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2 nding lectin from the common edible mushroom Agaricus bisporus (ABL) reversibly inhibits cell prolife
4 terologous promoters from the basidiomycetes Agaricus bisporus and Phanerochaete chrysosporium that w
5 eports arsenic analysis in Lentinula edodes, Agaricus bisporus and Pleurotus ostreatus before and aft
6 e similarity with fungal mannanases, such as Agaricus bisporus Cel4 (17.3% identity), Aspergillus acu
12 of dietary supplementation with Se-enriched Agaricus bisporus on cytosolic gluthathione peroxidase-1
15 ed and quantified in white button mushrooms (Agaricus bisporus) following treatment with pulsed UV (P
16 Here we show that a saprotrophic fungus (Agaricus bisporus) redistributes water from moist (-0.03
17 nt study, White Button and Honey Brown (both Agaricus bisporus), Shiitake (Lentinus edodes), Enoki (F
20 NAs were sequenced in the cultivated fungus, Agaricus bisporus, comprising 18 viruses each encoding a
22 ailable mainly in cultivated species such as Agaricus bisporus, Lentinus edodes and Pleurotus ostreat
23 employing tyrosinase and laccase, both from Agaricus bisporus, on green tea catechins, the oxidation
24 e stability of vitamin D2 in dried mushrooms Agaricus bisporus, Pleurotus ostreatus and Lentinula edo
25 sified, double-stranded RNA (dsRNA) virus of Agaricus bisporus, were associated with an RNA-dependent
29 Mushroom mycelia of Antrodia camphorata, Agaricus blazei, Hericium erinaceus and Phellinus linteu
31 mmobilization of pyranose dehydrogenase from Agaricus meleagris (AmPDH) with the dehydrogenase domain
32 sylated pyranose dehydrogenase (fdgPDH) from Agaricus meleagris recombinantly expressed in Pichia pas
33 infections may be ancient, preserved in wild Agaricus populations, which act as reservoirs for subseq
34 bers of viral RNAs were detected in multiple Agaricus samples; up to 24 in samples symptomatic for di
36 at SPR1 is a key enzyme in the adaptation of Agaricus to the humic-rich ecological niche formed durin
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