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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.
6       Inherited deficiency of the RNA lariat-debranching enzyme 1 (DBR1) is a rare etiology of brains
7  which inborn errors of the human RNA lariat-debranching enzyme 1 (DBR1) underlie brainstem viral enc
8  been named AtDBR1 (for Arabidopsis thaliana Debranching enzyme 1).
9 ells lacking both SpPrp18 and SpDbr1 (lariat debranching enzyme), a genetic background suitable for d
10 n accumulation when the only isoamylase-type debranching enzyme activity present is ISA1/ISA heterome
11 D-III) is caused by a deficiency of glycogen debranching enzyme (AGL) activity.
12 haracterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-alpha-glucan
13 haracterized by a deficiency in the glycogen debranching enzyme, amylo-1,6-glucosidase,4-alpha-glucan
14      These intronic sequences can escape the debranching enzyme and accumulate as lariats.
15           Although the ex vivo activities of debranching enzyme and lysosomal acid maltase, two major
16 form of a lariat and rapidly targeted by the debranching enzyme and nuclear exonucleases for lineariz
17 osin binding protein C (C-protein), glycogen debranching enzyme and ryanodine receptor 2 were also id
18     These data indicate that isoamylase-type debranching enzyme and SSIII work in a coordinated fashi
19 ene with sequence similarity to higher plant debranching enzymes, and both mutants lacked a chloropla
20 tide diversities, while pyrophosphatases and debranching enzymes are most conserved.
21 h/glycogen synthases, branching enzymes, and debranching enzymes) are differentially expressed in Mul
22 ity is that specific SSs, BEs, and/or starch debranching enzymes associate physically with each other
23  structure of the complex between the starch debranching enzyme barley limit dextrinase (LD), hydroly
24 t an enzyme of analogous nature to the plant debranching enzyme but of a different bacterial origin w
25 Saccharomyces cerevisiae, the absence of the debranching enzyme causes these lariat RNAs to accumulat
26 tered by mutations of isoamylase-type starch-debranching enzymes (DBE), although how these proteins a
27 pes of alpha(1-->6) glucan hydrolase (starch-debranching enzyme [DBE]).
28 ific isoamylase- and pullulanase-type starch-debranching enzymes (DBEs) present in developing maize (
29 e to alpha-(1-->6) glucan hydrolases (starch-debranching enzymes [DBEs]).
30  investigations of group II intron splicing, debranching enzyme (Dbr) activity, and other biochemical
31 he 2',5'-bonds must be hydrolyzed by the RNA debranching enzyme Dbr1 before spliced introns can be de
32    A new study shows that loss of the lariat debranching enzyme Dbr1 suppresses TDP-43 toxicity.
33        Using fission yeast cells lacking the debranching enzyme Dbr1, LaSSO not only accurately ident
34 TDN1 C-terminal region directly binds lariat debranching enzyme DBR1, whereas its N-terminal intrinsi
35 on in DBR1 (p.D262Y) encoding the RNA lariat-debranching enzyme DBR1, which is involved in the remova
36 ng new BP data from RNA sequencing of lariat debranching enzyme DBR1-mutated patients and from machin
37 ' linkage of these lariats is the RNA lariat debranching enzyme Dbr1.
38 lariat stability by knocking down the lariat debranching enzyme Dbr1.
39 spliceosome must be hydrolyzed by the intron debranching enzyme (Dbr1) before they can be metabolized
40 tudies in our laboratory showed that the RNA debranching enzyme (DBR1) is not required for early step
41 rpin RNA (shRNA) knockdown of the RNA lariat debranching enzyme (DBR1) led to a decrease in the produ
42  One of these host factors is the RNA lariat debranching enzyme (Dbr1), which cleaves the 2'-5' bond
43 ive disease, is caused by deficient glycogen debranching enzyme (GDE) activity.
44 ns of the AGL gene encoding for the glycogen debranching enzyme (GDE).
45                                     Glycogen debranching enzyme (gene symbol, AGL) is a multifunction
46 e show that c-di-GMP also binds the glycogen-debranching-enzyme, GlgX, uncovering a direct link betwe
47 eals from a need for effective inhibition of debranching enzymes having characteristic open active si
48           Here, we report that the human RNA debranching enzyme (hDBR1), when inappropriately regulat
49 , starch branching enzymes (BEs), and starch debranching enzymes; however, the molecular explanation
50      We now report the implication of starch debranching enzyme in the aggregation of semicrystalline
51 r abundance of oligosaccharide degrading and debranching enzymes in buffalo rumen metagenome and that
52  our goal was to evaluate the role of starch debranching enzymes in the determination of the structur
53 zyme families (oligosaccharide degrading and debranching enzymes) in digestion of coarse feed.
54                                       Lariat debranching enzyme is also necessary for siRNA productio
55                                  Because the debranching enzyme is conserved among eukaryotes, this a
56          Functions of isoamylase-type starch-debranching enzyme (ISA) proteins and complexes in maize
57                       Isoamylase-type starch debranching enzymes (ISA) play important roles in starch
58  indirect evidence that the heteromultimeric debranching enzyme ISA1-ISA2 is not involved in starch b
59 ubunit of heteromeric isoamylase-type starch-debranching enzyme (ISA1/ISA2 heteromer).
60             Conserved isoamylase-type starch debranching enzymes (ISAs), including the catalytic ISA1
61                                   The starch debranching enzymes isoamylase 1 and 2 (ISA1 and ISA2) a
62              Previous studies identified two debranching enzymes, isoamylase 3 (ISA3) and limit dextr
63 SS2, and SS3 (to vary chain lengths) and the debranching enzyme ISOAMYLASE1-ISOAMYLASE2 (ISA; to alte
64  genes on SBEIIa, starch synthase, or starch-debranching enzyme isoforms were observed.
65 ose pyrophosphorylase, starch synthases, and debranching enzymes, leading to varied chain lengths and
66 G (type 1 phosphatase-targeting subunit), or debranching enzyme, making it unlikely that these protei
67           This involved the recruitment of a debranching enzyme of chlamydial pathogen origin.
68              This enzyme was identified as a debranching enzyme of the isoamylase type.
69 addition of pregelatinized starch and starch-debranching enzymes produced by far the highest amount o
70 tein body and found to be enriched in starch debranching enzyme (pullulanase).
71 -fold increase in the activity of the starch debranching enzyme, pullulanase (limit dextrinase), the
72 enes encoding granule-bound starch synthase, debranching enzymes, pullulanase, and starch phosphoryla
73 that gene expression of LIMIT DEXTRINASE1, a debranching enzyme that cleaves branch points within sta
74 yces cerevisiae Dbr1 is a 405-amino acid RNA debranching enzyme that cleaves the 2'-5' phosphodiester
75  I, SBEIIb, and sugary1, the putative starch-debranching enzyme, were each highly enriched in the amy
76        The csrA gene did not affect glycogen debranching enzyme, which is now shown to be encoded by
77  action of the splicing machinery and lariat-debranching enzyme, which yield pre-miRNA-like hairpins.
78 rotein with domains characteristic of lariat debranching enzymes, which has been named AtDBR1 (for Ar