(Q25257372)

English

Does tumorigenesis select for or against mutations of the DNA repair-associated genes BRCA2 and MRE11?: considerations from somatic mutations in microsatellite unstable (MSI) gastrointestinal cancers

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

6 July 2017

Does tumorigenesis select for or against mutations of the DNA repair-associated genes BRCA2 and MRE11?: considerations from somatic mutations in microsatellite unstable (MSI) gastrointestinal cancers (English)

1 reference

Europe PubMed Central

6 July 2017

1 reference

based on heuristic

inferred from title

Elhaam Elghalbzouri-Maghrani

3

object named as

Elhaam Elghalbzouri-Maghrani

1 reference

Europe PubMed Central

6 July 2017

Małgorzata Z Zdzienicka

4

object named as

Malgorzata Z Zdzienicka

1 reference

Europe PubMed Central

6 July 2017

author name string

Michiel S van der Heijden

1

1 reference

Europe PubMed Central

6 July 2017

Jonathan R Brody

2

1 reference

Europe PubMed Central

6 July 2017

Scott E Kern

5

1 reference

Europe PubMed Central

6 July 2017

language of work or name

0 references

publication date

17 January 2006

1 reference

Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

6 July 2017

7

1 reference

Europe PubMed Central

6 July 2017

3

1 reference

Europe PubMed Central

6 July 2017

1

0 references

https://scigraph.springernature.com/pub.10.1186/1471-2156-7-3

0 references

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

7 April 2017

Abnormal cytokinesis in cells deficient in the breast cancer susceptibility protein BRCA2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

7 April 2017

Alterations of the double-strand break repair gene MRE11 in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

7 April 2017

Brca2 deficiency in the murine small intestine sensitizes to p53-dependent apoptosis and leads to the spontaneous deletion of stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

7 April 2017

BRCA2 is required for homology-directed repair of chromosomal breaks

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

7 April 2017

Hypersensitivity of tumor cell lines with microsatellite instability to DNA double strand break producing chemotherapeutic agent bleomycin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Mutations of an intronic repeat induce impaired MRE11 expression in primary human cancer with microsatellite instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Evidence for a direct association of hMRE11 with the human mismatch repair protein hMLH1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Mutations at coding repeat sequences in mismatch repair-deficient human cancers: toward a new concept of target genes for instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Human MRE11 is inactivated in mismatch repair-deficient cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Role of BRCA2 in control of the RAD51 recombination and DNA repair protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

BRCA2 is inactivated late in the development of pancreatic intraepithelial neoplasia: evidence and implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Mre11 is essential for the maintenance of chromosomal DNA in vertebrate cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 September 2017

Mutations at coding mononucleotide repeats in gastric cancer with the microsatellite mutator phenotype.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

31 May 2018

Three classes of genes mutated in colorectal cancers with chromosomal instability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Tumors with microsatellite instability: many mutations, targets and paradoxes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Evidence of selection for clones having genetic inactivation of the activin A type II receptor (ACVR2) gene in gastrointestinal cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Quantitative selection constants.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

The effect of mismatch repair deficiency on tumourigenesis; microsatellite instability affecting genes containing short repeated sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Frameshift somatic mutations in gastrointestinal cancer of the microsatellite mutator phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Microsatellite instability and mutations of the transforming growth factor beta type II receptor gene in colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1382246

28 November 2018

Splice variant lacking the transactivation domain of theBRCA2 gene and mutations in the splice acceptor site of intron 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short mononucleotide repeat sequence variability in mismatch repair-deficient cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic progression in sporadic endometrial and gastrointestinal cancers with high microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelotype of pancreatic adenocarcinoma using xenograft enrichment

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the BRCA2 gene in ovarian carcinomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A somatic BRCA2 mutation in RER+ endometrial carcinomas that specifically deletes the amino-terminal transactivation domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel sensitive method to detect frameshift mutations in exonic repeat sequences of cancer-related genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16417627

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2156-7-3

1 reference

Europe PubMed Central

6 July 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

6 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q25257372&oldid=1739691756"