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1 m against wild-caught, insecticide-resistant anophelines.
2 an primate models and highly conserved among anophelines.
3 ng anophelines and 57.74% for outdoor biting anophelines.
4                          The midgut-specific anopheline alanyl aminopeptidase N (AnAPN1) is highly co
5 ion of 68.27% was recorded for indoor biting anophelines and 57.74% for outdoor biting anophelines.
6 igm that malaria infection is pathogenic for anophelines and, instead suggests there are biological a
7 rives designed to target haplolethal loci in anophelines and, potentially, other metazoans.
8 e binding specificity of P47Rec from distant anophelines (Anopheles gambiae, Anopheles dirus, and Ano
9 fects of forest cover on larval habitats and anopheline assemblages in different seasons.
10 iables) effects on the composition of larval anopheline assemblages in the rainy season.
11 rainy season, with positive consequences for anopheline assemblages.
12 e root exudate allelochemicals could play on anopheline bionomics, with potential implications in mal
13  associated with a reduction of 68% of adult anopheline biting density and of 79% of the entomologica
14 oral consistency of spatial distribution and anopheline community composition presents an opportunity
15 riendly approaches to reduce malaria through anopheline control.
16                                          The anopheline density collected using CDC light traps was u
17 th derived characters that have coevolved in anophelines, driving the adaptation of a female 20E-inte
18 lostridium bifermentans strains collected in anopheline endemic areas on two continents indicates it
19                             This dynamism of anopheline genes and genomes may contribute to their fle
20  and gene models to 15 other newly assembled Anopheline genomes led to the discovery of a large numbe
21 secticide resistance in malaria-transmitting Anophelines has become an impediment and has created an
22 wever, natural Wolbachia infections in field anophelines have never been reported.
23 n volatiles that may play a critical role in anopheline host selection.
24 logical crosstalk" between the mammalian and anopheline hosts for Plasmodium functions to control par
25            The incidence density of infected anophelines in sites where the original forest cover dec
26 clusters we caught an average of 1.14 female anophelines inside hotspots and 0.47 in evaluation zones
27 clusters we caught an average of 0.90 female anophelines inside hotspots and 0.50 in evaluation zones
28 mosquito Anopheles gambiae, as well as other anophelines, is among the most effective methods to cont
29 tive at reducing the abundance of late-stage anopheline larvae (pooled reduction = - 35%), but not ov
30 hree CTSs showed an overall 82% reduction in anopheline larvae compared to no fish.
31                             DNA barcoding of anopheline larvae sampled in the 2019 wet season reveale
32 cal inoculation rate, breeding habitats with anopheline larvae, and larval density.
33  primary vectors, but represented only 2% of anopheline larvae.
34 ween environmental and spatial variables and anopheline larval presence.
35 reassignments were suggested for Neotropical anopheline malaria vectors, elevating four monophyletic
36 Nigeria studying the taxonomy and biology of anopheline malaria vectors.
37      The density ratio adjusted for baseline Anopheline mosquito density was 0.77 (95% CI: 0.45-1.29)
38 e Plasmodium parasites successfully invading Anopheline mosquito midguts following a blood meal.
39                                       Female anopheline mosquito reproduction is intimately linked to
40  spatial grid subdivided the study area into anopheline mosquito sampling units where mosquitoes were
41                                              Anopheline mosquito species are obligatory vectors for h
42 d Pfs47 suggest that adaptation to different Anopheline mosquito species drives Pv47 diversity by sel
43 ctor control, we sequenced the genomes of 16 anopheline mosquito species from diverse locations spann
44 nsmitted worldwide by more than 70 different anopheline mosquito species.
45 ection offers avenues for onward research in anopheline mosquito symbioses.
46 e to females of Anopheles stephensi, a major anopheline mosquito vector of human malaria in Asia.
47 The recent publication of the genome of this anopheline mosquito will have a profound impact on inqui
48 their injection into the skin by an infected anopheline mosquito.
49               In culicine (Culex, Aedes) and anopheline mosquitoes (Anopheles), embryo polarity rests
50                         Pyrethroid resistant Anopheline mosquitoes are now ubiquitous in Africa, thou
51                                              Anopheline mosquitoes are the obligatory vectors of Plas
52                                              Anopheline mosquitoes are the only vectors of human mala
53                                              Anopheline mosquitoes are the sole vectors for the Plasm
54                                              Anopheline mosquitoes are vectors of human malaria but a
55 tion and the presence of W. bancrofti DNA in anopheline mosquitoes before and after the introduction
56                              More than 2,400 anopheline mosquitoes belonging to 18 species were colle
57 od, the rate of detection of W. bancrofti in anopheline mosquitoes decreased from 1.8% to 0.4% (P=0.0
58                We have previously shown that anopheline mosquitoes expressing the SM1 peptide in the
59  studies and facilitation of mass storage of anopheline mosquitoes for release programs.
60 go sexual differentiation and development in anopheline mosquitoes for transmission to occur.
61                             To do so, female anopheline mosquitoes have to be fed on blood from P. vi
62 e of volunteers by the bites of membrane-fed anopheline mosquitoes infected with Plasmodium falciparu
63           Malaria is initiated when infected anopheline mosquitoes inoculate sporozoites as they prob
64                       Plasmodium invasion of anopheline mosquitoes is an obligatory step for malaria
65                            Outdoor biting by anopheline mosquitoes is one of the contributors to resi
66         Village-specific rates of bites from anopheline mosquitoes ranged from 6.4 to 61.3 bites per
67                                              Anopheline mosquitoes rely on their highly sensitive che
68 nopheles coluzzii, were identified among 235 anopheline mosquitoes that were captured during 617 noct
69 Rapid spread of insecticide resistance among anopheline mosquitoes threatens malaria elimination effo
70 rasite--'Laveran's germ'--was transmitted by anopheline mosquitoes to human beings to cause malaria.
71  as hypnozoites after transmission by female anopheline mosquitoes to human hosts.
72 r W. bancrofti elimination in areas in which anopheline mosquitoes transmit the parasite.
73                                              Anopheline mosquitoes were sampled from 80 sites to inve
74 laria parasite transmitted by African sylvan anopheline mosquitoes, adapted to humans.
75 development of pyrethroid resistance in some anopheline mosquitoes, and the emergence of artemisinin
76 uced into the germ line of both culicine and anopheline mosquitoes, and these transgenes can be expre
77 g membrane feeds of CTRP disruptant lines to Anopheline mosquitoes, despite the development of mature
78 tion of medically important insects, such as anopheline mosquitoes, is the single most important impe
79  of conservation in sequence and function in anopheline mosquitoes, makes fle an excellent target for
80 tages that persist within the insect vector, anopheline mosquitoes, or target mosquito midgut protein
81 opathogenic fungi can efficiently kill adult anopheline mosquitoes, the females of which are the obli
82           Such blood-feeding insects include anopheline mosquitoes, which transmit malaria-causing Pl
83 pathogenic sexual gametocytes infectious for anopheline mosquitoes.
84 Plasmodium parasites that are transmitted by anopheline mosquitoes.
85 ed protein and has orthologs in culicine and anopheline mosquitoes.
86 bodies may block malaria transmission to all anopheline mosquitoes.
87  this family of salivary anticoagulants from anopheline mosquitoes.
88 tablish inherited infections of Wolbachia in anopheline mosquitoes.
89 P008138 is a unique gene that only exists in Anopheline mosquitoes.
90  can contemplate the evolutionary history of anopheline mosquitoes.
91 laria is known to be transmitted strictly by anopheline mosquitoes.
92 ," which differs in evolutionarily divergent anopheline mosquitoes.
93 ptations relevant to malaria transmission in anopheline mosquitoes.
94 to the skin of a vertebrate host by infected anopheline mosquitoes.
95  of Plasmodium that is transmitted by female anopheline mosquitoes.
96 ce the efficiency of malaria transmission by anopheline mosquitoes.
97 perinfection from the bites of many infected anopheline mosquitoes.
98 sulting in the identification of over 20,000 Anopheline mosquitoes.
99 ial-like neurotoxin that selectively targets anopheline mosquitoes.
100 esulted in the identification of over 60,000 Anopheline mosquitoes.
101  Plasmodium protozoa that are transmitted by anopheline mosquitoes.
102 e-vector interactions and for studies on how anophelines of brackish water deal with the high fluctua
103 63-Glu-82 region (absent in orthologues from anophelines of the New World species A. albimanus and An
104 a multidimensional functionality of Ir76b in anopheline olfactory and gustatory pathways that directl
105 evel is helping to address questions such as anopheline phylogenetics and biogeography, the nature of
106                                      Natural anopheline populations exhibit much variation in ability
107  flow, and the propagation of gene drives in Anopheline populations.
108                          We report the first anopheline proteasome knockouts, and identify ribosome m
109 he most medically important yet understudied anopheline radiations, the Afrotropical Anopheles funest
110 inearity suggests that locating genes in one anopheline species based on gene order in another may be
111 ia vector in Asia and it is becoming a model Anopheline species for physiological and genetics studie
112 nd Plasmodium vivax across distantly related anopheline species in countries to which malaria is ende
113 The availability of genome sequences from 16 anopheline species provides unprecedented opportunities
114                                              Anopheline species richness and diversity decreased from
115              No impact on the composition of anopheline species was recorded.
116 g different Pfs47 haplotypes and these three anopheline species.
117 tical for Plasmodium adaptation to different anopheline species.
118 e sexes likely to have shaped the ability of anophelines to transmit malaria.
119 f) between the vertebrate human host and the anopheline vector results in differential expression of
120 y linked to the ecology and evolution of its anopheline vector.
121 on status affects energetic reserves of wild anopheline vectors and (iii) nutrient content and olfact
122                 Although behavior changes in anopheline vectors have been reported over the last deca
123 , the cultured germline tissues of two major Anopheline vectors of Plasmodium parasites are susceptib
124 le aquatic breeding habitats for P. knowlesi anopheline vectors.
125           A total of 3217 culicines and 1017 anophelines were collected, of which 388 were Anopheles
126 n size and gene content to other Neotropical anophelines, with 162 Mb and 12,446 protein-coding genes
127                                    While the Anopheline Y had previously been implicated in male mati

 
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