Ghanim G, Kellogg E, Nogales E, Rio D
Nat Struct Mol Biol. 2019; 26(11):1013-1022.
PMID: 31659330
PMC: 6948148.
DOI: 10.1038/s41594-019-0319-6.
Srivastava S, Dahal S, Naidu S, Anand D, Gopalakrishnan V, Kooloth Valappil R
DNA Res. 2017; 24(2):117-128.
PMID: 28431013
PMC: 5397610.
DOI: 10.1093/dnares/dsw059.
Srivastav S, Kelleher E
G3 (Bethesda). 2017; 7(5):1487-1497.
PMID: 28315830
PMC: 5427502.
DOI: 10.1534/g3.117.040634.
Sekelsky J
Genetics. 2017; 205(2):471-490.
PMID: 28154196
PMC: 5289830.
DOI: 10.1534/genetics.116.186759.
Francis M, Roche S, Cho M, Beall E, Min B, Panganiban R
Proc Natl Acad Sci U S A. 2016; 113(46):13003-13008.
PMID: 27799520
PMC: 5135294.
DOI: 10.1073/pnas.1613508113.
DNA Transposition at Work.
Hickman A, Dyda F
Chem Rev. 2016; 116(20):12758-12784.
PMID: 27187082
PMC: 6380494.
DOI: 10.1021/acs.chemrev.6b00003.
Mechanisms of DNA Transposition.
Hickman A, Dyda F
Microbiol Spectr. 2015; 3(2):MDNA3-0034-2014.
PMID: 26104718
PMC: 7422641.
DOI: 10.1128/microbiolspec.MDNA3-0034-2014.
P Transposable Elements in Drosophila and other Eukaryotic Organisms.
Majumdar S, Rio D
Microbiol Spectr. 2015; 3(2):MDNA3-0004-2014.
PMID: 26104714
PMC: 4399808.
DOI: 10.1128/microbiolspec.MDNA3-0004-2014.
Ku-mediated coupling of DNA cleavage and repair during programmed genome rearrangements in the ciliate Paramecium tetraurelia.
Marmignon A, Bischerour J, Silve A, Fojcik C, Dubois E, Arnaiz O
PLoS Genet. 2014; 10(8):e1004552.
PMID: 25166013
PMC: 4148214.
DOI: 10.1371/journal.pgen.1004552.
Is non-homologous end-joining really an inherently error-prone process?.
Betermier M, Bertrand P, Lopez B
PLoS Genet. 2014; 10(1):e1004086.
PMID: 24453986
PMC: 3894167.
DOI: 10.1371/journal.pgen.1004086.
The human THAP9 gene encodes an active P-element DNA transposase.
Majumdar S, Singh A, Rio D
Science. 2013; 339(6118):446-8.
PMID: 23349291
PMC: 3779457.
DOI: 10.1126/science.1231789.
Ku70 alleviates neurodegeneration in Drosophila models of Huntington's disease.
Tamura T, Sone M, Iwatsubo T, Tagawa K, Wanker E, Okazawa H
PLoS One. 2011; 6(11):e27408.
PMID: 22096569
PMC: 3210167.
DOI: 10.1371/journal.pone.0027408.
A segmental genomic duplication generates a functional intron.
Hellsten U, Aspden J, Rio D, Rokhsar D
Nat Commun. 2011; 2:454.
PMID: 21878908
PMC: 3265369.
DOI: 10.1038/ncomms1461.
Evidence based on studies of the mus309 mutant, deficient in DNA double-strand break repair, that meiotic crossing over in Drosophila melanogaster is a two-phase process.
Portin P
Genetica. 2010; 138(9-10):1033-45.
PMID: 20803348
DOI: 10.1007/s10709-010-9489-1.
The effect of the mus309 mutation, defective in DNA double-strand break repair, on crossing over in Drosophila melanogaster suggests a mechanism for the centromere effect of crossing over.
Portin P
Genetica. 2009; 138(3):333-42.
PMID: 19882364
DOI: 10.1007/s10709-009-9422-7.
Removal of the bloom syndrome DNA helicase extends the utility of imprecise transposon excision for making null mutations in Drosophila.
Witsell A, Kane D, Rubin S, McVey M
Genetics. 2009; 183(3):1187-93.
PMID: 19687136
PMC: 2778970.
DOI: 10.1534/genetics.109.108472.
Synthetic lethality of Drosophila in the absence of the MUS81 endonuclease and the DmBlm helicase is associated with elevated apoptosis.
Trowbridge K, McKim K, Brill S, Sekelsky J
Genetics. 2007; 176(4):1993-2001.
PMID: 17603121
PMC: 1950608.
DOI: 10.1534/genetics.106.070060.
Multiple functions of Drosophila BLM helicase in maintenance of genome stability.
McVey M, Andersen S, Broze Y, Sekelsky J
Genetics. 2007; 176(4):1979-92.
PMID: 17507683
PMC: 1950607.
DOI: 10.1534/genetics.106.070052.
Multiple-pathway analysis of double-strand break repair mutations in Drosophila.
Johnson-Schlitz D, Flores C, Engels W
PLoS Genet. 2007; 3(4):e50.
PMID: 17432935
PMC: 1851981.
DOI: 10.1371/journal.pgen.0030050.
DNA strand displacement, strand annealing and strand swapping by the Drosophila Bloom's syndrome helicase.
Weinert B, Rio D
Nucleic Acids Res. 2007; 35(4):1367-76.
PMID: 17272294
PMC: 1849897.
DOI: 10.1093/nar/gkl831.