(Q42734300)

6 November 2017

Early onset brain tumor and lymphoma in MSH2-deficient children (English)

1 reference

6 November 2017

1 reference

Gaëlle Bougeard

1

1 reference

6 November 2017

Françoise Charbonnier

2

1 reference

6 November 2017

Alexandre Moerman

3

1 reference

6 November 2017

Cosette Martin

4

1 reference

6 November 2017

Marie M Ruchoux

5

1 reference

6 November 2017

Nathalie Drouot

6

1 reference

6 November 2017

Thierry Frébourg

7

1 reference

6 November 2017

language of work or name

English

0 references

publication date

1 January 2003

1 reference

American Journal of Human Genetics

6 November 2017

1 reference

6 November 2017

72

1 reference

6 November 2017

1

1 reference

6 November 2017

213-216

1 reference

Association of p53 and MSH2 with recombinative repair complexes during S phase

6 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

Brain tumor-polyposis syndrome: two genetic diseases?

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

Mismatch repair in replication fidelity, genetic recombination, and cancer biology

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

The molecular basis of Turcot's syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

Extensive somatic microsatellite mutations in normal human tissue.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=378628

Detection of exon deletions and duplications of the mismatch repair genes in hereditary nonpolyposis colorectal cancer families using multiplex polymerase chain reaction of short fluorescent fragments

16 August 2018

1 reference

12 December 2020

MSH2 in contrast to MLH1 and MSH6 is frequently inactivated by exonic and promoter rearrangements in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Neurofibromatosis and early onset of cancers in hMLH1-deficient children

1 reference

12 December 2020

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

1 reference

12 December 2020

Identifiers

DOI

10.1086/345297

1 reference

6 November 2017

1 reference

6 November 2017

PubMed publication ID

12549480

1 reference