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1 OLE1 on the emerging human pathogenic fungus Candida parapsilosis.
2 been grouped with the more prevalent species Candida parapsilosis.
3 te was Candida albicans, and one isolate was Candida parapsilosis.
4 andida guilliermondii, Candida glabrata, and Candida parapsilosis.
5 Doogh including Rhodotorula mucilaginosa and Candida parapsilosis.
6 stribution was 55.6% Candida albicans, 14.4% Candida parapsilosis, 13.4% Candida glabrata, 10.1% Cand
7 42 Candida albicans, 25 Candida glabrata, 22 Candida parapsilosis, 14 Candida tropicalis, and 8 Candi
8 a albicans, followed by Candida glabrata and Candida parapsilosis (15%), Candida tropicalis (9%), and
9 s (38%), followed by Candida glabrata (29%), Candida parapsilosis (17%), and Candida tropicalis (10%)
10 icans (0.4%), Candida tropicalis (1.3%), and Candida parapsilosis (2.1%); however, 8.8% of C. glabrat
11 ates was as follows: Candida albicans (52%), Candida parapsilosis (23.7%), Candida glabrata (12.7%),
12 pp identified were Candida albicans (55.8%), Candida parapsilosis (29.4%), Candida glabrata (7.8%), a
13 isolates of Candida albicans, 9 isolates of Candida parapsilosis, 5 isolates of Candida krusei, 3 is
15 41 Candida albicans, 23 Candida glabrata, 20 Candida parapsilosis, 9 Candida tropicalis, and 1 each o
16 However, antibiotics promoted emergence of Candida parapsilosis, a collagenase-producing microorgan
17 ly related clade, Lodderomyces elongisporus, Candida parapsilosis, a new Candida sp., C. sojae, C. tr
18 n health care settings compared with that of Candida parapsilosis, a species known to colonize the sk
20 However, we found that the linear mtDNA of Candida parapsilosis also employs recombination for repl
21 ds towards Candida albicans, Candida krusei, Candida parapsilosis and Cryptococcus neoformans were in
22 al characterizations of Est3 homologues from Candida parapsilosis and Lodderomyces elongisporus, whic
23 Candida krusei, 10 Candida dubliniensis, 10 Candida parapsilosis, and 10 Cryptococcus neoformans iso
25 uding 28 (66.7%) Candida albicans, 8 (19.0%) Candida parapsilosis, and 5 (11.9%) Candida tropicalis i
26 tropicalis, 99.3% (95% CI, 98.7%-99.6%) for Candida parapsilosis, and 99.9% (95% CI, 99.7%-100.0%) f
27 nce is a concern for Nakaseomyces glabratus, Candida parapsilosis, and Candida auris and less so in C
28 solates of Candida glabrata, two isolates of Candida parapsilosis, and one isolate of Saccharomyces c
29 ecies of Candida albicans, Candida glabrata, Candida parapsilosis, Aspergillus fumigatus, and Aspergi
30 ata to propose zone size limits for tests of Candida parapsilosis ATCC 22019 (22 to 33 mm), C. tropic
31 ata to propose zone size limits for tests of Candida parapsilosis ATCC 22019 (28 to 37 mm), Candida a
32 proposed range for the suggested QC strains Candida parapsilosis ATCC 22019 and Candida krusei ATCC
33 ns isolates and two quality control strains (Candida parapsilosis ATCC 22019 and Candida krusei ATCC
34 mphotericin B, fluconazole, and flucytosine (Candida parapsilosis ATCC 22019 and Candida krusei ATCC
38 Antifungal susceptibility testing among 1740 Candida parapsilosis blood isolates submitted to a Unite
39 regarding the optimal antifungal regimen for Candida parapsilosis bloodstream infection (BSI) in view
41 Ten yeast bloodstream isolates identified as Candida parapsilosis by conventional methods grew as tur
42 trazolium metabolism in Candida albicans and Candida parapsilosis by using XTT [2,3-bis (2-methoxy-4-
43 aureus), Candida albicans (C. albicans) and Candida parapsilosis (C. parapsilosis) was investigated.
44 y identify Candida albicans, Candida krusei, Candida parapsilosis, Candida glabrata, and Candida trop
45 s, Streptococcus mutans, Candida tropicalis, Candida parapsilosis, Candida krusei, Candida glabrata,
46 non-Candida albicans Candida spp. (including Candida parapsilosis, Candida krusei, Candida guilliermo
47 icans, Candida glabrata, Candida tropicalis, Candida parapsilosis, Candida lusitaniae, Candida guilli
48 identify Candida albicans, Candida glabrata, Candida parapsilosis, Candida tropicalis, and Aspergillu
49 tible in Candida albicans, Candida glabrata, Candida parapsilosis, Candida tropicalis, and Candida kr
50 0543, Torulaspora delbrueckii CCMA 0684, and Candida parapsilosis CCMA 0544) singly and with co-inocu
55 phic and temporal trends in the isolation of Candida parapsilosis from clinical specimens and the in
56 lated Candida sojae, Candida viswanathii and Candida parapsilosis indicates loss of ancestral HIR-ass
65 sitive with AF only (two C. albicans and one Candida parapsilosis isolate); and 13 were positive with
67 isteria monocytogenes, Candida albicans, and Candida parapsilosis isolates were detected in volumes a
68 isolates, 70 Candida tropicalis isolates, 36 Candida parapsilosis isolates, 13 isolates of other Cand
69 s a sequence derived from the extreme end of Candida parapsilosis linear mtDNA, and sequence analysis
72 brata (n = 41), Candida tropicalis (n = 35), Candida parapsilosis (n = 29), Candida krusei (n = 32),
73 icans (n = 420), Candida glabrata (n = 112), Candida parapsilosis (n = 30), Candida krusei (n = 12),
75 brata (n = 96), Candida tropicalis (n = 51), Candida parapsilosis (n = 47), Candida krusei (n = 11),
76 fied as Candida dubliniensis, one isolate of Candida parapsilosis (n = 73) identified as Candida pell
77 one Candida membranaefaciens (identified as Candida parapsilosis), one Candida norvegensis (identifi
78 telomeres identified in three yeast species, Candida parapsilosis, Pichia philodendra and Candida sal
79 roperties of 14 isolates of the form species Candida parapsilosis representing three diverse genetic
82 estion of how the unit sized linear mtDNA of Candida parapsilosis terminating at both ends with array
84 Candida dubliniensis with all agents and for Candida parapsilosis when caspofungin or micafungin but