(Q75296796)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14732922%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

title

High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14732922%20AND%20SRC:MED&resulttype=core&format=json

esophageal squamous cell carcinoma

17 November 2019

main subject

1 reference

inferred from title

squamous cell carcinoma

1 reference

Nan Hu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14732922%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

Chaoyu Wang

2

1 reference

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17 November 2019

Hua Su

3

1 reference

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17 November 2019

Wen-Jun Li

4

1 reference

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17 November 2019

Michael R Emmert-Buck

5

1 reference

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17 November 2019

Guang Li

6

1 reference

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17 November 2019

Mark J Roth

7

1 reference

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17 November 2019

Ze-Zhong Tang

8

1 reference

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17 November 2019

Ning Lu

9

1 reference

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17 November 2019

Carol Giffen

10

1 reference

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17 November 2019

Paul S Albert

11

1 reference

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17 November 2019

Philip R Taylor

12

1 reference

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17 November 2019

Alisa M Goldstein

13

1 reference

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17 November 2019

publication date

1 March 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14732922%20AND%20SRC:MED&resulttype=core&format=json

Genes, Chromosomes and Cancer

17 November 2019

published in

1 reference

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17 November 2019

volume

39

1 reference

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17 November 2019

issue

3

1 reference

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17 November 2019

page(s)

205-216

1 reference

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Family history of oesophageal cancer in Shanxi Province, China

17 November 2019

cites work

1 reference

p16 INK4 Mutations and Altered Expression in Human Tumors and Cell Lines

21 January 2018

1 reference

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

21 January 2018

1 reference

7 January 2021

Frequency of homozygous deletion at p16/CDKN2 in primary human tumours

1 reference

7 January 2021

p16 tumor suppressor gene mutations in Chinese esophageal carcinomas in Hong Kong.

1 reference

7 January 2021

Low frequency of p16/CDKN2 gene mutations in esophageal carcinomas

1 reference

7 January 2021

p53 and p16/CDKN2 gene mutations in esophageal tumors from a high-incidence area in South Africa

1 reference

7 January 2021

Identification of novel regions of allelic loss from a genomewide scan of esophageal squamous-cell carcinoma in a high-risk Chinese population

1 reference

7 January 2021

High frequency allelic loss on chromosome 17p13.3-p11.1 in esophageal squamous cell carcinomas from a high incidence area in northern China

1 reference

7 January 2021

Highly frequent homozygous deletion of the p16 gene in esophageal cancer cell lines

1 reference

7 January 2021

p16 is a major inactivation target in hepatocellular carcinoma

1 reference

7 January 2021

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

1 reference

7 January 2021

Methylation of exon 2 of p16 is associated with late stage oesophageal cancer

1 reference

7 January 2021

Mutations in the CDKN2A ( p16INK4a ) gene in microdissected sporadic primary melanomas

1 reference

7 January 2021

Role of the p16 tumor suppressor gene in cancer

1 reference

7 January 2021

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

1 reference

7 January 2021

Genetic alterations in esophageal cancer and their relevance to etiology and pathogenesis: a review

1 reference

7 January 2021

Loss of heterozygosity on chromosome 9 andp16 (MTS1, CDKN2) gene mutations in esophageal cancers

1 reference

7 January 2021

A germline deletion of p14(ARF) but not CDKN2A in a melanoma-neural system tumour syndrome family

1 reference

7 January 2021

1 reference

7 January 2021

Intragenic mutations of CDKN2B and CDKN2A in primary human esophageal cancers.

1 reference

7 January 2021

Multiple types of aberrations in the p16 (INK4a) and the p15(INK4b) genes in 30 esophageal squamous-cell-carcinoma cell lines

1 reference

7 January 2021

Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China.

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.10315

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14732922%20AND%20SRC:MED&resulttype=core&format=json

17 November 2019

1 reference