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1 dence that the maize (Zea mays) nuclear gene Pentatricopeptide repeat 2263 (PPR2263) encoding a DYW d
2 ly, which includes tetratricopeptide repeat, pentatricopeptide repeat, and the recently identified oc
6 rans-acting small interfering RNA gene (TAS)-pentatricopeptide repeat-containing gene (PPR)-small int
10 ipts, mitochondrial RNA polymerase (POLRMT), pentatricopeptide repeat domain 3 protein (PTCD3), and a
12 Here, we found that Drosophila leucine-rich pentatricopeptide repeat domain-containing protein 1 (Dm
13 FACTOR1 (MTL1) protein, a new member of the Pentatricopeptide Repeat family, and show that it is ess
17 sess the respective importance of individual pentatricopeptide repeat motifs in PRORP2 for RNA bindin
18 eous RNase P (PRORP) possesses two domains - pentatricopeptide repeat (PPR) and metallonuclease (NYN)
19 typical metallonuclease domain tethered to a pentatricopeptide repeat (PPR) domain by a structural zi
22 putative RNA binding proteins in plants, the pentatricopeptide repeat (PPR) family, no physiologicall
23 AS1/2, produces tasiRNAs regulating a set of pentatricopeptide repeat (PPR) genes and has been charac
32 In this paper, we show that the E(+)-type pentatricopeptide repeat (PPR) protein SLO2, which lacks
33 this line is caused by lack of a chloroplast pentatricopeptide repeat (PPR) protein that we named SUP
44 end maturation posits that sequence-specific pentatricopeptide repeat (PPR) proteins define termini b
46 NA, a set of SSU ribosomal proteins, several pentatricopeptide repeat (PPR) proteins, and proteins no
49 king discernible motifs and approximately 20 pentatricopeptide repeat (PPR) RNA binding proteins.
50 Many proteins of unknown function, including pentatricopeptide repeat (PPR), tetratricopeptide repeat
51 vents in plant mitochondria and plastids are pentatricopeptide repeat (PPR)-containing proteins with
52 ied two independent defective genes encoding pentatricopeptide repeat (PPR)-like proteins [CELL WALL
53 F10 protein is characterized by a stretch of pentatricopeptide repeats (PPR) and a C-terminal extensi
54 family protein, ABC transporter G family and pentatricopeptide repeat protein are the major markers f
57 ere, we studied the functions of Arabidopsis PENTATRICOPEPTIDE REPEAT PROTEIN FOR GERMINATION ON NaCl
58 77 editing, like the essential site-specific pentatricopeptide repeat protein LOW PSII ACCUMULATION66
60 y been identified as a chloroplast-localized pentatricopeptide repeat protein that integrates informa
62 d to investigate the role of a PLS-subfamily pentatricopeptide repeat protein, Mitochondrial Editing
63 EME1), an Arabidopsis (Arabidopsis thaliana) pentatricopeptide repeat protein-encoding gene belonging
66 show here that GUN1, a chloroplast-localized pentatricopeptide-repeat protein, and ABI4, an Apetala 2
67 nd mitochondria of flowering plants requires pentatricopeptide repeat proteins (PPR proteins) for sit
68 affected in RNA editing have shown that many pentatricopeptide repeat proteins (PPRs) are required fo
69 ipts and target several transcripts encoding pentatricopeptide repeat proteins and proteins of unknow
71 ith genes encoding chloroplast ribosomal and pentatricopeptide repeat proteins well represented among
74 rtility genes) has identified genes encoding pentatricopeptide-repeat proteins as key regulators of p
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