Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21. (Q36135600)

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English	Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.	scientific article

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16 October 2019

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21 (English)

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16 October 2019

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Ian G. Campbell

7

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16 October 2019

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M Tavassoli

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16 October 2019

H Steingrimsdottir

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16 October 2019

E Pierce

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16 October 2019

X Jiang

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16 October 2019

M Alagoz

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16 October 2019

F Farzaneh

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16 October 2019

language of work or name

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1 July 1996

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16 October 2019

British Journal of Cancer

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16 October 2019

74

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16 October 2019

1

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16 October 2019

115-119

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16 October 2019

https://scigraph.springernature.com/pub.10.1038/bjc.1996.324

0 references

Frequent loss of heterozygosity on chromosome 6 in human ovarian carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 October 2017

A novel gene encoding a B-box protein within the BRCA1 region at 17q21.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 October 2017

MDM2 overexpression is rare in ovarian carcinoma irrespective of TP53 mutation status.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 October 2017

The 1993-94 Généthon human genetic linkage map

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 October 2017

Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 October 2017

Revised FIGO staging for gynaecological cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 July 2018

Frequent allelic losses and mutations of the p53 gene in human ovarian cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 July 2018

Frequent somatic mutations of the APC gene in human pancreatic cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 July 2018

Polymorphic sites within the MCC and APC loci reveal very frequent loss of heterozygosity in human small cell lung cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 July 2018

The APC gene, responsible for familial adenomatous polyposis, is mutated in human gastric cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

2 July 2018

Human epithelial ovarian cancer allelotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

23 September 2018

p53 mutation is a common genetic event in ovarian carcinoma.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

23 September 2018

A frequent deletion of chromosome 5q21 in advanced small cell and non-small cell carcinoma of the lung.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2074604

23 September 2018

Whole chromosome 17 loss in ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype of human ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation analysis of RASK and the ‘FLR exon’ of NF1 in sporadic ovarian carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity on chromosome 5 in sporadic ovarian carcinoma is a late event and is not associated with mutations in APC at 5q21-22

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation and overexpression of p53 in early-stage epithelial ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Very frequent loss of heterozygosity throughout chromosome 17 in sporadic ovarian carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

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/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spectrum of mutation and frequency of allelic deletion of the p53 gene in ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity on chromosomal segments 3p, 6q and 11p in human ovarian carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/8679443

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/BJC.1996.324

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8679443%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8679443%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8679443%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

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