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1 ting abundance of replete ticks (Dermacentor variabilis).
2 intramembrane cleaving proteases in Anabaena variabilis.
3 ied through a genome-wide survey in Anabaena variabilis.
4 ization levels between I. fasciculata and I. variabilis.
5 from Rhodosporidium toruloides and Anabaena variabilis.
6 se inhibitor (KPI) from the tick Dermacentor variabilis.
7 in the ovaries of the hard tick Dermacentor variabilis.
8 GJB4) in the etiology of erythrokeratodermia variabilis.
9 rived cells from a natural host, Dermacentor variabilis.
10 ions and from salivary glands of Dermacentor variabilis.
11 vel with the vnfD gene product from Anabaena variabilis.
12 een for cold-induced transcripts in Anabaena variabilis.
13 e in the pathogenesis of erythrokeratodermia variabilis.
14 essential for the V-nitrogenase system in A. variabilis.
15 e transport system, vupABC, were found in A. variabilis about 5 kb from the major cluster of genes en
16 s and a sporadic case of erythrokeratodermia variabilis, all of which were not found in controls.
18 otypic differences, both erythrokeratodermia variabilis and erythrokeratodermia with ataxia map to a
22 (Ulva pertusa), and cyanobacteria (Anabaena variabilis and Synechococcus) have been investigated by
23 genetic heterogeneity in erythrokeratodermia variabilis, and emphasize that intercellular communicati
24 e biological species as the benthic Bolivina variabilis, and geochemical evidence that this ecologica
25 ed States, Amblyomma americanum, Dermacentor variabilis, and Ixodes scapularis are among the principa
26 presented with localized erythrokeratodermia variabilis, and one with erythrokeratodermia and ataxia.
28 MITEs in the two bacterial genomes, Anabaena variabilis ATCC 29413 and Haloquadratum walsbyi DSM 1679
29 from cyanobacteria, in particular, Anabaena variabilis ATCC 29413 and Nostoc punctiforme ATCC 29133,
36 haplotype analyses place erythrokeratodermia variabilis between the marker D1S496 and D1S186 with a m
37 rved for the two active-site loops in the A. variabilis C503S/C565S double mutant, yielding a complet
40 to antigens from four other algae: Chlorella variabilis, Coccomyxa subellipsoidea, Nannochloropsis oc
41 three antimicrobials, especially the two D. variabilis defensin isoforms, are markedly different, il
42 itor from the American dog tick (Dermacentor variabilis) (DvKPI) is suppressed by small interfering R
43 31 cause the skin disease erythrokeratoderma variabilis (EKV) and hearing loss with or without neurop
45 a combination of SCA and erythrokeratodermia variabilis (EKV) in an autosomal dominant fashion was de
46 underlie the skin disease erythrokeratoderma variabilis (EKV) or sensorineural hearing loss with/with
50 of GJB4 in 13 unrelated erythrokeratodermia variabilis families without detectable mutations in GJB3
53 ase from the established erythrokeratodermia variabilis gene region indicating genetic heterogeneity
57 calcium-dependent protease PrcA of Anabaena variabilis, HreP forms a new subfamily of bacterial subt
59 Connexin 31, which causes erythrokeratoderma variabilis, induces ER stress and p63-dependent epiderma
64 One of these disorders, erythrokeratoderma variabilis, is associated with germline mutations in the
67 29 cells (mouse fibroblasts), implicating D. variabilis KPI as a bacteriostatic protein, a property t
70 rthermore, our in vitro studies show that D. variabilis KPI limits rickettsial colonization of L929 c
71 s anticoagulant properties indicates that D. variabilis KPI may be important for blood meal digestion
72 ole in the midgut during feeding and that D. variabilis KPI may be involved as part of the tick's def
76 and 8-heptadecene were detected in Chlorella variabilis NC64A (Trebouxiophyceae) and several Nannochl
78 n this case we reduced aggregation of the A. variabilis PAL by mutating two surface cysteine residues
79 l and biochemical characterization of the A. variabilis PAL C503S/C565S double mutant and carefully c
80 from the salivary glands of male Dermacentor variabilis persistently infected with A. marginale after
81 istics, and efficacy of recombinant Anabaena variabilis phenylalanine ammonia lyase (produced in Esch
82 re loaded with recombinant PAL from Anabaena variabilis (rAvPAL) and their ability to perform as bior
84 family, maps within the erythrokeratodermia variabilis region and is an attractive candidate gene.
85 ermacentor occidentalis Marx and 30 adult D. variabilis Say ticks, collected chiefly in southern Cali
87 sis demonstrated that these five putative A. variabilis site-2 proteases (S2Ps(Av)) have authentic pr
89 prise multiple operons; however, in Anabaena variabilis, the promoter for the first gene in the clust
90 and in Amblyomma americanum and Dermacentor variabilis ticks collected from a cattle herd in Missour
91 ysozyme, in the midguts and fat bodies of D. variabilis ticks that were challenged with R. montanensi
92 nactivation of rca reduced the ability of A. variabilis to elevate Rubisco activity under high light
93 salivary glands of the hard tick Dermacentor variabilis using a combination of gel filtration and hig
95 High-affinity transport of molybdate in A. variabilis was mediated by an ABC-type transport system
97 d in vivo and resulting mutant strains of A. variabilis were found to be incapable of synthesizing im
98 1 from Clostridium thermocellum and Anabaena variabilis, which are enzymatically indistinguishable fr
100 phore pathway in the cyanobacterium Anabaena variabilis, which was shown to be a bona fide DABA DC.
101 in this study, we show that challenge of D. variabilis with the spotted fever group rickettsia, Rick
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