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1 surgence in sleeping sickness (human African trypanosomiasis).
2 yma is a major pathogenetic event in African trypanosomiasis.
3 diseases such as malaria, toxoplasmosis, and trypanosomiasis.
4 and new developments in vaccination against trypanosomiasis.
5 nfections such as tuberculosis, malaria, and trypanosomiasis.
6 omising therapeutic target for human African trypanosomiasis.
7 tential novel drug targets for human African trypanosomiasis.
8 PTR1 may be a drug target for human African trypanosomiasis.
9 ment of new treatments against human African trypanosomiasis.
10 t and prevention of human and animal African trypanosomiasis.
11 ly reproducible mouse model of human African trypanosomiasis.
12 get for new compounds to treat human African trypanosomiasis.
13 infected animals in the acute mouse model of trypanosomiasis.
14 animals in the STIB900 acute mouse model of trypanosomiasis.
15 animals in the acute mouse model of African trypanosomiasis.
16 ion could have therapeutic potential against trypanosomiasis.
17 is definitively linked to host resistance in trypanosomiasis.
18 variant cross-specific immunity for African trypanosomiasis.
19 tory and regulatory mediators during African trypanosomiasis.
20 ng phase III clinical trials against African trypanosomiasis.
21 ibitors of therapeutic value against African trypanosomiasis.
22 mportant chemotherapeutic target for African trypanosomiasis.
23 ises the use of antifolates for treatment of trypanosomiasis.
24 imulation of the host immune response during trypanosomiasis.
25 to control tsetse flies and, hence, African trypanosomiasis.
26 mals in the STIB900 animal model for African trypanosomiasis.
27 developed for the treatment of human African trypanosomiasis.
28 es (PMCAs) of T. brucei, an agent of African trypanosomiasis.
29 r developing new serodiagnostics for African trypanosomiasis.
30 robial peptides for the treatment of African trypanosomiasis.
31 omes overcome host resistance during African trypanosomiasis.
32 fforts to develop effective vaccines against trypanosomiasis.
33 some in vivo activity in a model of African trypanosomiasis.
34 nisms of tropical diseases leishmaniasis and trypanosomiasis.
35 ic Th-cell responses in experimental African trypanosomiasis.
36 d compound for treatment of cancer, HIV, and trypanosomiasis.
37 pment of specific drugs and vaccines against trypanosomiasis.
38 chemotherapeutic target for the treatment of trypanosomiasis.
39 the parasites that cause malaria and African trypanosomiasis.
40 or T.b. gambiense, which cause human African trypanosomiasis.
41 inidae), vectors of Human and Animal African trypanosomiasis.
42 ackbone of the pharmacopoeia against African trypanosomiasis.
43 compounds for the treatment of human African trypanosomiasis.
44 peutic target for treatment of human African trypanosomiasis.
45 in the STIB900 mouse model for human African trypanosomiasis.
46 e blood meal of tsetse flies, the vector for trypanosomiasis.
47 ns as potential therapeutic drug targets for trypanosomiasis.
48 ucei is the causative agent of human African trypanosomiasis.
49 development of drugs to treat human African trypanosomiasis.
50 t of a combination therapy for human African trypanosomiasis.
51 oan responsible for human and animal African trypanosomiasis.
52 osoma brucei, the causative agent of African trypanosomiasis.
53 ead for development of drugs against African trypanosomiasis.
54 al target for the treatment of human African trypanosomiasis.
55 brucei, the causative agent of human African trypanosomiasis.
56 brucei, the causative agent of human African trypanosomiasis.
57 ed, with a particular focus on human African trypanosomiasis.
58 ed target for the treatment of human African trypanosomiasis.
59 osoma brucei is the causing agent of African trypanosomiasis.
61 the efficacy of treatment for human African trypanosomiasis, accurate tests that can discriminate re
62 brucei, the causative agent of human African trypanosomiasis, affects tens of thousands of sub-Sahara
66 serum samples from 85 patients with African trypanosomiasis and 146 control patients who had other p
69 to diseases such as malaria, leishmaniasis, trypanosomiasis and dysentery that are responsible for m
70 s TbCLK1 as a therapeutic target for African trypanosomiasis and establishes a new chemoproteomic too
71 rypanosoma brucei causes fatal human African trypanosomiasis and evades the host immune response by r
77 ithin the GlaxoSmithKline HAT (Human African Trypanosomiasis) and Chagas chemical boxes, two collecti
78 ABQ) library against the causative agents of trypanosomiasis, and cutaneous leishmaniasis, identifyin
79 causative agents of malaria, toxoplasmosis, trypanosomiasis, and leishmaniasis, contain a minimal ER
80 ucei, the protozoan parasite causing African trypanosomiasis, and the tsetse (Glossina) vector remain
82 All four main drugs used for human African trypanosomiasis are toxic, and melarsoprol, the only dru
83 ypanosoma brucei, which causes human African trypanosomiasis, as well as the livestock disease, nagan
84 nt option for reducing the impact of African trypanosomiasis but, although many effective methods hav
85 as new therapeutic targets for human African trypanosomiasis by both genetic and pharmacological mean
86 anti-inflammatory therapies in Human African trypanosomiasis by modulating the NK1 receptor as well a
87 lected parasitic diseases, including African trypanosomiasis caused by the protozoan, Trypanosoma bru
88 n, particularly in the case of Human African Trypanosomiasis caused by Trypanosoma brucei gambiense.
89 mes in two types: East African human African trypanosomiasis caused by Trypanosoma brucei rhodesiense
92 African sleeping sickness or human African trypanosomiasis, caused by Trypanosoma brucei spp., is r
93 soma cruzi , the etiologic agent of American trypanosomiasis (Chagas disease), exhibiting IC(50) valu
94 ishmania spp., which in humans cause African trypanosomiasis, Chagas disease, and leishmaniasis, resp
95 parum, the causative agents of human African trypanosomiasis, Chagas disease, leishmaniasis, and mala
96 ping world, including malaria, human African trypanosomiasis, Chagas disease, leishmaniasis, filarias
98 osoma brucei, the causative agent of African trypanosomiasis, contains a soluble, vacuolar pyrophosph
99 ber of reported cases, patients with African trypanosomiasis continue to present major challenges to
100 vivo efficacies in the acute mouse model of trypanosomiasis, curing 3/4 or 4/4 animals at 4 x 5 mg/k
103 ges resulting from an ongoing suppression of trypanosomiasis disease in cattle in an agropastoral com
104 oma brucei, the etiological agent of African trypanosomiasis, disease progression can be rapid or slo
112 Epidemics of both forms of human African trypanosomiasis (HAT) are confined to spatially stable f
120 ally validated drug target for human African trypanosomiasis (HAT), also called African sleeping sick
121 cei, the causative parasite of human African trypanosomiasis (HAT), also known as African sleeping si
123 worldwide; four in particular (human African trypanosomiasis (HAT), Chagas disease, cutaneous leishma
125 protozoan parasites that cause human African trypanosomiasis (HAT), depend on ornithine uptake and me
126 eir protective effects against human African trypanosomiasis (HAT), or African sleeping sickness.
128 ug target for the treatment of human African trypanosomiasis (HAT), raising interest in understanding
129 nity, the parasites that cause human African Trypanosomiasis (HAT), Trypanosoma brucei rhodesiense an
130 serum proteomic signature for human African trypanosomiasis (HAT), using a combination of surface-en
131 ts a promising drug target for human African trypanosomiasis (HAT), which is caused by the parasitic
132 site Trypanosoma brucei causes Human African trypanosomiasis (HAT), which threatens millions of peopl
142 historical focus of gambiense Human African Trypanosomiasis (HAT, sleeping sickness), a disease that
144 ve agent of sleeping sickness (Human African Trypanosomiasis, HAT), contains a kinetoplast with the m
146 protozoan and the causative agent of African trypanosomiasis, imports about a thousand proteins into
147 ine, which is currently being tested against trypanosomiasis in humans, and berenil, which is used in
151 be developed for treatment of human African trypanosomiasis in the near future, increasing attention
152 esults implicate both forms of human African trypanosomiasis in the selection and persistence of othe
153 ch is used clinically to treat human African trypanosomiasis, inhibits the first step in polyamine (s
159 ne control of variation in susceptibility to trypanosomiasis is known to occur in mice, where the C57
160 ecular target for treatment of human African trypanosomiasis is ornithine decarboxylase (ODC), which
162 eatment of both human and veterinary African trypanosomiasis is still, to a large extent, dependent o
165 amin, traditionally used in the treatment of trypanosomiasis, is under investigation in the treatment
167 e parasite Trypanasoma brucei causes African trypanosomiasis, known as sleeping sickness in humans an
168 and model analysis show that suppression of trypanosomiasis leads to increased cattle and human popu
169 brucei, the causative agent of human African trypanosomiasis, led to the identification of substitute
171 arasitic diseases (schistosomiasis, malaria, trypanosomiasis, leishmaniasis, and toxoplasmosis) and p
172 aturation, and Ig class switching in African trypanosomiasis may be partially regulated by unusual me
174 adenosine analogues as drugs against African trypanosomiasis, N(6)-, 2-amino-N(6)-, and N(2)-substitu
176 lsopp argues that those tasked with managing trypanosomiasis or committed to poverty alleviation in A
178 added to the pharmacopeia for human African trypanosomiasis (or sleeping sickness), orally dosed fex
185 ypanosoma cruziare the major agents of human trypanosomiasis; other Trypanosomaspecies can cause huma
186 osoma brucei, the causative agent of African trypanosomiasis, possesses a bona fide member of this fa
187 brucei, the causative agent of human African trypanosomiasis, possesses non-canonical mitochondrial p
188 brucei, the causative agent of human African trypanosomiasis, possesses two fatty acid synthesis path
190 d Central America, Chagas' disease (American trypanosomiasis) remains one of the most prevalent infec
191 n therapy for the treatment of human African trypanosomiasis, renewing interest in nitroheterocycle t
192 s of both early and late stage human African trypanosomiasis, representing a new lead for the develop
196 brucei, the causative agent of Human African Trypanosomiasis (sleeping sickness), yet little is known
197 site Trypanosoma brucei causes human African trypanosomiasis ("sleeping sickness") across sub-Saharan
198 resent front line drugs for treating African trypanosomiasis such as melarsoprol (Arsobal) and pentam
199 he analysis of these conflicting outcomes of trypanosomiasis suppression is used to illustrate the ne
200 hypothesis that these APOL1 variants reduce trypanosomiasis susceptibility, resulting in their posit
202 uch as malaria, dysentery, leishmaniasis and trypanosomiasis that are responsible for millions of dea
203 ally involved in the pathogenesis of African trypanosomiasis, the contributions to this disease of CD
204 brucei, the causative agent of human African trypanosomiasis, the NDR kinase, PK50, is expressed in p
205 ysis in the causative agent of human African trypanosomiasis, Trypanosoma brucei, has already shown t
207 soma brucei, the causative agent for African trypanosomiasis undergoes various stages of cellular dif
208 l, melarsoprol (a drug used for treatment of trypanosomiasis), upon induction of apoptosis in cell li
209 protozoan parasite that causes human African trypanosomiasis, uses antigenic variation as a major vir
210 ained from 61 patients in whom human African trypanosomiasis was cured, SL RNA detection had specific
213 nosoma cruzi causes Chagas disease (American trypanosomiasis), which threatens the lives of millions
214 es with faster progression of T.b. gambiense trypanosomiasis, while G1 associates with asymptomatic c
215 a novel test that can diagnose human African trypanosomiasis with high sensitivity and specificity.
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