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1 surgence in sleeping sickness (human African trypanosomiasis).
2 brucei, the causative agent of human African trypanosomiasis.
3 ed, with a particular focus on human African trypanosomiasis.
4 imization for the treatment of human African trypanosomiasis.
5 ed target for the treatment of human African trypanosomiasis.
6 osoma brucei is the causing agent of African trypanosomiasis.
7 yma is a major pathogenetic event in African trypanosomiasis.
8 nfections such as tuberculosis, malaria, and trypanosomiasis.
9 ful development of a promising drug to treat trypanosomiasis.
10 omising therapeutic target for human African trypanosomiasis.
11 tential novel drug targets for human African trypanosomiasis.
12 PTR1 may be a drug target for human African trypanosomiasis.
13 ment of new treatments against human African trypanosomiasis.
14 t and prevention of human and animal African trypanosomiasis.
15 ly reproducible mouse model of human African trypanosomiasis.
16 get for new compounds to treat human African trypanosomiasis.
17 infected animals in the acute mouse model of trypanosomiasis.
18 animals in the STIB900 acute mouse model of trypanosomiasis.
19 animals in the acute mouse model of African trypanosomiasis.
20 ion could have therapeutic potential against trypanosomiasis.
21 is definitively linked to host resistance in trypanosomiasis.
22 variant cross-specific immunity for African trypanosomiasis.
23 tory and regulatory mediators during African trypanosomiasis.
24 ng phase III clinical trials against African trypanosomiasis.
25 ibitors of therapeutic value against African trypanosomiasis.
26 mportant chemotherapeutic target for African trypanosomiasis.
27 ises the use of antifolates for treatment of trypanosomiasis.
28 imulation of the host immune response during trypanosomiasis.
29 to control tsetse flies and, hence, African trypanosomiasis.
30 mals in the STIB900 animal model for African trypanosomiasis.
31 developed for the treatment of human African trypanosomiasis.
32 es (PMCAs) of T. brucei, an agent of African trypanosomiasis.
33 r developing new serodiagnostics for African trypanosomiasis.
34 robial peptides for the treatment of African trypanosomiasis.
35 omes overcome host resistance during African trypanosomiasis.
36 onoallelic expression could be used to treat trypanosomiasis.
37 fforts to develop effective vaccines against trypanosomiasis.
38 some in vivo activity in a model of African trypanosomiasis.
39 nisms of tropical diseases leishmaniasis and trypanosomiasis.
40 ic Th-cell responses in experimental African trypanosomiasis.
41 d compound for treatment of cancer, HIV, and trypanosomiasis.
42 pment of specific drugs and vaccines against trypanosomiasis.
43 in the Excavate lineage that causes African trypanosomiasis.
44 chemotherapeutic target for the treatment of trypanosomiasis.
45 nd affecting the loss of fat mass in African trypanosomiasis.
46 pical climates and endemic diseases, notably trypanosomiasis.
47 the brain and prevent the onset of cerebral trypanosomiasis.
48 y process for the treatment of Human African Trypanosomiasis.
49 developed for the treatment of human African trypanosomiasis.
50 e dose of 20 mg kg(-1) were cured of stage 1 trypanosomiasis.
51 dose cure using acoziborole against African trypanosomiasis.
52 ific inhibitors for the treatment of African trypanosomiasis.
53 siense, the causative agent of Human African Trypanosomiasis.
54 protozoan parasite that causes human African trypanosomiasis.
55 e trypanosomes responsible for human African trypanosomiasis.
56 a in a stage 1 animal model of human African trypanosomiasis.
57 or T.b. gambiense, which cause human African trypanosomiasis.
58 treatments for both human and animal African trypanosomiasis.
59 brucei, the causative agent of human African trypanosomiasis.
60 diseases such as malaria, toxoplasmosis, and trypanosomiasis.
61 and new developments in vaccination against trypanosomiasis.
62 the parasites that cause malaria and African trypanosomiasis.
63 inidae), vectors of Human and Animal African trypanosomiasis.
64 hmaniasis, Chagas disease, and human African trypanosomiasis.
65 ackbone of the pharmacopoeia against African trypanosomiasis.
66 compounds for the treatment of human African trypanosomiasis.
67 peutic target for treatment of human African trypanosomiasis.
68 in the STIB900 mouse model for human African trypanosomiasis.
69 e blood meal of tsetse flies, the vector for trypanosomiasis.
70 ns as potential therapeutic drug targets for trypanosomiasis.
71 of the wider epidemiology of animal African trypanosomiasis.
72 ucei is the causative agent of human African trypanosomiasis.
73 development of drugs to treat human African trypanosomiasis.
74 t of a combination therapy for human African trypanosomiasis.
75 oan responsible for human and animal African trypanosomiasis.
76 osoma brucei, the causative agent of African trypanosomiasis.
77 ead for development of drugs against African trypanosomiasis.
78 al target for the treatment of human African trypanosomiasis.
79 a brucei spp. cause African human and animal trypanosomiasis, a burden on health and economy in Afric
80 re a key control component of African animal trypanosomiasis (AAT) in tsetse-infested areas of sub-Sa
84 the efficacy of treatment for human African trypanosomiasis, accurate tests that can discriminate re
85 brucei, the causative agent of human African trypanosomiasis, affects tens of thousands of sub-Sahara
90 serum samples from 85 patients with African trypanosomiasis and 146 control patients who had other p
91 tage or second-stage gambiense human African trypanosomiasis and a cerebrospinal fluid leucocyte coun
94 to diseases such as malaria, leishmaniasis, trypanosomiasis and dysentery that are responsible for m
95 s TbCLK1 as a therapeutic target for African trypanosomiasis and establishes a new chemoproteomic too
96 rypanosoma brucei causes fatal human African trypanosomiasis and evades the host immune response by r
97 panosomatid species, the causative agents of trypanosomiasis and leishmaniasis, are dependent on a fl
100 Trypanosoma brucei causes human African trypanosomiasis and regularly switches its major surface
101 Trypanosoma brucei causes human African trypanosomiasis and regularly switches its major surface
102 Trypanosoma brucei causes human African trypanosomiasis and regularly switches its major surface
103 we establish a mouse model of acute cerebral trypanosomiasis and we propose a mechanism whereby paras
104 ithin the GlaxoSmithKline HAT (Human African Trypanosomiasis) and Chagas chemical boxes, two collecti
106 ABQ) library against the causative agents of trypanosomiasis, and cutaneous leishmaniasis, identifyin
107 causative agents of malaria, toxoplasmosis, trypanosomiasis, and leishmaniasis, contain a minimal ER
108 ucei, the protozoan parasite causing African trypanosomiasis, and the tsetse (Glossina) vector remain
110 All four main drugs used for human African trypanosomiasis are toxic, and melarsoprol, the only dru
111 ypanosoma brucei, which causes human African trypanosomiasis, as well as the livestock disease, nagan
113 ical diseases such as leprosy, human African trypanosomiasis, Buruli ulcer, and visceral leishmaniasi
114 nt option for reducing the impact of African trypanosomiasis but, although many effective methods hav
115 as new therapeutic targets for human African trypanosomiasis by both genetic and pharmacological mean
116 anti-inflammatory therapies in Human African trypanosomiasis by modulating the NK1 receptor as well a
117 cutaneous), Chagas disease and human African trypanosomiasis cause substantial death and morbidity, p
118 lected parasitic diseases, including African trypanosomiasis caused by the protozoan, Trypanosoma bru
120 n, particularly in the case of Human African Trypanosomiasis caused by Trypanosoma brucei gambiense.
121 mes in two types: East African human African trypanosomiasis caused by Trypanosoma brucei rhodesiense
124 CBL0137 is a lead drug for human African trypanosomiasis, caused by Trypanosoma brucei Herein, we
125 African sleeping sickness or human African trypanosomiasis, caused by Trypanosoma brucei spp., is r
126 f species that cause leishmaniasis, American trypanosomiasis (Chagas disease), and African trypanosom
127 soma cruzi , the etiologic agent of American trypanosomiasis (Chagas disease), exhibiting IC(50) valu
128 ishmania spp., which in humans cause African trypanosomiasis, Chagas disease, and leishmaniasis, resp
129 parum, the causative agents of human African trypanosomiasis, Chagas disease, leishmaniasis, and mala
130 ping world, including malaria, human African trypanosomiasis, Chagas disease, leishmaniasis, filarias
133 osoma brucei, the causative agent of African trypanosomiasis, contains a soluble, vacuolar pyrophosph
134 ber of reported cases, patients with African trypanosomiasis continue to present major challenges to
135 vivo efficacies in the acute mouse model of trypanosomiasis, curing 3/4 or 4/4 animals at 4 x 5 mg/k
138 ges resulting from an ongoing suppression of trypanosomiasis disease in cattle in an agropastoral com
139 of severe anaemia, a debilitating feature of trypanosomiasis disease, which severely constrains cattl
140 oma brucei, the etiological agent of African trypanosomiasis, disease progression can be rapid or slo
143 pigs in endemic and historical human African trypanosomiasis foci in Guinea and Cote d'Ivoire, respec
147 d Trypanosoma brucei gambiense human African trypanosomiasis (gHAT) for elimination as a public healt
150 The diagnosis of gambiense human African trypanosomiasis (gHAT) typically involves 2 steps: a ser
151 vector-borne disease gambiense human African trypanosomiasis (gHAT, sleeping sickness) in the last tw
155 rug discovery pipeline for leishmaniasis and trypanosomiasis has been filling with novel chemical ent
159 Epidemics of both forms of human African trypanosomiasis (HAT) are confined to spatially stable f
161 cted tropical diseases such as human African trypanosomiasis (HAT) are prevalent primarily in tropica
169 ypanosoma brucei, which causes human African trypanosomiasis (HAT) or sleeping sickness, accumulates
172 d for drug development against human African trypanosomiasis (HAT), a disease caused by Trypanosoma b
175 ally validated drug target for human African trypanosomiasis (HAT), also called African sleeping sick
176 cei, the causative parasite of human African trypanosomiasis (HAT), also known as African sleeping si
179 worldwide; four in particular (human African trypanosomiasis (HAT), Chagas disease, cutaneous leishma
181 protozoan parasites that cause human African trypanosomiasis (HAT), depend on ornithine uptake and me
183 eir protective effects against human African trypanosomiasis (HAT), or African sleeping sickness.
186 ug target for the treatment of human African trypanosomiasis (HAT), raising interest in understanding
187 ted tropical diseases, such as human African trypanosomiasis (HAT), require novel treatments that can
188 nity, the parasites that cause human African Trypanosomiasis (HAT), Trypanosoma brucei rhodesiense an
189 serum proteomic signature for human African trypanosomiasis (HAT), using a combination of surface-en
190 ts a promising drug target for human African trypanosomiasis (HAT), which is caused by the parasitic
191 site Trypanosoma brucei causes Human African trypanosomiasis (HAT), which threatens millions of peopl
203 historical focus of gambiense Human African Trypanosomiasis (HAT, sleeping sickness), a disease that
205 ve agent of sleeping sickness (Human African Trypanosomiasis, HAT), contains a kinetoplast with the m
207 protozoan and the causative agent of African trypanosomiasis, imports about a thousand proteins into
208 ine, which is currently being tested against trypanosomiasis in humans, and berenil, which is used in
213 be developed for treatment of human African trypanosomiasis in the near future, increasing attention
214 esults implicate both forms of human African trypanosomiasis in the selection and persistence of othe
215 ch is used clinically to treat human African trypanosomiasis, inhibits the first step in polyamine (s
226 ne control of variation in susceptibility to trypanosomiasis is known to occur in mice, where the C57
227 ecular target for treatment of human African trypanosomiasis is ornithine decarboxylase (ODC), which
229 eatment of both human and veterinary African trypanosomiasis is still, to a large extent, dependent o
232 reatment of chronic Chagas disease (American trypanosomiasis) is the long time required to achieve co
233 osoma brucei, the causative agent of African trypanosomiasis, is characterized by its high rate of en
234 amin, traditionally used in the treatment of trypanosomiasis, is under investigation in the treatment
236 e parasite Trypanasoma brucei causes African trypanosomiasis, known as sleeping sickness in humans an
237 and model analysis show that suppression of trypanosomiasis leads to increased cattle and human popu
238 brucei, the causative agent of human African trypanosomiasis, led to the identification of substitute
240 arasitic diseases (schistosomiasis, malaria, trypanosomiasis, leishmaniasis, and toxoplasmosis) and p
241 aturation, and Ig class switching in African trypanosomiasis may be partially regulated by unusual me
243 adenosine analogues as drugs against African trypanosomiasis, N(6)-, 2-amino-N(6)-, and N(2)-substitu
245 lsopp argues that those tasked with managing trypanosomiasis or committed to poverty alleviation in A
248 added to the pharmacopeia for human African trypanosomiasis (or sleeping sickness), orally dosed fex
256 ypanosoma cruziare the major agents of human trypanosomiasis; other Trypanosomaspecies can cause huma
257 oma cruzi is the causative agent of American trypanosomiasis, otherwise known as Chagas disease.
258 the neglected tropical disease human African trypanosomiasis, otherwise known as sleeping sickness.
259 osoma brucei, the causative agent of African trypanosomiasis, possesses a bona fide member of this fa
260 brucei, the causative agent of human African trypanosomiasis, possesses non-canonical mitochondrial p
261 brucei, the causative agent of human African trypanosomiasis, possesses two fatty acid synthesis path
263 d Central America, Chagas' disease (American trypanosomiasis) remains one of the most prevalent infec
264 n therapy for the treatment of human African trypanosomiasis, renewing interest in nitroheterocycle t
265 s of both early and late stage human African trypanosomiasis, representing a new lead for the develop
270 brucei, the causative agent of Human African Trypanosomiasis (sleeping sickness), yet little is known
274 site Trypanosoma brucei causes human African trypanosomiasis ("sleeping sickness") across sub-Saharan
276 resent front line drugs for treating African trypanosomiasis such as melarsoprol (Arsobal) and pentam
277 he analysis of these conflicting outcomes of trypanosomiasis suppression is used to illustrate the ne
278 hypothesis that these APOL1 variants reduce trypanosomiasis susceptibility, resulting in their posit
280 uch as malaria, dysentery, leishmaniasis and trypanosomiasis that are responsible for millions of dea
281 ally involved in the pathogenesis of African trypanosomiasis, the contributions to this disease of CD
282 brucei, the causative agent of human African trypanosomiasis, the NDR kinase, PK50, is expressed in p
283 the situation has improved for human African trypanosomiasis, there remains an urgent need for new me
287 ysis in the causative agent of human African trypanosomiasis, Trypanosoma brucei, has already shown t
289 soma brucei, the causative agent for African trypanosomiasis undergoes various stages of cellular dif
290 he pathogen causing Human and Animal African trypanosomiasis, undergoes a complex developmental progr
291 l, melarsoprol (a drug used for treatment of trypanosomiasis), upon induction of apoptosis in cell li
292 protozoan parasite that causes human African trypanosomiasis, uses antigenic variation as a major vir
293 ained from 61 patients in whom human African trypanosomiasis was cured, SL RNA detection had specific
294 a, visceral leishmaniasis, and human African trypanosomiasis, we used mathematical transmission model
297 nosoma cruzi causes Chagas disease (American trypanosomiasis), which threatens the lives of millions
299 es with faster progression of T.b. gambiense trypanosomiasis, while G1 associates with asymptomatic c
300 a novel test that can diagnose human African trypanosomiasis with high sensitivity and specificity.