(Q55029059)

15 June 2018

title

Infrequent somatic mutation of the MTS1 gene in primary bladder carcinomas. (English)

1 reference

15 June 2018

author name string

M Kai

1

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15 June 2018

H Arakawa

2

1 reference

15 June 2018

Y Sugimoto

3

1 reference

15 June 2018

Y Murata

4

1 reference

15 June 2018

M Ogawa

5

1 reference

15 June 2018

Y Nakamura

6

1 reference

15 June 2018

publication date

1 March 1995

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15 June 2018

number of pages

3

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

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15 June 2018

volume

86

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15 June 2018

page(s)

249-251

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15 June 2018

issue

3

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15 June 2018

A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4

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1 reference

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

16 June 2018

1 reference

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

Somatic mutations of the MTS (multiple tumor suppressor) 1/CDK4l (cyclin-dependent kinase-4 inhibitor) gene in human primary non-small cell lung carcinomas

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

Germline p16 mutations in familial melanoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

DNA typing from single hairs

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

Preliminary mapping of the deleted region of chromosome 9 in bladder cancer.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5920817

Role of chromosome 9 in human bladder cancer.

13 August 2018

1 reference

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Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus

13 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1995.TB03047.X

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

21 January 2018

1 reference

12 December 2020

Chromosome 9 allelic losses and microsatellite alterations in human bladder tumors

1 reference

12 December 2020

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

1 reference

12 December 2020

Homozygous deletions of 9p21 in primary human bladder tumors detected by comparative multiplex polymerase chain reaction

1 reference

12 December 2020

Allelotype of human bladder cancer

1 reference

12 December 2020

10.1111/J.1349-7006.1995.TB03047.X

Identifiers

DOI

1 reference

15 June 2018

PMCID

5920817

1 reference

15 June 2018

PubMed ID

7744694

1 reference

15 June 2018