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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 ndividuals, together with decreased glycogen branching enzyme 1 (GBE1) activity, indicated an additio
11  and (3) controls the levels of the glycogen branching enzyme 1 (GBE1) consistent with a glycogen-sto
12                                     Glycogen branching enzyme 1 (GBE1) plays an essential role in gly
13                                   The starch branching enzyme 1 (sbe1) gene is the first region downs
14 e variant in GBE1, encoding 1,4-alpha-glucan branching enzyme 1, to be associated with lower white ma
15 ated with the recessive allele of the starch branching enzyme 2b (sbeIIb).
16                                          The branching enzyme, 3-hydroxy-3-methylglutaryl synthase (H
17 e asked if this motif could be essential for branching enzyme action.We used site-directed mutagenesi
18 ain magnetic resonance imaging, and glycogen branching enzyme activity and GBE1 molecular analysis.
19                            Residual glycogen branching enzyme activity was 16% and 30% of normal in l
20 synthase (GS), glycogenin (GN), and glycogen branching enzyme and forms particles that range in size
21 phorylation sites are conserved in all plant branching enzymes and are located at opposite openings o
22                        We thereby identified branching enzymes and FUT1 (required for Fucalpha1-->2Ga
23 synthetic enzyme (starch/glycogen synthases, branching enzymes, and debranching enzymes) are differen
24 es the notion that the catalytic centers for branching enzymes are exclusively located in the central
25 that some of the starch synthases and starch-branching enzymes are trapped inside the starch granule
26 nitiated from UDP-GlcNAc by the medial-Golgi branching enzymes as well as the trans-Golgi poly-LacNAc
27 , we investigated the functions of different branching enzyme (BE) types by expressing proteins from
28                                          The branching enzyme belongs to the amylolytic family, a gro
29                                              Branching enzymes (BEs) confer to alpha-glucans, the pri
30 em, including starch synthases (SSs), starch branching enzymes (BEs), and starch debranching enzymes;
31 y-N-acetyllactosamines through the loss of I-branching enzyme, beta1,6 N-acetylglucosaminyltransferas
32 er epithelial cancers that have up-regulated branching enzymes but diminished expression of H antigen
33                                              Branching enzyme catalyzes the formation of alpha-1,6 br
34 ve sequences for glycogen synthase, glycogen branching enzyme, chitin synthase, and for the first enz
35                    Glycogen synthase and the branching enzyme complete the synthesis of the polysacch
36 heir different requirements for the O-glycan branching enzyme core 2 beta1,6-N-acetylglucosaminyltran
37 osomal recessive condition known as Glycogen Branching Enzyme Deficiency (GBED) is the result of one
38   The neuromuscular presentation of glycogen branching enzyme deficiency includes a severe infantile
39 s (e.g. phosphorylase-b-kinase deficiency or branching enzyme deficiency), whereas they form long lis
40 thophysiologic features of human adult-onset branching enzyme deficiency.
41 siological features of two human variants of branching enzyme deficiency.
42                                              Branching enzymes differ from other amylolytic enzymes i
43 of trypanosome TbGT10 and higher-eukaryote I-branching enzyme (EC 2.4.1.150), which belong to glycosy
44 port the 2.3-A crystal structure of glycogen branching enzyme from Escherichia coli.
45 cid sequence identity with those of glycogen-branching enzymes from such animals as mouse, horse, and
46 of cDNAs encoding two closely related starch branching enzymes from the same species.
47 ve disease resulting from deficient glycogen-branching enzyme (GBE) activity.
48 ka1) mRNAs, along with those of the glycogen branching enzyme (GBE) and the phosphorylase b kinase al
49 stems and are often associated with glycogen branching enzyme (GBE) deficiency.
50 isorder caused by deficiency of the glycogen branching enzyme (GBE).
51 isorder caused by deficiency of the glycogen-branching enzyme (GBE).
52 downregulated and the levels of the glycogen branching enzyme (Gbe1) and muscle-type PhKalpha subunit
53 osomal recessive disorder caused by glycogen branching enzyme (GBE1) deficiency, resulting in the acc
54 by loss-of-function variants in the glycogen branching enzyme (GBE1) gene, essential for glycogen bio
55                                     Glycogen branching enzymes (GBEs) have been used to generate new
56 nched glycans catalyzed principally by the I-branching enzyme GCNT2 are now indicated in several mali
57 well-known c.986A>C mutation in the glycogen branching enzyme gene (GBE1) but harbored no other known
58 ure analysis, a conserved position unique to branching enzymes has been identified.
59                                              Branching enzyme I and II isoforms from maize endosperm
60 icant levels of starch synthase I and starch branching enzyme II (BEII) remained granule associated.
61 thesis, starch synthase II (SSII) and starch branching enzyme IIa (SBEIIa).
62 e amylose-extender (Ae) gene encoding starch-branching enzyme IIb (SBEIIb) in maize is predominantly
63                                       Starch branching enzyme IIb (SBEIIb) plays a crucial role in am
64 s starch synthase IIa (SSIIa), SSIII, starch branching enzyme IIb (SBEIIb), and SBEIIa for assembly i
65  waxy protein, starch synthase I, and starch-branching enzyme IIb, remained refractory to proteolysis
66 n identified as starch synthase I and starch branching enzyme IIb, respectively.
67 f mutating the OsSBEIIb gene encoding starch branching enzyme IIb, which is required for amylopectin
68 enesis of the Glu-459 residue in the E. coli branching enzyme in order to determine the significance
69 t revealed that SBEIIa is the primary active branching enzyme in the leaf and that in its absence pla
70                       GlgB (alpha-1,4-glucan branching enzyme) is the key enzyme involved in the bios
71 ing glucosaminyl (N-acetyl) transferase 2, I-branching enzyme, is overexpressed in highly metastatic
72 of heterologous glucan synthase and a glucan branching enzyme, may in future enable elevated yields o
73 e transporters SLC7A9, SLC7A11, and N-glycan branching enzymes MGAT4B, MGAT4C in Neoaves suggests a s
74  (glycogen synthase) and DeltaglgB (glycogen-branching enzyme) mutants are glycogen-deficient and exh
75                                 The specific branching enzyme present had a significant effect on the
76   Full length cDNAs encoding a second starch branching enzyme (SBE A) isoform have been isolated from
77                                   Two starch branching enzyme (SBE) cDNAs were identified in an Arabi
78 Expression of the maize (Zea mays L.) starch branching enzyme (SBE) genes Sbe1 and Sbe2 were characte
79 dies indicated that the deficiency of starch-branching enzyme (SBE) Ia in the single mutant sbe1a::Mu
80                                       Starch-branching enzyme (SBE), a glucosyl transferase, is requi
81 fic activities of starch synthase and starch-branching enzyme (SBE), but not the cytosolic marker alc
82                                       Starch-branching enzymes (SBE) alter starch structure by breaki
83                The genes encoding the starch-branching enzymes (SBE) SBEI, SBEIIa, and SBEIIb in maiz
84                                       Starch branching enzymes (SBE) which catalyse the formation of
85 like Kidney beans have an isoforms of Starch-Branching-Enzyme (SBE) helps in converting amylose to am
86 arch synthases, SSI, SSII, SSIII; and starch branching enzyme, SBE, between others), except starch sy
87 maize (Zea mays L.) three isoforms of starch-branching enzyme (SBEI, SBEIIa, and SBEIIb) are involved
88                                       Starch-branching enzymes (SBEs) catalyze the formation of alpha
89                                       Starch branching enzymes (SBEs) play important roles in plant s
90 hat of all the other amylase family enzymes, branching enzyme shares the structure of all three domai
91  of the oligosaccharides modeled well in the branching enzyme structure, an approximate 50 degrees ro
92  discovered by cloning cDNAs that the core 2 branching enzyme, termed core 2 beta-1,6-N-acetylglucosa
93 s from CPS10A, thereby identifying WcrG as a branching enzyme that acts on the product of WcrD.
94 PM2B, which respectively encode the glycogen branching enzyme, the glycogen phosphatase laforin and t
95 ltaneously inhibiting two isoforms of starch branching enzyme to below 1% of the wild-type activities
96 ice lacking both core 1 extension and core 2 branching enzymes to assess the functions of O-glycan-bo
97      Oligosaccharide binding was modeled for branching enzyme using the enzyme-oligosaccharide comple
98 e, soluble starch synthase, and other starch branching enzymes were up-regulated, either in their nat