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Genome Biol. 2002 Sep 19;3(10):research0052. Epub 2002 Sep 19.

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Identifying related L1 retrotransposons by analyzing 3' transduced sequences.

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Genome Biol. 2003;4(5):R30. Epub 2003 Apr 16.

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Genomic rearrangements by LINE-1 insertion-mediated deletion in the human and chimpanzee lineages.

Han K, Sen SK, Wang J, Callinan PA, Lee J, Cordaux R, Liang P, Batzer MA.

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More active human L1 retrotransposons produce longer insertions.

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Nucleic Acids Res. 2004 Jan 23;32(2):502-10. Print 2004.

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Endonuclease-independent insertion provides an alternative pathway for L1 retrotransposition in the human genome.

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Characterization of pre-insertion loci of de novo L1 insertions.

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Genomic characterization of recent human LINE-1 insertions: evidence supporting random insertion.

Ovchinnikov I, Troxel AB, Swergold GD.

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[Analysis, identification and correction of some errors of model refseqs appeared in NCBI Human Gene Database by in silico cloning and experimental verification of novel human genes]

Zhang DL, Ji L, Li YD.

Yi Chuan Xue Bao. 2004 May;31(5):431-43. Chinese.

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Genomic deletions created upon LINE-1 retrotransposition.

Gilbert N, Lutz-Prigge S, Moran JV.

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A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element.

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The insertional history of an active family of L1 retrotransposons in humans.

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Whole genome computational comparative genomics: A fruitful approach for ascertaining Alu insertion polymorphisms.

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Tandem insertions of Alu elements.

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LINE-1 preTa elements in the human genome.

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Frequent human genomic DNA transduction driven by LINE-1 retrotransposition.

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Acquisition of endonuclease specificity during evolution of L1 retrotransposon.

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Endonuclease-independent LINE-1 retrotransposition at mammalian telomeres.

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