(Q28257407)

1

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Renee L Vander Laan

2

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Aswathi Suresh

3

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Thomas E Wilson

Journal of Biological Chemistry

4

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language of work or name

English

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publication date

12 August 2005

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published in

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volume

280

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issue

32

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page(s)

29030-7

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cites work

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DNA breaks promote genomic instability by impeding proper chromosome segregation.

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Yeast DNA ligase IV mediates non-homologous DNA end joining

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Hairpin opening and overhang processing by an Artemis/DNA-dependent protein kinase complex in nonhomologous end joining and V(D)J recombination

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Efficient processing of DNA ends during yeast nonhomologous end joining. Evidence for a DNA polymerase beta (Pol4)-dependent pathway

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Sibling rivalry: competition between Pol X family members in V(D)J recombination and general double strand break repair

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Requirement of mammalian DNA polymerase-beta in base-excision repair.

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Lack of N regions in antigen receptor variable region genes of TdT-deficient lymphocytes

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Mice lacking TdT: mature animals with an immature lymphocyte repertoire

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Implication of DNA polymerase lambda in alignment-based gap filling for nonhomologous DNA end joining in human nuclear extracts.

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Association of DNA polymerase mu (pol mu) with Ku and ligase IV: role for pol mu in end-joining double-strand break repair

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A biochemically defined system for mammalian nonhomologous DNA end joining

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Mycobacterial Ku and ligase proteins constitute a two-component NHEJ repair machine

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A role for FEN-1 in nonhomologous DNA end joining: the order of strand annealing and nucleolytic processing events

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Rejoining of DNA double-strand breaks as a function of overhang length

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Uncoupling of 3'-phosphatase and 5'-kinase functions in budding yeast. Characterization of Saccharomyces cerevisiae DNA 3'-phosphatase (TPP1).

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Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications

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Yeast Mre11 and Rad1 proteins define a Ku-independent mechanism to repair double-strand breaks lacking overlapping end sequences

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A structural solution for the DNA polymerase lambda-dependent repair of DNA gaps with minimal homology

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Lesion bypass by human DNA polymerase mu reveals a template-dependent, sequence-independent nucleotidyl transferase activity.

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The Y-family of DNA polymerases

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DNA damage control by novel DNA polymerases: translesion replication and mutagenesis

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The role of DNA polymerase activity in human non-homologous end joining

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Mammalian base excision repair by DNA polymerases delta and epsilon

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Long patch base excision repair with purified human proteins. DNA ligase I as patch size mediator for DNA polymerases delta and epsilon

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The fifth essential DNA polymerase phi in Saccharomyces cerevisiae is localized to the nucleolus and plays an important role in synthesis of rRNA

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Polymerase mu is a DNA-directed DNA/RNA polymerase

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DNA polymerase lambda, a novel DNA repair enzyme in human cells.

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Processing and joining of DNA ends coordinated by interactions among Dnl4/Lif1, Pol4, and FEN-1.

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Involvement of human polynucleotide kinase in double-strand break repair by non-homologous end joining

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Xrcc4 physically links DNA end processing by polynucleotide kinase to DNA ligation by DNA ligase IV

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The frameshift infidelity of human DNA polymerase lambda. Implications for function.

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A physical and functional interaction between yeast Pol4 and Dnl4-Lif1 links DNA synthesis and ligation in nonhomologous end joining

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DNA polymerase lambda can elongate on DNA substrates mimicking non-homologous end joining and interact with XRCC4-ligase IV complex

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