(Q33901652)

29 July 2017

Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer (English)

1 reference

29 July 2017

Sigbjörnsdottir BI

1

1 reference

29 July 2017

Ragnarsson G

2

1 reference

29 July 2017

Agnarsson BA

3

1 reference

29 July 2017

Huiping C

4

1 reference

29 July 2017

Barkardottir RB

5

1 reference

29 July 2017

Egilsson V

6

1 reference

29 July 2017

Ingvarsson S

7

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 May 2000

1 reference

Journal of Medical Genetics

29 July 2017

1 reference

29 July 2017

37

1 reference

29 July 2017

342-347

1 reference

29 July 2017

5

1 reference

Double-strand break repair deficiency and radiation sensitivity in BRCA2 mutant cancer cells

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Involvement of Brca2 in DNA repair

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Chromosome imbalance at the 3p14 region in human breast tumours: high frequency in patients with inherited predisposition due to BRCA2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Allelic loss of chromosomal arm 8p in breast cancer progression.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Deletion mapping and linkage analysis provide strong indication for the involvement of the human chromosome region 8p12-p22 in breast carcinogenesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Study of a single BRCA2 mutation with high carrier frequency in a small population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Developmental expression of Brca2 colocalizes with Brca1 and is associated with proliferation and differentiation in multiple tissues.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Identification of the breast cancer susceptibility gene BRCA2

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Allelotyping of ductal carcinoma in situ of the breast: deletion of loci on 8p, 13q, 16q, 17p and 17q.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

The 1993-94 Généthon human genetic linkage map

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Evaluation of survival data and two new rank order statistics arising in its consideration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

A simple salting out procedure for extracting DNA from human nucleated cells

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Allelotype of colorectal carcinomas

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Human epithelial ovarian cancer allelotype.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Deletion mapping in colorectal cancer of a putative tumour suppressor gene in 8p22-p21.3.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Deletion mapping of chromosome 8 in cancers of the urinary bladder using restriction fragment length polymorphisms and microsatellite polymorphisms.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Different tumor types from BRCA2 carriers show wild-type chromosome deletions on 13q12-q13

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Loss of chromosome arm 8p loci in prostate cancer: mapping by quantitative allelic imbalance

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Deletion mapping reveals two regions of chromosome 8 allele loss in colorectal carcinomas.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734587

Frequent loss of heterozygosity for loci on chromosome 8p in hepatocellular carcinoma, colorectal cancer, and lung cancer

29 October 2018

1 reference

12 December 2020

Deletion mapping of the short arm of chromosome 8 in non-small cell lung carcinoma

1 reference

12 December 2020

Allelic loss at chromosome band 8p21.3-p22 is associated with progression of hepatocellular carcinoma

1 reference

12 December 2020

Homozygous deletion and frequent allelic loss of chromosome 8p22 loci in human prostate cancer

1 reference

12 December 2020

Loss of heterozygosity and linkage analysis in breast carcinoma: indication for a putative third susceptibility gene on the short arm of chromosome 8

1 reference

12 December 2020

Loss of heterozygosity from the short arm of chromosome 8 is an early event in breast cancers

1 reference

12 December 2020

Chromosome 17q-linkage seems to be infrequent in Icelandic families at risk of breast cancer

1 reference

12 December 2020

Loss of heterozygosity on the short arm of chromosome 8 in male breast carcinomas

1 reference

12 December 2020

Loss of heterozygosity from the short arm of chromosome 8 is associated with invasive behavior in breast cancer

1 reference

12 December 2020

Strong indication for a breast cancer susceptibility gene on chromosome 8p12-p22: linkage analysis in German breast cancer families

1 reference

12 December 2020

Distinct somatic genetic changes associated with tumor progression in carriers of BRCA1 and BRCA2 germ-line mutations

1 reference

12 December 2020

High incidence of loss of heterozygosity at chromosome 17p13 in breast tumours from BRCA2 mutation carriers

1 reference

12 December 2020

Inherited BRCA2 mutation associated with high grade breast cancer

1 reference

12 December 2020

BRCA2 and p53 mutations in primary breast cancer in relation to genetic instability

1 reference

12 December 2020

High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation

1 reference

12 December 2020

Somatic genetic alterations inBRCA2-associated and sporadic male breast cancer

1 reference

12 December 2020

Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.37.5.342

1 reference

29 July 2017

1 reference

29 July 2017

1 reference