(Q36617800)

English

Prognostic significance of loss of heterozygosity at loci on chromosome 17p13.3-ter in sporadic breast cancer is evidence for a putative tumour suppressor gene

scientific article published on May 1999

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Prognostic significance of loss of heterozygosity at loci on chromosome 17p13.3-ter in sporadic breast cancer is evidence for a putative tumour suppressor gene (English)

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

sporadic breast cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Liscia DS

1

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Morizio R

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Venesio T

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Palenzona C

4

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Donadio M

5

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Callahan R

6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

language of work or name

0 references

publication date

1 May 1999

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

British Journal of Cancer

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

80

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

5-6

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

821-826

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.bjc.6690427

0 references

High levels of loss at the 17p telomere suggest the close proximity of a tumour suppressor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

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=2362303

30 September 2017

Identification of two candidate tumor suppressor genes on chromosome 17p13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

30 September 2017

Allelic loss on distal chromosome 17p is associated with poor prognosis in a group of Brazilian breast cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

30 September 2017

p53 activates expression of HIC-1, a new candidate tumour suppressor gene on 17p13.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

30 September 2017

A meta-analysis of reported correlations between prognostic factors in breast cancer: Does axillary lymph node metastasis represent biology or chronology?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

30 September 2017

Hereditary cancer, oncogenes, and antioncogenes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

28 June 2018

Evidence implicating at least two genes on chromosome 17p in breast carcinogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

28 June 2018

Inherited p53 gene mutations in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

28 June 2018

Dinucleotide repeat polymorphism mapping to the critical region for lissencephaly (17p13.3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

20 September 2018

Human ABR encodes a protein with GAPrac activity and homology to the DBL nucleotide exchange factor domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

20 September 2018

Suppression of tumorigenicity of breast cancer cells by transfer of human chromosome 17 does not require transferred BRCA1 and p53 genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

20 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2362303

21 October 2018

Current status of Milan adjuvant chemotherapy trials for node-positive and node-negative breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cotranslation of activated mutant p53 with wild type drives the wild-type p53 protein into the mutant conformation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four separate regions on chromosome 17 show loss of heterozygosity in familial breast carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detailed analysis of loss of heterozygosity on chromosome band 17p13 in breast carcinoma on the basis of a high-resolution physical map with 29 markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for a second tumor suppressor gene on 17p linked to high S-phase index in primary human breast carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spatial organization of ABR and CRK genes on human chromosome band 17p13.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detailed mapping and loss of heterozygosity analysis suggests a suppressor locus involved in sporadic breast cancer within a distal region of chromosome band 17p13.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The p53 gene in breast cancer: prognostic value of complementary DNA sequencing versus immunohistochemistry

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele loss on short arm of chromosome 17 in breast cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/10360661

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non-canonical E box and acts as a transcriptional repressor.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.BJC.6690427

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.BJC.6690427

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

0 references

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