(Q74073284)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

alternative mRNA splicing, via spliceosome

8 November 2019

main subject

1 reference

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

author name string

T L Chan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

S T Yuen

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

J W Ho

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

A S Chan

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

K Kwan

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

L P Chung

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

P W Lam

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

C W Tse

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

language of work or name

English

0 references

publication date

1 May 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

issue

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

page(s)

2976-2981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11420710%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.onc.1204376

8 November 2019

exact match

0 references

cites work

Clues to the pathogenesis of familial colorectal cancer

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7 January 2021

Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer

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7 January 2021

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

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7 January 2021

Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes

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7 January 2021

Frequent microsatellite instability and mismatch repair gene mutations in young Chinese patients with colorectal cancer

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7 January 2021

Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells

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7 January 2021

Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls

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7 January 2021

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

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7 January 2021

Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome

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7 January 2021

Distinct clinical features associated with microsatellite instability in colorectal cancers of young patients.

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7 January 2021

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

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7 January 2021

Microsatellite instability-a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

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7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

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7 January 2021

Microsatellite instability and mutation of DNA mismatch repair genes in gliomas.

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7 January 2021

Genetic instability occurs in the majority of young patients with colorectal cancer

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7 January 2021

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

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7 January 2021

Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients

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7 January 2021

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

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7 January 2021

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

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7 January 2021

Founding mutations and Alu-mediated recombination in hereditary colon cancer

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7 January 2021

Transcripts with splicings of exons 15 and 16 of the hMLH1 gene in normal lymphocytes: implications in RNA-based mutation screening of hereditary non-polyposis colorectal cancer

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7 January 2021

GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells

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7 January 2021

Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer

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7 January 2021

An economic method for the fluorescent labeling of PCR fragments.

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7 January 2021

Microsatellite instability in cancer of the proximal colon

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7 January 2021

Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer

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7 January 2021

MSH2 genomic deletions are a frequent cause of HNPCC

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7 January 2021

Colorectal carcinoma in Hong Kong: epidemiology and genetic mutations.

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7 January 2021