(Q53600981)

English

A de novo MLH1 germ line mutation in a 31-year-old colorectal cancer patient.

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

A de novo MLH1 germ line mutation in a 31-year-old colorectal cancer patient. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

colorectal cancer

1 reference

based on heuristic

inferred from title

author name string

Martina Plasilova

1

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Jian Zhang

2

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Roberta Okhowat

3

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Giancarlo Marra

4

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Markus Mettler

5

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Hansjakob Mueller

6

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Karl Heinimann

7

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

publication date

1 December 2006

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

45

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

12

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

1106-1110

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

Cancer risk in mutation carriers of DNA-mismatch-repair genes

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Lynch syndrome: form, function, proteins, and basketball

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Recurrent germline mutation in MSH2 arises frequently de novo

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Hereditary colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

The hamartomatous polyposis syndromes: a clinical and molecular review

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20374

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GCC.20374

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 May 2018

http://europepmc.org/abstract/MED/16955466

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