Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers (Q36951846)

17 August 2017

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

1 reference

17 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

chromosomal deletion syndrome

9 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

tumor suppressor gene

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

1 reference

R. F. Boynton

1

1 reference

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9 October 2022

P. L. Blount

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

J. Yin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

V. L. Brown

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

Y. Huang

5

1 reference

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9 October 2022

Y. Tong

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

T. McDaniel

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

C. Newkirk

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

J. H. Resau

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

W. H. Raskind

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

R. C. Haggitt

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

B. J. Reid

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

S. J. Meltzer

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

9 October 2022

language of work or name

English

0 references

publication date

1 April 1992

1 reference

PMCID

48872

17 August 2017

15 April 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1565631

9 October 2022

number of pages

4

1 reference

full work available at URL

inferred from page(s)

https://europepmc.org/articles/PMC48872

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

https://europepmc.org/articles/PMC48872?pdf=render

9 October 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1565631

Proceedings of the National Academy of Sciences of the United States of America

9 October 2022

published in

1 reference

17 August 2017

89

1 reference

17 August 2017

8

1 reference

17 August 2017

3385-3388

1 reference

Mutation and cancer: statistical study of retinoblastoma

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Loss of heterozygosity on chromosomes 3, 13, and 17 in small-cell carcinoma and on chromosome 3 in adenocarcinoma of the lung

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Genetic alterations during colorectal-tumor development

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Frequent mutation of the p53 gene in human esophageal cancer

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Reduction to homozygosity involving p53 in esophageal cancers demonstrated by the polymerase chain reaction

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Identification of a Gene Located at Chromosome 5q21 that Is Mutated in Colorectal Cancers

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Identification of deletion mutations and three new genes at the familial polyposis locus

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Identification of FAP locus genes from chromosome 5q21

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Identification and characterization of the familial adenomatous polyposis coli gene

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Frequent loss of heterozygosity at the retinoblastoma locus in human esophageal cancers

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Gardner syndrome in a man with an interstitial deletion of 5q.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Amplification of the hst-1 gene in human esophageal carcinomas.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Coamplification of the hst-1 and int-2 genes in human cancers.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Localization of the gene for familial adenomatous polyposis on chromosome 5.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

High incidence of amplification of the epidermal growth factor receptor gene in human squamous carcinoma cell lines.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Chromosome 5 allele loss in human colorectal carcinomas.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Activation of c-Ki-ras in human gastrointestinal dysplasias determined by direct sequencing of polymerase chain reaction products.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Mucoepidermoid tumor of the parotid gland showing a translocation (3;8)(p21;q12) and a deletion (5)(q22) as sole chromosome abnormalities.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Frequent loss of heterozygosity on chromosomes 1q, 5q, and 17p in human gastric carcinomas.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Allelotype study of primary hepatocellular carcinoma

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

The gene for familial polyposis coli maps to the long arm of chromosome 5.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Amplification of the EGF receptor and c-myc genes in human esophageal cancers

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Allelotype of renal cell carcinoma

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

Smoking and drinking in relation to cancers of the oral cavity, pharynx, larynx, and esophagus in northern Italy

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=48872

17p allelic deletions and p53 protein overexpression in Barrett's adenocarcinoma

20 October 2018

1 reference

12 December 2020

Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma

1 reference

12 December 2020

Deletion of 17p and amplification of the int-2 gene in esophageal carcinomas

1 reference

12 December 2020

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

1 reference

12 December 2020

Chromosome 5 abnormalities in acute lymphoblastic leukemia

1 reference

12 December 2020

No evidence for point mutations in codons 12, 13, and 61 of the ras gene in a high-incidence area for esophageal and gastric cancers

1 reference

12 December 2020

Involvement of chromosomes 3 and 5 in renal cell carcinoma

1 reference

12 December 2020

Prevalence and characteristics of Barrett esophagus in patients with adenocarcinoma of the esophagus or esophagogastric junction

1 reference

12 December 2020

Barrett's esophagus. Correlation between flow cytometry and histology in detection of patients at risk for adenocarcinoma

1 reference

12 December 2020

Adenocarcinoma of the esophagus and/or gastric cardia

1 reference

12 December 2020

Comparative features of esophageal and gastric adenocarcinomas: recent changes in type and frequency

1 reference

12 December 2020

MCC, a candidate familial polyposis gene in 5q.21, shows frequent allele loss in colorectal and lung cancer

1 reference

12 December 2020

Frequent loss of heterozygosity on chromosomes 6q, 11, and 17 in human ovarian carcinomas

1 reference

12 December 2020

5q deletion. The sole chromosome change in a carcinoma of the bladder

1 reference

12 December 2020

Loss of heterozygosity on the short arm of chromosome 3 in carcinoma of the uterine cervix

1 reference

12 December 2020

Loss of heterozygosity in human germinal tumors

1 reference

12 December 2020

Rapid detection of ras oncogenes in human tumors: applications to colon, esophageal, and gastric cancer

1 reference

12 December 2020

Purification of DNA from formaldehyde fixed and paraffin embedded human tissue

1 reference

12 December 2020

Amplification of epidermal growth factor receptor gene but no evidence of ras mutations in primary human esophageal cancers

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.89.8.3385

1 reference

17 August 2017

0 references

1 reference

17 August 2017

1 reference

PMCID

48872