New mammalian cellular systems to study mutations introduced at the break site by non-homologous end-joining.

[1]  M. Rocchi,et al.  Insertion of telomeric repeats at intrachromosomal break sites during primate evolution. , 2004, Genome research.

[2]  Yunmei Ma,et al.  The mechanism of vertebrate nonhomologous DNA end joining and its role in V(D)J recombination. , 2004, DNA repair.

[3]  C. Desmaze,et al.  Impact of the KU80 pathway on NHEJ-induced genome rearrangements in mammalian cells. , 2004, Molecular cell.

[4]  P. Chartrand,et al.  Genomic DNA is captured and amplified during double-strand break (DSB) repair in human cells , 2004, Oncogene.

[5]  S. Kuhfittig-Kulle,et al.  Pathways of DNA double-strand break repair and their impact on the prevention and formation of chromosomal aberrations , 2004, Cytogenetic and Genome Research.

[6]  K. Valerie,et al.  Regulation and mechanisms of mammalian double-strand break repair , 2003, Oncogene.

[7]  Yunmei Ma,et al.  Mechanism and regulation of human non-homologous DNA end-joining , 2003, Nature Reviews Molecular Cell Biology.

[8]  G. Maga,et al.  Human DNA polymerase lambda possesses terminal deoxyribonucleotidyl transferase activity and can elongate RNA primers: implications for novel functions. , 2003, Journal of molecular biology.

[9]  D. Ramsden,et al.  Association of DNA Polymerase μ (pol μ) with Ku and Ligase IV: Role for pol μ in End-Joining Double-Strand Break Repair , 2002, Molecular and Cellular Biology.

[10]  S. Jackson,et al.  Sensing and repairing DNA double-strand breaks. , 2002, Carcinogenesis.

[11]  Yunmei Ma,et al.  Hairpin Opening and Overhang Processing by an Artemis/DNA-Dependent Protein Kinase Complex in Nonhomologous End Joining and V(D)J Recombination , 2002, Cell.

[12]  J. Hoeijmakers,et al.  Different types of V(D)J recombination and end‐joining defects in DNA double‐strand break repair mutant mammalian cells , 2002, European journal of immunology.

[13]  D. Papadopoulo,et al.  The influence of DNA double-strand break structure on end-joining in human cells. , 2001, Nucleic acids research.

[14]  A. Waldman,et al.  Promiscuous patching of broken chromosomes in mammalian cells with extrachromosomal DNA. , 2001, Nucleic acids research.

[15]  C. Azzalin,et al.  Human intrachromosomal telomeric-like repeats: sequence organization and mechanisms of origin , 2001, Chromosoma.

[16]  J. Haber Partners and pathwaysrepairing a double-strand break. , 2000, Trends in genetics : TIG.

[17]  T. Kirchhoff,et al.  DNA polymerase mu (Pol mu), homologous to TdT, could act as a DNA mutator in eukaryotic cells. , 2000, The EMBO journal.

[18]  J. Murnane,et al.  Chromosome healing in mouse embryonic stem cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[19]  J. Hoeijmakers,et al.  Molecular mechanisms of DNA double strand break repair. , 1998, Trends in cell biology.

[20]  Y. Yamaguchi-Iwai,et al.  Homologous recombination and non‐homologous end‐joining pathways of DNA double‐strand break repair have overlapping roles in the maintenance of chromosomal integrity in vertebrate cells , 1998, The EMBO journal.

[21]  M. Jasin,et al.  Homology-directed repair is a major double-strand break repair pathway in mammalian cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[22]  M. Brenneman,et al.  Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination , 1997, Molecular and cellular biology.

[23]  J. Haber,et al.  Cell cycle and genetic requirements of two pathways of nonhomologous end-joining repair of double-strand breaks in Saccharomyces cerevisiae , 1996, Molecular and cellular biology.

[24]  D. Scherman,et al.  A versatile vector for gene and oligonucleotide transfer into cells in culture and in vivo: polyethylenimine. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[25]  P. Rouet,et al.  Introduction of double-strand breaks into the genome of mouse cells by expression of a rare-cutting endonuclease. , 1994, Molecular and cellular biology.

[26]  E. Mucciolo,et al.  Telomeric and nontelomeric (TTAGGG)n sequences in gene amplification and chromosome stability. , 1994, Genomics.

[27]  J. Phillips,et al.  Illegitimate recombination induced by DNA double-strand breaks in a mammalian chromosome , 1994, Molecular and cellular biology.

[28]  J. Lamb,et al.  De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16). , 1993, American journal of human genetics.

[29]  B. Dujon,et al.  Recognition and cleavage site of the intron-encoded omega transposase. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[30]  B. Hirt Selective extraction of polyoma DNA from infected mouse cell cultures. , 1967, Journal of molecular biology.

[31]  A. Baiker,et al.  A vector based on the SV40 origin of replication and chromosomal S/MARs replicates episomally in CHO cells. , 1999, Nucleic acids research.

[32]  A. Coquelle,et al.  Interstitial deletions and intrachromosomal amplification initiated from a double‐strand break targeted to a mammalian chromosome , 1998, The EMBO journal.

[33]  C. Greider Telomere length regulation. , 1996, Annual review of biochemistry.

[34]  A. S. Waldman,et al.  Repair of a specific double-strand break generated within a mammalian chromosome by yeast endonuclease I-SceI. , 1994, Nucleic acids research.