Coupled Homologous and Nonhomologous Repair of a Double-Strand Break Preserves Genomic Integrity in Mammalian Cells
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[1] Philippe Soriano,et al. Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice. , 1991, Genes & development.
[2] H. Puchta. Double-strand break-induced recombination between ectopic homologous sequences in somatic plant cells. , 1999, Genetics.
[3] M. Lieber,et al. The nonhomologous DNA end joining pathway is important for chromosome stability in primary fibroblasts , 1999, Current Biology.
[4] J. Haber,et al. Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae , 1999, Microbiology and Molecular Biology Reviews.
[5] C. Schmid,et al. Alu: structure, origin, evolution, significance and function of one-tenth of human DNA. , 1996, Progress in nucleic acid research and molecular biology.
[6] M. Jasin,et al. Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations. , 1998, Genes & development.
[7] G. Gloor,et al. Gene conversion in mitotically dividing cells: a view from Drosophila. , 1998, Trends in genetics : TIG.
[8] A. Belmaaza,et al. One-sided invasion events in homologous recombination at double-strand breaks. , 1994, Mutation research.
[9] 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.
[10] K. Kinzler,et al. The Genetic Basis of Human Cancer , 1997 .
[11] F Liang,et al. Chromosomal double-strand break repair in Ku80-deficient cells. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[12] R. Tebbs,et al. Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[13] F. Alt,et al. Impairment of V(D)J recombination in double-strand break repair mutants. , 1993, Science.
[14] Jack W. Szostak,et al. The double-strand-break repair model for recombination , 1983, Cell.
[15] S. Sowerby,et al. The BCR gene recombines preferentially with Alu elements in complex BCR-ABL translocations of chronic myeloid leukaemia. , 1998, Human molecular genetics.
[16] J. Haber,et al. Lack of chromosome territoriality in yeast: promiscuous rejoining of broken chromosome ends. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[17] M. Jasin,et al. Sister chromatid gene conversion is a prominent double‐strand break repair pathway in mammalian cells , 2000, The EMBO journal.
[18] J. Haber,et al. Double-strand break repair in the absence of RAD51 in yeast: a possible role for break-induced DNA replication. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[19] K. Schwarz,et al. DNA ligase IV is essential for V(D)J recombination and DNA double-strand break repair in human precursor lymphocytes. , 1998, Molecular cell.
[20] P. Rouet,et al. Double-strand breaks at the target locus stimulate gene targeting in embryonic stem cells. , 1995, Nucleic acids research.
[21] M. McDonald,et al. BCR gene recombines with genomically distinct sites on band 11Q13 in complex BCR-ABL translocations of chronic myeloid leukemia. , 1996, Oncogene.
[22] J. Hoeijmakers,et al. Disruption of Mouse RAD54 Reduces Ionizing Radiation Resistance and Homologous Recombination , 1997, Cell.
[23] M. Jasin,et al. Loss of heterozygosity induced by a chromosomal double-strand break. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[24] Christine Richardson,et al. Frequent chromosomal translocations induced by DNA double-strand breaks , 2000, Nature.
[25] L. Thompson,et al. XRCC3 promotes homology-directed repair of DNA damage in mammalian cells. , 1999, Genes & development.
[26] J. Hoeijmakers,et al. Homologous and non‐homologous recombination differentially affect DNA damage repair in mice , 2000, The EMBO journal.
[27] J. Lamerdin,et al. XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages. , 1998, Molecular cell.
[28] L. Hartwell,et al. Sister chromatids are preferred over homologs as substrates for recombinational repair in Saccharomyces cerevisiae. , 1992, Genetics.
[29] H. Puchta. Repair of genomic double‐strand breaks in somatic plant cells by one‐sided invasion of homologous sequences , 1998 .
[30] M. Monk,et al. HPRT-deficient (Lesch–Nyhan) mouse embryos derived from germline colonization by cultured cells , 1987, Nature.
[31] F. Alt,et al. Ku70-deficient embryonic stem cells have increased ionizing radiosensitivity, defective DNA end-binding activity, and inability to support V(D)J recombination. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[32] M. Capecchi,et al. Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells , 1987, Cell.
[33] R. Liskay,et al. The effects of insertions on mammalian intrachromosomal recombination. , 1994, Genetics.
[34] M. Jasin,et al. Mammalian XRCC2 promotes the repair of DNA double-strand breaks by homologous recombination , 1999, Nature.
[35] M. Caligiuri,et al. The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[36] J. Haber. DNA recombination: the replication connection. , 1999, Trends in biochemical sciences.
[37] J. Phillips,et al. Illegitimate recombination induced by DNA double-strand breaks in a mammalian chromosome , 1994, Molecular and cellular biology.
[38] B. Dujon,et al. Induction of homologous recombination in mammalian chromosomes by using the I-SceI system of Saccharomyces cerevisiae , 1995, Molecular and cellular biology.
[39] A. Berns,et al. Consecutive inactivation of both alleles of the pim-1 proto-oncogene by homologous recombination in embryonic stem cells , 1990, Nature.
[40] A. Borkhardt,et al. A DNA damage repair mechanism is involved in the origin of chromosomal translocations t(4;11) in primary leukemic cells , 1999, Oncogene.
[41] 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.
[42] 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.
[43] F. Alt,et al. A targeted DNA-PKcs-null mutation reveals DNA-PK-independent functions for KU in V(D)J recombination. , 1998, Immunity.
[44] C. Jackson-Cook,et al. Highly conservative reciprocal translocations formed by apparent joining of exchanged DNA double-strand break ends. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[45] A. Nussenzweig,et al. Hypersensitivity of Ku80-deficient cell lines and mice to DNA damage: the effects of ionizing radiation on growth, survival, and development. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[46] S M Burgess,et al. Collisions between yeast chromosomal loci in vivo are governed by three layers of organization. , 1999, Genes & development.
[47] Stylianos E. Antonarakis,et al. The nature and mechanisms of human gene mutation , 1995 .
[48] F. Alt,et al. Growth retardation and leaky SCID phenotype of Ku70-deficient mice. , 1997, Immunity.
[49] A. Giaccia,et al. scid mutation in mice confers hypersensitivity to ionizing radiation and a deficiency in DNA double-strand break repair. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[50] 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.
[51] B. Koller,et al. Brca1 controls homology-directed DNA repair. , 1999, Molecular cell.
[52] M. Caligiuri,et al. ALL-1 tandem duplication in acute myeloid leukemia with a normal karyotype involves homologous recombination between Alu elements. , 1994, Cancer research.
[53] Thomas Ried,et al. DNA repair protein Ku80 suppresses chromosomal aberrations and malignant transformation , 2000, Nature.
[54] H. Klein,et al. Yeast intrachromosomal recombination: long gene conversion tracts are preferentially associated with reciprocal exchange and require the RAD1 and RAD3 gene products. , 1989, Genetics.
[55] A. Berns,et al. Highly efficient gene targeting in embryonic stem cells through homologous recombination with isogenic DNA constructs. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[56] F. Alt,et al. Late embryonic lethality and impaired V (D)J recombination in mice lacking DNA ligase IV , 1998, Nature.