戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 ting abundance of replete ticks (Dermacentor variabilis).
2 essential for the V-nitrogenase system in A. variabilis.
3 dentatus/Laevistrombus canarium/Ministrombus variabilis.
4 laris, Amblyomma americanum, and Dermacentor variabilis.
5 eplicate within a single strain of Chlorella variabilis.
6 ization levels between I. fasciculata and I. variabilis.
7 rived cells from a natural host, Dermacentor variabilis.
8 intramembrane cleaving proteases in Anabaena variabilis.
9 ied through a genome-wide survey in Anabaena variabilis.
10  from Rhodosporidium toruloides and Anabaena variabilis.
11 se inhibitor (KPI) from the tick Dermacentor variabilis.
12  in the ovaries of the hard tick Dermacentor variabilis.
13 thered Synechocystis cells and killed off T. variabilis.
14 GJB4) in the etiology of erythrokeratodermia variabilis.
15 ions and from salivary glands of Dermacentor variabilis.
16 vel with the vnfD gene product from Anabaena variabilis.
17 een for cold-induced transcripts in Anabaena variabilis.
18 e in the pathogenesis of erythrokeratodermia variabilis.
19 ), Comamonas thiooxydans (9%), Acinetobacter variabilis (7%), Pseudomonas aeruginosa, and Pseudomonas
20 e transport system, vupABC, were found in A. variabilis about 5 kb from the major cluster of genes en
21 s and a sporadic case of erythrokeratodermia variabilis, all of which were not found in controls.
22      The similarity of the vnfEN genes of A. variabilis and A. vinelandii was not strong.
23 nitor feeding behaviors of adult Dermacentor variabilis and Amblyomma americanum in real-time.
24 otypic differences, both erythrokeratodermia variabilis and erythrokeratodermia with ataxia map to a
25                                   Rhizomucor variabilis and Hormographiella aspergillata rarely cause
26 ndosymbionts (Chlorella heliozoae, Chlorella variabilis and Micractinium conductrix).
27 tous nitrogen-fixing cyanobacteria, Anabaena variabilis and Nostoc punctiforme.
28  (Ulva pertusa), and cyanobacteria (Anabaena variabilis and Synechococcus) have been investigated by
29 genetic heterogeneity in erythrokeratodermia variabilis, and emphasize that intercellular communicati
30 e biological species as the benthic Bolivina variabilis, and geochemical evidence that this ecologica
31 ed States, Amblyomma americanum, Dermacentor variabilis, and Ixodes scapularis are among the principa
32 presented with localized erythrokeratodermia variabilis, and one with erythrokeratodermia and ataxia.
33 topology, Absidia corymbifera and Rhizomucor variabilis appear to be misplaced taxonomically.
34 ins and identified previously as Dermacentor variabilis are the recently described species, Dermacent
35 MITEs in the two bacterial genomes, Anabaena variabilis ATCC 29413 and Haloquadratum walsbyi DSM 1679
36  from cyanobacteria, in particular, Anabaena variabilis ATCC 29413 and Nostoc punctiforme ATCC 29133,
37                                     Anabaena variabilis ATCC 29413 fixes nitrogen in specialized cell
38                                     Anabaena variabilis ATCC 29413 is a filamentous heterocystous cya
39                                     Anabaena variabilis ATCC 29413 is unusual in that it has two Mo-d
40                  The cyanobacterium Anabaena variabilis ATCC 29413 uses nitrate and atmospheric N2 as
41 utant strains of the cyanobacterium Anabaena variabilis ATCC 29413.
42 rate specificity from that known in Anabaena variabilis ATCC 29413.
43  in the heterocystous cyanobacteria Anabaena variabilis ATTC 29413 using the acetylene reduction assa
44 haplotype analyses place erythrokeratodermia variabilis between the marker D1S496 and D1S186 with a m
45 rved for the two active-site loops in the A. variabilis C503S/C565S double mutant, yielding a complet
46                                           A. variabilis C503S/C565S PAL is shown to be both more ther
47                        Examination of the A. variabilis C503S/C565S PAL structure, combined with anal
48 n lesions reminiscent of erythrokeratodermia variabilis, caused by mutations in connexin (Cx) genes.
49 to antigens from four other algae: Chlorella variabilis, Coccomyxa subellipsoidea, Nannochloropsis oc
50                        Furthermore, Anabaena variabilis cultures grown in Mo or V media achieved simi
51  three antimicrobials, especially the two D. variabilis defensin isoforms, are markedly different, il
52 itor from the American dog tick (Dermacentor variabilis) (DvKPI) is suppressed by small interfering R
53 31 cause the skin disease erythrokeratoderma variabilis (EKV) and hearing loss with or without neurop
54          The skin disease erythrokeratoderma variabilis (EKV) has been shown to be associated with mu
55 a combination of SCA and erythrokeratodermia variabilis (EKV) in an autosomal dominant fashion was de
56 underlie the skin disease erythrokeratoderma variabilis (EKV) or sensorineural hearing loss with/with
57 ases, including familial erythrokeratodermia variabilis (EKV).
58                          Erythrokeratodermia variabilis (EKV, OMIM 133200) is an autosomal dominant g
59                          Erythrokeratodermia variabilis et progressiva (EKVP) is a rare, inherited sk
60 d congenital alopecia-1, erythrokeratodermia variabilis et progressiva, or inflammatory linear verruc
61  of GJB4 in 13 unrelated erythrokeratodermia variabilis families without detectable mutations in GJB3
62 l as computation, we characterized Chlorella variabilis FAP reaction intermediates on time scales fro
63      The filamentous cyanobacterium Anabaena variabilis fixes nitrogen in the presence of vanadium (V
64                                     Anabaena variabilis fixes nitrogen under aerobic growth condition
65 ploitation of the nitrogen-fixing Trichormus variabilis, for survival in nitrogen-deficient environme
66 ase from the established erythrokeratodermia variabilis gene region indicating genetic heterogeneity
67                                           A. variabilis grew better with increasing concentrations of
68                                     Anabaena variabilis grows heterotrophically using fructose, while
69                  The cyanobacterium Anabaena variabilis has two Mo-nitrogenases that function under d
70  calcium-dependent protease PrcA of Anabaena variabilis, HreP forms a new subfamily of bacterial subt
71             Expression of nifB2:lacZ from A. variabilis in anaerobic vegetative cells of Anabaena sp.
72 Connexin 31, which causes erythrokeratoderma variabilis, induces ER stress and p63-dependent epiderma
73                       We report a case of A. variabilis invasive wound infection in a 21-year-old mal
74                          Erythrokeratodermia variabilis is an autosomal dominant genodermatosis chara
75                                Apophysomyces variabilis is an emerging fungal pathogen that can cause
76 r miehei-Rhizomucor pusillus clade, while R. variabilis is nested within Mucor.
77   One of these disorders, erythrokeratoderma variabilis, is associated with germline mutations in the
78  isolates (three A. trapeziformis and two A. variabilis isolates).
79                                  In Anabaena variabilis it was shown that a NifE-N fusion protein enc
80 terized an AHGD from marine bacterium Vibrio variabilis JCM 19239 (VvAHGD).
81 29 cells (mouse fibroblasts), implicating D. variabilis KPI as a bacteriostatic protein, a property t
82 kettsia montanensis, results in sustained D. variabilis KPI gene expression in the midgut.
83          Interestingly, we observe little D. variabilis KPI gene expression in the salivary gland and
84 rthermore, our in vitro studies show that D. variabilis KPI limits rickettsial colonization of L929 c
85 s anticoagulant properties indicates that D. variabilis KPI may be important for blood meal digestion
86 ole in the midgut during feeding and that D. variabilis KPI may be involved as part of the tick's def
87             However, our demonstration of D. variabilis KPI's anticoagulant properties indicates that
88 rotein, a property that may be related to D. variabilis KPI's trypsin inhibitory capability.
89  other Ixodid ticks, most proteins in the D. variabilis midgut cDNA library were intracellular.
90 discovered photodecarboxylase from Chlorella variabilis NC64A ( CvFAP) bears the promise for the effi
91 and 8-heptadecene were detected in Chlorella variabilis NC64A (Trebouxiophyceae) and several Nannochl
92 re compared to PBCV-1 and its host Chlorella variabilis NC64A predicted proteomes.
93 infects the unicellular green alga Chlorella variabilis NC64A.
94 A virus that infects the microalga Chlorella variabilis NC64A.
95 that only infect the Syngen 2-3 strain of C. variabilis (OSy viruses).
96 n this case we reduced aggregation of the A. variabilis PAL by mutating two surface cysteine residues
97 l and biochemical characterization of the A. variabilis PAL C503S/C565S double mutant and carefully c
98 from the salivary glands of male Dermacentor variabilis persistently infected with A. marginale after
99 istics, and efficacy of recombinant Anabaena variabilis phenylalanine ammonia lyase (produced in Esch
100 s-specific preferences for location, with D. variabilis preferentially biting the head and neck and A
101 re loaded with recombinant PAL from Anabaena variabilis (rAvPAL) and their ability to perform as bior
102 d to sustain a normal growth rate for the A. variabilis rca mutant.
103  family, maps within the erythrokeratodermia variabilis region and is an attractive candidate gene.
104 ermacentor occidentalis Marx and 30 adult D. variabilis Say ticks, collected chiefly in southern Cali
105                        The vnfEN genes of A. variabilis showed greater similarity to the vnfDK genes
106 sis demonstrated that these five putative A. variabilis site-2 proteases (S2Ps(Av)) have authentic pr
107 uded one field population of Neohydatothrips variabilis (soybean thrips [ST]) from the United States.
108 , atopic dermatitis, and erythrokeratodermia variabilis, suggesting a contributory role for epidermal
109 replication cycle in one strain of Chlorella variabilis, systematic challenges emerged.
110 rine sponges Ircinia fasciculata and Ircinia variabilis that live in sympatry.
111 prise multiple operons; however, in Anabaena variabilis, the promoter for the first gene in the clust
112  and in Amblyomma americanum and Dermacentor variabilis ticks collected from a cattle herd in Missour
113 ysozyme, in the midguts and fat bodies of D. variabilis ticks that were challenged with R. montanensi
114 nactivation of rca reduced the ability of A. variabilis to elevate Rubisco activity under high light
115 salivary glands of the hard tick Dermacentor variabilis using a combination of gel filtration and hig
116 re tethered to polysaccharide capsules of T. variabilis using nanotubular structures, presumably for
117            The patient first developed an R. variabilis var. regularior palate infection and later de
118   High-affinity transport of molybdate in A. variabilis was mediated by an ABC-type transport system
119 mal dominant skin disease erythrokeratoderma variabilis was segregating.
120 d in vivo and resulting mutant strains of A. variabilis were found to be incapable of synthesizing im
121 ris, two Ixodes brunneus, and 35 Dermacentor variabilis) were tested for Borrelia spp., Rickettsia sp
122 1 from Clostridium thermocellum and Anabaena variabilis, which are enzymatically indistinguishable fr
123                                     Anabaena variabilis, which can fix nitrogen by using an alternati
124 phore pathway in the cyanobacterium Anabaena variabilis, which was shown to be a bona fide DABA DC.
125  in this study, we show that challenge of D. variabilis with the spotted fever group rickettsia, Rick

 
Page Top