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1 cleavage of the 2',5' linkage by recombinant debranching enzyme.
2 eletion of DBR1, which encodes an RNA lariat debranching enzyme.
3 or to genes up-regulated by deletion of the debranching enzyme.
4 Pullulanase is a well-known starch-debranching enzyme.
5 pyrophosphorylase, and starch branching and debranching enzymes.
7 ells lacking both SpPrp18 and SpDbr1 (lariat debranching enzyme), a genetic background suitable for d
8 n accumulation when the only isoamylase-type debranching enzyme activity present is ISA1/ISA heterome
10 haracterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-alpha-glucan
11 haracterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-alpha-glucan
13 osin binding protein C (C-protein), glycogen debranching enzyme and ryanodine receptor 2 were also id
14 These data indicate that isoamylase-type debranching enzyme and SSIII work in a coordinated fashi
15 ene with sequence similarity to higher plant debranching enzymes, and both mutants lacked a chloropla
17 h/glycogen synthases, branching enzymes, and debranching enzymes) are differentially expressed in Mul
18 ity is that specific SSs, BEs, and/or starch debranching enzymes associate physically with each other
19 structure of the complex between the starch debranching enzyme barley limit dextrinase (LD), hydroly
20 t an enzyme of analogous nature to the plant debranching enzyme but of a different bacterial origin w
21 Saccharomyces cerevisiae, the absence of the debranching enzyme causes these lariat RNAs to accumulat
22 tered by mutations of isoamylase-type starch-debranching enzymes (DBE), although how these proteins a
24 ific isoamylase- and pullulanase-type starch-debranching enzymes (DBEs) present in developing maize (
26 investigations of group II intron splicing, debranching enzyme (Dbr) activity, and other biochemical
27 he 2',5'-bonds must be hydrolyzed by the RNA debranching enzyme Dbr1 before spliced introns can be de
30 spliceosome must be hydrolyzed by the intron debranching enzyme (Dbr1) before they can be metabolized
31 tudies in our laboratory showed that the RNA debranching enzyme (DBR1) is not required for early step
32 rpin RNA (shRNA) knockdown of the RNA lariat debranching enzyme (DBR1) led to a decrease in the produ
35 eals from a need for effective inhibition of debranching enzymes having characteristic open active si
37 , starch branching enzymes (BEs), and starch debranching enzymes; however, the molecular explanation
39 r abundance of oligosaccharide degrading and debranching enzymes in buffalo rumen metagenome and that
40 our goal was to evaluate the role of starch debranching enzymes in the determination of the structur
46 indirect evidence that the heteromultimeric debranching enzyme ISA1-ISA2 is not involved in starch b
51 SS2, and SS3 (to vary chain lengths) and the debranching enzyme ISOAMYLASE1-ISOAMYLASE2 (ISA; to alte
53 G (type 1 phosphatase-targeting subunit), or debranching enzyme, making it unlikely that these protei
57 -fold increase in the activity of the starch debranching enzyme, pullulanase (limit dextrinase), the
58 that gene expression of LIMIT DEXTRINASE1, a debranching enzyme that cleaves branch points within sta
59 yces cerevisiae Dbr1 is a 405-amino acid RNA debranching enzyme that cleaves the 2'-5' phosphodiester
60 I, SBEIIb, and sugary1, the putative starch-debranching enzyme, were each highly enriched in the amy
62 action of the splicing machinery and lariat-debranching enzyme, which yield pre-miRNA-like hairpins.
63 rotein with domains characteristic of lariat debranching enzymes, which has been named AtDBR1 (for Ar
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