ライフサイエンスコーパス: anopheline

1 m against wild-caught, insecticide-resistant anophelines.

2 an primate models and highly conserved among anophelines.

3 The midgut-specific anopheline alanyl aminopeptidase N (AnAPN1) is highly co

4 th derived characters that have coevolved in anophelines, driving the adaptation of a female 20E-inte

5 This dynamism of anopheline genes and genomes may contribute to their fle

6 and gene models to 15 other newly assembled Anopheline genomes led to the discovery of a large numbe

7 wever, natural Wolbachia infections in field anophelines have never been reported.

8 n volatiles that may play a critical role in anopheline host selection.

9 logical crosstalk" between the mammalian and anopheline hosts for Plasmodium functions to control par

10 clusters we caught an average of 1.14 female anophelines inside hotspots and 0.47 in evaluation zones

11 clusters we caught an average of 0.90 female anophelines inside hotspots and 0.50 in evaluation zones

12 Nigeria studying the taxonomy and biology of anopheline malaria vectors.

13 e Plasmodium parasites successfully invading Anopheline mosquito midguts following a blood meal.

14 Anopheline mosquito species are obligatory vectors for h

15 ctor control, we sequenced the genomes of 16 anopheline mosquito species from diverse locations spann

16 nsmitted worldwide by more than 70 different anopheline mosquito species.

17 e to females of Anopheles stephensi, a major anopheline mosquito vector of human malaria in Asia.

18 The recent publication of the genome of this anopheline mosquito will have a profound impact on inqui

19 their injection into the skin by an infected anopheline mosquito.

20 Pyrethroid resistant Anopheline mosquitoes are now ubiquitous in Africa, thou

21 Anopheline mosquitoes are the obligatory vectors of Plas

22 Anopheline mosquitoes are the only vectors of human mala

23 Anopheline mosquitoes are vectors of human malaria but a

24 tion and the presence of W. bancrofti DNA in anopheline mosquitoes before and after the introduction

25 More than 2,400 anopheline mosquitoes belonging to 18 species were colle

26 od, the rate of detection of W. bancrofti in anopheline mosquitoes decreased from 1.8% to 0.4% (P=0.0

27 We have previously shown that anopheline mosquitoes expressing the SM1 peptide in the

28 go sexual differentiation and development in anopheline mosquitoes for transmission to occur.

29 e of volunteers by the bites of membrane-fed anopheline mosquitoes infected with Plasmodium falciparu

30 Plasmodium invasion of anopheline mosquitoes is an obligatory step for malaria

31 Village-specific rates of bites from anopheline mosquitoes ranged from 6.4 to 61.3 bites per

32 rasite--'Laveran's germ'--was transmitted by anopheline mosquitoes to human beings to cause malaria.

33 r W. bancrofti elimination in areas in which anopheline mosquitoes transmit the parasite.

34 development of pyrethroid resistance in some anopheline mosquitoes, and the emergence of artemisinin

35 uced into the germ line of both culicine and anopheline mosquitoes, and these transgenes can be expre

36 g membrane feeds of CTRP disruptant lines to Anopheline mosquitoes, despite the development of mature

37 tion of medically important insects, such as anopheline mosquitoes, is the single most important impe

38 tages that persist within the insect vector, anopheline mosquitoes, or target mosquito midgut protein

39 opathogenic fungi can efficiently kill adult anopheline mosquitoes, the females of which are the obli

40 bodies may block malaria transmission to all anopheline mosquitoes.

41 tablish inherited infections of Wolbachia in anopheline mosquitoes.

42 can contemplate the evolutionary history of anopheline mosquitoes.

43 laria is known to be transmitted strictly by anopheline mosquitoes.

44 ptations relevant to malaria transmission in anopheline mosquitoes.

45 to the skin of a vertebrate host by infected anopheline mosquitoes.

46 of Plasmodium that is transmitted by female anopheline mosquitoes.

47 ce the efficiency of malaria transmission by anopheline mosquitoes.

48 perinfection from the bites of many infected anopheline mosquitoes.

49 this family of salivary anticoagulants from anopheline mosquitoes.

50 63-Glu-82 region (absent in orthologues from anophelines of the New World species A. albimanus and An

51 evel is helping to address questions such as anopheline phylogenetics and biogeography, the nature of

52 Natural anopheline populations exhibit much variation in ability

53 inearity suggests that locating genes in one anopheline species based on gene order in another may be

54 ia vector in Asia and it is becoming a model Anopheline species for physiological and genetics studie

55 nd Plasmodium vivax across distantly related anopheline species in countries to which malaria is ende

56 The availability of genome sequences from 16 anopheline species provides unprecedented opportunities

57 e sexes likely to have shaped the ability of anophelines to transmit malaria.

58 Although behavior changes in anopheline vectors have been reported over the last deca

59 , the cultured germline tissues of two major Anopheline vectors of Plasmodium parasites are susceptib

60 A total of 3217 culicines and 1017 anophelines were collected, of which 388 were Anopheles

61 While the Anopheline Y had previously been implicated in male mati