Frameshift mismatch recognition by the human MutS alpha complex (Q47791002)

5 February 2018

title

Frameshift mismatch recognition by the human MutS alpha complex (English)

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5 February 2018

author name string

Macpherson P

series ordinal

1

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5 February 2018

Humbert O

series ordinal

2

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5 February 2018

Karran P

series ordinal

3

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5 February 2018

language of work or name

English

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publication date

1 July 1998

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5 February 2018

published in

Mutation Research

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5 February 2018

volume

408

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5 February 2018

issue

1

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5 February 2018

page(s)

55-66

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5 February 2018

Mismatch repair in replication fidelity, genetic recombination, and cancer biology

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7 January 2021

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

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

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

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7 January 2021

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

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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

hMutSbeta, a heterodimer of hMSH2 and hMSH3, binds to insertion/deletion loops in DNA

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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

Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair

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7 January 2021

Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage

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7 January 2021

An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair.

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7 January 2021

A mismatch recognition defect in colon carcinoma confers DNA microsatellite instability and a mutator phenotype

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7 January 2021

Mutator phenotypes in human colorectal carcinoma cell lines

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Kinds and locations of mutations arising spontaneously in the coding region of theHPRT gene of finite-life-span diploid human fibroblasts

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Spectrum of spontaneously occurring mutations in the hprt gene of V79 Chinese hamster cells

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7 January 2021

Spontaneous mutation spectrum in the hprt gene in human lymphoblastoid TK6 cells

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7 January 2021

Molecular analysis of mutations in mutator colorectal carcinoma cell lines

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7 January 2021

Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype

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7 January 2021

Frameshift mutations and the genetic code. This paper is dedicated to Professor Theodosius Dobzhansky on the occasion of his 66th birthday

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Repair of DNA heteroduplexes containing small heterologous sequences in Escherichia coli

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Mismatch repair defects and O6-methylguanine-DNA methyltransferase expression in acquired resistance to methylating agents in human cells

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7 January 2021

BAX frameshift mutations in cell lines derived from human haemopoietic malignancies are associated with resistance to apoptosis and microsatellite instability

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7 January 2021

Mutations of GTBP in genetically unstable cells

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7 January 2021

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

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7 January 2021

Appropriate Partners Make Good Matches

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7 January 2021

DNA-mismatch repair. The intricacies of eukaryotic spell-checking

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7 January 2021

Binding of insertion/deletion DNA mismatches by the heterodimer of yeast mismatch repair proteins MSH2 and MSH3.

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7 January 2021

Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability

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7 January 2021

Microsatellite instability in the insulin–like growth factor II receptor gene in gastrointestinal tumours

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7 January 2021

Somatic frameshift mutations in the BAX gene in colon cancers of the microsatellite mutator phenotype.

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Selection for beta 2-microglobulin mutation in mismatch repair-defective colorectal carcinomas.

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10.1016/S0921-8777(98)00017-2

Identifiers

DOI

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5 February 2018

1 reference

5 February 2018