Isolation and characterization of the human mismatch repair gene hMSH2 promoter region (Q36790595)

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scientific article published on January 1996

Language	Label	Description	Also known as
English	Isolation and characterization of the human mismatch repair gene hMSH2 promoter region	scientific article published on January 1996

Statements

scholarly article

1 reference

Europe PubMed Central

16 August 2017

Isolation and characterization of the human mismatch repair gene hMSH2 promoter region (English)

1 reference

Europe PubMed Central

16 August 2017

DNA mismatch repair

1 reference

based on heuristic

inferred from title

author name string

S J Scherer

1

1 reference

Europe PubMed Central

16 August 2017

T Seib

2

1 reference

Europe PubMed Central

16 August 2017

G Seitz

3

1 reference

Europe PubMed Central

16 August 2017

S Dooley

4

1 reference

Europe PubMed Central

16 August 2017

C Welter

5

1 reference

Europe PubMed Central

16 August 2017

language of work or name

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based on heuristic

inferred from title

publication date

1 January 1996

1 reference

Europe PubMed Central

16 August 2017

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Europe PubMed Central

16 August 2017

97

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Europe PubMed Central

16 August 2017

1

1 reference

Europe PubMed Central

16 August 2017

114-116

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Europe PubMed Central

16 August 2017

https://scigraph.springernature.com/pub.10.1007/bf00218844

0 references

Stalking the start of colon cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic instability of microsatellites in endometrial carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

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Microsatellite instability in Muir-Torre syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial colonic cancer without antecedent polyposis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clues to the pathogenesis of familial colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

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Direct sequencing of terminal regions of genomic P1 clones. A general strategy for the design of sequence-tagged site markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of a mutL homolog in hereditary colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a locus predisposing to human colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8557250

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00218844

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

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