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1 muscle and Deinococcus geothermalis glycogen branching enzyme.
2 red to avoid steric clashes with Trp(298) of branching enzyme.
3 ssed in the absence of the endogenous glucan-branching enzyme.
4 ialyltransferases, and at least one O-linked branching enzyme.
5 roup H expression together with up-regulated branching enzymes.
6 f a conserved Cys-containing domain in plant branching enzymes.
7 P-GlcNAc, the donor substrate shared by Mgat branching enzymes.
8 he glucan chains further or for branching by branching enzymes.
9 the significance of the conserved Asp/Glu in branching enzymes.
10                                     Glycogen branching enzyme 1 (GBE1) plays an essential role in gly
11                                   The starch branching enzyme 1 (sbe1) gene is the first region downs
12                                          The branching enzyme, 3-hydroxy-3-methylglutaryl synthase (H
13 e asked if this motif could be essential for branching enzyme action.We used site-directed mutagenesi
14 ain magnetic resonance imaging, and glycogen branching enzyme activity and GBE1 molecular analysis.
15                            Residual glycogen branching enzyme activity was 16% and 30% of normal in l
16 synthase (GS), glycogenin (GN), and glycogen branching enzyme and forms particles that range in size
17 phorylation sites are conserved in all plant branching enzymes and are located at opposite openings o
18                        We thereby identified branching enzymes and FUT1 (required for Fucalpha1-->2Ga
19 synthetic enzyme (starch/glycogen synthases, branching enzymes, and debranching enzymes) are differen
20 es the notion that the catalytic centers for branching enzymes are exclusively located in the central
21 that some of the starch synthases and starch-branching enzymes are trapped inside the starch granule
22 nitiated from UDP-GlcNAc by the medial-Golgi branching enzymes as well as the trans-Golgi poly-LacNAc
23 , we investigated the functions of different branching enzyme (BE) types by expressing proteins from
24                                          The branching enzyme belongs to the amylolytic family, a gro
25 em, including starch synthases (SSs), starch branching enzymes (BEs), and starch debranching enzymes;
26 er epithelial cancers that have up-regulated branching enzymes but diminished expression of H antigen
27                                              Branching enzyme catalyzes the formation of alpha-1,6 br
28 ve sequences for glycogen synthase, glycogen branching enzyme, chitin synthase, and for the first enz
29                    Glycogen synthase and the branching enzyme complete the synthesis of the polysacch
30 heir different requirements for the O-glycan branching enzyme core 2 beta1,6-N-acetylglucosaminyltran
31   The neuromuscular presentation of glycogen branching enzyme deficiency includes a severe infantile
32 s (e.g. phosphorylase-b-kinase deficiency or branching enzyme deficiency), whereas they form long lis
33 siological features of two human variants of branching enzyme deficiency.
34 thophysiologic features of human adult-onset branching enzyme deficiency.
35                                              Branching enzymes differ from other amylolytic enzymes i
36 port the 2.3-A crystal structure of glycogen branching enzyme from Escherichia coli.
37 cid sequence identity with those of glycogen-branching enzymes from such animals as mouse, horse, and
38 of cDNAs encoding two closely related starch branching enzymes from the same species.
39 ve disease resulting from deficient glycogen-branching enzyme (GBE) activity.
40 ka1) mRNAs, along with those of the glycogen branching enzyme (GBE) and the phosphorylase b kinase al
41 stems and are often associated with glycogen branching enzyme (GBE) deficiency.
42 isorder caused by deficiency of the glycogen branching enzyme (GBE).
43 isorder caused by deficiency of the glycogen-branching enzyme (GBE).
44 downregulated and the levels of the glycogen branching enzyme (Gbe1) and muscle-type PhKalpha subunit
45 well-known c.986A>C mutation in the glycogen branching enzyme gene (GBE1) but harbored no other known
46 ure analysis, a conserved position unique to branching enzymes has been identified.
47                                              Branching enzyme I and II isoforms from maize endosperm
48 icant levels of starch synthase I and starch branching enzyme II (BEII) remained granule associated.
49 thesis, starch synthase II (SSII) and starch branching enzyme IIa (SBEIIa).
50 e amylose-extender (Ae) gene encoding starch-branching enzyme IIb (SBEIIb) in maize is predominantly
51                                       Starch branching enzyme IIb (SBEIIb) plays a crucial role in am
52 s starch synthase IIa (SSIIa), SSIII, starch branching enzyme IIb (SBEIIb), and SBEIIa for assembly i
53  waxy protein, starch synthase I, and starch-branching enzyme IIb, remained refractory to proteolysis
54 n identified as starch synthase I and starch branching enzyme IIb, respectively.
55 enesis of the Glu-459 residue in the E. coli branching enzyme in order to determine the significance
56 t revealed that SBEIIa is the primary active branching enzyme in the leaf and that in its absence pla
57                       GlgB (alpha-1,4-glucan branching enzyme) is the key enzyme involved in the bios
58 ing glucosaminyl (N-acetyl) transferase 2, I-branching enzyme, is overexpressed in highly metastatic
59  (glycogen synthase) and DeltaglgB (glycogen-branching enzyme) mutants are glycogen-deficient and exh
60                                 The specific branching enzyme present had a significant effect on the
61   Full length cDNAs encoding a second starch branching enzyme (SBE A) isoform have been isolated from
62                                   Two starch branching enzyme (SBE) cDNAs were identified in an Arabi
63 Expression of the maize (Zea mays L.) starch branching enzyme (SBE) genes Sbe1 and Sbe2 were characte
64 dies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu
65                                       Starch-branching enzyme (SBE), a glucosyl transferase, is requi
66 fic activities of starch synthase and starch-branching enzyme (SBE), but not the cytosolic marker alc
67                                       Starch-branching enzymes (SBE) alter starch structure by breaki
68                The genes encoding the starch-branching enzymes (SBE) SBEI, SBEIIa, and SBEIIb in maiz
69                                       Starch branching enzymes (SBE) which catalyse the formation of
70 like Kidney beans have an isoforms of Starch-Branching-Enzyme (SBE) helps in converting amylose to am
71 maize (Zea mays L.) three isoforms of starch-branching enzyme (SBEI, SBEIIa, and SBEIIb) are involved
72                                       Starch-branching enzymes (SBEs) catalyze the formation of alpha
73                                       Starch branching enzymes (SBEs) play important roles in plant s
74 hat of all the other amylase family enzymes, branching enzyme shares the structure of all three domai
75  of the oligosaccharides modeled well in the branching enzyme structure, an approximate 50 degrees ro
76  discovered by cloning cDNAs that the core 2 branching enzyme, termed core 2 beta-1,6-N-acetylglucosa
77 s from CPS10A, thereby identifying WcrG as a branching enzyme that acts on the product of WcrD.
78 ltaneously inhibiting two isoforms of starch branching enzyme to below 1% of the wild-type activities
79 ice lacking both core 1 extension and core 2 branching enzymes to assess the functions of O-glycan-bo
80      Oligosaccharide binding was modeled for branching enzyme using the enzyme-oligosaccharide comple

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