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1 he most commonly occurring repeat is the Alu short interspersed element.
2 etions within the oligo(dA)-rich tail of the short interspersed element.
3 stly at intergenic sites located on long and short interspersed elements.
4 GCAGA repeat unit from within a subset of B1 short interspersed elements.
5 self-mobilization and trans-mobilization of short interspersed elements and processed pseudogenes, h
6 are associated with Alu elements and SINEs (short interspersed elements) and which have been postula
7 nmethylated and a large fraction of abundant short interspersed elements are also methylation free.
8 rticle endogenous retrovirus elements and B2 short interspersed elements, but it does not appear to h
9 nvolved versus normal skin, including an Alu-short interspersed element-derived siRNA which was 17-fo
10 Alu elements are the most successful SINEs (Short INterspersed Elements) in primate genomes and have
12 ue primarily to a continuing series of SINE (short interspersed element) insertions into this locus.
17 ts are primate-specific members of the SINE (short interspersed element) retroposon family, which com
21 ements represent the first identified walnut short interspersed element (SINE) and terminal-repeat re
22 cell stresses upon the expression of the Bm1 short interspersed element (SINE) family in cultured sil
23 rotransposons represents the most successful short interspersed element (SINE) in primates and CpG di
24 0 bp in length, making it the shortest known short interspersed element (SINE) in primates, and harbo
26 CTCF, housekeeping genes, transfer RNAs and short interspersed element (SINE) retrotransposons, indi
27 ghly significant (P<.0001) enrichment of Alu short interspersed element (SINE) sequences near or with
29 mon 3' end with a highly transcribed 0.55 kb short interspersed element (SINE)-like element previousl
30 ITS1 and ITS2) and intergenic spacers (IGS), Short INterspersed Elements (SINE), as well as mitochond
31 orphisms and include 16,221 dimorphic canine short interspersed elements (SINECs) and 1,121 dimorphic
37 four assays based upon PCR amplification of short interspersed elements (SINEs) for species-specific
40 stions concern why mobile, highly repetitive short interspersed elements (SINEs) have been tolerated
41 ne new roles for lncRNAs as well as B and ID short interspersed elements (SINEs) in mice that undoubt
42 are the most active and predominant type of short interspersed elements (SINEs) in the human genome.
45 me rearrangements, an over-representation of short interspersed elements (SINEs) probably linked to h
46 we show that human Alu RNA, transcribed from short interspersed elements (SINEs), is a transacting tr
47 ough an RNA intermediate, are categorized as short interspersed elements (SINEs), long interspersed e
49 s of non-autonomous retroposons belonging to short interspersed elements that are specific to the pri
50 proximately 100 precursors of composite SVA (short interspersed element, variable number of tandem re
51 ers revealed that they have a human-specific short interspersed element-variable number of tandem rep
52 presents the first conclusive application of short interspersed elements, which are considered nearly