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1 aily headache patients overuse analgesics or ergots.
2 ced sensitization, whereas the high affinity ergot agonists bromocriptine and lisuride did not.
3 ndole nucleus in the first committed step of ergot alkaloid biosynthesis.
4  that controls this critical branch point of ergot alkaloid biosynthesis.
5 n C. purpurea by its clustering with another ergot alkaloid biosynthetic gene, dmaW.
6 identified for the first time as significant ergot alkaloid components within the C. africana sclerot
7 synthetic pathway of cycloclavine, a complex ergot alkaloid containing a cyclopropyl moiety.
8 e strains of N. fumigata and three different ergot alkaloid mutants derived by previous gene knockout
9               Cycloclavine is a clavine-type Ergot alkaloid noteworthy for its unique pentacyclic ske
10 olites including products of a branch of the ergot alkaloid pathway called fumigaclavines.
11  identify the ergot species by molecular and ergot alkaloid profile analysis, to determine the ergot
12  alkaloid profile analysis, to determine the ergot alkaloid profile in pure honeydew and in infected
13  by previous gene knockouts and differing in ergot alkaloid profiles.
14 amine and aldehyde to form the D ring of the ergot alkaloid structural framework.
15 s developed for low-picogram detection of an ergot alkaloid, cabergoline, in coyote plasma extracts.
16  Dihydroergosine was identified as the major ergot alkaloid.
17 d to be safe for feed consumption, since the ergot alkaloids and the regulated mycotoxins were below
18          The biosynthesis of the N. fumigata ergot alkaloids and their relation to those produced by
19 ped molecularly imprinted polymer toward six ergot alkaloids and their respective epimers is describe
20                                          The ergot alkaloids are a diverse class of fungal-derived in
21 d the matrix effect of each of the 12 tested ergot alkaloids as well as a cross-reactivity study with
22                       The data indicate that ergot alkaloids contribute to virulence of N. fumigata i
23                                              Ergot alkaloids festuclavine 2 and agroclavine 3 derive
24                     Concise syntheses of the Ergot alkaloids rugulovasine A (3a), rugulovasine B (3b)
25                           Elimination of all ergot alkaloids significantly reduced virulence of N. fu
26 olites have been described as toxins such as ergot alkaloids that have potent psychotropic activity.
27          We investigated the contribution of ergot alkaloids to virulence of N. fumigata by measuring
28 nes) to 10(4.0) L/kg(oc) (positively charged ergot alkaloids).
29                                          The ergot alkaloids, a class of fungal-derived natural produ
30 alkaloids are associated with the symbionts: ergot alkaloids, indolediterpenes (lolitrems), peramine,
31                                              Ergot alkaloids, secondary metabolites produced by filam
32 ne-I aldehyde 1 represents a branch point in ergot biosynthesis.
33 he Old Yellow Enzyme homologue EasA from the ergot biosynthetic gene cluster of Aspergillus fumigatus
34 ed with dihydroergotamine mesylate (DHE), an ergot derivative that is especially effective in non-res
35 ing lysergic acid dimethylamide (DAM-57), an ergot derivative, and its deuterated isotopologues; we a
36  vasoconstrictor properties (ie, triptans or ergot derivatives).
37                   Ropinirole, which is a non-ergot dopamine agonist derivative, exerts therapeutic be
38 elegiline (Spearman's rho 0.22, p=0.005) and ergot dopamine agonists (0.24, p=0.006) but not correlat
39  to 5-hydroxytryptamine (5-HT)(2)-preferring ergot drugs (ergotamine, methysergide).
40 vular 5-HT(2B) receptors by norfenfluramine, ergot drugs, or 5-HT released from carcinoid tumors (wit
41 human pathogen Sporothrix schenckii, and the ergot fungus Claviceps purpurea.
42  Enzyme encoded in the Aspergillus fumigatus ergot gene cluster catalyzes reduction of the alpha,beta
43                                      Sorghum ergot is a disease caused commonly by C. africana.
44 e treatment is either specific (triptans and ergots) or non-specific (analgesics).
45   The aims of the study were to identify the ergot species by molecular and ergot alkaloid profile an
46 art disease and valvulopathy associated with ergot use.
47                                     In 2015, ergot was identified for the first time in sorghum field
48 te migraine-specific medication [triptans or ergots] was used to treat a headache of any severity or

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