(Q79198468)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574162%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

title

The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14574162%20AND%20SRC:MED&resulttype=core&format=json

20 December 2019

1 reference

4

1 reference

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20 December 2019

10

Pål Møller

1 reference

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20 December 2019

author name string

Astrid T Stormorken

1

1 reference

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20 December 2019

Wolfram Müller

2

1 reference

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20 December 2019

Annika Lindblom

3

1 reference

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20 December 2019

Steinar Aase

5

1 reference

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20 December 2019

Inger Marie Bowitz Lothe

6

1 reference

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20 December 2019

Tove Norèn

7

1 reference

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20 December 2019

Juul T Wijnen

8

1 reference

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20 December 2019

Gabriela Möslein

9

1 reference

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20 December 2019

publication date

1 January 2003

1 reference

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20 December 2019

1 reference

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20 December 2019

volume

2

1 reference

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20 December 2019

issue

1

1 reference

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20 December 2019

page(s)

9-13

1 reference

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https://scigraph.springernature.com/pub.10.1023/a:1023362205205

20 December 2019

exact match

0 references

cites work

MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

12 December 2020

Lack of MSH2 and MSH6 characterizes endometrial but not colon carcinomas in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

1 reference

12 December 2020

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Proximal adenomas in hereditary non-polyposis colorectal cancer are prone to rapid malignant transformation

1 reference

12 December 2020

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis

1 reference

12 December 2020

Expression of wild-type p53 is not compatible with continued growth of p53-negative tumor cells

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation of a mutL homolog in hereditary colon cancer

1 reference

12 December 2020

Mismatch repair deficiency associated with overexpression of the MSH3 gene

1 reference

12 December 2020

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

12 December 2020

Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes

1 reference

12 December 2020

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

1 reference

12 December 2020

Steady-state regulation of the human DNA mismatch repair system.

1 reference

12 December 2020

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

1 reference

12 December 2020

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

12 December 2020

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

1 reference

12 December 2020