(Q34386209)

English

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria (English)

1 reference

Europe PubMed Central

1 August 2017

colorectal cancer

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

colorectal carcinoma

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

DNA mismatch repair

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based on heuristic

inferred from title

author name string

Kruse R

1

1 reference

Europe PubMed Central

1 August 2017

Rütten A

2

1 reference

Europe PubMed Central

1 August 2017

Lamberti C

3

1 reference

Europe PubMed Central

1 August 2017

Hosseiny-Malayeri HR

4

1 reference

Europe PubMed Central

1 August 2017

Wang Y

5

1 reference

Europe PubMed Central

1 August 2017

Ruelfs C

6

1 reference

Europe PubMed Central

1 August 2017

Jungck M

7

1 reference

Europe PubMed Central

1 August 2017

Mathiak M

8

1 reference

Europe PubMed Central

1 August 2017

Ruzicka T

9

1 reference

Europe PubMed Central

1 August 2017

Hartschuh W

10

1 reference

Europe PubMed Central

1 August 2017

Bisceglia M

11

1 reference

Europe PubMed Central

1 August 2017

Friedl W

12

1 reference

Europe PubMed Central

1 August 2017

Propping P

13

1 reference

Europe PubMed Central

1 August 2017

language of work or name

0 references

publication date

1 July 1998

1 reference

Europe PubMed Central

1 August 2017

American Journal of Human Genetics

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Europe PubMed Central

1 August 2017

63

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Europe PubMed Central

1 August 2017

63-70

1 reference

Europe PubMed Central

1 August 2017

1

1 reference

Europe PubMed Central

1 August 2017

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Microsatellite instability analysis: a multicenter study for reliability and quality control.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Molecular basis of HNPCC: mutations of MMR genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Obstructive jejunal adenocarcinoma in the Muir-Torre syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Muir-Torre syndrome: a variant of the cancer family syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

The Muir-Torre syndrome: a 25-year retrospect

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

6 July 2018

Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

28 July 2018

Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

27 October 2018

[Muir-Torre syndrome. Diagnostic criteria and review of the literature]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377247

27 October 2018

The Cancer Family Syndrome Rare Cutaneous Phenotypic Linkage of Torre's Syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muir-Torre syndrome. Histologic spectrum of sebaceous proliferations

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muir-Torre Syndrome: A Case Report

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-step screening method for the most common mutations in familial adenomatous polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability in Muir-Torre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muir-Torre syndrome: clinical features and molecular genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9634524

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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