(Q40801508)

23 September 2017

title

Analysis of microsatellite instability and hypermutation of immunoglobulin variable genes in Werner syndrome (English)

1 reference

23 September 2017

Rosner K

1

1 reference

23 September 2017

Winter DB

2

1 reference

23 September 2017

Skovgaard GL

3

1 reference

23 September 2017

Oshima J

4

1 reference

23 September 2017

Gearhart PJ

5

1 reference

23 September 2017

Bohr VA

6

1 reference

23 September 2017

publication date

1 August 2001

1 reference

Mechanisms of Ageing and Development

23 September 2017

published in

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23 September 2017

volume

122

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23 September 2017

issue

11

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23 September 2017

page(s)

1121-1133

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Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus

23 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Werner syndrome protein: biochemical properties and functional interactions

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Mammalian DNA mismatch repair

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Homologous recombination is elevated in some Werner-like syndromes but not during normal in vitro or in vivo senescence of mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Sequence of the human immunoglobulin diversity (D) segment locus: a systematic analysis provides no evidence for the use of DIR segments, inverted D segments, "minor" D segments or D-D recombination

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Mutator phenotype of Werner syndrome is characterized by extensive deletions

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Increased frequency of 6-thioguanine-resistant peripheral blood lymphocytes in Werner syndrome patients.

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Werner's syndrome: analysis of 15 cases with a review of the Japanese literature

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Immunoglobulin heavy chain gene expression in peripheral blood B lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Functional interaction between Ku and the werner syndrome protein in DNA end processing

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Cytogenetic aspects of Werner's syndrome lymphocyte cultures

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Homozygosity mapping of the Werner syndrome locus (WRN)

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Mismatch Repair Deficiency in Phenotypically Normal Human Cells

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Impaired S-phase transit of Werner syndrome cells expressed in lymphoblastoid cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Impact of age on hypermutation of immunoglobulin variable genes in humans

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Third complementarity-determining region of mutated VH immunoglobulin genes contains shorter V, D, J, P, and N components than non-mutated genes

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Somatic hypermutation of immunoglobulin genes is independent of the Bloom's syndrome DNA helicase

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

The role of clonal selection and somatic mutation in autoimmunity

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Genetic control of microsatellite stability

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Werner's syndrome; report of two cases

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Microsatellite instability in tumors as a model to study the process of microsatellite mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Abnormal telomere dynamics of B-lymphoblastoid cell strains from Werner's syndrome patients transformed by Epstein-Barr virus

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

High frequency of somatically mutated IgM molecules in the human adult blood B cell repertoire

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Immunoglobulin heavy chain junctional diversity in young and aged humans

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

Preferential utilization of specific immunoglobulin heavy chain diversity and joining segments in adult human peripheral blood B lymphocytes

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

A time-efficient, linear-space local similarity algorithm

1 reference

https://api.crossref.org/works/10.1016%2FS0047-6374%2801%2900256-1

7 January 2021

10.1016/S0047-6374(01)00256-1

Identifiers

DOI

1 reference

23 September 2017

1 reference