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1 discovered more than 340 yr ago in the human louse.
2  egg production and reproduction in the book louse.
3 be greatest in the cooler temperature of the louse.
4  of cement glands in the adult female salmon louse.
5 poE is significantly upregulated at the body louse (28 degrees C) versus the human host (37 degrees C
6 ere, we present genome sequences of the body louse and its primary bacterial endosymbiont Candidatus
7  lysine 27 on histone H3 (H3K27) in the gene louses and through regulation of specific miRNAs.
8                     Bartonella quintana is a louse-borne bacterium that remains a neglected cause of
9  Relapsing fever (RF) is caused by tick- and louse-borne Borrelia spp., is characterized by recurrent
10 ission, it is possible that we are missing a louse-borne branch of the alphaviruses.
11 tralis, R. rickettsii, and R. akari with the louse-borne R. prowazekii.
12 tted pathogen B. miyamotoi, and the agent of louse-borne relapsing fever (B. recurrentis).
13 odies will allow serological confirmation of louse-borne relapsing fever and determination of disease
14  The hallmark of disease caused by tick- and louse-borne relapsing fever due to Borrelia infection is
15                                        Human louse-borne relapsing fever occurs in sporadic outbreaks
16 serum samples obtained from 42 patients with louse-borne relapsing fever were tested with an indirect
17 t Borrelia recurrentis genomes, the agent of louse-borne relapsing fever, dating from 2300 to 600 yea
18 ponent of Borrelia recurrentis, the agent of louse-borne relapsing fever.
19 thogens have transitioned from tick-borne to louse-borne transmission, which often involves genome re
20                                              Louse-borne trench fever caused by Bartonella quintana i
21  commissions identified that the disease was louse-borne.
22 erium, Tenacibaculum, Pseudomonas) with high louse burdens.
23                                      The sea louse Caligus rogercresseyi has become one of the main c
24 enate, an essential vitamin deficient in the louse diet.
25                 The genome of the obligatory louse endosymbiont Candidatus Riesia pediculicola encode
26  (hbpC and hbpB) predominates in a simulated louse environment (high heme), and subgroup II (hbpA, hb
27 tana transcriptional program within the body louse environment.
28 is study, we report that the Atlantic salmon louse expresses three full-length MVP paralogues (LsMVP1
29 h concern, known to be transmitted from body louse feces via scratching.
30                       Saliva injected during louse feeding induces pruritis and local inflammation in
31 ize matters, we measured three components of louse fitness: attachment, feeding, and escape from host
32                                        Avian louse flies (Hippoboscidae: Ornithomyinae) are blood-fee
33 nsistent with previous work, we propose that louse flies could serve as valuable sentinels for monito
34        Our findings suggest that the role of louse flies in transmitting the investigated bacterial p
35  the first report of these bacteria in avian louse flies.
36 n the intention-to-treat population who were louse-free 1 day after treatment (day 2) and remained so
37 than patients receiving vehicle control were louse-free on day 2 (94.9% vs. 31.3%), day 8 (85.2% vs.
38 Compared with other insect genomes, the body louse genome contains significantly fewer genes associat
39                               Thus, the body louse genome project offers unique information and tools
40 ents of the Pediculus humanus corporis (body louse) gut and the human vasculature.
41                                     The body louse has the smallest known insect genome, spanning 108
42 of putative accessory salivary glands in the louse head.
43  bacterial community associated with the sea louse, however, it is unknown if these microorganisms sh
44                                         Head-louse infestation remains a public health problem.
45 matic review first identified trials on head-louse infestation; 49 were selected and their methodolog
46 omplicates the public health problem of head-louse infestations and drives the need for continuing de
47 ive than vehicle control in eliminating head-louse infestations at 1, 7, and 14 days after treatment.
48 e efficient than placebo at eliminating body louse infestations by day 14; however, this difference w
49                                        Human louse is an ectoparasite that causes pediculosis and tra
50                               The human body louse, its primary endosymbiont, and the bacterial patho
51 Atlantic salmon (Salmo salar) against salmon louse (Lepeophtheirus salmonis) infestations.
52 n hbpC transcript levels in response to the "louse-like" temperature of 30 degrees C.
53 Furthermore, when this strain is grown at a "louse-like" temperature, an inversion of the transcript
54 nscription of irr (a >5-fold decrease) at a "louse-like" temperature, suggesting that Irr may functio
55 rcular mitochondrial chromosomes of the body louse may be linked to the loss of the gene encoding the
56 louse Pediculus humanus capitis and the body louse P. h. humanus.
57 s gambiae and Culex quinquefasciatus, a body louse Pediculus humanus and a tick species Ixodes scapul
58 ction of the mycetomic bacterium of the head louse Pediculus humanus capitis and the body louse P. h.
59                                        Human louse Pediculus humanus is a cosmopolitan obligatory blo
60 s an obligatory parasite of humans, the body louse (Pediculus humanus humanus) is an important vector
61        Human ectoparasites, such as the body louse (Pediculus humanus humanus), have largely been dis
62 uefasciatus), tick (Ixodes scapularis), body louse (Pediculus humanus), kissing bug (Rhodnius prolixu
63 ganisms, and another compared the human body louse, Pediculus humanus humanus, against itself and sel
64 d Pediculus humanus corporis (Ph; human body louse) PINK1 resolves an N-terminal helix, revealing the
65              The rounded shape optimizes the louse's ability to withstand external pressure by redist
66                                     The body louse's high level of susceptibility to infection by gra
67 tracted RNA and protein from two of the body louse's morphologically distinct sets of salivary glands
68 rt body deformations, thereby increasing the louse's resilience in the deep sea environment.
69                             Analysis of body louse salivary gene products and proteins revealed that
70 ss the potential physiological importance of louse salivary proteins, and consider possible explanati
71 proteomic characterization of the human body louse sialome, discuss the potential physiological impor
72 he complex nature of GABA receptors in human louse that could help in understanding the resistance pa
73 mimetabolous insects, the genome of the body louse thus provides a reference for studies of holometab
74 d optimal designs to standardize future head-louse treatment trials, thereby obtaining valid conclusi
75 o stressors that are encountered in the body louse vector environment, a decreased temperature and an
76  has adapted to both the human host and body louse vector niches, producing persistent infection with
77 ted human bloodstream to the hemin-rich body louse vector.
78 e transition from the human host to the body louse vector.
79  the pathogen in the human host and the body louse vector; e.g., we observed a dramatic (>100-fold) i