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 s are dependent on stimulation with the cyst life cycle stage.
2 ssential to the medically relevant T. brucei life cycle stage.
3 rect comparison of protection against either life cycle stage.
4 sary for the growth and replication of every life cycle stage.
5 nctions in the mammalian infective T. brucei life cycle stage.
6 containing asparagine-linked glycans of this life cycle stage.
7 imerase levels are close to limiting in this life cycle stage.
8 ion phenotypes at specific developmental and life cycle stages.
9 anscribed to an equal extent in all parasite life cycle stages.
10 g glucose transporter mRNA levels in the two life cycle stages.
11 RNAs are expressed at similar levels in both life cycle stages.
12 release nanosilver (impact) during multiple life cycle stages.
13 map with base-level resolution at different life cycle stages.
14 editosome proteins are adjusted between the life cycle stages.
15 , exposure routes and pathways and for other life cycle stages.
16 d that the 20S editosomes differ between the life cycle stages.
17 y set by processes operating at the earliest life cycle stages.
18 of PAT inhibitors against multiple parasite life cycle stages.
19 t the in vivo functions of PAT in Plasmodium life cycle stages.
20 upon the growth environment in two different life cycle stages.
21 cluster, with several expressed at multiple life cycle stages.
22 is apparently dispensable for growth in both life cycle stages.
23 ol enrichment and cell metabolism in the two life cycle stages.
24 as profiled and compared with other parasite life cycle stages.
25 the protein is essential for growth in both life cycle stages.
26 g of this most elusive of the parasites many life cycle stages.
27 essential in both bloodstream and procyclic life cycle stages.
28 ty against the liver and gametocyte parasite life-cycle stages.
29 on of antigens expressed in pre-erythrocytic life-cycle stages.
30 timalarial drug discovery targeting multiple life-cycle stages.
31 is indispensable during the sexual mosquito life-cycle stages.
32 ere differentially expressed between the two life-cycle stages.
33 nalyses, and protein characterization of its life-cycle stages.
34 cruzi genome were identified across the four life-cycle stages.
36 d and interact with each other in both major life cycle stages and show similar distributions at Pol
38 erstanding of the preerythrocytic Plasmodium life cycle stages and the development of preerythrocytic
39 kinase, PK50, is expressed in proliferative life cycle stages and was shown to complement a yeast ND
40 housekeeping genes (expressed during several life-cycle stages) and mating-related genes, while the s
41 ammalian host) and procyclic (insect vector) life cycle stages, and KHARON is thus critical for paras
42 loodstream form (BF) and procyclic form (PF) life cycle stages, and this correlates with the differen
43 the activities of parasites in these various life-cycle stages are likely to be reflected in changes
45 reactivity against Pf proteins based on the life cycle stage at which proteins are expressed, subcel
47 e mechanisms of flagellum length regulation, life cycle stage differentiation and trypanosomatid divi
48 ent or exflagellation, suggesting that these life cycle stages do not utilize host-derived glycerol a
49 on haploid genotypes during less conspicuous life cycle stages, e.g., competition among sperm/pollen
50 size, shape, and form yet transition through life cycle stages, each having a distinct morphology.
51 e eggs, because exposure of the host to this life-cycle stage elicits a polarized Th2 response to egg
52 eal-time qPCR has confirmed the differential life-cycle stage expression of a set of selected lincRNA
54 emerging evidence suggests that the parasite life cycle stage impacts the modulation of apoptosis and
55 d culture conditions and was lethal for this life cycle stage in the presence of hydrogen peroxide.
56 nd differences might exist between different life cycle stages in relation to the regulation of cell
58 se results highlight the importance of early life cycle stages in tropical forest community dynamics.
59 for the identification of distinct parasite life-cycle stages in the tsetse, trypanosome differentia
60 rom those of eggs confirm that each of these life cycle stages induces a unique pattern of cytokine e
61 pvs25 that is expressed in gametocytes, the life cycle stage infectious to mosquitoes, were first de
62 observation that differentiation of parasite life cycle stages involves structural and functional reo
63 parameters determine the timing of seasonal life cycle stages is constrained by limited long-term da
64 ghly expressed cysteine protease during both life cycle stages measured, with a dramatic expression i
65 ce a chitin-rich cell wall during any of the life cycle stages observed and therefore do not conform
66 se regulator CtrA are not expressed during a life cycle stage of Caulobacter crescentus when the regu
67 aria infection is caused by sporozoites, the life cycle stage of Plasmodium that is transmitted by fe
69 sumption for supply chain production at each life cycle stage of the well was estimated using the eco
70 importance of ASL to purine salvage by both life cycle stages of L. donovani and authenticate ASL as
71 is established that AAH is expressed in both life cycle stages of L. donovani, whereas subcellular fr
72 nd salvage to pyrimidine homeostasis in both life cycle stages of Leishmania donovani, individual mut
75 tal and adult mice to the trophic and cystic life cycle stages of Pneumocystis murina The adult and n
77 on and have differential effects between the life cycle stages of T. brucei that differentially edit
79 its spectrum of activities against multiple life cycle stages of the human malaria parasite Plasmodi
80 efects in surface glycoproteins in different life cycle stages of the parasite highlights the essenti
81 transcripts and protein are expressed in all life cycle stages of the parasite within the vertebrate
86 e no known functions or homologues, and most life cycle stages of this haploid eukaryotic parasite ar
90 Here, I analyse the swimming of the insect life cycle stages of two human parasites; Trypanosoma br
91 of highly potent compounds against the blood life-cycle stage of the human malaria parasite Plasmodiu
92 The high density of GPI structures at all life-cycle stages of African trypanosomes and Leishmania
94 be facilitated by intervention at different life-cycle stages of the parasite, including the obligat
96 um of antimalarial activity against multiple life-cycle stages of the Plasmodium parasite, with good
99 ir relationship with their host at different life-cycle stages or in response to changing environment
100 We wondered whether the insect and mammalian life cycle stages possess chemically different lipid raf
101 e differentially phosphorylated in different life-cycle stages, possibly indicative for unique forms
105 hierarchical regulatory model in tissue and life cycle stage-specific silencing by NuRD complexes.
107 tes between bloodstream-form and insect-form life cycle stages that are adapted to survive in the mam
108 A expression libraries were constructed from life cycle stages that are critical for establishment of
109 rall, we expand our view of the sex-specific life cycle stages that can drive sex chromosome evolutio
110 constitutively expressed at 37 degrees C in life cycle stages that live in the mammalian host (micro
112 gulation has focussed on comparisons between life-cycle stages that exist in the blood of mammalian h
114 invade hepatocytes and develop into the next life cycle stage, the exoerythrocytic, or liver, stage.
115 ng and exon skipping were active in multiple life cycle stages to change exon structure in the deduce
116 of studying the trypanosomatid intracellular life cycle stages to gain a better understanding of the
118 ess to the surface plasma membrane in insect life-cycle-stage trypanosomes but, remarkably, AQP2 was
119 abilities with EHS risks across nanomaterial life-cycle stages using empirical knowledge in the field
121 n G antibodies to PfEMP-1, expressed on both life cycle stages, were measured in residents from an ar
122 te Leishmania during the transformation of a life cycle stage with a 9+2 axoneme (the promastigote) t
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。