(Q55325234)

2 July 2018

title

Loss of heterozygosity on the short arm of chromosome 9 without p16 gene mutation in gastric carcinomas. (English)

1 reference

2 July 2018

1 reference

K Sakata

1

1 reference

2 July 2018

G Tamura

2

1 reference

2 July 2018

C Maesawa

3

1 reference

2 July 2018

Y Suzuki

4

1 reference

2 July 2018

M Terashima

5

1 reference

2 July 2018

K Satoh

6

1 reference

2 July 2018

Y Eda

7

1 reference

2 July 2018

A Suzuki

8

1 reference

2 July 2018

S Sekiyama

9

1 reference

2 July 2018

R Satodate

10

1 reference

2 July 2018

publication date

1 April 1995

1 reference

2 July 2018

number of pages

3

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

1 reference

2 July 2018

volume

86

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2 July 2018

page(s)

333-335

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2 July 2018

issue

4

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2 July 2018

A cell cycle regulator potentially involved in genesis of many tumor types

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Deletions of the cyclin-dependent kinase-4 inhibitor gene in multiple human cancers

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Frequent somatic mutation of the MTS1/CDK4I (multiple tumor suppressor/cyclin-dependent kinase 4 inhibitor) gene in esophageal squamous cell carcinoma.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Homozygous loss of the interferon genes defines the critical region on 9p that is deleted in lung cancers.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

p53 mutations in human cancers

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas.

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Homozygous deletions within human chromosome band 9p21 in melanoma

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

Dinucleotide repeat polymorphism at the IFNA locus (9p22)

3 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920828

P16 gene in uncultured tumours

3 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1995.TB03060.X

Frequent loss of chromosome 9p21-22 early in head and neck cancer progression

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7775254

12 December 2020

inferred from PubMed ID database lookup

Rates of p16 (MTS1) mutations in primary tumors with 9p loss

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7775254

12 December 2020

inferred from PubMed ID database lookup

Open questions on p16

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/7775254

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1111/J.1349-7006.1995.TB03060.X

1 reference

2 July 2018

PMCID

5920828

1 reference

2 July 2018

PubMed ID

7775254

1 reference

2 July 2018