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1 sary for the growth and replication of every life cycle stage.
2 nctions in the mammalian infective T. brucei life cycle stage.
3 containing asparagine-linked glycans of this life cycle stage.
4 imerase levels are close to limiting in this life cycle stage.
5 t switch their host range according to their life cycle stage.
6 s are dependent on stimulation with the cyst life cycle stage.
7 ssential to the medically relevant T. brucei life cycle stage.
8 rect comparison of protection against either life cycle stage.
9 a role during an early, prereplication virus life-cycle stage.
10 o interrogate U-indel editing in EMF and MCF life cycle stages.
11 is apparently dispensable for growth in both life cycle stages.
12 as profiled and compared with other parasite life cycle stages.
13 the protein is essential for growth in both life cycle stages.
14 g of this most elusive of the parasites many life cycle stages.
15 essential in both bloodstream and procyclic life cycle stages.
16 ion phenotypes at specific developmental and life cycle stages.
17 anscribed to an equal extent in all parasite life cycle stages.
18 c premises of different parasite species and life cycle stages.
19 g glucose transporter mRNA levels in the two life cycle stages.
20 RNAs are expressed at similar levels in both life cycle stages.
21 istinct functional consequences in different life cycle stages.
22 ciding with the most energetically demanding life cycle stages.
23 ducible APX is essential for survival of all life cycle stages.
24 n specific hosts or tissues, or at different life cycle stages.
25 ns that can be targeted in multiple parasite life cycle stages.
26 e evaluation of F(1) hybrid fitness in early life cycle stages.
27 ythrocytic, and sexual erythrocytic parasite life cycle stages.
28 nd stack recycling lowers impacts across all life cycle stages.
29 ESB and is expressed only in VSG-expressing life cycle stages.
30 complex crystal formation in coccolithophore life cycle stages.
31 ol enrichment and cell metabolism in the two life cycle stages.
32 release nanosilver (impact) during multiple life cycle stages.
33 map with base-level resolution at different life cycle stages.
34 editosome proteins are adjusted between the life cycle stages.
35 , exposure routes and pathways and for other life cycle stages.
36 d that the 20S editosomes differ between the life cycle stages.
37 y set by processes operating at the earliest life cycle stages.
38 of PAT inhibitors against multiple parasite life cycle stages.
39 t the in vivo functions of PAT in Plasmodium life cycle stages.
40 upon the growth environment in two different life cycle stages.
41 cluster, with several expressed at multiple life cycle stages.
42 nalyses, and protein characterization of its life-cycle stages.
43 cruzi genome were identified across the four life-cycle stages.
44 f merozoites, one of three motile Plasmodium life-cycle stages.
45 evelop probabilities of flaring at different life-cycle stages.
46 transcriptomes to determine gene use across life-cycle stages.
47 nteractions (PPIs) to study proteins in mRNA life-cycle stages.
48 ty against the liver and gametocyte parasite life-cycle stages.
49 on of antigens expressed in pre-erythrocytic life-cycle stages.
50 timalarial drug discovery targeting multiple life-cycle stages.
51 is indispensable during the sexual mosquito life-cycle stages.
52 , there were significant differences between life-cycle stages.
53 ere differentially expressed between the two life-cycle stages.
54 roliferative cells differentiate to the next life cycle stage?
56 shows activity against liver and gametocyte life cycle stages and demonstrates in vivo efficacy in P
58 d and interact with each other in both major life cycle stages and show similar distributions at Pol
60 erstanding of the preerythrocytic Plasmodium life cycle stages and the development of preerythrocytic
61 kinase, PK50, is expressed in proliferative life cycle stages and was shown to complement a yeast ND
62 d emissions mitigation strategies at varying life-cycle stages and can be adapted to other materials
63 housekeeping genes (expressed during several life-cycle stages) and mating-related genes, while the s
65 e impact of these changes on motility across life cycle stages, and how such changes might serve to f
66 ammalian host) and procyclic (insect vector) life cycle stages, and KHARON is thus critical for paras
67 loodstream form (BF) and procyclic form (PF) life cycle stages, and this correlates with the differen
69 the activities of parasites in these various life-cycle stages are likely to be reflected in changes
71 10% for totals and up to 25% for individual life cycle stages, as standard in carbon footprinting an
72 tion of resting spores, a heavily silicified life cycle stage associated with carbon export due to ra
73 reactivity against Pf proteins based on the life cycle stage at which proteins are expressed, subcel
74 mbic crystals can be produced by the haploid life cycle stage but are thought to be formed extracellu
77 tudy of these protein-vRNA interactions in a life cycle stage-dependent manner, as well as providing
78 e mechanisms of flagellum length regulation, life cycle stage differentiation and trypanosomatid divi
79 ent or exflagellation, suggesting that these life cycle stages do not utilize host-derived glycerol a
80 on haploid genotypes during less conspicuous life cycle stages, e.g., competition among sperm/pollen
81 size, shape, and form yet transition through life cycle stages, each having a distinct morphology.
82 e eggs, because exposure of the host to this life-cycle stage elicits a polarized Th2 response to egg
83 eal-time qPCR has confirmed the differential life-cycle stage expression of a set of selected lincRNA
85 emerging evidence suggests that the parasite life cycle stage impacts the modulation of apoptosis and
86 diversity of mRNA molecules across different life-cycle stages impacts their functionality but has re
87 d culture conditions and was lethal for this life cycle stage in the presence of hydrogen peroxide.
89 diversification is disproportionate between life cycle stages in mushroom-forming fungi, so that the
90 nd differences might exist between different life cycle stages in relation to the regulation of cell
93 se results highlight the importance of early life cycle stages in tropical forest community dynamics.
94 for the identification of distinct parasite life-cycle stages in the tsetse, trypanosome differentia
95 from subcellular to system levels across all life cycle stages, in intact animals and regenerating bo
96 rom those of eggs confirm that each of these life cycle stages induces a unique pattern of cytokine e
98 pvs25 that is expressed in gametocytes, the life cycle stage infectious to mosquitoes, were first de
99 observation that differentiation of parasite life cycle stages involves structural and functional reo
100 phological reorganization into the preceding life cycle stage is thought to be restricted to a few sp
101 parameters determine the timing of seasonal life cycle stages is constrained by limited long-term da
104 ism for crystal morphogenesis in the diploid life cycle stage led to the emergence of the intricately
105 hat promote or limit regeneration in certain life cycle stages may pinpoint the most critical factors
106 ghly expressed cysteine protease during both life cycle stages measured, with a dramatic expression i
107 lopment of antiretrovirals that act on virus life cycle stages not targeted by drugs currently in use
108 o identify antiretrovirals that act on viral life cycle stages not targeted by drugs in use, such as
109 ce a chitin-rich cell wall during any of the life cycle stages observed and therefore do not conform
110 se regulator CtrA are not expressed during a life cycle stage of Caulobacter crescentus when the regu
111 aria infection is caused by sporozoites, the life cycle stage of Plasmodium that is transmitted by fe
114 sumption for supply chain production at each life cycle stage of the well was estimated using the eco
115 the direction of the complex depends on the life cycle stage of this digenetic parasite: in the midg
118 importance of ASL to purine salvage by both life cycle stages of L. donovani and authenticate ASL as
119 is established that AAH is expressed in both life cycle stages of L. donovani, whereas subcellular fr
120 nd salvage to pyrimidine homeostasis in both life cycle stages of Leishmania donovani, individual mut
124 tal and adult mice to the trophic and cystic life cycle stages of Pneumocystis murina The adult and n
126 on and have differential effects between the life cycle stages of T. brucei that differentially edit
128 its spectrum of activities against multiple life cycle stages of the human malaria parasite Plasmodi
129 efects in surface glycoproteins in different life cycle stages of the parasite highlights the essenti
130 we studied endogenous TcHTE in the different life cycle stages of the parasite to gain insight into i
131 transcripts and protein are expressed in all life cycle stages of the parasite within the vertebrate
132 i HDAC8 (SmHDAC8) is highly expressed in all life cycle stages of the parasite, and selective inhibit
137 oteins (GPI-APs) play essential roles in all life cycle stages of the parasites, including developmen
138 are 5' modification-independent, across five life cycle stages of the rodent parasite Strongyloides v
140 e no known functions or homologues, and most life cycle stages of this haploid eukaryotic parasite ar
144 Here, I analyse the swimming of the insect life cycle stages of two human parasites; Trypanosoma br
146 of highly potent compounds against the blood life-cycle stage of the human malaria parasite Plasmodiu
147 The high density of GPI structures at all life-cycle stages of African trypanosomes and Leishmania
149 be facilitated by intervention at different life-cycle stages of the parasite, including the obligat
151 um of antimalarial activity against multiple life-cycle stages of the Plasmodium parasite, with good
154 a company had reported a PCF's breakdown to life cycle stages or only the total emissions (10.9% ave
155 ir relationship with their host at different life-cycle stages or in response to changing environment
156 We wondered whether the insect and mammalian life cycle stages possess chemically different lipid raf
157 e differentially phosphorylated in different life-cycle stages, possibly indicative for unique forms
164 ories of parameters were assessed, including life cycle stages, reproductive traits, and external mor
165 hierarchical regulatory model in tissue and life cycle stage-specific silencing by NuRD complexes.
167 Additionally, the mechanism of action and life-cycle stage specificity of the four antimalarials i
168 to appropriately differentiate into distinct life cycle stages, such as the transition from its repli
169 tes between bloodstream-form and insect-form life cycle stages that are adapted to survive in the mam
170 A expression libraries were constructed from life cycle stages that are critical for establishment of
171 rall, we expand our view of the sex-specific life cycle stages that can drive sex chromosome evolutio
172 constitutively expressed at 37 degrees C in life cycle stages that live in the mammalian host (micro
174 gulation has focussed on comparisons between life-cycle stages that exist in the blood of mammalian h
176 invade hepatocytes and develop into the next life cycle stage, the exoerythrocytic, or liver, stage.
177 ll cycle of the Trypanosoma brucei procyclic life cycle stage, three subcycles emerge that control th
178 y contributing to the formation of different life-cycle stages, tissue differentiation and metabolism
179 ng and exon skipping were active in multiple life cycle stages to change exon structure in the deduce
180 of studying the trypanosomatid intracellular life cycle stages to gain a better understanding of the
182 ess to the surface plasma membrane in insect life-cycle-stage trypanosomes but, remarkably, AQP2 was
183 i, a flagellated protozoan parasite, between life cycle stages typically occurs through an asymmetric
184 were evaluated throughout the cradle-to-gate life-cycle stage using a life cycle assessment-material
185 abilities with EHS risks across nanomaterial life-cycle stages using empirical knowledge in the field
187 n G antibodies to PfEMP-1, expressed on both life cycle stages, were measured in residents from an ar
188 tial abatement measures throughout different life cycle stages while focusing on the role of banked f
189 ability to identify CO(2)e emission hot-spot life-cycle stages will be instrumental in identifying pa
190 te Leishmania during the transformation of a life cycle stage with a 9+2 axoneme (the promastigote) t
191 ome with unknown functions, to specific mRNA life-cycle stages, with nearly half associated with mult