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1 A (miRNA), short-interfering RNA (siRNA) and Piwi-interacting RNA.
2 obile genetic elements, acting together with Piwi-interacting RNAs.
3 RNA intermediates to achieve optimally sized piwi-interacting RNAs.
4 enomenon to paramutation that is mediated by piwi-interacting RNAs.
6 nd micro-RNA pathways; whereas PIWIs bind to PIWI-interacting RNAs and regulate germ line development
9 fs that are overrepresented in comparison to Piwi-interacting RNAs and transcription start site-assoc
12 r-dependent miRNAs and the Dicer-independent Piwi-interacting RNAs, associate with Argonaute family p
13 A second endogenous small RNA class, the Piwi-interacting RNAs, bind Piwi proteins and suppress t
14 , these results define PNLDC1 as a mammalian piwi-interacting RNA biogenesis factor that protects the
15 ce, here we show that PNLDC1 is required for piwi-interacting RNA biogenesis, transposon silencing, a
16 have shown that proteins involved in piRNA (PIWI-interacting RNA) biogenesis are necessary for retro
17 ld), known epigenetic regulators (2.3-fold), piwi-interacting RNA clusters (3.6-fold) and curated tra
20 ll as a large population of putative piRNAs (piwi-interacting RNAs) had dynamic accumulation profiles
21 d small interfering RNAs (siRNAs) in plants, Piwi-interacting RNAs in animals and siRNAs in Drosophil
24 ng RNAs requires a critical step of trimming piwi-interacting RNA intermediates to achieve optimally
25 rimming and causes accumulation of untrimmed piwi-interacting RNA intermediates with 3' end extension
26 previously that Piwi plays a crucial role in Piwi-interacting RNA-mediated epigenetic regulation and
28 uted to the nuage proteins, which engage the Piwi-interacting RNA pathway and other posttranscription
30 "cancer/testis antigens" (CTAs), and piRNA (PIWI-interacting RNA) pathway proteins are found among C
32 are sterile, and phenocopy mutations in the PIWI interacting RNA (piRNA) pathway, which silences tra
33 The Piwi protein subfamily is essential for Piwi-interacting RNA (piRNA) biogenesis, transposon sile
34 nsposon insertions negatively correlate with Piwi-interacting RNA (piRNA) levels for most transposon
36 mutant animals, we probed the roles of known Piwi-interacting RNA (piRNA) pathway components in the i
38 spite exciting progress in understanding the Piwi-interacting RNA (piRNA) pathway in the germ line, l
43 , to participate in the previously described PIWI-interacting RNA (piRNA) pathway that promotes trans
44 facets-1)(Kr(If-1)) allele, we show that the Piwi-interacting RNA (piRNA) pathway, but not the short
45 ermline-specific RNAi mechanism known as the Piwi-interacting RNA (piRNA) pathway, which specifically
48 uman extracellular RNAs including microRNAs, piwi-interacting RNA (piRNA), and small nucleolar RNAs.
49 erfering RNA (siRNA), micro-RNA (miRNA), and piwi-interacting RNA (piRNA), play important roles in ma
50 f proteins containing tudor domains with the piwi-interacting RNA (piRNA)-binding Piwi proteins, and
51 binds the histone ubiquitin ligase RNF8 in a Piwi-interacting RNA (piRNA)-independent manner, and MIW
53 NAs map within annotated genes, but some are PIWI-interacting RNA (piRNA)-like and map to piRNA clust
54 singly, zuc/MitoPLD activity is required for Piwi-interacting RNA (piRNA)-mediated silencing of trans
55 PIWI-directed gene silencing, we employed a Piwi-interacting RNA (piRNA)-targeted reporter assay in
57 on a 180-kb heterochromatic locus producing Piwi-interacting RNAs (piRNA cluster), the flamenco (fla
62 lencing effectors for approximately 26-32 nt Piwi-interacting RNAs (piRNAs) [1], and piwi mutants exh
65 include small interfering RNAs (siRNAs) and PIWI-interacting RNAs (piRNAs) and are implicated in nuc
66 ermore, we showed that tsRNAs are similar to Piwi-interacting RNAs (piRNAs) and demonstrated that ts-
68 In Drosophila, Piwi proteins associate with Piwi-interacting RNAs (piRNAs) and protect the germline
70 ures our current understandings of mammalian PIWI-interacting RNAs (piRNAs) and their role in TE regu
87 Short deletions over sites with homology to PIWI-interacting RNAs (piRNAs) are sufficient to comprom
93 interfering RNAs (siRNAs) as well as animal piwi-interacting RNAs (piRNAs) from degradation and 3' t
95 The conserved Piwi family of proteins and piwi-interacting RNAs (piRNAs) have a central role in ge
96 ince their discovery less than a decade ago, Piwi-interacting RNAs (piRNAs) have been shown to repres
100 iRNAs), small interfering RNAs (siRNAs), and piwi-interacting RNAs (piRNAs) impact numerous biologica
101 We also report detection of virus-derived PIWI-interacting RNAs (piRNAs) in Drosophila melanogaste
102 dentification and characterization of 12,903 Piwi-interacting RNAs (piRNAs) in Drosophila, showing th
103 ssion of retrotranspons with the presence of piwi-interacting RNAs (piRNAs) in fetal male germ cells
104 p to low-copy, intergenic regions similar to PIWI-interacting RNAs (piRNAs) in mammalian testis.
106 oding RNAs (sncRNAs), microRNAs (miRNAs) and PIWI-interacting RNAs (piRNAs) in particular, define sev
114 azoan germline, piwi proteins and associated piwi-interacting RNAs (piRNAs) provide a defense system
123 mall interfering RNAs) and Piwi proteins and Piwi-interacting RNAs (piRNAs) suggest novel functions f
124 ughters show a markedly different content of Piwi-interacting RNAs (piRNAs) targeting each element, d
125 RNAs) and siRNAs, whereas the latter targets piwi-interacting RNAs (piRNAs) that are 2'-O-methylated
126 vered a class of noncoding small RNAs called PIWI-interacting RNAs (piRNAs) that are abundantly expre
127 n Piwi proteins, MIWI and MILI, partner with Piwi-interacting RNAs (piRNAs) that are depleted of repe
129 ound approximately 23- to 30-nucleotide (nt) PIWI-interacting RNAs (piRNAs) that are processed from s
130 amily proteins, carry approximately 24-30-nt Piwi-interacting RNAs (piRNAs) that mediate gonadal defe
132 y 29 to 30 nucleotides in length, are called Piwi-interacting RNAs (piRNAs), 94% of which map to 100
134 Piwi Argonaute protein PRG-1 and associated Piwi-interacting RNAs (piRNAs), as well as by proteins t
136 ous small interfering RNAs (endo-siRNAs) and Piwi-interacting RNAs (piRNAs), have been shown to play
137 on the role of small RNAs, and in particular piwi-interacting RNAs (piRNAs), in the epigenetic regula
139 ous small interfering RNAs (endo-siRNAs) and Piwi-interacting RNAs (piRNAs), play essential roles in
140 iRNAs, other bilaterian small RNAs, known as Piwi-interacting RNAs (piRNAs), protect the genome from
142 UTE/PIWI protein family member that binds to Piwi-interacting RNAs (piRNAs), strongly and specificall
143 TEs) in flies and vertebrates is mediated by Piwi-interacting RNAs (piRNAs), which are approximately
144 e numerous long noncoding RNAs (lncRNAs) and Piwi-interacting RNAs (piRNAs), yet the functions of the
151 nd silencing recently exemplified by piRNAs (piwi-interacting RNAs), position effect variegation, X-c
155 the mechanism of biogenesis for tRNA-derived Piwi-interacting RNAs (td-piRNAs) expressed in Bombyx Bm
158 re matched by small regulatory RNAs, such as piwi-interacting RNAs, which play a potent role in both
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