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2 crude mixtures of laccase enzymes from fungi Agaricus bisporus (Ab) and Myceliopthora thermophila (Mt
3 nding lectin from the common edible mushroom Agaricus bisporus (ABL) reversibly inhibits cell prolife
5 cts were assessed from two edible mushrooms, Agaricus bisporus (brown) and Pleurotus ostreatus (oyste
7 terologous promoters from the basidiomycetes Agaricus bisporus and Phanerochaete chrysosporium that w
8 eports arsenic analysis in Lentinula edodes, Agaricus bisporus and Pleurotus ostreatus before and aft
9 upling was also performed with laccases from Agaricus bisporus and Trametes versicolor, resulting in
10 current data on the bioactive properties of Agaricus bisporus as well as the recent research for the
11 e similarity with fungal mannanases, such as Agaricus bisporus Cel4 (17.3% identity), Aspergillus acu
17 of dietary supplementation with Se-enriched Agaricus bisporus on cytosolic gluthathione peroxidase-1
18 nutritional composition of fresh samples of Agaricus bisporus Portobello (a highly commercialized sp
22 Early publications utilizing tyrosinase from Agaricus bisporus(abTYR) showed the potential to convert
23 gen of the commercial white button mushroom (Agaricus bisporus) and is the causal agent of dry bubble
24 M retarded cap browning of button mushrooms (Agaricus bisporus) by 78.35, 31.40, 30.91, 27.17, and 32
25 ed and quantified in white button mushrooms (Agaricus bisporus) following treatment with pulsed UV (P
27 Here we show that a saprotrophic fungus (Agaricus bisporus) redistributes water from moist (-0.03
28 SNP) on shelf-life of white button mushroom (Agaricus bisporus) stored at 4+/-1 degrees C for 7-days.
29 nt study, White Button and Honey Brown (both Agaricus bisporus), Shiitake (Lentinus edodes), Enoki (F
32 ery of functional proteins and peptides from Agaricus bisporus, A. brunnescens, Lentinula edodes, Ple
33 nd phenolic compounds from edible mushrooms (Agaricus bisporus, Cantharellus cibarius, and Lentinula
35 NAs were sequenced in the cultivated fungus, Agaricus bisporus, comprising 18 viruses each encoding a
36 the taste compounds of five mushroom species Agaricus bisporus, Lactarius trivialis, Cantharellus cib
38 ailable mainly in cultivated species such as Agaricus bisporus, Lentinus edodes and Pleurotus ostreat
39 employing tyrosinase and laccase, both from Agaricus bisporus, on green tea catechins, the oxidation
40 e stability of vitamin D2 in dried mushrooms Agaricus bisporus, Pleurotus ostreatus and Lentinula edo
41 rooms, especially of the most common species Agaricus bisporus, represents an increasingly important
43 sified, double-stranded RNA (dsRNA) virus of Agaricus bisporus, were associated with an RNA-dependent
47 racterize mixtures of goat milk proteins and Agaricus blazei Murrill (ABM) extracts (aqueous, AE and
49 Mushroom mycelia of Antrodia camphorata, Agaricus blazei, Hericium erinaceus and Phellinus linteu
51 mmobilization of pyranose dehydrogenase from Agaricus meleagris (AmPDH) with the dehydrogenase domain
52 sylated pyranose dehydrogenase (fdgPDH) from Agaricus meleagris recombinantly expressed in Pichia pas
53 infections may be ancient, preserved in wild Agaricus populations, which act as reservoirs for subseq
54 bers of viral RNAs were detected in multiple Agaricus samples; up to 24 in samples symptomatic for di
57 cal differences between fruitbodies of three Agaricus subrufescens mushroom strains [from Japan (JP),
58 at SPR1 is a key enzyme in the adaptation of Agaricus to the humic-rich ecological niche formed durin