戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 acquisition of cyanobacterial symbionts by a marine sponge.
2 sylceramide (alpha-GalCer), derived from the marine sponge.
3 enome report of a cultivated symbiont from a marine sponge.
4 tor (KAR) ligands originally isolated from a marine sponge.
5 ivated bacteria that exist as symbionts in a marine sponge.
6  potent anticancer agent originally found in marine sponges.
7 e they are part of the microbiome of healthy marine sponges.
8 47 may act as a chemical offense molecule in marine sponges.
9  pathway through symbiotic microorganisms of marine sponges.
10 stence of new structural classes of PBDEs in marine sponges.
11 nthetic bacteria associated with beetles and marine sponges.
12 towards discovering similar systems in other marine sponges.
13     A first and short total synthesis of the marine sponge 2,3'-bis(indolyl)ethylamine (2,3'-BIEA) al
14 aryl-pyrazin-2-one core was derived from the marine sponge alkaloid family of hamacanthins.
15                                          The marine sponge alkaloid leucettamine B was recently ident
16 of 2-aminoimidazolin-4-ones derived from the marine sponge alkaloid Leucettamine B, have been develop
17 g found in fungi, vascular and lower plants, marine sponges and algae, and insects.
18 ated from terrestrial cyanobacteria and from marine sponges and gastropods.
19            The isonitrile moiety is found in marine sponges and some microbes, where it plays a role
20 tural products isolated from fungal species, marine sponges, and cactaceous species.
21 osome-scale genomes for a ctenophore and two marine sponges, and for three unicellular relatives of a
22                                              Marine sponges are hosts to large, diverse communities o
23                                              Marine sponges are major habitat-forming organisms in co
24                                              Marine sponges are prolific sources of bioactive natural
25                                              Marine sponges are the source of numerous bioactive natu
26 ether Shark Bay bottlenose dolphins that use marine sponges as hunting tools (spongers) are culturall
27          In this study, a biosurfactant from marine sponge associated bacteria MS48 was used to effec
28 ew class of knotted cyclic peptides from the marine sponge Axinella sp.
29 symbiosum found living in association with a marine sponge, Axinella mexicana.
30             These include glycolipids from a marine sponge, bacterial glycolipids, normal endogenous
31 n which lives in specific association with a marine sponge, belongs to a recently recognized nontherm
32 abilizing agent originally isolated from the marine sponge Cacospongia mycofijiensis.
33 66 was identified in a saline extract of the marine sponge, Callyspongia sp.
34 is study we established the first continuous marine sponge cell line, originating from G. barretti.
35      Although many have attempted to culture marine sponge cells in vitro to create a scalable produc
36 sing the axial cores of silica spicules in a marine sponge chemically and spatially direct the polyme
37    While no sulfated GAGs have been found in marine sponges, chondroitin sulfate (CS) and heparan sul
38 and enigmimide A (5), were isolated from the marine sponge Cinachyrella enigmatica.
39 ed from a Papua New Guinea collection of the marine sponge Cinachyrella enigmatica.
40 ccharide fragment of the naturally occurring marine sponge clarhamnoside.
41 B (2) have been isolated from the Philippine marine sponge Clathria (Thalysias) abietina.
42                                          The marine sponge constituent aaptamine (1) has been convert
43  of such 1H-benzo[de][1,6]-naphthyridine (1) marine sponge constituents at position C-9 has been deve
44 anisms that are sessile or slow moving, some marine sponges contain aversive compounds that defend th
45  are a small subset of the oroidin family of marine sponge-derived alkaloids and are, for the most pa
46 ion of NKT cells is greatly augmented by the marine sponge-derived glycolipid alpha-galactosylceramid
47  cells recognize glycolipid Ags, such as the marine sponge-derived glycosphingolipid alpha-galactosyl
48                 Although presentation of the marine sponge-derived lipid alphaGalCer to type I NKT ce
49  we describe the structure and function of a marine sponge-derived MPL agonist, thrombocorticin (ThC)
50  iNKT cells with glycolipid Ags, such as the marine sponge-derived reagent alpha-galactosylceramide (
51 HLO) assay has been employed to discover new marine-sponge-derived bioactive compounds.
52  (+)-18-epi-latrunculol A, a congener of the marine-sponge-derived latrunculins A and B, is reported.
53                    Because alpha-GalCer is a marine-sponge-derived ligand, our study here shows that
54 ed architecture found in the spicules of the marine sponge Euplectella aspergillum.
55 a pyrrole-imidazole alkaloid obtained from a marine sponge, exhibits potent in vitro activity against
56 sly identified from the silica skeleton of a marine sponge, for enzyme variants capable of synthesizi
57 en) derivatives are bioactive alkaloids from marine sponges found to induce Ca(2+) release from stria
58                                          The marine sponge glycolipid alpha-galactosylceramide (alpha
59 mpound, adociasulfate-2, was isolated from a marine sponge, Haliclona (also known as Adocia) species,
60  hamigeran diterpenoids from the New Zealand marine sponge Hamigera tarangaensis are described.
61 the glassy skeletal elements (spicules) of a marine sponge, has led to the development of new low-tem
62 e (alpha-GalCer), originally isolated from a marine sponge, has potent immunomodulatory activities in
63          We previously demonstrated that the marine sponge Hymeniacidon heliophila displayed signific
64                                          The marine sponge Ianthella basta synthesizes at least 25 te
65 adin-5, a brominated macro-dilactam from the marine sponge Ianthella basta, enhances release of Ca2+
66 de analogues from two taxonomically distinct marine sponges including two Auletta spp. and one Jaspis
67                       Bacteria isolated from marine sponges, including the Silicibacter-Ruegeria (SR)
68  as cyclosporin A blocks tissue rejection in marine sponges indicates that the cellular mechanisms fo
69     Hemiasterlin, a tripeptide isolated from marine sponges, induces microtubule depolymerization and
70 nalog of a natural steroidal alkaloid from a marine sponge, inhibits Tat-mediated transactivation of
71                             The Indo-Pacific marine sponge Ircinia ramosa has been found to contain t
72 a have been reported for the closely related marine sponges Ircinia fasciculata and Ircinia variabili
73 tionation of the crude methanol extract of a marine sponge, Ircinia sp., yielded tedanolide C (1), a
74 dermolide (DDM), a polyketide macrolide from marine sponge, is a potent microtubule assembly promoter
75          Laulimalide, a natural product from marine sponges, is a microtubule-stabilizing agent that
76 s an antimitotic macrolide isolated from the marine sponge Leiodermatium sp. whose potentially novel
77 stigation of a new species of the deep-water marine sponge Leiodermatium, collected by manned submers
78 irst total synthesis of the antiinflammatory marine sponge metabolite (+)-cacospongionolide B has bee
79 tal synthesis of the architecturally complex marine sponge metabolite (-)-enigmazole A has been achie
80 zepines that are structurally related to the marine sponge metabolite hymenialdisine.
81                            We identified the marine sponge metabolite latonduine as a corrector.
82 e previously shown that ilimaquinone (IQ), a marine sponge metabolite, causes complete vesiculation o
83  The total syntheses of the antiinflammatory marine sponge metabolites (+)-cacospongionolide B and E
84 thesis and stereochemical elucidation of the marine sponge metabolites (4R,6R)-plakilactone C, (4R,6R
85  short synthesis of the hydantoin-containing marine sponge metabolites axinohydantoins is described.
86          A new asymmetric synthesis of these marine sponge metabolites is described herein, featuring
87  membrane-anchored epitopes derived from the marine sponge Microciona prolifera has been explored by
88 study tissue acceptance and rejection in the marine sponge Microciona prolifera.
89 Ruegeria sp. strain KLH11, isolated from the marine sponge Mycale laxissima, produces a complex profi
90 ed 2-aminoimidazolin-4-ones (inspired by the marine sponge natural product Leucettamine B) developed
91 ide, a cytotoxic macrolide isolated from the marine sponge Neopeltidae.
92                              Extracts of the marine sponge Niphates digitalis collected in Dominica s
93 ing potent antifungal activity reported from marine sponges of the genera Microscleroderma and Theone
94                                              Marine sponges often house small-molecule-producing symb
95 codermolide, a promising anticancer agent of marine sponge origin, has been completed in 11.1% overal
96 , a 14-membered macrolides isolated from the marine sponge Phakellia fusca Thiele, which was collecte
97 oles B-F, were isolated from extracts of the marine sponge Phorbas amaranthus along with the known am
98 15), have been isolated from extracts of the marine sponge Phorbas sp. collected in Howe Sound Britis
99 olated in only 90 microg yield from the same marine sponge, Phorbas sp. that also provided phorboxazo
100        The family of silicatein enzymes from marine sponges (phylum Porifera) is unique in nature for
101  13 oxygenated polyketides isolated from the marine sponge Plakinastrella mamillaris allowed the disc
102 active fractions derived from the Australian marine sponge Plakortis lita .
103 ing pairs sampled from eight species of wild marine sponges (Porifera).
104                            Here, we document marine sponge presenting associated with visual and acou
105 d of using light or heat as a driving force, marine sponges promote cycloaddition with a more versati
106                               A screening of marine sponges revealed that crude extracts of Psammocin
107 f the natural product rhizochalin C from the marine sponge Rhizochalina incrustata.
108 ound as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and fruit fly, wher
109                  Here, we report suvanine, a marine sponge sesterterpene, as an antagonist of the mam
110 opapuamides B-D, have been isolated from the marine sponge Siliquariaspongia mirabilis.
111 rins, mollenynes B-E, were isolated from the marine sponge Spirastrella mollis collected from Hogsty
112 e/2-propanol (1:1) extract of the Indonesian marine sponge Strepsichordaia aliena, twelve new 20, 24-
113 ro5-Tyr6-cis-Pro7]) isolated from the Fijian marine sponge Stylotella aurantium are reported.
114 re isolated from the n-hexane extract of the marine sponge Svenzea flava collected at Great Inagua Is
115 yrroles (BrPyr) are synthesized naturally by marine sponge symbionts and produced anthropogenically a
116 wo cyclic diarylheptanoids isolated from the marine sponge Tedania ignis.
117 e of an undecapeptide natural product from a marine sponge, termed halichondamide A, that is morphed
118 ilicatein, an enzymatic biocatalyst from the marine sponge Tethya aurantia, is demonstrated to cataly
119 y connection in the skeletal elements of the marine sponge Tethya aurantia.
120 lectella aspergillum, is a sediment-dwelling marine sponge that is anchored into the sea floor by a f
121 ic natural product biosynthetic potential in marine sponges that was not detected by traditional natu
122 miasterlin is a natural product derived from marine sponges that, like other structurally diverse pep
123 totheonella gemina" live associated with the marine sponge Theonella swinhoei Y, the source of numero
124 -inhabit the chemically and microbially rich marine sponge Theonella swinhoei.
125 w polyhydroxylated steroid isolated from the marine sponge Theonella swinhoei.
126 rization of conicasterol E isolated from the marine sponge Theonella swinhoei.
127  from 11 cultivated archaeal species and one marine sponge tissue sample that contained essentially a
128                                Although this marine sponge toxin is known to inhibit protein phosphat
129                      We report here that the marine sponge toxin, latrunculin B, which blocks photopo
130                   Only adult males presented marine sponges, typically doing so in the presence of se
131 es that can suppress immune cell function in marine sponges using secreted ankyrin proteins.
132          The crude extract of Hemimycale sp. marine sponge was evaluated as a cytotoxic drug against
133 Pateamine A, a natural product isolated from marine sponge, was recently reported to inhibit eukaryot
134 metagenomics data from seven field-collected marine sponges were analyzed.
135 d in the extracellular aggregation factor of marine sponges, which mediates species-specific cell agg
136 OH-XeA, and araguspongin C isolated from the marine sponge Xestospongia species also inhibit IP(3)-me
137  (JA), a bioactive compound derived from the marine sponge Xestospongia, in PDAC.
138 ) and B (7) were also isolated from the same marine sponge (Zyzzya sp.).

 
Page Top