(Q51038828)

English

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden.

scientific article published in April 2004

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

0 references

Irina Golovleva

6

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

Henrik Grönberg

7

object named as

Henrik Grönberg

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

Elke Holinski-Feder

4

object named as

Elke Holinski-Feder

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

author name string

Kristina Cederquist

1

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

Monica Emanuelsson

2

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

Ingela Göransson

3

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

Yvonne Müller-Koch

5

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

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publication date

1 April 2004

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

International Journal of Cancer

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

109

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

3

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

370-376

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Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

A role for MLH3 in hereditary nonpolyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mutation in the mismatch repair gene Msh6 causes cancer susceptibility

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations.

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Do MSH6 mutations contribute to double primary cancers of the colorectum and endometrium?

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approach

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mutations in hMSH6 alone are not sufficient to cause the microsatellite instability in colorectal cancer cell lines.

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

The molecular basis of Turcot's syndrome

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

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/10.1002%2FIJC.11718

21 January 2018

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Finnish mutations in Swedish HNPCC families

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Microsatellite instability in the insulin–like growth factor II receptor gene in gastrointestinal tumours

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

A population based cohort study of patients with multiple colon and endometrial cancer: Correlation of microsatellite instability (msi) status, age at diagnosis and cancer risk

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

Excess of hMLH1 germline mutations in Swiss families with hereditary non-polyposis colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FIJC.11718

21 January 2018

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

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1126/SCIENCE.7761852

Identifiers

10.1002/IJC.11718

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 March 2018

http://europepmc.org/abstract/MED/14961575

ResearchGate publication ID

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