(Q22254326)

1 July 2017

Multiple mutations and frameshifts are the hallmark of defective hPMS2 in pZ189-transfected human tumor cells (English)

1 reference

PMS1 homolog 2, mismatch repair system component

1 July 2017

1 reference

GOA release 2020-03-11

1 reference

single base insertion or deletion binding

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

S Ceccotti

1

S

Ceccotti

1 reference

1 July 2017

C Ciotta

2

C

Ciotta

1 reference

1 July 2017

G Fronza

3

G

Fronza

1 reference

1 July 2017

E Dogliotti

4

E

Dogliotti

1 reference

1 July 2017

M Bignami

5

M

Bignami

1 reference

1 July 2017

language of work or name

English

0 references

publication date

1 July 2000

1 reference

1 July 2017

8

1 reference

inferred from page(s)

published in

Nucleic Acids Research

1 reference

1 July 2017

28

1 reference

1 July 2017

13

1 reference

1 July 2017

2577-2584

1 reference

MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability

1 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Eukaryotic DNA mismatch repair

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Isolation of MutSbeta from human cells and comparison of the mismatch repair specificities of MutSbeta and MutSalpha

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

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

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Sequence-dependent mutations in a shuttle vector plasmid replicated in a mismatch repair deficient human cell line

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Effect of hMSH6 cDNA expression on the phenotype of mismatch repair-deficient colon cancer cell line HCT15.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Characterization of distinct human endometrial carcinoma cell lines deficient in mismatch repair that originated from a single tumor

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Single gene complementation of the hPMS2 defect in HEC-1-A endometrial carcinoma cells.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Structural intermediates of deletion mutagenesis: a role for palindromic DNA

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Rearrangement and mutagenesis of a shuttle vector plasmid after passage in mammalian cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Multiple point mutations in a shuttle vector propagated in human cells: evidence for an error-prone DNA polymerase activity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Restricted ultraviolet mutational spectrum in a shuttle vector propagated in xeroderma pigmentosum cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Statistical test for the comparison of samples from mutational spectra

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Spectra of spontaneous mutations at the hprt locus in colorectal carcinoma cell lines defective in mismatch repair.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

O6-methylguanine residues elicit DNA repair synthesis by human cell extracts.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

A mutator phenotype characterizes one of two complementation groups in human cells tolerant to methylation damage.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Mechanisms of spontaneous and induced frameshift mutation in bacteriophage T4.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

A shuttle vector plasmid for studying carcinogen-induced point mutations in mammalian cells

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Mutagenesis by hydrogen peroxide treatment of mammalian cells: a molecular analysis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Mutagenesis by transient misalignment.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Reversal of methylation tolerance by transfer of human chromosome 2.

19 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Computer program for the analysis of mutational spectra: application to p53 mutations.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=102707

Mediating mismatch repair

29 November 2018

1 reference

12 December 2020

O6-methylguanine in DNA inhibits replication in vitro by human cell extracts

1 reference

12 December 2020

Molecular analysis of mutations in mutator colorectal carcinoma cell lines

1 reference

12 December 2020

Processing of O6-methylguanine by mismatch correction in human cell extracts

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/28.13.2577

1 reference

journals/nar/CeccottiCFDB00

1 July 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

0 references

1 reference