A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype (Q33772742)

29 July 2017

title

A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype (English)

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29 July 2017

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B Vogelstein

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29 July 2017

K W Kinzler

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29 July 2017

N C Nicolaides

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29 July 2017

S J Littman

series ordinal

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29 July 2017

P Modrich

series ordinal

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29 July 2017

language of work or name

English

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publication date

1 March 1998

1 reference

Molecular and Cellular Biology

29 July 2017

published in

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29 July 2017

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29 July 2017

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29 July 2017

page(s)

1635-1641

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Functional Domains of the Saccharomyces cerevisiae Mlh1p and Pms1p DNA Mismatch Repair Proteins and Their Relevance to Human Hereditary Nonpolyposis Colorectal Cancer-Associated Mutations

29 July 2017

cites work

1 reference

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4 July 2018

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Molecular cloning of the N-terminus of GTBP

4 July 2018

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Cisplatin and adriamycin resistance are associated with MutLalpha and mismatch repair deficiency in an ovarian tumor cell line

4 July 2018

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4 July 2018

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Analysis of the 5' region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene

4 July 2018

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Genomic organization of the human PMS2 gene family.

4 July 2018

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

4 July 2018

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Hypermutability and mismatch repair deficiency in RER+ tumor cells

4 July 2018

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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

4 July 2018

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

4 July 2018

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

4 July 2018

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Mutation of a mutL homolog in hereditary colon cancer

4 July 2018

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Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

4 July 2018

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MLH1, PMS1, and MSH2 interactions during the initiation of DNA mismatch repair in yeast

4 July 2018

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

4 July 2018

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Mismatch repair, genetic stability, and cancer

4 July 2018

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The molecular basis of Turcot's syndrome

4 July 2018

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Mismatch Repair Deficiency in Phenotypically Normal Human Cells

4 July 2018

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Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

4 July 2018

1 reference

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Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

4 July 2018

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

4 July 2018

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

4 July 2018

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A versatile in vivo and in vitro eukaryotic expression vector for protein engineering

4 July 2018

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Mispair specificity of methyl-directed DNA mismatch correction in vitro

4 July 2018

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Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines

4 July 2018

1 reference

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Positive autoregulation of c-myb expression via Myb binding sites in the 5' flanking region of the human c-myb gene

4 July 2018

1 reference

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The Jun family members, c-Jun and JunD, transactivate the human c-myb promoter via an Ap1-like element.

4 July 2018

1 reference

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Mismatch repair and cancer

4 July 2018

1 reference

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

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9488480

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1128/MCB.18.3.1635

1 reference

29 July 2017

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29 July 2017

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