ライフサイエンスコーパス: Trypanosoma

1 Crithidia, Trypanosoma and Leishmania are all members of the order

2 (T) confined to pathogenic protozoa such as Trypanosoma and Leishmania JBP1 has two known functional

3 ection system of parasitic protozoa, such as trypanosoma and leishmania parasites.

4 ypanosomatids, which include human pathogens Trypanosoma and Leishmania This makes Paratrypanosoma un

5 estral characters such as peptidases between Trypanosoma and Leishmania, genomic differences that wer

6 ude medically important members of the genus Trypanosoma and Leishmania, the 26/28S large subunit rib

7 African trypanosomes (Trypanosoma) are vector-borne haemoparasites that surviv

8 Most of the samples were active against Trypanosoma b.

9 ng drug target within the parasitic protozoa Trypanosoma brucei (T. brucei), the causative agent for

10 tal disease caused by the protozoan parasite Trypanosoma brucei (Tb).

11 Nonetheless, the GMPR of Trypanosoma brucei (TbGMPR) includes a unique structure

12 rominent defence of the unicellular parasite Trypanosoma brucei against the host immune system is a d

13 Structural studies performed in Trypanosoma brucei already highlighted the numerous pecu

14 The flagellated eukaryote Trypanosoma brucei alternates between the insect vector

15 The compounds were assessed for Trypanosoma brucei and Leishmania major PTR1 inhibition

16 ct life cycle stages of two human parasites; Trypanosoma brucei and Leishmania mexicana.

17 el can be applied to the characterization of Trypanosoma brucei and Leishmania spp. ribosomes as well

18 in two well-studied kinetoplastid parasites, Trypanosoma brucei and Leishmania, focusing on recent wo

19 wledge largely stems from the human pathogen Trypanosoma brucei and mouse experimental models.

20 In Trypanosoma brucei and related kinetoplastids, gene expr

21 zation of this channel to acidocalcisomes of Trypanosoma brucei and suggest that caution should be ex

22 The parasitic trypanosomes Trypanosoma brucei and T. cruzi are responsible for sign

23 roducts exhibit significant activity against Trypanosoma brucei and T. cruzi, featuring favorable dru

24 ickness, is caused by the protozoan parasite Trypanosoma brucei and transmitted through the bite of i

25 We also compare Trypanosoma brucei and Trypanosoma congolense, parasites

26 Mutations in the Trypanosoma brucei aquaporin AQP2 are associated with re

27 Mitochondrial ribosomes of Trypanosoma brucei are composed of 9S and 12S rRNAs, eub

28 cells but were effective in cell cultures of Trypanosoma brucei brucei (EC(50) = 1-15 muM) and elimin

29 h a single-digit micromolar activity against Trypanosoma brucei brucei (EC50 = 2.97 muM), thus being

30 on by several protozoan parasites, including Trypanosoma brucei brucei Endocytosis and acidification

31 ate immunity against the veterinary pathogen Trypanosoma brucei brucei is conferred by trypanosome ly

32 e glycerol kinase and alternative oxidase of Trypanosoma brucei brucei.

33 RNase H1 loss is tolerated by the parasite Trypanosoma brucei but no work has examined the function

34 rotozoan parasites Plasmodium falciparum and Trypanosoma brucei by microscopy imaging, proving that t

35 Trypanosoma brucei causes African sleeping sickness for

36 Trypanosoma brucei causes African trypanosomiasis and co

37 Trypanosoma brucei causes fatal human African trypanosom

38 Trypanosoma brucei causes human African trypanosomiasis

39 Trypanosoma brucei causes human African trypanosomiasis

40 The protist parasite Trypanosoma brucei causes Human African trypanosomiasis

41 The protozoan parasite Trypanosoma brucei causes the fatal illness human Africa

42 A defining feature of Trypanosoma brucei cell shape is the lateral attachment

43 Trypanosoma brucei CRK9 is an essential cyclin-dependent

44 ly assembled flagellum in the human parasite Trypanosoma brucei depends on the faithful duplication a

45 Survival of Trypanosoma brucei depends upon switches in its protecti

46 al metabolic remodeling is a hallmark of the Trypanosoma brucei digenetic life cycle because the inse

47 The human parasite Trypanosoma brucei does not synthesize heme de novo and

48 generates functional mitochondrial mRNAs in Trypanosoma brucei Editing is catalyzed by three distinc

49 Trypanosoma brucei encodes three paralogue single-protei

50 Unlike other type II TKs, the Trypanosoma brucei enzyme (TbTK) is a tandem protein wit

51 Trypanosoma brucei evades the host immune system through

52 ad of important trypanosome variants such as Trypanosoma brucei evansi that exploit mechanical transm

53 clusion ensures that the African trypanosome Trypanosoma brucei exclusively expresses only 1 of thous

54 screens were undertaken in bloodstream form Trypanosoma brucei exposed to the antifolates methotrexa

55 The bloodstream form of the human pathogen Trypanosoma brucei expresses oligomannose, paucimannose,

56 Trypanosoma brucei faces relentless immune attack in the

57 segmented gene conversion, is fundamental in Trypanosoma brucei for both VSG gene switching and for g

58 ine reductase 1 with phenotypic screening on Trypanosoma brucei for hit identification.

59 st Trypanosoma, including the human pathogen Trypanosoma brucei gambiense and Trypanosoma cruzi paras

60 uman African trypanosomiasis (HAT) caused by Trypanosoma brucei gambiense can be diagnosed in the ear

61 The World Health Organization targeted Trypanosoma brucei gambiense human African trypanosomias

62 Infection rates of Trypanosoma brucei gambiense in tsetse are extremely low

63 to replace the current treatment regimen for Trypanosoma brucei gambiense infections, following a pos

64 Human African trypanosomiasis caused by Trypanosoma brucei gambiense is a parasitic infection th

65 e of Human African Trypanosomiasis caused by Trypanosoma brucei gambiense.

66 this effect in an important human pathogen, Trypanosoma brucei gambiense.

67 number of constitutive origins mapped in the Trypanosoma brucei genome is less than the minimum requi

68 l for growth and infectivity of the parasite Trypanosoma brucei However, the mechanism by which TbIP(

69 ausative agent of African sleeping sickness, Trypanosoma brucei In mitochondria of this pathogen, mos

70 eptor (TfR) of the bloodstream form (BSF) of Trypanosoma brucei is a heterodimer comprising glycosylp

71 Trypanosoma brucei is a kinetoplastid parasite that caus

72 Trypanosoma brucei is a parasitic protozoan that undergo

73 Trypanosoma brucei is a protist parasite causing sleepin

74 Trypanosoma brucei is a protozoan parasite that evades i

75 The African trypanosome Trypanosoma brucei is a single-celled eukaryote with a s

76 Trypanosoma brucei is an extracellular parasite that cau

77 The basal body in the human parasite Trypanosoma brucei is structurally equivalent to the cen

78 The parasite Trypanosoma brucei is the causative agent of African sle

79 The unicellular parasite Trypanosoma brucei is transmitted between mammals by tse

80 The mitochondrion of the parasitic protozoan Trypanosoma brucei lacks tRNA genes and therefore import

81 The mitochondrion of the parasitic protozoan Trypanosoma brucei lacks tRNA genes, and thus imports al

82 screen with 176 individual bloodstream form Trypanosoma brucei lines identified PKs required for pro

83 es, putative stem-loops from L. donovani and Trypanosoma brucei nucleobase transporter mRNAs were not

84 Trypanosoma brucei parasites successfully evade the host

85 rican trypanosomiasis is a disease caused by Trypanosoma brucei parasites with limited treatment opti

86 allelic exclusion and antigenic variation in Trypanosoma brucei parasites.

87 Trypanosoma brucei possesses a highly complex RNA editin

88 Trypanosoma brucei PRMT7 (TbPRMT7) is a protein arginine

89 ation of the proliferative cell cycle of the Trypanosoma brucei procyclic life cycle stage, three sub

90 volutionarily early divergent human parasite Trypanosoma brucei proliferates through binary cell fiss

91 The major Trypanosoma brucei protein arginine methyltransferase, T

92 Cardiolipin depletion-induced changes in the Trypanosoma brucei proteome.

93 The infectious metacyclic forms of Trypanosoma brucei result from a complex development in

94 ition of the cysteine proteases rhodesain of Trypanosoma brucei rhodesiense and falcipain-2 of Plasmo

95 logues possess micromolar activities against Trypanosoma brucei rhodesiense and Leishmania donovani a

96 ent manner and demonstrated activity against Trypanosoma brucei rhodesiense bloodstream forms, which

97 r proteins that contribute to virulence, and Trypanosoma brucei rhodesiense EVs contain the serum res

98 stance to most African trypanosomes, but not Trypanosoma brucei rhodesiense or T.b. gambiense, which

99 gnized as a strong inhibitor of rhodesain of Trypanosoma brucei rhodesiense, endowed with a k(second)

100 ch as Plasmodium falciparum, Lassa Virus and Trypanosoma brucei rhodesiense, has resulted in elevated

101 c markers in CSF from patients infected with Trypanosoma brucei rhodesiense, using 1H nuclear magneti

102 ite concentrations in patients infected with Trypanosoma brucei rhodesiense, using liquid chromatogra

103 We report X-ray structures of Trypanosoma brucei S-adenosylmethionine decarboxylase al

104 ved following RNAi-mediated silencing of the Trypanosoma brucei SODA ortholog suggests that SODA is e

105 Trypanosoma brucei spp. cause African human and animal t

106 sites Trypanosoma cruzi, Leishmania spp. and Trypanosoma brucei spp., respectively.

107 Trypanosoma brucei stumpy forms are the only stage that

108 Humans are susceptible to two Trypanosoma brucei subspecies but protected from other t

109 the procyclic and bloodstream form stages of Trypanosoma brucei that yields viable and proliferative

110 Here, we show that in the PAM of Trypanosoma brucei the function of Pam18 has been replac

111 ing the cell cycle of the protozoan parasite Trypanosoma brucei The source of components required to

112 rin uptake, we determined the structure of a Trypanosoma brucei transferrin receptor in complex with

113 ow that cytosine 32 in the anticodon loop of Trypanosoma brucei tRNA(Thr) is methylated to 3-methylcy

114 Mitochondrial mRNAs in Trypanosoma brucei undergo extensive insertion and delet

115 ghly motile and versatile protozoan pathogen Trypanosoma brucei undergoes a complex life cycle in the

116 Trypanosoma brucei undergoes cytokinesis uni-directional

117 Trypanosoma brucei uses multiple mechanisms to evade det

118 ve-site residues of PRMT7 from the protozoan Trypanosoma brucei We have designed 26 single and double

119 ulation of glycosomes in live procyclic form Trypanosoma brucei When added to cells, this fluorescent

120 Here, we identify the Trypanosoma brucei ZC3H39/40 RNA-binding proteins as reg

121 tozoa (Leishmania spp., Plasmodium spp., and Trypanosoma brucei).

122 We examined BBSome functions in Trypanosoma brucei, a flagellated protozoan parasite tha

123 Differentiation of Trypanosoma brucei, a flagellated protozoan parasite, be

124 rganisms belonging to the phylum euglenozoa: Trypanosoma brucei, a lethal human parasite, and Euglena

125 mography structures of the 96-nm repeat from Trypanosoma brucei, a protozoan parasite in the Excavate

126 In Trypanosoma brucei, an ancient unicellular eukaryote, on

127 e biosynthesis pathway of the human parasite Trypanosoma brucei, an early branching eukaryote that la

128 Trypanosoma brucei, an early divergent microbial eukaryo

129 ential for growth of the parasitic protozoan Trypanosoma brucei, enabling the study of its function i

130 In Trypanosoma brucei, genes are arranged in Polycistronic

131 th sleeping sickness, caused by the parasite Trypanosoma brucei, have disruptions in both sleep timin

132 ed to TbKHC1, an orphan kinesin H chain from Trypanosoma brucei, inhibited T. musculi excreted/secret

133 receptor of the African trypanosome species, Trypanosoma brucei, is expressed when the parasite is in

134 OM protein of the early diverging protozoan Trypanosoma brucei, is signal-anchored.

135 In Trypanosoma brucei, mitochondrial pre-mRNAs undergo 3'-5

136 In Trypanosoma brucei, most mitochondrial mRNAs undergo edi

137 In Trypanosoma brucei, most mitochondrial mRNAs undergo int

138 the causative agent, the protozoan parasite Trypanosoma brucei, occurs through receptor-mediated end

139 e effects of the sleeping sickness parasite, Trypanosoma brucei, on sleep patterns in mice, under bot

140 In Trypanosoma brucei, PE synthesis has been shown to occur

141 To identify new chemotypes against Trypanosoma brucei, previously we identified 797 potent

142 Trypanosoma brucei, protozoan parasites that cause human

143 t that CRK1, a G1 cyclin-dependent kinase in Trypanosoma brucei, regulates anterograde protein traffi

144 ains of TR from the basal eukaryotic species Trypanosoma brucei, revealing the ancestry of TR compris

145 ruzi, the causative agent of Chagas disease; Trypanosoma brucei, the causative agent of African sleep

146 13b ortholog in the evolutionarily divergent Trypanosoma brucei, the causative agent of African sleep

147 , which had been identified as a hit against Trypanosoma brucei, the causative agent of human African

148 es (PKs) are a class of druggable targets in Trypanosoma brucei, the causative agent of Human African

149 point for the synthesis of new hits against Trypanosoma brucei, the causative agent of human African

150 Here, we show that Trypanosoma brucei, the causative agent of human sleepin

151 The parasite Trypanosoma brucei, the causative agent of sleeping sick

152 Trypanosoma brucei, the causative agent of sleeping sick

153 Trypanosoma brucei, the etiologic agent of African Sleep

154 In the sleeping sickness parasite Trypanosoma brucei, the kinetoplast is a chain mail-like

155 In Trypanosoma brucei, the proteins that make up the kineto

156 In Trypanosoma brucei, the small noncoding TBsRNA-10 was fi

157 resistant strains of the protozoal pathogens Trypanosoma brucei, Trypanosoma congolense and Leishmani

158 nt parasites and include the human pathogens Trypanosoma brucei, Trypanosoma cruzi, and Leishmania sp

159 The trypanosomatids Trypanosoma brucei, Trypanosoma cruzi, and Leishmania sp

160 nd biogenesis of the array, with emphasis on Trypanosoma brucei, Trypanosoma cruzi, and Leishmania, w

161 pathway and its enzymes have been studied in Trypanosoma brucei, Trypanosoma cruzi, and various Leish

162 The sleeping sickness parasite, Trypanosoma brucei, uses quorum sensing (QS) to balance

163 its application to the pathogenic protozoan, Trypanosoma brucei, using hyperpolarized (13)C1 pyruvate

164 The protozoan parasite Trypanosoma brucei, which causes devastating diseases in

165 An example is Trypanosoma brucei, which causes human African trypanoso

166 Tsetse flies transmit Trypanosoma brucei, which is the parasite that causes hu

167 in the causative agent of sleeping sickness, Trypanosoma brucei, with that of human erythrocytes, and

168 ammalian cells, CL synthesis is essential in Trypanosoma brucei.

169 ndidates, Xpo-t and Xpo-5 for tRNA export in Trypanosoma brucei.

170 ke and the modulation of drug sensitivity in Trypanosoma brucei.

171 in tRNAs from Bacillus subtilis, plants and Trypanosoma brucei.

172 orthologue, PNT1, in the parasitic protozoon Trypanosoma brucei.

173 by RNA polymerase I (Pol I) in the parasite Trypanosoma brucei.

174 diting in kinetoplastid protists typified by Trypanosoma brucei.

175 ents in the large ribosomal subunit (60S) of Trypanosoma brucei.

176 e boundaries of previously annotated CDSs in Trypanosoma brucei.

177 As and is unique for kinetoplastids, such as Trypanosoma brucei.

178 P2 in either the cytosol or mitochondrion of Trypanosoma brucei.

179 ith either of two subspecies of the parasite Trypanosoma brucei.

180 ositol pyrophosphate biosynthetic pathway in Trypanosoma brucei: inositol polyphosphate multikinase (

181 of unicellular parasitic flagellate protozoa.Trypanosoma bruceispecies and Trypanosoma cruziare the m

182 We report a way to selectively kill Trypanosoma by blocking glycosomal/peroxisomal import th

183 ection model of zebrafish (Danio rerio) with Trypanosoma carassii.

184 the protozoal pathogens Trypanosoma brucei, Trypanosoma congolense and Leishmania mexicana.

185 o-infections with other trypanosome species (Trypanosoma congolense and Trypanosoma vivax) are common

186 mal African trypanosomiasis (AAT), caused by Trypanosoma congolense and Trypanosoma vivax, remains on

187 fectious diseases, their role in immunity to Trypanosoma congolense has not been investigated.

188 Here we show that in Trypanosoma congolense this receptor is instead expresse

189 st the principal causative organisms of AAT: Trypanosoma congolense, and Trypanosoma vivax.

190 We also compare Trypanosoma brucei and Trypanosoma congolense, parasites that share a common pa

191 Trypanosoma cruzi (T. cruzi) infection is endemic in Lat

192 the authors present a 2.5-A structure of the Trypanosoma cruzi 60S ribosomal subunit and propose a mo

193 disease is caused by the protozoan parasite Trypanosoma cruzi and affects 5-8 million people in Lati

194 time for the simultaneous detection of anti-Trypanosoma cruzi and anti-Leishmania infantum antibodie

195 Chagas disease is caused by the parasite Trypanosoma cruzi and is an important cause of morbidity

196 have been considered as virulence factors of Trypanosoma cruzi and Leishmania spp., and have been dem

197 gondii and kinetoplastid protozoa, including Trypanosoma cruzi and Leishmania spp., cause millions of

198 centrating on Mycobacterium tuberculosis and Trypanosoma cruzi as examples of bacterial and parasitic

199 The Trypanosoma cruzi ascorbate peroxidase is, by sequence a

200 ole and posaconazole have not been tested in Trypanosoma cruzi carriers.

201 reference perspective, cruzain, an essential Trypanosoma cruzi cysteine protease, is highly homologou

202 To successfully infect, Trypanosoma cruzi evades and modulates the host immune r

203 In contrast, as a model eukaryote, Trypanosoma cruzi exhibits two individual putative ortho

204 The protozoan Trypanosoma cruzi has a complicated dual-host life cycle

205 e extreme genetic diversity of the protozoan Trypanosoma cruzi has been proposed to be associated wit

206 Oral transmission of Trypanosoma cruzi has gained relevance because of its as

207 Vertical transmission of Trypanosoma cruzi infection accounts for a growing propo

208 Congenital Trypanosoma cruzi infection accounts for an estimated 22

209 response plays a crucial role in controlling Trypanosoma cruzi infection and parasite burden, but it

210 Trypanosoma cruzi infection drives the expansion of rema

211 nic Chagas disease cardiomyopathy, caused by Trypanosoma cruzi infection, is a major cause of heart f

212 In chronic Trypanosoma cruzi infection, the cause of Chagas disease

213 Trypanosoma cruzi infection, which is the etiological ag

214 o be relevant in the context of experimental Trypanosoma cruzi infection.

215 eviously described in immune response during Trypanosoma cruzi infection.

216 In chronic Trypanosoma cruzi infections, parasite burden is control

217 Trypanosoma cruzi infects many cell types but preferenti

218 Trypanosoma cruzi is a unicellular parasite and the etio

219 Trypanosoma cruzi is an intracellular protozoan parasite

220 The insect-transmitted protozoan parasite Trypanosoma cruzi is the causative agent of Chagas disea

221 Trypanosoma cruzi is the causative agent of chronic chag

222 Trypanosoma cruzi is the causative pathogen of Chagas di

223 Trypanosoma cruzi is the etiological agent of Chagas dis

224 of the protozoans Leishmania tarentolae and Trypanosoma cruzi mitoribosomes.

225 Trypanosoma cruzi parasites are the causative agents of

226 The diversity of Trypanosoma cruzi parasites infecting humans is still po

227 an pathogen Trypanosoma brucei gambiense and Trypanosoma cruzi parasites.

228 s were identified as potential inhibitors of Trypanosoma cruzi replication, a parasite responsible fo

229 es, we determined the 2.5-A structure of the Trypanosoma cruzi ribosome large subunit by single-parti

230 Trypanosoma cruzi species is categorized into six discre

231 s from a screen against the related parasite Trypanosoma cruzi Subsequent optimization of the chemica

232 Congenital Trypanosoma cruzi transmission is now estimated to accou

233 pest insect that has the ability to transmit Trypanosoma cruzi under experimental laboratory conditio

234 as disease, caused by the protozoan parasite Trypanosoma cruzi, affects 7 million people in Latin Ame

235 gas disease is a chronic infection caused by Trypanosoma cruzi, an intracellular protozoan parasite.

236 infections due to Toxoplasma gondii (n = 3), Trypanosoma cruzi, and Leishmania species.

237 The trypanosomatids Trypanosoma brucei, Trypanosoma cruzi, and Leishmania spp. are flagellate eu

238 lude the human pathogens Trypanosoma brucei, Trypanosoma cruzi, and Leishmania spp., which in humans

239 array, with emphasis on Trypanosoma brucei, Trypanosoma cruzi, and Leishmania, which cause life-thre

240 mes have been studied in Trypanosoma brucei, Trypanosoma cruzi, and various Leishmania species.

241 ng infection with the intracellular parasite Trypanosoma cruzi, as evidenced by transcriptome and cyt

242 The protozoan agent, Trypanosoma cruzi, comprises six genetic lineages, TcI-T

243 sed by infection with the protozoan parasite Trypanosoma cruzi, is a leading cause of heart disease (

244 Chagas disease, caused by Trypanosoma cruzi, is a major public health issue.

245 used by the intracellular protozoan parasite Trypanosoma cruzi, is a public health problem affecting

246 ysteine protease of the parasitic protozoan, Trypanosoma cruzi, is an important drug target for Chaga

247 Chagas disease, caused by the protozoan Trypanosoma cruzi, is endemic in Latin America and affec

248 Chagas disease, caused by the parasite Trypanosoma cruzi, is endemic in Latin America.

249 s' disease, caused by the protozoan parasite Trypanosoma cruzi, is the most common cause of cardiac-r

250 y infection with the kinetoplastid parasites Trypanosoma cruzi, Leishmania spp. and Trypanosoma bruce

251 a novel mechanism used by diverse pathogens (Trypanosoma cruzi, Listeria monocytogenes, and adenoviru

252 mice with the myotropic Colombiana strain of Trypanosoma cruzi, parasites persisted in tissue at low

253 uM against neglected Chagas' disease causing Trypanosoma cruzi, respectively.

254 of fire ants against the protozoan parasite Trypanosoma cruzi, the aetiologic agent of Chagas diseas

255 The Triatominae are vectors for Trypanosoma cruzi, the aetiological agent of the neglect

256 Using a murine model of infection with Trypanosoma cruzi, the causal agent of Chagas cardiomyop

257 ted with AT during part of their life cycle: Trypanosoma cruzi, the causative agent of Chagas disease

258 The release of EVs by Trypanosoma cruzi, the causative agent of Chagas disease

259 Trypanosoma cruzi, the causative agent of Chagas disease

260 (NMT), an essential and druggable target in Trypanosoma cruzi, the causative agent of Chagas' diseas

261 Trypanosoma cruzi, the causing agent of Chagas disease,

262 We report here that Trypanosoma cruzi, the etiologic agent of Chagas disease

263 Methods for genetic manipulation of Trypanosoma cruzi, the etiologic agent of Chagas disease

264 Trypanosoma cruzi, the etiological agent of Chagas disea

265 Trypanosoma cruzi, the etiological agent of Chagas disea

266 Trypanosoma cruzi, the parasitic agent of Chagas disease

267 role of CD43 in the immune response against Trypanosoma cruzi, the protozoan parasite that causes Ch

268 Transmitted by a protozoan named Trypanosoma cruzi, this infection triggers a chronic inf

269 g resistance of the Chagas disease parasite, Trypanosoma cruzi, to current therapies are not well und

270 elivers Gzms into three protozoan parasites (Trypanosoma cruzi, Toxoplasma gondii and Leishmania majo

271 C(50) within the low nanomolar range against Trypanosoma cruzi, with very high selectivity toward the

272 ar why only a proportion of children born to Trypanosoma cruzi-infected mothers acquire the infection

273 hmania-like flagellum attachment zone, and a Trypanosoma cruzi-like cytostome are ancestral features,

274 in the activation and functional profile of Trypanosoma cruzi-specific DN T cells.

275 n the infective stages of the human parasite Trypanosoma cruzi.

276 CI 2.2-6.8) were estimated to be infected by Trypanosoma cruzi.

277 the kinetoplastidea including Leishmania and Trypanosoma cruzi.

278 used by the kinetoplastid protozoan parasite Trypanosoma cruzi.

279 T. brucei bloodstream forms, Leishmania and Trypanosoma cruzi.

280 disease is caused by the protozoan parasite Trypanosoma cruzi.

281 gas disease caused by the protozoan parasite Trypanosoma cruzi.

282 easy discrimination of Leishmania major and Trypanosoma cruzi.

283 idate clathrin-associated proteins (CAPs) in Trypanosoma cruzi; the cohort includes orthologs of many

284 llate protozoa.Trypanosoma bruceispecies and Trypanosoma cruziare the major agents of human trypanoso

285 testing identified the infecting species as Trypanosoma evansi.Despite relapsing 6 weeks after compl

286 The parasitic protists of the Trypanosoma genus infect humans and domestic mammals, ca

287 s show significant cellular activity against Trypanosoma, including the human pathogen Trypanosoma br

288 range of available chemotherapeutics against Trypanosoma is limited, and the existing therapies are p

289 Trypanosoma is unable to synthesize purines de novo and

290 hosts) trypanosomatid species of the genera Trypanosoma, Leishmania, and Phytomonas, but only fragme

291 Trypanosoma lewisi is a member of the Stercorarian group

292 examination of blood revealed infection with Trypanosoma METHODS: Microscopic observation, polymerase

293 ced in macrophages during mouse infection by Trypanosoma musculi, a natural parasite of this host.

294 Trypanosoma protists are pathogens leading to a spectrum

295 Trypanosoma protozoan parasites are the causative agents

296 identify PEX14 as an "Achilles' heel" of the Trypanosoma suitable for the development of new therapie

297 Trypanosoma vivax is a related, livestock pathogen whose

298 panosome species (Trypanosoma congolense and Trypanosoma vivax) are common in animals, generating the

299 (AAT), caused by Trypanosoma congolense and Trypanosoma vivax, remains one of the most important liv

300 rganisms of AAT: Trypanosoma congolense, and Trypanosoma vivax.