Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein (Q59273299)

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6 November 2019

title

Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein (English)

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6 November 2019

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Carlos Alberto Vaccaro

2

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6 November 2019

Wael M Abdel-Rahman

3

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6 November 2019

Päivi Peltomäki

9

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6 November 2019

Minna Nyström

10

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6 November 2019

author name string

Tiina E Raevaara

1

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6 November 2019

Esteban Mocetti

4

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6 November 2019

Shashi Bala

5

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6 November 2019

Karin E Lönnqvist

6

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6 November 2019

Reetta Kariola

7

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6 November 2019

Henry T Lynch

8

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6 November 2019

language of work or name

English

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publication date

1 August 2003

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6 November 2019

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6 November 2019

volume

125

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6 November 2019

issue

2

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6 November 2019

page(s)

501-509

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Genetic mapping of a locus predisposing to human colorectal cancer

6 November 2019

cites work

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Clues to the pathogenesis of familial colorectal cancer

7 January 2021

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Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations

7 January 2021

1 reference

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

7 January 2021

1 reference

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New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

7 January 2021

1 reference

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MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis

7 January 2021

1 reference

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Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

7 January 2021

1 reference

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The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study

7 January 2021

1 reference

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Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer

7 January 2021

1 reference

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Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer

7 January 2021

1 reference

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Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1.

7 January 2021

1 reference

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Functional analysis of hMLH1 variants and HNPCC-related mutations using a human expression system

7 January 2021

1 reference

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The molecular basis of Turcot's syndrome

7 January 2021

1 reference

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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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

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

7 January 2021

1 reference

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Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer

7 January 2021

1 reference

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

7 January 2021

1 reference

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

7 January 2021

1 reference

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The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

7 January 2021

1 reference

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Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindreds

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae

7 January 2021

1 reference

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Mutator phenotypes conferred by MLH1 overexpression and by heterozygosity for mlh1 mutations.

7 January 2021

1 reference

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Functional analysis of human MLH1 and MSH2 missense variants and hybrid human-yeast MLH1 proteins in Saccharomyces cerevisiae

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

Mutations within the hMLH1 and hPMS2 subunits of the human MutLalpha mismatch repair factor affect its ATPase activity, but not its ability to interact with hMutSalpha

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0016-5085%2803%2900905-3

The interaction of DNA mismatch repair proteins with human exonuclease I

7 January 2021

1 reference

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10.1016/S0016-5085(03)00905-3

7 January 2021

Identifiers

DOI

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6 November 2019

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