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1 cteria, we analyzed six members of the genus Cyanothece.
2                                    Wild-type Cyanothece 51142 can produce hydrogen at rates as high a
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        Unlike non-diazotrophic clock models, Cyanothece 51142 exhibits conspicuous self-sustained rhy
6  cells, we determined that the thylakoids in Cyanothece 51142 form a dense and complex network that e
7                             The 5,460,377-bp Cyanothece 51142 genome has a unique arrangement of one
8           We expressed the c-psbA4 gene from Cyanothece 51142 in a 4E-3 mutant strain of the model no
9                                              Cyanothece 51142 performs oxygenic photosynthesis and ni
10 portant information regarding the ability of Cyanothece 51142 to accomplish metabolic compartmentaliz
11 cadian clock in the now genetically amenable Cyanothece 51142, a unicellular, nitrogen-fixing cyanoba
12 or almost all central metabolic processes in Cyanothece 51142.
13 ly identified lectin from the cyanobacterium Cyanothece(7424), and elucidated its glycan specificity
14 ript levels for a limited number of genes in Cyanothece and other unicellular diazotrophic cyanobacte
15  processes, the intracellular environment of Cyanothece oscillates between aerobic and anaerobic cond
16               The unicellular cyanobacterium Cyanothece sp. American Type Culture Collection (ATCC) 5
17 The unicellular, diazotrophic cyanobacterium Cyanothece sp. ATCC 51142 demonstrated important modific
18 900 features were reproducibly detected from Cyanothece sp. ATCC 51142 metabolite extracts.
19 icellular diazotrophic cyanobacteria such as Cyanothece sp. ATCC 51142 produce oxygen and can also fi
20 ernating oxygenic and microoxic processes of Cyanothece sp. ATCC 51142 under continuous high irradian
21                                              Cyanothece sp. ATCC 51142, a member of this genus, has b
22                            Here, we describe Cyanothece sp. ATCC 51142, a unicellular, diazotrophic c
23 in unicellular cyanobacterial cells, such as Cyanothece sp. ATCC 51142, are capable of nitrogen fixat
24 e have sequenced to completion the genome of Cyanothece sp. ATCC 51142, the first such organism.
25 ed to investigate light-driven metabolism in Cyanothece sp. ATCC 51142, with a particular focus on re
26 e model for the diazotrophic cyanobacterium, Cyanothece sp. ATCC 51142.
27 d membranes in a unicellular cyanobacterium, Cyanothece sp. ATCC 51142.
28  metabolite extracts from the cyanobacterium Cyanothece sp. ATCC 51142.
29  the unicellular diazotrophic cyanobacterium Cyanothece sp. ATCC 51142.
30 oth dark- and light-induced H(2) effluxes by Cyanothece sp. Miami BG 043511 and establish their respe
31 ried cells of the ACC-forming cyanobacterium Cyanothece sp. PCC 7425 to probe the molecular environme
32 d barium (Ba) by two cyanobacterial strains, Cyanothece sp. PCC7425 and Gloeomargarita lithophora, bo
33                                 In contrast, Cyanothece sp. PCC7425 showed neither a preferential acc
34                                      Indeed, Cyanothece sp. strain ATCC 51142 has developed an expens
35                                              Cyanothece sp. strain ATCC 51142 is a unicellular, diazo
36 the unicellular, diazotrophic cyanobacterium Cyanothece sp. strain ATCC 51142 under N(2)-fixing condi
37                                              Cyanothece sp. strain ATCC 51142, a unicellular, diazotr
38  nitrogen-fixing unicellular cyanobacterium, Cyanothece sp. strain BH68K.
39                                              Cyanothece sp. strain PCC 7822 is a unicellular, diazotr
40 nclude that in unicellular diazotrophs, like Cyanothece sp. strain PCC 7822, the HupLS complex helps
41  respiration and nitrogen fixation among the Cyanothece spp. strains that were grown under identical