ライフサイエンスコーパス: human bite

1 d from populations in the Middle East, where human-biting and other adaptations to human environments

2 bite humans but are more important than the human biting "bridge" vector, Ixodes scapularis, in main

3 and rodents; occasionally spilling over into humans bitten by infectious fleas.

4 ion of diverse pathogens by the aggressively human-biting deer tick may have a unique impact on publi

5 to food-processing technologies modified the human bite from an edge-to-edge configuration to one tha

6 A total of 250 adults of this human-biting, generalist tick were collected from contig

7 xt of two previously observed shifts towards human biting in Ae. aegypti differ; climate was likely t

8 r mosquito evolution, causing a shift toward human-biting in many large cities by 2050.

9 Our findings suggest that human-biting in this important disease vector originally

10 arbon dioxide (CO(2)), behaviorally activate human-biting mosquitoes to search for a host, the mechan

11 rgin of 50%, vector density indicated by the human biting rate (bites/person/night) was non-inferior

12 ations between seroprevalence with Anopheles human biting rate (HBR) and malaria transmission measure

13 tomology surveys to estimate household-level human biting rate (HBR), expressed as the number of fema

14 We propose updated definitions for the human biting rate and entomological inoculation rates.

15 The MN-MS model is used to determine how human biting rate of mosquitoes, known to be able to tra

16 ensities, which are directly proportional to human biting rates (the number of bites, per person, per

17 nd entomological indicators of transmission (human biting rates and entomological inoculation rates [

18 ission intensities, computed as a product of human biting rates and prevalence of Plasmodium sporozoi

19 ongitudinal entomological surveys of outdoor human biting rates by mosquitoes and experimental measur

20 We argue that human biting rates convey more use- ful information for

21 o 37.0) times higher human-behavior adjusted human biting rates due to An. funestus.

22 under steady state conditions, including the human biting rates, parasite dispersal, the "vectorial c

23 l can be compared using sporozoite rates and human biting rates, which are commonly measured.

24 humans, yielding intrinsic heterogeneity in human biting risk.

25 Phlebotomus papatasi saliva, the only other human-biting sand fly in the ISC.

26 In human bite studies, one or two IC haplotypes compromised

27 The predominant human-biting tick throughout the southeastern United Sta

28 The primary human-biting ticks in this region are Ixodes scapularis,