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1 nes) to 10(4.0) L/kg(oc) (positively charged ergot alkaloids).
2  Dihydroergosine was identified as the major ergot alkaloid.
3 , dragmacidins, isoryanodane diterpenes, and ergot alkaloids.
4                                          The ergot alkaloids, a class of fungal-derived natural produ
5 d to be safe for feed consumption, since the ergot alkaloids and the regulated mycotoxins were below
6          The biosynthesis of the N. fumigata ergot alkaloids and their relation to those produced by
7 ped molecularly imprinted polymer toward six ergot alkaloids and their respective epimers is describe
8                                          The ergot alkaloids are a class of natural products known fo
9                                          The ergot alkaloids are a diverse class of fungal-derived in
10 d the matrix effect of each of the 12 tested ergot alkaloids as well as a cross-reactivity study with
11 ndole nucleus in the first committed step of ergot alkaloid biosynthesis.
12  that controls this critical branch point of ergot alkaloid biosynthesis.
13 n C. purpurea by its clustering with another ergot alkaloid biosynthetic gene, dmaW.
14 s developed for low-picogram detection of an ergot alkaloid, cabergoline, in coyote plasma extracts.
15 e scaffold, as are present in members of the ergot alkaloid class of natural products.
16 identified for the first time as significant ergot alkaloid components within the C. africana sclerot
17 synthetic pathway of cycloclavine, a complex ergot alkaloid containing a cyclopropyl moiety.
18                       The data indicate that ergot alkaloids contribute to virulence of N. fumigata i
19                                              Ergot alkaloids (EA) are mycotoxins produced by Clavicep
20                                              Ergot alkaloids (EAs) are a group of mycotoxins that con
21                                              Ergot alkaloids festuclavine 2 and agroclavine 3 derive
22                    The mean recovery rate of ergot alkaloids in spiked whole rye grain was close to 1
23 rized all-in-one 2LabsToGo system to analyze ergot alkaloids in whole rye samples.
24 ales) that produce the bioactive metabolites ergot alkaloids, indole diterpene alkaloids, and swainso
25            Here, we report the occurrence of ergot alkaloids, indole diterpene alkaloids, and swainso
26 alkaloids are associated with the symbionts: ergot alkaloids, indolediterpenes (lolitrems), peramine,
27 nations of oxytocin, carbetocin, carboprost, ergot alkaloids, misoprostol, and tranexamic acid were i
28 e strains of N. fumigata and three different ergot alkaloid mutants derived by previous gene knockout
29 plemented by the synthesis of the polycyclic ergot alkaloid natural product xylanigripone A.
30                                              Ergot alkaloids, naturally occurring mycotoxins of Clavi
31               Cycloclavine is a clavine-type Ergot alkaloid noteworthy for its unique pentacyclic ske
32 olites including products of a branch of the ergot alkaloid pathway called fumigaclavines.
33                           Reconstituting the ergot alkaloid pathway in a strain strongly amenable for
34           Reaction of the isocyanide with an ergot alkaloid precursor results in carbon-carbon bond f
35 e fescue toxicosis (FT) is caused by grazing ergot alkaloid-producing endophyte (Epichloe coenophiala
36  identify the ergot species by molecular and ergot alkaloid profile analysis, to determine the ergot
37  alkaloid profile analysis, to determine the ergot alkaloid profile in pure honeydew and in infected
38  by previous gene knockouts and differing in ergot alkaloid profiles.
39 al pharmacological agents, such as oxytocin, ergot alkaloids, prostaglandins, and tranexamic acid, ha
40                     Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b)
41                                              Ergot alkaloids, secondary metabolites produced by filam
42                           Elimination of all ergot alkaloids significantly reduced virulence of N. fu
43 amine and aldehyde to form the D ring of the ergot alkaloid structural framework.
44 olites have been described as toxins such as ergot alkaloids that have potent psychotropic activity.
45          We investigated the contribution of ergot alkaloids to virulence of N. fumigata by measuring
46                             Detectability of ergot alkaloids was proven to be below the current maxim
47           Results of screening whole rye for ergot alkaloids were successfully verified by comparison