Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts (Q39443467)

12 September 2017

Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts (English)

1 reference

12 September 2017

1 reference

1 reference

1 reference

7

Hugo W Tilanus

1 reference

12 September 2017

9

Winand N M Dinjens

1 reference

12 September 2017

Jurjen J Boonstra

1

1 reference

12 September 2017

Ronald van Marion

2

1 reference

12 September 2017

Hannie J C W Douben

3

1 reference

12 September 2017

Jerry S Lanchbury

4

1 reference

12 September 2017

Kirsten M Timms

5

1 reference

12 September 2017

Victor Abkevich

6

1 reference

12 September 2017

Annelies de Klein

8

1 reference

12 September 2017

12 November 2011

1 reference

Genes, Chromosomes and Cancer

12 September 2017

1 reference

12 September 2017

51

1 reference

12 September 2017

3

1 reference

12 September 2017

272-282

1 reference

Chromosomal abnormalities and novel disease-related regions in progression from Barrett's esophagus to esophageal adenocarcinoma

12 September 2017

1 reference

Inactivation of the Wwox gene accelerates forestomach tumor progression in vivo

21 January 2018

1 reference

The landscape of somatic copy-number alteration across human cancers

21 January 2018

1 reference

Signatures of mutation and selection in the cancer genome

21 January 2018

1 reference

The RUNX genes: gain or loss of function in cancer

21 January 2018

1 reference

Verification and unmasking of widely used human esophageal adenocarcinoma cell lines.

21 January 2018

1 reference

A survey of homozygous deletions in human cancer genomes

21 January 2018

1 reference

Application of Nexus copy number software for CNV detection and analysis

21 January 2018

1 reference

Establishment of cell lines from adenocarcinomas of the esophagus and gastric cardia growing in vivo and in vitro

21 January 2018

1 reference

FHIT gene therapy prevents tumor development in Fhit-deficient mice.

21 January 2018

1 reference

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

21 January 2018

1 reference

Integrative analysis of array-comparative genomic hybridisation and matched gene expression profiling data reveals novel genes with prognostic significance in oesophageal adenocarcinoma

21 January 2018

1 reference

Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.

21 January 2018

1 reference

E-cadherin germline mutations in familial gastric cancer.

21 January 2018

1 reference

DPC4, a candidate tumor suppressor gene at human chromosome 18q21.1

21 January 2018

1 reference

Cadherin and catenin alterations in human cancer

21 January 2018

1 reference

High incidence of somatic mutations in the AML1/RUNX1 gene in myelodysplastic syndrome and low blast percentage myeloid leukemia with myelodysplasia

21 January 2018

1 reference

Four human breast cancer cell lines with biallelic inactivating alpha-catenin gene mutations

21 January 2018

1 reference

Switch from alphavbeta5 to alphavbeta6 integrin expression protects squamous cell carcinomas from anoikis

21 January 2018

1 reference

New roles for integrins in squamous-cell carcinoma

21 January 2018

1 reference

21 January 2018

Cancer statistics, 2009

1 reference

Overexpression of Slug is associated with malignant progression of esophageal adenocarcinoma.

21 January 2018

1 reference

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

21 January 2018

1 reference

Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)

21 January 2018

1 reference

Deletion at fragile sites is a common and early event in Barrett's esophagus.

21 January 2018

1 reference

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

21 January 2018

1 reference

Causal relationship between the loss of RUNX3 expression and gastric cancer

21 January 2018

1 reference

Single nucleotide polymorphism-based genome-wide chromosome copy change, loss of heterozygosity, and aneuploidy in Barrett's esophagus neoplastic progression

21 January 2018

1 reference

Oncogenic transcription factors in the human acute leukemias

21 January 2018

1 reference

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

21 January 2018

1 reference

A molecular signature of metastasis in primary solid tumors

21 January 2018

1 reference

Cloning and characterisation of ITGAV, the genomic sequence for human cell adhesion protein (vitronectin) receptor alpha subunit, CD51

21 January 2018

1 reference

The RIN: an RNA integrity number for assigning integrity values to RNA measurements

21 January 2018

1 reference

21 January 2018

1 reference

P-cadherin promotes cell-cell adhesion and counteracts invasion in human melanoma

21 January 2018

1 reference

The human alphaE-catenin gene CTNNA1: mutational analysis and rare occurrence of a truncated splice variant

21 January 2018

1 reference

E-cadherin gene mutations are rare in adenocarcinomas of the oesophagus

21 January 2018

1 reference

Genome-Wide Copy Number Analysis in Esophageal Adenocarcinoma Using High-Density Single-Nucleotide Polymorphism Arrays

21 January 2018

1 reference

Integration of somatic deletion analysis of prostate cancers and germline linkage analysis of prostate cancer families reveals two small consensus regions for prostate cancer genes at 8p

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Genome-wide analysis of genetic alterations in Barrett's adenocarcinoma using single nucleotide polymorphism arrays

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GCC.20952

1 reference

12 September 2017

1 reference