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1 more frequently as complex loci of tandemly repeated genes.
2 onsiderably between single-copy and 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
8 Phylogenetic analyses further reveal that repeated gene conversion of CEACAM extracellular domains
11 evolution in which new genes are created by repeated gene duplication and some duplicate genes are m
14 ated genes, the p200 cluster, which arose by repeated gene duplications and which encodes a large fam
17 RNA: the RNU1 and RNU2 loci contain tandemly repeated genes encoding U1 and U2 small nuclear RNAs (sn
20 ican lineages were complex, involving either repeated gene flow among geographically disparate groups
22 U1, RNU2, and RN5S) each containing tandemly repeated genes for an abundant small RNA (U1, U2, and 5S
23 mal genes, transposon remnants, and tandemly repeated genes (HXT6/7, ENA1/2/5, and CUP1-1/-2) that we
24 esults suggest that template switching among repeated genes is a potent driver of genome instability
25 t many phytoplasma genomes appear to contain repeated genes organized in units of approximately 20 kb
27 olymerase I (pol I) transcribes the tandemly repeated genes that encode the precursor of 18S, 5.8S an
28 composed of hundreds of ribosomal DNA (rDNA) repeated genes that form large chromosomal clusters, who
29 approach and found to contain three tandemly repeated genes with the structures of nucleotide binding