(Q39737975)

14 September 2017

Signatures of mutation and selection in the cancer genome (English)

1 reference

14 September 2017

1 reference

14 September 2017

Sarah Edkins

0 references

Sara Widaa

object named as

Sara Widaa

0 references

Gillian L Dalgliesh

0 references

Bin T Teh

0 references

P Andrew Futreal

1 reference

14 September 2017

Gemma Buck

0 references

Michael R Stratton

1 reference

14 September 2017

Calli Latimer

1 reference

14 September 2017

Helen Davies

1 reference

14 September 2017

Sajani Swamy

1 reference

14 September 2017

Jonathon Hinton

1 reference

14 September 2017

David Beare

1 reference

14 September 2017

Graham R Bignell

1 reference

14 September 2017

Chris D Greenman

1 reference

14 September 2017

Adam P Butler

1 reference

14 September 2017

Jenny M Andrews

1 reference

14 September 2017

Lina Chen

1 reference

14 September 2017

Ciara Fahey

1 reference

14 September 2017

Beiyuan Fu

1 reference

14 September 2017

Fengtang Yang

1 reference

14 September 2017

Peter J Campbell

1 reference

14 September 2017

language of work or name

English

0 references

publication date

1 February 2010

1 reference

14 September 2017

1 reference

14 September 2017

463

1 reference

14 September 2017

7283

1 reference

14 September 2017

893-898

1 reference

Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

14 September 2017

start time

1 February 2010

1 reference

April 2022 Public Data File from Crossref

copyrighted

0 references

cites work

PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Sample type bias in the analysis of cancer genomes

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Replication stress induces genome-wide copy number changes in human cells that resemble polymorphic and pathogenic variants

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

RETRACTED: A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Mutational inactivation of PTPRD in glioblastoma multiforme and malignant melanoma

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Conspirators in a capital crime: co-deletion of p18INK4c and p16INK4a/p14ARF/p15INK4b in glioblastoma multiforme

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Somatic mutations affect key pathways in lung adenocarcinoma

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Integrated detection and population-genetic analysis of SNPs and copy number variation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Copy number variation and evolution in humans and chimpanzees

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Feedback circuit among INK4 tumor suppressors constrains human glioblastoma development

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Human chromosome fragility

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Characterizing the cancer genome in lung adenocarcinoma

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Definition of the zebrafish genome using flow cytometry and cytogenetic mapping.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Chromosome fragility: molecular mechanisms and cellular consequences

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

The consensus coding sequences of human breast and colorectal cancers

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Roles of FHIT and WWOX fragile genes in cancer

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

ATR Regulates Fragile Site Stability

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Hypermutation of multiple proto-oncogenes in B-cell diffuse large-cell lymphomas

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Human mitogen-activated protein kinase kinase 4 as a candidate tumor suppressor

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Expression of wild-type alpha-catenin protein in cells with a mutant alpha-catenin gene restores both growth regulation and tumor suppressor activities

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

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

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

The cytoplasmic domain of the cell adhesion molecule uvomorulin associates with three independent proteins structurally related in different species

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

p15Ink4b is a critical tumour suppressor in the absence of p16Ink4a

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Chromosome 5q deletion and epigenetic suppression of the gene encoding alpha-catenin (CTNNA1) in myeloid cell transformation

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Structural evidence for the authenticity of the human retinoblastoma gene

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Two levels of protection for the B cell genome during somatic hypermutation.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Somatic frameshift mutations in the MBD4 gene of sporadic colon cancers with mismatch repair deficiency.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

The alphaE-catenin gene (CTNNA1) acts as an invasion-suppressor gene in human colon cancer cells

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype.

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

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

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3145113

Evaluation of candidate tumour suppressor genes on chromosome 18 in colorectal cancers

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20164919

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Novel aphidicolin-inducible common fragile site FRA9G maps to 9p22.2, within the C9orf39 gene

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20164919

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NATURE08768

1 reference

14 September 2017

1 reference

14 September 2017

PubMed publication ID

20164919

1 reference