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1 cteria, we analyzed six members of the genus Cyanothece.
3 ed with other nitrogen-fixing cyanobacteria, Cyanothece 51142 contains the largest intact contiguous
4 expression patterns of nearly 5,000 genes in Cyanothece 51142 during two consecutive diurnal periods.
5 cells, we determined that the thylakoids in Cyanothece 51142 form a dense and complex network that e
9 portant information regarding the ability of Cyanothece 51142 to accomplish metabolic compartmentaliz
11 ly identified lectin from the cyanobacterium Cyanothece(7424), and elucidated its glycan specificity
12 ript levels for a limited number of genes in Cyanothece and other unicellular diazotrophic cyanobacte
13 processes, the intracellular environment of Cyanothece oscillates between aerobic and anaerobic cond
15 The unicellular, diazotrophic cyanobacterium Cyanothece sp. ATCC 51142 demonstrated important modific
17 icellular diazotrophic cyanobacteria such as Cyanothece sp. ATCC 51142 produce oxygen and can also fi
18 ernating oxygenic and microoxic processes of Cyanothece sp. ATCC 51142 under continuous high irradian
21 in unicellular cyanobacterial cells, such as Cyanothece sp. ATCC 51142, are capable of nitrogen fixat
23 ed to investigate light-driven metabolism in Cyanothece sp. ATCC 51142, with a particular focus on re
27 oth dark- and light-induced H(2) effluxes by Cyanothece sp. Miami BG 043511 and establish their respe
28 d barium (Ba) by two cyanobacterial strains, Cyanothece sp. PCC7425 and Gloeomargarita lithophora, bo
32 the unicellular, diazotrophic cyanobacterium Cyanothece sp. strain ATCC 51142 under N(2)-fixing condi
36 nclude that in unicellular diazotrophs, like Cyanothece sp. strain PCC 7822, the HupLS complex helps
37 respiration and nitrogen fixation among the Cyanothece spp. strains that were grown under identical
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