Published in Proc Natl Acad Sci U S A on March 16, 1999
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Shaping and reshaping of salmonid genomes by amplification of tRNA-derived retroposons during evolution. Proc Natl Acad Sci U S A (1991) 1.51
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A novel family of short interspersed repetitive elements (SINEs) from cichlids: the patterns of insertion of SINEs at orthologous loci support the proposed monophyly of four major groups of cichlid fishes in Lake Tanganyika. Mol Biol Evol (1998) 1.21
Novel Alu-type repeat in artiodactyls. Nucleic Acids Res (1987) 1.20
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Chicken repeat 1 elements contain a pol-like open reading frame and belong to the non-long terminal repeat class of retrotransposons. Proc Natl Acad Sci U S A (1993) 1.09
Determination of the entire sequence of turtle CR1: the first open reading frame of the turtle CR1 element encodes a protein with a novel zinc finger motif. Mol Biol Evol (1997) 1.09
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The 3' ends of tRNA-derived SINEs originated from the 3' ends of LINEs: a new example from the bovine genome. J Mol Evol (1997) 0.97
SINE cousins: the 3'-end tails of the two oldest and distantly related families of SINEs are descended from the 3' ends of LINEs with the same genealogical origin. Mol Biol Evol (1998) 0.91
A highly repetitive and transcribable sequence in the tortoise genome is probably a retroposon. Eur J Biochem (1990) 0.90
A new family of repetitive, retroposon-like sequences in the genome of the rainbow trout. Eur J Biochem (1988) 0.88
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Phylogenetic and familial estimates of mitochondrial substitution rates: study of control region mutations in deep-rooting pedigrees. Am J Hum Genet (2001) 1.59
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. Proc Natl Acad Sci U S A (1991) 1.56
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Use of gamma irradiation to eliminate DNA contamination for PCR. Nucleic Acids Res (1990) 1.09
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High resolution deletion mapping reveals frequent allelic losses at the DNA mismatch repair loci hMLH1 and hMSH3 in non-small cell lung cancer. Int J Cancer (1998) 1.03
Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families. Genomics (1992) 1.01
A young Alu subfamily amplified independently in human and African great apes lineages. Nucleic Acids Res (1994) 1.01
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Linkage mapping by simultaneous screening of multiple polymorphic loci using Alu oligonucleotide-directed PCR. Proc Natl Acad Sci U S A (1992) 0.99
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Deletions in the dystrophin gene: analysis of Duchenne and Becker muscular dystrophy patients in Quebec. Hum Genet (1992) 0.93
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Magnesium ion inner sphere complex in the anticodon loop of phenylalanine transfer ribonucleic acid. Biochemistry (1982) 0.91
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Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution. Genomics (1994) 0.89
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Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. Hum Genet (1992) 0.87
Are CpG sites mutation hot spots in the dystrophin gene? Hum Mol Genet (1994) 0.84
Detection of a mutator phenotype in cancer cells by inter-Alu polymerase chain reaction. Cancer Res (1996) 0.84
Small cytoplasmic Ro RNA pseudogene and an Alu repeat in the human alpha-1 globin gene. Nucleic Acids Res (1988) 0.84
Mechanism of codon recognition by transfer RNA studied with oligonucleotides larger than triplets. Nucleic Acids Res (1985) 0.83
Codon-induced transfer ribonucleic acid association: quantitative analysis by sedimentation equilibrium. Biochemistry (1982) 0.82
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