The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours (Q79198468)

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scientific article published on 01 January 2003

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English	The inframe MSH2 codon 596 deletion is linked with HNPCC and associated with lack of MSH2 protein in tumours	scientific article published on 01 January 2003

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

title

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

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

main subject

Lynch syndrome

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inferred from title

author

Ketil R. Heimdal

series ordinal

4

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Pål Møller

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10

object named as

Pål Møller

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

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20 December 2019

Annika Lindblom

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3

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Annika Lindblom

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

author name string

Astrid T Stormorken

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Wolfram Müller

series ordinal

2

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Steinar Aase

series ordinal

5

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Inger Marie Bowitz Lothe

series ordinal

6

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Europe PubMed Central

PubMed publication ID

14574162

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

retrieved

20 December 2019

Tove Norèn

series ordinal

7

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Juul T Wijnen

series ordinal

8

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Gabriela Möslein

series ordinal

9

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

publication date

1 January 2003

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

published in

Familial Cancer

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

volume

2

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stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

page(s)

9-13

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Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

cites work

MSH2 genomic deletions are a frequent cause of HNPCC

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation of a mutL homolog in hereditary colon cancer

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair deficiency associated with overexpression of the MSH3 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cancer risk associated with germline DNA mismatch repair gene mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID 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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/14574162

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1023362205205

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

Dimensions Publication ID

1028388557

0 references

PubMed publication ID

14574162

1 reference

stated in

Europe PubMed Central

PubMed publication ID

14574162

reference URL

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

retrieved

20 December 2019

 

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