DOI: 10.1006/geno.1998.5595. Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher Eukaryotes

Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher Eukaryotes

10.1006/geno.1998.5595

Crossref journal-article

Elsevier BV

Genomics (78)

Bibliography

Kitao, S., Ohsugi, I., Ichikawa, K., Goto, M., Furuichi, Y., & Shimamoto, A. (1998). Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher Eukaryotes. Genomics, 54(3), 443â452.

Authors 6

Saori Kitao (first)
Itaru Ohsugi (additional)
Koji Ichikawa (additional)
Makoto Goto (additional)
Yasuhiro Furuichi (additional)
Akira Shimamoto (additional)

References 32 Referenced 195

10.1016/0092-8674(95)90105-1 / Cell / The Bloom's syndrome gene product is homologous to RecQ helicases by Ellis (1995)
{'key': '10.1006/geno.1998.5595_GE985595RF2', 'first-page': '1019', 'article-title': 'Somatic intragenic recombination within the mutated locusBLM', 'volume': '57', 'author': 'Ellis', 'year': '1995', 'journal-title': 'Am. J. Hum. Genet.'} / Am. J. Hum. Genet. / Somatic intragenic recombination within the mutated locusBLM by Ellis (1995)
10.1097/00005792-196605000-00001 / Medicine / Werner's syndrome: A review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process by Epstein (1966)
10.1073/pnas.86.15.5893 / Proc. Natl. Acad. Sci. USA / Mutator phenotype of Werner syndrome is characterized by extensive deletions by Fukuchi (1989)
10.1128/MCB.14.12.8391 / Mol. Cell. Biol. / The yeast type I topoisomerase Top3 interacts with Sgs1, a DNA helicase homolog: A potential eukaryotic reverse gyrase by Gangloff (1994)
10.1007/BF00702855 / Hum. Genet. / Spontaneous and induced chromosomal instability in Werner syndrome by Gebhardt (1988)
10.1097/00005792-199311000-00003 / Medicine / Bloom syndrome: A Mendelian prototype of somatic mutational disease by German (1993)
10.1093/nar/17.12.4713 / Nucleic Acids Res. / Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomes by Gorbalenya (1989)
10.1016/S0047-6374(97)00111-5 / Mech. Ageing Dev. / Hierarchical deterioration of body systems in Werner's syndrome: Implications for normal ageing by Goto (1997)
10.1111/j.1399-0004.1981.tb00660.x / Clin. Genet. / Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literature by Goto (1981)
{'key': '10.1006/geno.1998.5595_GE985595RF11', 'first-page': '239', 'article-title': "Excess of rare cancers in Werner's syndrome (adult progeria)", 'volume': '5', 'author': 'Goto', 'year': '1996', 'journal-title': "Cancer Epidemiol. Biomarker's Prev."} / Cancer Epidemiol. Biomarker's Prev. / Excess of rare cancers in Werner's syndrome (adult progeria) by Goto (1996)
10.1073/pnas.94.8.3860 / Proc. Natl. Acad. Sci. USA / RecQ DNA helicase is a suppressor of illegitimate recombination inEscherichia coli. by Hanada (1997)
10.1126/science.270.5244.1945 / Science / An STS-based map of the human genome by Hudson (1995)
10.1006/geno.1997.4661 / Genomics / Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescencein situ by Imamura (1997)
10.1006/bbrc.1997.7648 / Biochem. Biophys. Res. Commn. / BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal by Kaneko (1997)
10.1038/352290c0 / Nature / Similarities in RNA helicases by Koonin (1991)
10.1073/pnas.91.3.1173 / Proc. Natl. Acad. Sci. USA / DNA double-strand break repair: Genetic determinants of flanking crossing-over by Kusano (1994)
10.1038/ng0897-335 / Nat. Genet. / Impaired nuclear localization of defective DNA helicases in Werner's syndrome by Matsumoto (1997)
{'key': '10.1006/geno.1998.5595_GE985595RF19', 'first-page': '71', 'article-title': "Characterization of the nuclear localization signal in the DNA helicase involved in Werner's syndrome", 'volume': '1', 'author': 'Matsumoto', 'year': '1998', 'journal-title': 'Int. J. Mol. Med.'} / Int. J. Mol. Med. / Characterization of the nuclear localization signal in the DNA helicase involved in Werner's syndrome by Matsumoto (1998)
10.1128/MCB.17.12.6868 / Mol. Cell. Biol. / Role ofSchizosaccharomyces pombe by Murray (1997)
10.1073/pnas.94.11.5831 / Proc. Natl. Acad. Sci. USA / Positionally cloned human disease genes: Patterns of evolutionary conservation and functional motifs by Mushegian (1997)
10.1007/BF00425434 / Mol. Gen. Genet. / TherecQEscherichia coli by Nakayama (1985)
10.1007/s004390050599 / Hum. Genet. / An apoptosis-inducing genotoxin differentiates heterozygotic carriers for Werner helicase mutations from wild-type and homozygous mutants by Ogburn (1997)
10.1016/S0021-9258(18)43957-9 / J. Biol. Chem. / Cloning and characterization of RECQL, a potential human homologue of theEscherichia coli by Puranam (1994)
10.1093/nar/22.22.4566 / Nucleic Acids Res. / Molecular cloning of cDNA encoding human DNA helicase Q1 which has homology toEscherichia coli by Seki (1994)
10.1073/pnas.93.20.10913 / Proc. Natl. Acad. Sci. USA / A unique human gene that spans over 230 kb in the human chromosome 8p11–12 and codes multiple family proteins sharing RNA-binding motifs by Shimamoto (1996)
10.1093/emboj/16.10.2682 / EMBO J. / rqh1+ by Stewart (1997)
10.1016/0092-8674(95)90335-6 / Cell / Sgs1: A eukaryotic homolog ofE. coliin vivo by Watt (1995)
10.1006/geno.1998.5245 / Genomics / Human calumenin gene (CALU by Yabe (1998)
10.1073/pnas.95.15.8733 / Proc. Natl. Acad. Sci. USA / Bloom's and Werner's syndrome genes suppress hyperrecombination in yeastsgs1 by Yamagata (1998)
10.1126/science.272.5259.258 / Science / Positional cloning of the Werner's syndrome gene by Yu (1996)
10.1073/pnas.93.12.6091 / Proc. Natl. Acad. Sci. USA / Cell cycle-dependent modulation of telomerase activity in tumor cells by Zhu (1996)

Dates

Type	When
Created	22 years, 10 months ago (Oct. 7, 2002, 10:19 a.m.)
Deposited	4 years, 4 months ago (May 3, 2021, 6:57 a.m.)
Indexed	1 week ago (Aug. 29, 2025, 6:21 a.m.)
Issued	26 years, 9 months ago (Dec. 1, 1998)
Published	26 years, 9 months ago (Dec. 1, 1998)
Published Print	26 years, 9 months ago (Dec. 1, 1998)

Funders 0

None

BibTeX

@article{Kitao_1998, title={Cloning of Two New Human Helicase Genes of the RecQ Family: Biological Significance of Multiple Species in Higher Eukaryotes}, volume={54}, ISSN={0888-7543}, url={http://dx.doi.org/10.1006/geno.1998.5595}, DOI={10.1006/geno.1998.5595}, number={3}, journal={Genomics}, publisher={Elsevier BV}, author={Kitao, Saori and Ohsugi, Itaru and Ichikawa, Koji and Goto, Makoto and Furuichi, Yasuhiro and Shimamoto, Akira}, year={1998}, month=dec, pages={443–452} }

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  "subtitle": [],
  "short-title": [],
  "issued": {
    "date-parts": [
      [
        1998,
        12
      ]
    ]
  },
  "references-count": 32,
  "journal-issue": {
    "issue": "3",
    "published-print": {
      "date-parts": [
        [
          1998,
          12
        ]
      ]
    }
  },
  "alternative-id": [
    "S0888754398955951"
  ],
  "URL": "http://dx.doi.org/10.1006/geno.1998.5595",
  "relation": {},
  "ISSN": [
    "0888-7543"
  ],
  "subject": [],
  "container-title-short": "Genomics",
  "published": {
    "date-parts": [
      [
        1998,
        12
      ]
    ]
  }
}