(Q36431320)

English

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers

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scholarly article

1 reference

Europe PubMed Central

14 August 2017

Absence of methylation of CpG dinucleotides within the promoter of the breast cancer susceptibility gene BRCA2 in normal tissues and in breast and ovarian cancers (English)

1 reference

Europe PubMed Central

14 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Michael Stratton

3

object named as

Stratton MR

1 reference

Europe PubMed Central

14 August 2017

Richard Wooster

2

object named as

Wooster R

1 reference

Europe PubMed Central

14 August 2017

author name string

Collins N

1

1 reference

Europe PubMed Central

14 August 2017

language of work or name

0 references

publication date

1 January 1997

1 reference

Europe PubMed Central

14 August 2017

British Journal of Cancer

1 reference

Europe PubMed Central

14 August 2017

76

1 reference

Europe PubMed Central

14 August 2017

1150-1156

1 reference

Europe PubMed Central

14 August 2017

9

1 reference

Europe PubMed Central

14 August 2017

https://scigraph.springernature.com/pub.10.1038/bjc.1997.526

0 references

Mutation analysis in the BRCA2 gene in primary breast cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Low incidence of BRCA2 mutations in breast carcinoma and other cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

BRCA2 mutations in primary breast and ovarian cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Identification of the breast cancer susceptibility gene BRCA2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Loss of heterozygosity in sporadic breast tumours at the BRCA2 locus on chromosome 13q12-q13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Silencing of the E-cadherin invasion-suppressor gene by CpG methylation in human carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Mutations in the p53 gene occur in diverse human tumour types

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

CpG-rich islands and the function of DNA methylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

Somatic mutations in the neurofibromatosis 1 gene in human tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

APC mutations occur early during colorectal tumorigenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

30 September 2017

CpG methylation inactivates the promoter activity of the human retinoblastoma tumor-suppressor gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

28 June 2018

Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

28 June 2018

BRCA1 mutations in primary breast and ovarian carcinomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

21 September 2018

Somatic mutations in the BRCA1 gene in sporadic ovarian tumours.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

21 September 2018

A somatic BRCA1 mutation in an ovarian tumour.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

21 September 2018

Infrequent mutation of theWT1 gene in 77 Wilms' tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2228118

4 December 2018

Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of loss of heterozygosity at loci from chromosome arm 13q suggests a possible involvement of BRCA2 in sporadic breast tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural rearrangement of the retinoblastoma gene in human breast carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

At least four different chromosomal regions are involved in loss of heterozygosity in human breast carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic loss in ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of three regions on chromosome 17q in primary human breast carcinomas which are frequently deleted

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the BRCA2 gene in ovarian carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic and germline mutations of the BRCA2 gene in sporadic ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/9365162

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/BJC.1997.526

1 reference

Europe PubMed Central

14 August 2017

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0 references

1 reference

Europe PubMed Central

14 August 2017

1 reference

Europe PubMed Central

14 August 2017

ResearchGate publication ID

0 references

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