(Q38305431)

2 September 2017

title

Extensive gene conversion at the PMS2 DNA mismatch repair locus (English)

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2 September 2017

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7

David T Bonthron

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Eamonn Sheridan

6

object named as

Eamonn Sheridan

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author name string

Bruce E Hayward

1

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2 September 2017

Michel De Vos

2

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2 September 2017

Elizabeth M A Valleley

3

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2 September 2017

Ruth S Charlton

4

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2 September 2017

Graham R Taylor

5

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2 September 2017

Eamonn Sheridan

6

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2 September 2017

publication date

1 May 2007

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2 September 2017

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2 September 2017

volume

28

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2 September 2017

issue

5

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2 September 2017

page(s)

424-430

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Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability

2 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

PMS2 mutations in childhood cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Discovery of human inversion polymorphisms by comparative analysis of human and chimpanzee DNA sequence assemblies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Germline PMS2 mutations: one hit or two?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

PMS2 mutations in HNPCC

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Cloning, characterization and chromosomal assignment of the human genes homologous to yeast PMS1, a member of mismatch repair genes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Intense and highly localized gene conversion activity in human meiotic crossover hot spots

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Drastic genetic instability of tumors and normal tissues in Turcot syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Genomic organization of the human PMS2 gene family.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20457

7 January 2021

Identifiers

DOI

10.1002/HUMU.20457

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2 September 2017

1 reference