(Q80776604)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18301448%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

title

No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients (English)

1 reference

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3 January 2020

1 reference

11

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3 January 2020

12

Peter Propping

1 reference

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3 January 2020

Brigitte Royer-Pokora

8

object named as

Brigitte Royer-Pokora

1 reference

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3 January 2020

author name string

Verena Steinke

1

1 reference

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3 January 2020

Nils Rahner

2

1 reference

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3 January 2020

Monika Morak

3

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3 January 2020

Gisela Keller

4

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3 January 2020

Hans K Schackert

5

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3 January 2020

Heike Görgens

6

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3 January 2020

Wolff Schmiegel

7

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3 January 2020

Wolfgang Dietmaier

9

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3 January 2020

Matthias Kloor

10

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3 January 2020

Stefan Aretz

13

1 reference

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3 January 2020

German HNPCC Consortium

14

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3 January 2020

publication date

27 February 2008

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European Journal of Human Genetics

3 January 2020

published in

1 reference

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3 January 2020

volume

16

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3 January 2020

issue

5

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3 January 2020

page(s)

587-592

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https://scigraph.springernature.com/pub.10.1038/ejhg.2008.26

3 January 2020

exact match

0 references

cites work

Hereditary colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Human MutY homolog, a DNA glycosylase involved in base excision repair, physically and functionally interacts with mismatch repair proteins human MutS homolog 2/human MutS homolog 6

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Deficient DNA mismatch repair: a common etiologic factor for colon cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP).

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Germline susceptibility to colorectal cancer due to base-excision repair gene defects

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

The role of MYH and microsatellite instability in the development of sporadic colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Germline mutations in the MYH gene in Swedish familial and sporadic colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

MUTYH and the mismatch repair system: partners in crime?

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: Meeting Highlights and Bethesda Guidelines

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Involvement of hMSH6 in the development of hereditary and sporadic colorectal cancer revealed by immunostaining is based on germline mutations, but rarely on somatic inactivation

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

A novel mutation detection approach of hMLH1 and hMSH2 genes for screening of colorectal cancer.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Frequency of the Common MYH Mutations (G382D and Y165C) in MMR Mutation Positive and Negative HNPCC Patients

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2008.26

7 January 2021

Identifiers

DOI

10.1038/EJHG.2008.26

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18301448%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

1 reference