(Q42437998)

English

No evidence of mutation in the human PTC gene, responsible for nevoid basal cell carcinoma syndrome, in human primary squamous cell carcinomas of the esophagus and lung

scientific article published on March 1997

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

No evidence of mutation in the human PTC gene, responsible for nevoid basal cell carcinoma syndrome, in human primary squamous cell carcinomas of the esophagus and lung (English)

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

nevoid basal cell carcinoma syndrome

1 reference

based on heuristic

inferred from title

author name string

K Suzuki

1

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

Y Daigo

2

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

S Fukuda

3

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

T Tokino

4

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

M Isomura

5

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

K Isono

6

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

B Wainwright

7

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

Y Nakamura

8

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

publication date

1 March 1997

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

number of pages

4

1 reference

based on heuristic

inferred from page(s)

Japanese Journal of Cancer Research

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

88

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

3

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

225-228

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Human homolog of patched, a candidate gene for the basal cell nevus syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

A mammalian patched homolog is expressed in target tissues of sonic hedgehog and maps to a region associated with developmental abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Detailed deletion mapping in squamous cell carcinomas of the esophagus narrows a region containing a putative tumor suppressor gene to about 200 kilobases on distal chromosome 9q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Altered expression of the cyclin D1 and retinoblastoma genes in human esophageal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Fine genetic mapping of the gene for nevoid basal cell carcinoma syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Localization of the gene for the nevoid basal cell carcinoma syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Accumulation of genetic alterations during esophageal carcinogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

Frequent mutation of the p53 gene in human esophageal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

3 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921385

16 August 2018

Difference of allelotype between squamous cell carcinoma and adenocarcinoma of the lung

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

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/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of 17p, mutation of the p53 gene, and overexpression of p53 protein in esophageal squamous cell carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple self-healing squamous epitheliomata (ESS1) mapped to chromosome 9q22-q31 in families with common ancestry

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High incidence of coamplification of hst-1 and int-2 genes in human esophageal carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered messenger RNA and unique mutational profiles of p53 and Rb in human esophageal carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Significance of int-2/hst-1 coamplification as a prognostic factor in patients with esophageal squamous carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype of human bladder cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype study of esophageal carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An allelotype of squamous carcinoma of the head and neck using microsatellite markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/9140104

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1111/J.1349-7006.1997.TB00370.X

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 June 2018

http://europepmc.org/abstract/PMC/5921385

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