Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients (Q40701745)

22 September 2017

title

Chromosomal instability in B-lymphoblasotoid cell lines from Werner and Bloom syndrome patients (English)

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22 September 2017

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Masamitsu Honma

1

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22 September 2017

Satoshi Tadokoro

2

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22 September 2017

Hiroko Sakamoto

3

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22 September 2017

Hideyuki Tanabe

4

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22 September 2017

Masanobu Sugimoto

5

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22 September 2017

Yasuhiro Furuichi

6

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22 September 2017

Takatomo Satoh

7

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22 September 2017

Toshio Sofuni

8

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22 September 2017

Makoto Goto

9

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22 September 2017

Makoto Hayashi

10

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22 September 2017

language of work or name

English

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publication date

1 September 2002

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22 September 2017

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22 September 2017

volume

520

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22 September 2017

issue

1-2

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22 September 2017

page(s)

15-24

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A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

22 September 2017

cites work

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

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7 January 2021

Mutation-causing mutations

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Positional cloning of the Werner's syndrome gene

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

The Bloom's syndrome gene product is homologous to RecQ helicases

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

The Werner syndrome protein is a DNA helicase

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Bloom's and Werner's syndrome genes suppress hyperrecombination in yeast sgs1 mutant: implication for genomic instability in human diseases

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Mutator phenotype of Werner syndrome is characterized by extensive deletions

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants

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7 January 2021

Werner syndrome lymphoblastoid cells are sensitive to camptothecin-induced apoptosis in S-phase

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Differential effects of cytotoxic drugs on mortal and immortalized B-lymphoblastoid cell lines from normal and Werner's syndrome patients

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7 January 2021

Werner's syndrome cell lines are hypersensitive to camptothecin-induced chromosomal damage

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7 January 2021

https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

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7 January 2021

Frequency of variant erythrocytes at the glycophorin-A locus in two Bloom's syndrome patients

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7 January 2021

Cancer predisposition caused by elevated mitotic recombination in Bloom mice

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7 January 2021

Multicolor Spectral Karyotyping of Human Chromosomes

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Functional interaction of p53 and BLM DNA helicase in apoptosis

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

A proposal for a simple way to distinguish aneugens from clastogens in the in vitro micronucleus test

1 reference

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7 January 2021

Illegitimate recombination leading to allelic loss and unbalanced translocation in p53-mutated human lymphoblastoid cells

1 reference

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7 January 2021

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

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7 January 2021

Cytogenetic studies using various clastogens in two patients with Werner syndrome and control individuals.

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7 January 2021

Clonal analysis of stable chromosome rearrangements in Bloom's syndrome fibroblasts

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7 January 2021

Evidence for chromosome instability in vivo in bloom syndrome: Increased numbers of micronuclei in exfoliated cells

1 reference

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7 January 2021

Inherited defects in DNA repair and susceptibility to DNA-damaging agents

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Immortalization of immunologically committed Epstein-Barr virus-transformed human B-lymphoblastoid cell lines accompanied by a strong telomerase activity

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Reconsideration of senescence, immortalization and telomere maintenance of Epstein-Barr virus-transformed human B-lymphoblastoid cell lines

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Possible association of BLM in decreasing DNA double strand breaks during DNA replication

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https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Chromosome instability in lymphocytes from a patient with Werner's syndrome is not associated with DNA repair defects

1 reference

https://api.crossref.org/works/10.1016%2FS1383-5718%2802%2900144-4

7 January 2021

Spontaneous and X-ray-induced chromosomal aberrations in Werner syndrome cells detected by FISH using chromosome-specific painting probes

1 reference

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7 January 2021

Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome

1 reference

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7 January 2021

10.1016/S1383-5718(02)00144-4

Identifiers

DOI

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22 September 2017

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