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1 sequence specificity [symbol: see text] from Microbacterium ammoniaphilum have been cloned in Escheri
2 rs of the genera Mycobacterium, Rhodococcus, Microbacterium and Gordonia.
3 genera Eubacterium, Flavobacterium, Kocuria, Microbacterium, and Porphyromonas and the related Strept
4                                  Contrarily, Microbacterium, and Rhizobium were significantly higher
5 cribe the first case of bacteremia caused by Microbacterium binotii in a patient with sickle cell ane
6  paraoxydans, should be included in this new Microbacterium clade alongside the four novel ISS strain
7                                              Microbacterium deferre sp. nov.
8                                              Microbacterium laevaniformans strain OR221 was isolated
9 -benzylhydantoin transport protein Mhp1 from Microbacterium liquefaciens comprises a five-helix inver
10 ily, the Mhp1 benzyl-hydantoin permease from Microbacterium liquefaciens, allowed us to construct and
11  Na(+)-coupled hydantoin symporter Mhp1 from Microbacterium liquefaciens.
12 r sodium-linked transport of hydantoins from Microbacterium liquefaciens.
13 CS1 benzyl-hydantoin transporter, Mhp1, from Microbacterium liquefaciens.
14    This article describes the isolation of a Microbacterium maritypicum riboflavin catabolic strain,
15 f a new Microbacterium species, herein named Microbacterium meiriae.
16 C. elegans that is resistant to infection by Microbacterium nematophilum and to binding of the biofil
17                                              Microbacterium nematophilum causes a deleterious infecti
18                                 Infection by Microbacterium nematophilum identified bus (bacterially
19 a new species of coryneform bacterium, named Microbacterium nematophilum n. sp., which fortuitously c
20 te the C. elegans response to infection with Microbacterium nematophilum We show that this receptor,
21 pomorphs, display resistance to infection by Microbacterium nematophilum, a pathogen of rhabditid nem
22 s cause resistance to the bacterial pathogen Microbacterium nematophilum, and most of these mutations
23  also resistant to infection by the pathogen Microbacterium nematophilum, due to failure of the bacte
24 ed susceptibility to the C. elegans pathogen Microbacterium nematophilum.
25            A representative daptide BGC from Microbacterium paraoxydans DSM 15019 was selected for ex
26 idization values with the closest recognized Microbacterium paraoxydans DSM 15019(T), delineating new
27 ing species, Aldercreutzia equolifaciens and Microbacterium schleiferi, generate BH4 and are present
28 ANI; > 83% dDDH) between the ISS strains and Microbacterium sp. LTR1 strain isolated from the larva s
29 famethoxazole (SMX) during biodegradation by Microbacterium sp. strain BR1 (ipso-hydroxylation) and u
30 ., Bacillus pumilus., Pantoea agglomerance., Microbacterium sp., and Serratia marcescens), and their
31 mucus coats trout commensal isolates such as Microbacterium sp., Staphylococcus warneri, Flectobacill
32                     To date, only 6 sporadic Microbacterium species (formerly coryneform Centers for
33       All isolates were identified at CDC as Microbacterium species and had identical DNA banding pat
34                                              Microbacterium species are non-spore-forming, Gram-posit
35                   To assess risk factors for Microbacterium species infection, a retrospective cohort
36 and potential for nosocomial transmission of Microbacterium species remain unknown.
37 ith LTR1 represent distinct strains of a new Microbacterium species, herein named Microbacterium meir
38                       There are more than 35 Microbacterium species, some of which are pathogenic in
39       This outbreak demonstrates significant Microbacterium species-associated morbidity and mortalit
40 ochemistry of adhesion to a host tissue by a Microbacterium species.
41 droxylase from the cold-adapted marine ultra-microbacterium Sphingopyxis alaskensis (Sa) and found th
42 ole (SMX) metabolization in pure cultures of Microbacterium strain BR1.
43             Common bacterial genera included Microbacterium, Terribacillus, and JABEUN01 (an Acidimic
44 _P_3B and F6_8S_P_3C, belonging to the genus Microbacterium were isolated from the walls of crew quar
45 led that Staphylococcus, Granulicatella, and Microbacterium were significantly enriched in BCO chicke
46 the genera Arthrobacter, Brevibacterium, and Microbacterium, which could not be identified to the spe