypomethylation in human bladder cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Characterization of human and mouse H19 regulatory sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Involvement of IGF-II in human cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

28 July 2018

Relaxation of imprinted genes in human cancer.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Methylation sequencing analysis refines the region of H19 epimutation in Wilms tumor

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0500037102

21 January 2018

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

29 October 2018

Loss of imprinting of IGF2 sense and antisense transcripts in Wilms' tumor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=554791

29 October 2018

Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of IGF2 and H19 in osteosarcoma is accompanied by reciprocal methylation changes of a CTCF-binding site

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple method for simultaneous R- or G-banding and fluorescence in situ hybridization of small single-copy genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promoter-specific IGF2 imprinting status and its plasticity during human liver development

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic heterogeneity at imprinted loci in normal populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15743916

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1073/PNAS.0500037102

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2005PNAS..102.4085P

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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