Abundant copy-number loss of CYCLOPS and STOP genes in gastric adenocarcinoma (Q36778202)

16 August 2017

Abundant copy-number loss of CYCLOPS and STOP genes in gastric adenocarcinoma (English)

1 reference

16 August 2017

1 reference

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14 June 2020

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14 June 2020

Ioana Cutcutache

1 reference

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14 June 2020

Alice Yingting Wu

1 reference

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14 June 2020

Yuka Suzuki

1 reference

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14 June 2020

John Richard McPherson

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14 June 2020

Zhengdeng Lei

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14 June 2020

Shenli Zhang

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14 June 2020

Wai Keong Wong

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14 June 2020

Khee Chee Soo

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14 June 2020

Weng Hoong Chan

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14 June 2020

London Lucien Ooi

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14 June 2020

Roy Welsch

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14 June 2020

Patrick Tan

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14 June 2020

publication date

24 July 2015

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16 August 2017

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14 June 2020

volume

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14 June 2020

issue

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14 June 2020

page(s)

453-465

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Creative Commons Attribution 4.0 International

14 June 2020

start time

24 July 2015

1 reference

April 2022 Public Data File from Crossref

copyrighted

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cites work

Homozygous deletions at 3p22, 5p14, 6q15, and 9p21 result in aberrant expression of tumor suppressor genes in gastric cancer

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Identification of molecular subtypes of gastric cancer with different responses to PI3-kinase inhibitors and 5-fluorouracil

29 September 2017

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29 September 2017

Cancer genome landscapes

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Cancer vulnerabilities unveiled by genomic loss

29 September 2017

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Recurrent hemizygous deletions in cancers may optimize proliferative potential

29 September 2017

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The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity

29 September 2017

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A comprehensive survey of genomic alterations in gastric cancer reveals systematic patterns of molecular exclusivity and co-occurrence among distinct therapeutic targets

29 September 2017

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Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity

29 September 2017

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Intrinsic subtypes of gastric cancer, based on gene expression pattern, predict survival and respond differently to chemotherapy

29 September 2017

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GPHMM: an integrated hidden Markov model for identification of copy number alteration and loss of heterozygosity in complex tumor samples using whole genome SNP arrays

29 September 2017

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Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008

29 September 2017

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29 September 2017

Global cancer statistics

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High resolution ArrayCGH and expression profiling identifies PTPRD and PCDH17/PCH68 as tumor suppressor gene candidates in laryngeal squamous cell carcinoma.

29 September 2017

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Allele-specific copy number analysis of tumors

29 September 2017

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TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays

29 September 2017

1 reference

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Prognostic significance of genetic alterations detected by high-density single nucleotide polymorphism array in gastric cancer.

29 September 2017

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The landscape of somatic copy-number alteration across human cancers

29 September 2017

1 reference

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A catalog of genes homozygously deleted in human lung cancer and the candidacy of PTPRD as a tumor suppressor gene.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6.

29 September 2017

1 reference

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The tyrosine phosphatase PTPRD is a tumor suppressor that is frequently inactivated and mutated in glioblastoma and other human cancers

29 September 2017

1 reference

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Mutational inactivation of PTPRD in glioblastoma multiforme and malignant melanoma

29 September 2017

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Genomic imbalances in 5918 malignant epithelial tumors: an explorative meta-analysis of chromosomal CGH data

29 September 2017

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Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma

29 September 2017

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Aberrant splicing of the PTPRD gene mimics microdeletions identified at this locus in neuroblastomas

29 September 2017

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Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis

29 September 2017

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Adjusting batch effects in microarray expression data using empirical Bayes methods

29 September 2017

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Homozygous deletion and reduced expression of the DOCK8 gene in human lung cancer.

29 September 2017

1 reference

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Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

29 September 2017

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A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

29 September 2017

1 reference

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A census of human cancer genes

29 September 2017

1 reference

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Relationship between inactivation of p16 gene and gastric carcinoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Chromosomal imbalances in gastric cancer. Correlation with histologic subtypes and tumor progression

29 September 2017

1 reference

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CDKN2A mutation and deletion status in thin and thick primary melanoma

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Allelotype of gastric adenocarcinoma.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

The CDKN2A (p16) gene and human cancer.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Frequent mutation of p16 in squamous cell carcinoma of the head and neck.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

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=4824836

Intragenic homozygous deletions of MTS1 gene in gastric cancer in Taiwan.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Frequent silence of chromosome 9p, homozygous DOCK8, DMRT1 and DMRT3 deletion at 9p24.3 in squamous cell carcinoma of the lung.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Relationship between alterations of p16(INK4a) and p14(ARF) genes of CDKN2A locus and gastric carcinogenesis.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Allelic deletions of MCC/APC and p53 are frequent late events in human gastric carcinogenesis.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4824836

Numerical aberrations of chromosome 8 in gastric cancer detected by fluorescence in situ hybridization

5 September 2018

1 reference

12 December 2020

Frequent loss of heterozygosity at the DCC locus in gastric cancer

1 reference

12 December 2020

Allelotype of adenoma and differentiated adenocarcinoma of the stomach

1 reference

12 December 2020

Genetic alterations in gastrinomas and nonfunctioning pancreatic neuroendocrine tumors: an analysis of p16/MTS1 tumor suppressor gene inactivation

1 reference

12 December 2020

1 reference

12 December 2020

10.1007/S10120-015-0514-Z

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26205786%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26205786%20AND%20SRC:MED&resulttype=core&format=json

14 June 2020

PubMed publication ID

26205786

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26205786%20AND%20SRC:MED&resulttype=core&format=json