(Q28586687)

English

Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications

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scholarly article

1 reference

PubMed publication ID

31 January 2017

Different mismatch repair deficiencies all have the same effects on somatic hypermutation: intact primary mechanism accompanied by secondary modifications (English)

1 reference

PubMed publication ID

31 January 2017

1 reference

GOA release 2020-03-11

Mismatch repair endonuclease PMS2

1 reference

GOA release 2020-03-11

DNA mismatch repair

1 reference

based on heuristic

inferred from title

author name string

N. Kim

1

1 reference

PubMed publication ID

31 January 2017

G. Bozek

2

1 reference

PubMed publication ID

31 January 2017

J. C. Lo

3

1 reference

PubMed publication ID

31 January 2017

U. Storb

4

1 reference

PubMed publication ID

31 January 2017

language of work or name

0 references

publication date

5 July 1999

1 reference

PubMed publication ID

31 January 2017

Journal of Experimental Medicine

1 reference

PubMed publication ID

31 January 2017

190

1 reference

PubMed publication ID

31 January 2017

1

1 reference

PubMed publication ID

31 January 2017

21–30

1 reference

PubMed publication ID

31 January 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2195558/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Hypermutation in Ig V genes from mice deficient in the MLH1 mismatch repair protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Severe attenuation of the B cell immune response in Msh2-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Hot spot focusing of somatic hypermutation in MSH2-deficient mice suggests two stages of mutational targeting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and not with the hypermutation process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient in the MSH2 mismatch repair protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Transcription-coupled repair deficiency and mutations in human mismatch repair genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

17 March 2017

A hypermutable insert in an immunoglobulin transgene contains hotspots of somatic mutation and sequences predicting highly stable structures in the RNA transcript

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

The role of DNA repair in somatic hypermutation of immunoglobulin genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

The molecular basis of somatic hypermutation of immunoglobulin genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

Transcription-coupled repair and human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

Mechanisms and biological effects of mismatch repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

29 September 2017

Somatic hypermutation of immunoglobulin genes is linked to transcription.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

3 June 2018

Somatic hypermutation in the heavy chain locus correlates with transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

27 November 2018

Somatic hypermutation of an artificial test substrate within an Ig kappa transgene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

27 November 2018

Mismatch repair co-opted by hypermutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

27 November 2018

Analysis of the frequency and pattern of somatic mutations within nonproductively rearranged human variable heavy chain genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

27 November 2018

Di- and trinucleotide target preferences of somatic mutagenesis in normal and autoreactive B cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2195558

27 November 2018

Elements regulating somatic hypermutation of an immunoglobulin κ gene: Critical role for the intron enhancer/matrix attachment region

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic hypermutation of VHS107 genes is not associated with gene conversion among family members

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The germinal center reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic hypermutation of immunoglobulin genes is linked to transcription initiation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic hypermutation of Ig genes in patients with xeroderma pigmentosum (XP-D)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolated human germinal center centroblasts have an intact mismatch repair system

1 reference

https://pubmed.ncbi.nlm.nih.gov/10429667

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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0 references

PubMed publication ID

1 reference

PubMed publication ID

31 January 2017

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