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1 r proteins (e.g., helicases, chelatases, and copines).
2 ng properties similar to those of Paramecium copine.
3 7, a secretory vesicle-binding protein, as a copine.
4 in-protein interaction for the VWA domain of copines.
5 of unknown function were identified, such as Copine 1 and PICOT, whose developmental regulation was p
6            Mutation of the Arabidopsis CPN1 (COPINE 1) gene causes a humidity-sensitive lesion mimic
7 volved in signalling, such as importin 7 and copine 1, cytoplasmic intermediate filament (IF) protein
8                                 However, the copine amino acid sequences lack the traditional kinase
9                        The highest levels of copine are found in the spleen.
10                                          The copines are a newly identified class of calcium-dependen
11                                          The copines are a novel group of Ca(2+)-dependent, phospholi
12                                          The copines are a widely distributed class of calcium-depend
13                                              Copines are calcium-dependent membrane-binding proteins
14                                              Copines are calcium-responsive, phospholipid-binding pro
15 athway for calcium signaling because we find copines are capable of interacting with a wide variety o
16                                              Copines are highly conserved proteins with lipid-binding
17                 The biological roles of most copines are not understood and the biochemical propertie
18     However, the biological functions of the copines are unknown.
19     A consensus sequence for the coiled-coil copine-binding site was derived and found to have predic
20                 In the majority of cases the copine binds to a domain of the target protein that is p
21        The full-length sequences reveal that copines consist of two C2 domains at the N terminus foll
22 rties and distribution of a native mammalian copine, copine I.
23 dicted transmembrane domain and a C-terminal copine domain and binds to the M-line/dense body protein
24                                          The copine domain of RGLG2 exhibited the strongest interacti
25                       Antibodies specific to copine domain protein atypical-1 (CPNA-1), as well as a
26                                    Thus, the copine family in Arabidopsis may have effects in promoti
27                gem-4 encodes a member of the copine family of Ca(2+)-dependent phosphatidylserine bin
28                                          The copines, first described by Creutz et al., comprise a tw
29                              The Arabidopsis copine gene BON1/CPN1 is a negative regulator of cell de
30                              The Arabidopsis copine gene BON1/CPN1 was previously shown to negatively
31                            It belongs to the copine gene family, which is conserved from protozoa to
32 mutant combinations we show that these three copine genes have overlapping functions essential for th
33  as in other organisms, there is a family of copine genes, BON1, 2 and 3.
34 mecium was found to have two closely related copine genes, CPN1 and CPN2.
35            The major protein obtained, named copine, had a mass of 55 kDa, bound phosphatidylserine b
36 data bases indicate the presence of multiple copine homologs in green plants, nematodes, and humans.
37 ally competed by Ca(2+), suggesting that the copine I A domain may be a functional MIDAS metal bindin
38                                              Copine I exhibits Mn(2+) binding activity that is strong
39 antiserum raised against a fragment of human copine I was used to identify chromobindin 17, a secreto
40                             A human homolog, copine I, was expressed in bacteria as a fusion protein
41 d distribution of a native mammalian copine, copine I.
42                                              Copine-I abolishes NF-kappaB transcription by inducing e
43                                 Knockdown of copine-I by siRNA increases tumor necrosis factor alpha-
44 ha-stimulated NF-kappaB transcription, while copine-I expression blocks endogenous transcription.
45              Our work provides evidence that copine-I regulates the half-life of NF-kappaB transcript
46                                              Copine-I stimulates endoproteolysis of p65 within a cons
47                    In this study we identify copine-I, a calcium phospholipid-binding protein, as a n
48  had correspondingly high kinase activity in copine III antiserum immunoprecipitate.
49 ified endogenous copine III, and recombinant copine III expressed in Saccharomyces cerevisiae.
50 ted in all in vitro kinase assays containing copine III immunoprecipitate or purified copine III.
51                  Therefore, the data suggest copine III may possess an intrinsic kinase activity and
52 no acid analysis revealed phosphorylation of copine III on serine and threonine residues.
53         Cell lines expressing high levels of copine III protein had correspondingly high kinase activ
54                                     The 5 kb copine III transcript is expressed ubiquitously as deter
55 pine III, chromatography-purified endogenous copine III, and recombinant copine III expressed in Sacc
56 performed with immunoprecipitated endogenous copine III, chromatography-purified endogenous copine II
57 ing copine III immunoprecipitate or purified copine III.
58 fy, partially microsequence, and clone human copine III.
59                                    Roles for copine in binding membranes and target proteins or small
60                              Purified native copine is a 58 kDa monomer that exhibits Ca(2+) self-ass
61 f a 920-base pair partial cDNA revealed that copine is a novel protein that contains a C2 domain like
62           We also show that interaction with copines may result in recruitment of target proteins to
63                     We provide evidence that copines, members of a ubiquitous family of calcium-depen
64       Here, we describe a humidity-sensitive copine mutant in Arabidopsis.
65 lysis reveals an unanticipated regulation of copine protein localization and function by calcium and
66                                          The copine target proteins were identified by yeast two-hybr
67 to have predictive value for identifying new copine targets.
68                     A protocol for purifying copine to homogeneity from bovine spleen is described.
69 ory vesicles, as well the general ability of copines to bind phospholipid bilayers in a calcium-depen
70 f a CRH-1/CREB transcriptional target (gem-4 Copine), which parallels the effects of human Shank copy
71 No enzymatic function has been attributed to copines yet.

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