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A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer

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A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer (English)

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3

Annika Lindblom

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author name string

Xiao-Lei Zhou

series ordinal

1

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Barbro Werelius

series ordinal

2

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language of work or name

English

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publication date

2004

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published in

Breast Cancer Research

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volume

6

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page(s)

R187-90

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issue

3

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cites work

Low frequency of E-cadherin alterations in familial breast cancer

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stated in

PubMed Central

reference URL

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7 April 2017

A widely expressed transcription factor with multiple DNA sequence specificity, CTCF, is localized at chromosome segment 16q22.1 within one of the smallest regions of overlap for common deletions in breast and prostate cancers

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=400671

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7 April 2017

Tumor-associated zinc finger mutations in the CTCF transcription factor selectively alter tts DNA-binding specificity

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=400671

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7 April 2017

CTCF, a candidate trans-acting factor for X-inactivation choice

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=400671

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7 April 2017

CTCF is a uniquely versatile transcription regulator linked to epigenetics and disease

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=400671

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7 April 2017

High frequency of skewed X inactivation in young breast cancer patients

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=400671

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28 September 2017

Skewed X inactivation in X-linked disorders

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PubMed Central

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28 September 2017

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

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PubMed Central

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28 September 2017

BRCA2 germline mutations in Swedish breast cancer families.

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21 January 2018

Allelic loss of 16q23.2-24.2 is an independent marker of good prognosis in primary breast cancer

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PubMed Central

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28 November 2018

Loss of heterozygosity in familial breast carcinomas

1 reference

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PubMed Central

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28 November 2018

Deletions on chromosome 16 in primary familial breast carcinomas are associated with development of distant metastases

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PubMed Central

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28 November 2018

At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer

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21 January 2018

Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers

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21 January 2018

Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer

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21 January 2018

First BRCA1 and BRCA2 gene testing implemented in the health care system of Stockholm

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21 January 2018

CTCF Gene Mutations in Invasive Ductal Breast Cancer

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21 January 2018

A region on the long arm of chromosome 16 is frequently deleted in metastatic node-negative breast cancer

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15084242

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/15084242

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1186/BCR774

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Dimensions Publication ID

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ResearchGate publication ID

8619541

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Springer Nature article ID

10.1186/bcr774

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(Q24794792)

A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer

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