(Q22008619)

7 February 2023

I Ohsugi

2

I

Ohsugi

1 reference

7 February 2023

K Ichikawa

3

K

Ichikawa

1 reference

7 February 2023

M Goto

4

M

Goto

1 reference

7 February 2023

Y Furuichi

5

Y

Furuichi

1 reference

7 February 2023

A Shimamoto

6

A

Shimamoto

1 reference

BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal

7 February 2023

language of work or name

English

0 references

publication date

15 December 1998

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published in

Genomics

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volume

54

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issue

3

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page(s)

443-52

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cites work

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Human calumenin gene (CALU): cDNA isolation and chromosomal mapping to 7q32

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

The recQ gene of Escherichia coli K12: molecular cloning and isolation of insertion mutants

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Spontaneous and induced chromosomal instability in Werner syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Sgs1: a eukaryotic homolog of E. coli RecQ that interacts with topoisomerase II in vivo and is required for faithful chromosome segregation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Similarities in RNA helicases

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Impaired nuclear localization of defective DNA helicases in Werner's syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Mutator phenotype of Werner syndrome is characterized by extensive deletions

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

DNA double-strand break repair: genetic determinants of flanking crossing-over

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Cell cycle-dependent modulation of telomerase activity in tumor cells.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

A unique human gene that spans over 230 kb in the human chromosome 8p11-12 and codes multiple family proteins sharing RNA-binding motifs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Positionally cloned human disease genes: patterns of evolutionary conservation and functional motifs

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

RecQ DNA helicase is a suppressor of illegitimate recombination in Escherichia coli

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology to Escherichia coli Rec Q helicase and localization of the gene at chromosome 12p12

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

1 reference

7 January 2021

An STS-based map of the human genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Positional cloning of the Werner's syndrome gene

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: a potential eukaryotic reverse gyrase

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Role of Schizosaccharomyces pombe RecQ Homolog, Recombination, and Checkpoint Genes in UV Damage Tolerance

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1998.5595

7 January 2021

Identifiers

DOI

10.1006/GENO.1998.5595

0 references