| P2093 | author name string | Masumi Abe | |
| | Yao Xu | |
| | Katheryn Meek | |
| | Eric Hendrickson | |
| | Jessica A Neal | |
| P2860 | cites work | A vector based on the SV40 origin of replication and chromosomal S/MARs replicates episomally in CHO cells | Q24548417 |
| | ATM damage response and XLF repair factor are functionally redundant in joining DNA breaks | Q24596775 |
| | RNA-guided human genome engineering via Cas9 | Q24598394 |
| | A human XRCC4-XLF complex bridges DNA | Q24630031 |
| | XRCC4's interaction with XLF is required for coding (but not signal) end joining | Q24630098 |
| | Molecular Mechanism of V(D)J Recombination from Synaptic RAG1-RAG2 Complex Structures | Q27321738 |
| | Non-homologous end-joining partners in a helical dance: structural studies of XLF-XRCC4 interactions | Q27674365 |
| | Autophosphorylation of the catalytic subunit of the DNA-dependent protein kinase is required for efficient end processing during DNA double-strand break repair | Q27919641 |
| | DNA-PK autophosphorylation facilitates Artemis endonuclease activity | Q27919702 |
| | The catalytic subunit of DNA-dependent protein kinase regulates proliferation, telomere length, and genomic stability in human somatic cells | Q28115800 |
| | DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation | Q28206029 |
| | Roles of nonhomologous DNA end joining, V(D)J recombination, and class switch recombination in chromosomal translocations | Q28247857 |
| | The response to and repair of RAG-mediated DNA double-strand breaks | Q28256889 |
| | A severe combined immunodeficiency mutation in the mouse | Q28274531 |
| | The ataxia telangiectasia mutated kinase controls Igκ allelic exclusion by inhibiting secondary Vκ-to-Jκ rearrangements | Q36603553 |
| | 53BP1 facilitates long-range DNA end-joining during V(D)J recombination | Q36682376 |
| | Complementary functions of ATM and H2AX in development and suppression of genomic instability | Q36756926 |
| | A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining. | Q37036037 |
| | RAG: a recombinase diversified | Q37171099 |
| | MRN complex function in the repair of chromosomal Rag-mediated DNA double-strand breaks | Q37234327 |
| | Formation of dynamic gamma-H2AX domains along broken DNA strands is distinctly regulated by ATM and MDC1 and dependent upon H2AX densities in chromatin. | Q37347174 |
| | Aberrantly resolved RAG-mediated DNA breaks in Atm-deficient lymphocytes target chromosomal breakpoints in cis. | Q37416485 |
| | The RAG2 C-terminus and ATM protect genome integrity by controlling antigen receptor gene cleavage | Q37519459 |
| | DNA double-strand break repair in a cellular context | Q38196085 |
| | Functional overlaps between XLF and the ATM-dependent DNA double strand break response | Q38199848 |
| | V(D)J Recombination: Mechanism, Errors, and Fidelity | Q38535955 |
| | PRKDC mutations in a SCID patient with profound neurological abnormalities | Q38955848 |
| | DNA-PK is essential only for coding joint formation in V(D)J recombination | Q39724861 |
| | Deficiency in the catalytic subunit of DNA-dependent protein kinase causes down-regulation of ATM. | Q40449393 |
| | Unraveling the complexities of DNA-dependent protein kinase autophosphorylation | Q40603571 |
| | DNA uptake and repair enzyme access to transfected DNA is under reported by gene expression | Q40640079 |
| | SCID in Jack Russell terriers: a new animal model of DNA-PKcs deficiency | Q40787847 |
| | Signal joint formation is also impaired in DNA-dependent protein kinase catalytic subunit knockout cells | Q40848620 |
| | Analyses of TCRB rearrangements substantiate a profound deficit in recombination signal sequence joining in SCID foals: implications for the role of DNA-dependent protein kinase in V(D)J recombination | Q40905044 |
| | A kinase-negative mutation of DNA-PK(CS) in equine SCID results in defective coding and signal joint formation | Q41116024 |
| | V(D)J recombination in mammalian cell mutants defective in DNA double-strand break repair | Q41549015 |
| | Impairment of V(D)J recombination in double-strand break repair mutants | Q41560292 |
| | Not All SCID Pigs Are Created Equally: Two Independent Mutations in the Artemis Gene Cause SCID in Pigs. | Q41666062 |
| | DNA-PKcs and ATM co-regulate DNA double-strand break repair | Q42007528 |
| | Extrachromosomal DNA substrates in pre-B cells undergo inversion or deletion at immunoglobulin V-(D)-J joining signals | Q45246384 |
| | H2AX prevents DNA breaks from progressing to chromosome breaks and translocations | Q46904251 |
| | The defect in murine severe combined immune deficiency: joining of signal sequences but not coding segments in V(D)J recombination | Q48313594 |
| | DNA-PKcs mutations in dogs and horses: allele frequency and association with neoplasia | Q48316202 |
| | Severe combined immunodeficiency in Frisian Water Dogs caused by a RAG1 mutation | Q58243743 |
| | Rag mutations reveal robust alternative end joining | Q59098597 |
| | V(D)J recombination: a functional definition of the joining signals | Q69721561 |
| | Characterization of coding ends in thymocytes of scid mice: Implications for the mechanism of V(D)J recombination | Q71843533 |
| | A targeted DNA-PKcs-null mutation reveals DNA-PK-independent functions for KU in V(D)J recombination | Q77398644 |
| | RAG1 and RAG2 form a stable postcleavage synaptic complex with DNA containing signal ends in V(D)J recombination | Q28307236 |
| | Targeted disruption of the catalytic subunit of the DNA-PK gene in mice confers severe combined immunodeficiency and radiosensitivity | Q28506163 |
| | RAG-1 and ATM coordinate monoallelic recombination and nuclear positioning of immunoglobulin loci | Q28508203 |
| | Crystal structure of the V(D)J recombinase RAG1-RAG2 | Q30622421 |
| | Molecular and biochemical characterisation of DNA-dependent protein kinase-defective rodent mutant irs-20 | Q32082716 |
| | ATM prevents the persistence and propagation of chromosome breaks in lymphocytes | Q33289263 |
| | RAG2's acidic hinge restricts repair-pathway choice and promotes genomic stability | Q33558920 |
| | Histone H2AX stabilizes broken DNA strands to suppress chromosome breaks and translocations during V(D)J recombination | Q33591110 |
| | Analysis of variable (diversity) joining recombination in DNAdependent protein kinase (DNA-PK)-deficient mice reveals DNA-PK-independent pathways for both signal and coding joint formation | Q33597709 |
| | Both V(D)J recombination and radioresistance require DNA-PK kinase activity, though minimal levels suffice for V(D)J recombination | Q33616301 |
| | Equine severe combined immunodeficiency: a defect in V(D)J recombination and DNA-dependent protein kinase activity. | Q33702830 |
| | Intermediates in V(D)J recombination: a stable RAG1/2 complex sequesters cleaved RSS ends. | Q33948953 |
| | Requirement for the kinase activity of human DNA-dependent protein kinase catalytic subunit in DNA strand break rejoining | Q33958394 |
| | ATM-deficient thymic lymphoma is associated with aberrant tcrd rearrangement and gene amplification | Q33979941 |
| | The ataxia telangiectasia mutated and cyclin D3 proteins cooperate to help enforce TCRβ and IgH allelic exclusion | Q34146558 |
| | Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation. | Q34320792 |
| | XLF regulates filament architecture of the XRCC4·ligase IV complex | Q34433470 |
| | ATM stabilizes DNA double-strand-break complexes during V(D)J recombination. | Q34541828 |
| | Ataxia telangiectasia-mutated protein and DNA-dependent protein kinase have complementary V(D)J recombination functions | Q34549990 |
| | Ataxia telangiectasia mutated (Atm) and DNA-PKcs kinases have overlapping activities during chromosomal signal joint formation | Q34550115 |
| | V(D)J recombination: RAG proteins, repair factors, and regulation | Q34667417 |
| | XR-C1, a new CHO cell mutant which is defective in DNA-PKcs, is impaired in both V(D)J coding and signal joint formation | Q34669732 |
| | Aberrant V(D)J recombination in ataxia telangiectasia mutated-deficient lymphocytes is dependent on nonhomologous DNA end joining. | Q34805011 |
| | DNA-dependent protein kinase activity is absent in xrs-6 cells: implications for site-specific recombination and DNA double-strand break repair | Q34868235 |
| | Catalytic subunit of DNA-dependent protein kinase: impact on lymphocyte development and tumorigenesis | Q34992049 |
| | Inhibition of homologous recombination by DNA-dependent protein kinase requires kinase activity, is titratable, and is modulated by autophosphorylation | Q35077127 |
| | H2AX prevents CtIP-mediated DNA end resection and aberrant repair in G1-phase lymphocytes. | Q35148396 |
| | Unique and redundant functions of ATM and DNA-PKcs during V(D)J recombination | Q35159001 |
| | PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity. | Q35806314 |
| | N-terminal constraint activates the catalytic subunit of the DNA-dependent protein kinase in the absence of DNA or Ku. | Q35888831 |
| | Linking double-stranded DNA breaks to the recombination activating gene complex directs repair to the nonhomologous end-joining pathway | Q36089263 |
| | Redundant and nonredundant functions of ATM and H2AX in αβ T-lineage lymphocytes | Q36106641 |
| | Defects in coding joint formation in vivo in developing ATM-deficient B and T lymphocytes. | Q36229444 |
| | Biochemistry of V(D)J recombination. | Q36397181 |
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3032-3042 | |
| P577 | publication date | 2016-02-26 | |
| P1433 | published in | Journal of Immunology | Q3521441 |
| P1476 | title | Restoration of ATM Expression in DNA-PKcs-Deficient Cells Inhibits Signal End Joining | |
| P478 | volume | 196 | |