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1 that guide post-transcriptional silencing by Aubergine.
2 izes and binds the sDMAs of the Piwi protein Aubergine.
3 ng the entire Tudor structure, interact with Aubergine.
4 pted in stocks heterozygous for mutations in aubergine, a gene whose protein product is involved in R
5 e to the perinuclear nuage and interact with Aubergine, a PIWI class protein.
6 nts profiled were tomato, pepper, chilli and aubergine, all members of the Solanaceae family.
7  ping-pong cycle, in which the PIWI proteins Aubergine and Ago3 increase the abundance of pre-existin
8  to contain two of the three PIWI proteins - Aubergine and Argonaute 3 (AGO3) - that are essential fo
9    The Piwi-interacting RNA (piRNA) proteins Aubergine and Argonaute 3, known to suppress transposons
10 cells, PIWI-interacting RNAs (piRNAs) direct Aubergine and Argonaute3 to cleave transposon transcript
11 nds on two genes involved in RNAi phenomena, aubergine and spindle-E (spn-E), for its nuage localizat
12                                 Mutations in aubergine and spindle-E, members of the PIWI/PAZ and DE-
13     Our data suggest that in polar granules, Aubergine and Tudor are assembled into distinct phases,
14 ution microscopy, we show that surprisingly, Aubergine and Tudor form distinct clusters within the sa
15                       Instead, Piwi requires Aubergine (and presumably secondary piRNA) for proper lo
16 ree gonad-specific Argonaute proteins (Piwi, Aubergine, and Argonaute 3).
17 three Drosophila Piwi proteins--called Piwi, Aubergine, and Argonaute 3--Piwi is the only member of t
18 ge into the Zucchini-dependent production of Aubergine- and Piwi-bound piRNAs on the mitochondrial su
19  components, including the ping-pong factors Aubergine, Argonaute-3, and Vasa, leading to assembly of
20 tion, the survival and viral titers of Piwi, Aubergine, Argonaute-3, and Zucchini mutant flies were s
21                                 Instead, fly Aubergine as well as its homologs, Siwi in silkmoth and
22            In Drosophila, two Piwi proteins, Aubergine (Aub) and Argonaute-3 (Ago3), localize to peri
23 all three PIWI proteins in Drosophila; Piwi, Aubergine (Aub) and Argonaute3 (Ago3) during early embry
24 RNA cleavage--catalyzed by the PIWI proteins Aubergine (Aub) and Argonaute3 (Ago3) in Drosophila mela
25 dor domain protein Qin and the PIWI proteins Aubergine (Aub) and Argonaute3 (Ago3).
26 n association with Argonaute family proteins Aubergine (Aub) and Argonaute3 (AGO3).
27 e now identified the Argonaute family member Aubergine (Aub) as a nos localization factor.
28                          Piwi family protein Aubergine (Aub) maintains genome integrity in late germ
29  relies on three Piwi family proteins--Piwi, Aubergine (Aub), and Ago3--acting in concert with their
30 line- P-element-induced wimpy testis (Piwi), Aubergine (Aub), and Argonaute 3 (Ago3).
31              We also found that mutations in aubergine (aub), another gene implicated in the rasiRNA
32  especially those loaded on the Piwi protein Aubergine (Aub), are transmitted to the germ plasm to in
33                                              Aubergine (Aub), Argonaute 3 (Ago3), and components of t
34 domains, associates physically with Piwi and Aubergine (Aub), stabilizing these proteins via a gonad-
35 osophila Piwi protein and find that Piwi and Aubergine bind RNAs that are predominantly antisense to
36                In the granules, Piwi protein Aubergine binds to a scaffold protein Tudor, which conta
37                                        While aubergine-dependence is conferred upon oskar mRNA by seq
38 rosophila rasiRNA pathway genes armitage and aubergine disrupt embryonic axis specification, triggeri
39 formation of distinct clusters, we show that Aubergine forms homo-oligomers and using all purified Tu
40                                              Aubergine glycans contain abundant heteroxylan epitopes,
41 the embryonic oosome, while small Oskar/Vasa/Aubergine granules coalesce interiorly.
42                                  Previously, aubergine has been implicated in dorsoventral patterning
43          We have isolated two new alleles of aubergine in a novel genetic screen and have shown that
44  Nature, Vourekas et al. (2016) suggest that Aubergine in complex with piRNAs may provide a low-speci
45      In this report, we describe the role of aubergine in oskar translation.
46 n a novel genetic screen and have shown that aubergine is also required for posterior body patterning
47 stent with its presence in these structures, Aubergine is required for pole cell formation independen
48                                        Thus, aubergine is required to enhance oskar translation.
49 rsicoides, which we use to shed light on the Aubergine locus responsible for anthocyanin production.
50 MYB genes sheds light on the identity of the Aubergine locus underlying anthocyanin production.
51 oskar mRNA by sequences in the oskar 3' UTR, aubergine may influence oskar translation through an int
52 tterning, as the small fraction of eggs from aubergine- mothers that are fertilized develop into embr
53 ted in dorsoventral patterning, as eggs from aubergine mutant mothers are ventralized and seldom fert
54                                              aubergine mutants fail to translate oskar mRNA efficient
55 of oskar protein is significantly reduced in aubergine mutants.
56                                     Although aubergine mutations do not appear to affect the stabilit
57                                              aubergine mutations exert their effects in the female ge
58 n loop in which an antisense piRNA, bound to Aubergine or Piwi protein, triggers production of a sens
59  silencing as a result of mutations in piwi, aubergine, or spindle-E (homeless), which encode RNAi co
60                           We have found that Aubergine protein is related to eukaryotic translation i
61 wn polar granule components, Vasa and Oskar, Aubergine remains cytoplasmic after pole cell formation,
62 d that the Tudor domain protein Qin prevents Aubergine's cleavage products from becoming Piwi-bound p
63  unexpected from these interacting proteins: Aubergine shell around the Tudor core.
64     Among the findings, some of the earliest aubergine (Solanum melongena) seeds in the Levant repres
65                    Lines derived from mutant aubergine stocks reestablish the P cytotype quickly, unl
66  parenchyma tissues of four fruits - tomato, aubergine, strawberry and apple - we have dissected cell
67  Drosophila piRNAs bound to the PIWI protein Aubergine typically begin with uridine (1U), while piRNA
68                   In addition, we found that Aubergine was recruited to the posterior pole in a vas-d