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1 onsiderably between single-copy and tandemly-repeated genes.
2 more frequently as complex loci of tandemly repeated genes.
3 amilies and maintaining similarities between repeated genes.
5 e culture, our study shows that the tandemly repeated genes are also prone to hypermethylation and ep
10 evolution in which new genes are created by repeated gene duplication and some duplicate genes are m
12 ated genes, the p200 cluster, which arose by repeated gene duplications and which encodes a large fam
15 RNA: the RNU1 and RNU2 loci contain tandemly repeated genes encoding U1 and U2 small nuclear RNAs (sn
18 ican lineages were complex, involving either repeated gene flow among geographically disparate groups
19 U1, RNU2, and RN5S) each containing tandemly repeated genes for an abundant small RNA (U1, U2, and 5S
20 mal genes, transposon remnants, and tandemly repeated genes (HXT6/7, ENA1/2/5, and CUP1-1/-2) that we
21 esults suggest that template switching among repeated genes is a potent driver of genome instability
22 t many phytoplasma genomes appear to contain repeated genes organized in units of approximately 20 kb
24 olymerase I (pol I) transcribes the tandemly repeated genes that encode the precursor of 18S, 5.8S an
25 approach and found to contain three tandemly repeated genes with the structures of nucleotide binding
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