(Q40762457)

23 September 2017

title

Mutation frequency in coding and non-coding repeat sequences in mismatch repair deficient cells derived from normal human tissue (English)

1 reference

23 September 2017

1 reference

3

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23 September 2017

Bacon AL

1

1 reference

23 September 2017

Farrington SM

series ordinal

2

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23 September 2017

language of work or name

English

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publication date

1 November 2001

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23 September 2017

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23 September 2017

volume

20

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23 September 2017

issue

51

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23 September 2017

page(s)

7464-7471

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Clues to the pathogenesis of familial colorectal cancer

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Sequence interruptions confer differential stability at microsatellite alleles in mismatch repair-deficient cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Genetic instability and darwinian selection in tumours

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Resistance to TGF-beta1 correlates with a reduction of TGF-beta type II receptor expression in Burkitt's lymphoma and Epstein-Barr virus-transformed B lymphoblastoid cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

HNPCC associated with germline mutation in the TGF-beta type II receptor gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Mismatch Repair Deficiency in Phenotypically Normal Human Cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Mutation analysis of coding sequences of the entire transforming growth factor beta type II receptor gene in sporadic human colon cancer using genomic DNA and intron primers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Mechanisms of inactivation of mismatch repair genes in human colorectal cancer cell lines: the predominant role of hMLH1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

Role of BAX mutations in mismatch repair-deficient colorectal carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

inferred from DOI database lookup

7 January 2021

based on heuristic

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1204973

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.ONC.1204973

1 reference

Dimensions Publication ID

23 September 2017

1019871097

0 references

1 reference