BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal
about
Human RecQ5beta, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3alpha and 3beta.Telomere and ribosomal DNA repeats are chromosomal targets of the bloom syndrome DNA helicaseThe C-terminal domain of the Bloom syndrome DNA helicase is essential for genomic stabilityRecQ helicases: caretakers of the genomeDNA IR-Double Strand Breaks (DSBs) and cellular response via ATMLocalization of the Bloom syndrome helicase to punctate nuclear structures and the nuclear matrix and regulation during the cell cycle: comparison with the Werner's syndrome helicase.Crystal structure of the Bloom's syndrome helicase indicates a role for the HRDC domain in conformational changesNLStradamus: a simple Hidden Markov Model for nuclear localization signal prediction.Regulation of BLM Nucleolar LocalizationMultiple genetic pathways involving the Caenorhabditis elegans Bloom's syndrome genes him-6, rad-51, and top-3 are needed to maintain genome stability in the germ line.Recruitment of HRDC domain of WRN and BLM to the sites of DNA damage induced by mitomycin C and methyl methanesulfonate.Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene.Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiaeRoles of RecQ family helicases in the maintenance of genome stability.DNA-based carrier screening in the Ashkenazi Jewish population.Clinical features of Bloom syndrome and function of the causative gene, BLM helicase.The DNA helicase activity of BLM is necessary for the correction of the genomic instability of bloom syndrome cellsRNF138 interacts with RAD51D and is required for DNA interstrand crosslink repair and maintaining chromosome integrityStructural mechanisms of human RecQ helicases WRN and BLM.Chromosomal instability associated with a novel BLM frameshift mutation (c.1980-1982delAA) in two unrelated Tunisian families with Bloom syndrome.A novel frameshift mutation in BLM gene associated with high sister chromatid exchanges (SCE) in heterozygous family members.Semiquantitative evaluation of mRNAs for the membranous form of immunoglobulin heavy chain is useful for investigating the etiology in CVID.Purification and enzymatic characterization of Gallus gallus BLM helicase.
P2860
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P2860
BLM (the causative gene of Bloom syndrome) protein translocation into the nucleus by a nuclear localization signal
description
1997 nî lūn-bûn
@nan
1997 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
BLM (the causative gene of Blo ...... a nuclear localization signal
@ast
BLM (the causative gene of Blo ...... a nuclear localization signal
@en
BLM (the causative gene of Blo ...... a nuclear localization signal
@en-gb
BLM (the causative gene of Blo ...... a nuclear localization signal
@nl
type
label
BLM (the causative gene of Blo ...... a nuclear localization signal
@ast
BLM (the causative gene of Blo ...... a nuclear localization signal
@en
BLM (the causative gene of Blo ...... a nuclear localization signal
@en-gb
BLM (the causative gene of Blo ...... a nuclear localization signal
@nl
prefLabel
BLM (the causative gene of Blo ...... a nuclear localization signal
@ast
BLM (the causative gene of Blo ...... a nuclear localization signal
@en
BLM (the causative gene of Blo ...... a nuclear localization signal
@en-gb
BLM (the causative gene of Blo ...... a nuclear localization signal
@nl
P2093
P3181
P356
P1476
BLM (the causative gene of Blo ...... a nuclear localization signal
@en
P2093
A Shimamoto
K Kasahara
N Shimozawa
S Hayakawa
T Matsumoto
P304
P3181
P356
10.1006/BBRC.1997.7648
P407
P577
1997-11-17T00:00:00Z