Distinct pathways of nonhomologous end joining that are differentially regulated by DNA-dependent protein kinase-mediated phosphorylation.
about
Effects of camptothecin on double-strand break repair by non-homologous end-joining in DNA mismatch repair-deficient human colorectal cancer cell linesThe role of NBS1 in DNA double strand break repair, telomere stability, and cell cycle checkpoint controlInhibition of homologous recombination by variants of the catalytic subunit of the DNA-dependent protein kinase (DNA-PKcs)Phosphorylation of linker histones by DNA-dependent protein kinase is required for DNA ligase IV-dependent ligation in the presence of histone H1.DNA-PKcs deficiency leads to persistence of oxidatively induced clustered DNA lesions in human tumor cells.Double-strand break repair deficiency in NONO knockout murine embryonic fibroblasts and compensation by spontaneous upregulation of the PSPC1 paralog.Lig4 and rad54 are required for repair of DNA double-strand breaks induced by P-element excision in DrosophilaChoosing the right path: does DNA-PK help make the decision?The role of the non-homologous end-joining pathway in lymphocyte development.The DNA-dependent protein kinase: the director at the end.Linking double-stranded DNA breaks to the recombination activating gene complex directs repair to the nonhomologous end-joining pathwayThe role of DNA dependent protein kinase in synapsis of DNA ends.DNA-dependent protein kinase and XRCC4-DNA ligase IV mobilization in the cell in response to DNA double strand breaks.Characterization of DNA binding and pairing activities associated with the native SFPQ·NONO DNA repair protein complex.SFPQ•NONO and XLF function separately and together to promote DNA double-strand break repair via canonical nonhomologous end joining.Sequences in PSF/SFPQ mediate radioresistance and recruitment of PSF/SFPQ-containing complexes to DNA damage sites in human cells.Involvement of p54(nrb), a PSF partner protein, in DNA double-strand break repair and radioresistance.Non-homologous end joining requires that the DNA-PK complex undergo an autophosphorylation-dependent rearrangement at DNA ends.Cell-type specific role of the RNA-binding protein, NONO, in the DNA double-strand break response in the mouse testes.Identification of the Polypyrimidine Tract Binding Protein-associated Splicing Factor·p54(nrb) Complex as a Candidate DNA Double-strand Break Rejoining Factor
P2860
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P2860
Distinct pathways of nonhomologous end joining that are differentially regulated by DNA-dependent protein kinase-mediated phosphorylation.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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name
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@en
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@nl
type
label
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@en
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@nl
prefLabel
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@en
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@nl
P2093
P2860
P356
P1476
Distinct pathways of nonhomolo ...... nase-mediated phosphorylation.
@en
P2093
Catherine L Bladen
Durga Udayakumar
Farlyn Z Hudson
William S Dynan
P2860
P304
41631-41635
P356
10.1074/JBC.M306470200
P407
P577
2003-08-12T00:00:00Z