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PAXX and XLF DNA repair factors are functionally redundant in joining DNA breaks in a G1-arrested progenitor B-cell line

Proceedings of the National Academy of Sciences - PNAS, 2016-09, Vol.113 (38), p.10619-10624

2016

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Precise and in situ genetic humanization of 6 Mb of mouse immunoglobulin genes

Proceedings of the National Academy of Sciences - PNAS, 2014-04, Vol.111 (14), p.5147-5152

2014

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role for the NAD-dependent deacetylase Sirt1 in the regulation of autophagy

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (9), p.3374-3379

2008

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Transcription-associated processes cause DNA double-strand breaks and translocations in neural stem/progenitor cells

Proceedings of the National Academy of Sciences - PNAS, 2016-02, Vol.113 (8), p.2258-2263

2016

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DNA double-strand break response factors influence end-joining features of IgH class switch and general translocation junctions

Proceedings of the National Academy of Sciences - PNAS, 2018-01, Vol.115 (4), p.762-767

2018

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Highly sensitive and unbiased approach for elucidating antibody repertoires

Proceedings of the National Academy of Sciences - PNAS, 2016-07, Vol.113 (28), p.7846-7851

2016

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Functional redundancy between the XLF and DNA-PKcs DNA repair factors in V(D)J recombination and nonhomologous DNA end joining

Proceedings of the National Academy of Sciences - PNAS, 2013-02, Vol.110 (6), p.2234-2239

2013

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Neural sirtuin 6 (Sirt6) ablation attenuates somatic growth and causes obesity

Proceedings of the National Academy of Sciences - PNAS, 2010-12, Vol.107 (50), p.21790-21794

2010

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Alternative end-joining catalyzes robust IgH locus deletions and translocations in the combined absence of ligase 4 and Ku70

Proceedings of the National Academy of Sciences - PNAS, 2010-02, Vol.107 (7), p.3034-3039

2010

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Developmental Defects and p53 Hyperacetylation in Sir2 Homolog (SIRT1)-Deficient Mice

Proceedings of the National Academy of Sciences - PNAS, 2003-09, Vol.100 (19), p.10794-10799

2003

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Ataxia telangiectasia-mutated protein and DNA-dependent protein kinase have complementary V(D)J recombination functions

Proceedings of the National Academy of Sciences - PNAS, 2011-02, Vol.108 (5), p.2028-2033

2011

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Robust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1)

Proceedings of the National Academy of Sciences - PNAS, 2012-02, Vol.109 (7), p.2473-2478

2012

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Complete Correction of Murine Artemis Immunodeficiency by Lentiviral Vector-Mediated Gene Transfer

Proceedings of the National Academy of Sciences - PNAS, 2006-10, Vol.103 (44), p.16406-16411

2006

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Antisense transcripts from immunoglobulin heavy-chain locus V(D)J and switch regions

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (10), p.3843-3848

2008

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Defective DNA repair and increased genomic instability in Cernunnos-XLF-deficient murine ES cells

Proceedings of the National Academy of Sciences - PNAS, 2007-03, Vol.104 (11), p.4518-4523

2007

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Parp3 promotes long-range end joining in murine cells

Proceedings of the National Academy of Sciences - PNAS, 2018-10, Vol.115 (40), p.10076-10081

2018

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Integrity of the AID serine-38 phosphorylation site is critical for class switch recombination and somatic hypermutation in mice

Proceedings of the National Academy of Sciences - PNAS, 2009-02, Vol.106 (8), p.2717-2722

2009

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Increased Ionizing Radiation Sensitivity and Genomic Instability in the Absence of Histone H2AX

Proceedings of the National Academy of Sciences - PNAS, 2002-06, Vol.99 (12), p.8173-8178

2002

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Ku70-Deficient Embryonic Stem Cells have Increased Ionizing Radiosensitivity, Defective DNA End-Binding Activity, and Inability to Support V(D)J Recombination

Proceedings of the National Academy of Sciences - PNAS, 1997-07, Vol.94 (15), p.8076-8081

1997

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Homozygous DNA ligase IV R278H mutation in mice leads to leaky SCID and represents a model for human LIG4 syndrome

Proceedings of the National Academy of Sciences - PNAS, 2010-02, Vol.107 (7), p.3024-3029

2010

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53BP1 and p53 Synergize to Suppress Genomic Instability and Lymphomagenesis

Proceedings of the National Academy of Sciences - PNAS, 2006-02, Vol.103 (9), p.3310-3315

2006

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Recombination and Transcription of the Endogenous Ig Heavy Chain Locus Is Effected by the Ig Heavy Chain Intronic Enhancer Core Region in the Absence of the Matrix Attachment Regions

Proceedings of the National Academy of Sciences - PNAS, 1999-02, Vol.96 (4), p.1526-1531

1999

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Vav3 is Regulated during the Cell Cycle and Effects Cell Division

Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (7), p.4313-4318

2002

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The Nonhomologous End-Joining Pathway of DNA Repair Is Required for Genomic Stability and the Suppression of Translocations

Proceedings of the National Academy of Sciences - PNAS, 2000-06, Vol.97 (12), p.6630-6633

2000

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Genetic Interactions between ATM and the Nonhomologous End-Joining Factors in Genomic Stability and Development

Proceedings of the National Academy of Sciences - PNAS, 2001-03, Vol.98 (6), p.3243-3248

2001

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PAXX and XLF DNA repair factors are functionally redundant in joining DNA breaks in a G1-arrested progenitor B-cell line

Precise and in situ genetic humanization of 6 Mb of mouse immunoglobulin genes

role for the NAD-dependent deacetylase Sirt1 in the regulation of autophagy

Transcription-associated processes cause DNA double-strand breaks and translocations in neural stem/progenitor cells

DNA double-strand break response factors influence end-joining features of IgH class switch and general translocation junctions

Highly sensitive and unbiased approach for elucidating antibody repertoires

Functional redundancy between the XLF and DNA-PKcs DNA repair factors in V(D)J recombination and nonhomologous DNA end joining

Neural sirtuin 6 (Sirt6) ablation attenuates somatic growth and causes obesity

Alternative end-joining catalyzes robust IgH locus deletions and translocations in the combined absence of ligase 4 and Ku70

Developmental Defects and p53 Hyperacetylation in Sir2 Homolog (SIRT1)-Deficient Mice

Ataxia telangiectasia-mutated protein and DNA-dependent protein kinase have complementary V(D)J recombination functions

Robust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1)

Complete Correction of Murine Artemis Immunodeficiency by Lentiviral Vector-Mediated Gene Transfer

Antisense transcripts from immunoglobulin heavy-chain locus V(D)J and switch regions

Defective DNA repair and increased genomic instability in Cernunnos-XLF-deficient murine ES cells

Parp3 promotes long-range end joining in murine cells

Integrity of the AID serine-38 phosphorylation site is critical for class switch recombination and somatic hypermutation in mice

Increased Ionizing Radiation Sensitivity and Genomic Instability in the Absence of Histone H2AX

Ku70-Deficient Embryonic Stem Cells have Increased Ionizing Radiosensitivity, Defective DNA End-Binding Activity, and Inability to Support V(D)J Recombination

Homozygous DNA ligase IV R278H mutation in mice leads to leaky SCID and represents a model for human LIG4 syndrome

53BP1 and p53 Synergize to Suppress Genomic Instability and Lymphomagenesis

Recombination and Transcription of the Endogenous Ig Heavy Chain Locus Is Effected by the Ig Heavy Chain Intronic Enhancer Core Region in the Absence of the Matrix Attachment Regions

Vav3 is Regulated during the Cell Cycle and Effects Cell Division

The Nonhomologous End-Joining Pathway of DNA Repair Is Required for Genomic Stability and the Suppression of Translocations

Genetic Interactions between ATM and the Nonhomologous End-Joining Factors in Genomic Stability and Development

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