ライフサイエンスコーパス: niger

1 n athletes (from Burkina Faso, Cameroon, and Niger).

2 opus oligosporus and by >21% for SSF with A. niger.

3 m uncomplicated severe acute malnutrition in Niger.

4 estigate nest construction in the ant Lasius niger.

5 e case-based meningitis surveillance data in Niger.

6 ngitis cases and 549 deaths were reported in Niger.

7 l gene expression in colonies of Aspergillus niger.

8 glucoamylase from newly isolated Aspergillus niger.

9 ryzae, Aspergillus fumigatus and Aspergillus niger.

10 well as one from the saprotroph Aspergillus niger.

11 itis at both national and district levels in Niger.

12 e from 1986 through 2006 for 38 districts in Niger.

13 lysate of the filamentous fungus Aspergillus niger.

14 scape for the filamentous fungus Aspergillus niger.

15 ified all mold isolates tested except for A. niger.

16 ty are highly correlated for three cities in Niger.

17 cies recovered, followed by A. flavus and A. niger.

18 r randomized trial of 12 villages in Maradi, Niger.

19 es formosus, Rhizopus oryzae and Aspergillus niger.

20 sponse in the filamentous fungus Aspergillus niger.

21 gy to lower the level of PDI in the ER of A. niger.

22 inant gene has been expressed in Aspergillus niger.

23 uringiensis, Bacillus subtilis, and Bacillus niger.

24 active site of glucoamylase from Aspergillus niger.

25 d be applied to the isozyme from Aspergillus niger.

26 were time dependent in batch cultures of A. niger.

27 erases (FAE-III and CinnAE) from Aspergillus niger.

28 temperature-sensitive mutant of Aspergillus niger.

29 nitial deployment in Burkina Faso, Mali, and Niger.

30 rity of the repeated regions derived from H. niger.

31 mportant causes of meningitis in children in Niger.

32 solanaceae Nicotiana tabacum and Hyoscyamus niger.

33 ildren from an antibiotic-naive community in Niger.

34 e rotavirus gastroenteritis among infants in Niger.

35 Zymes) of the filamentous fungus Aspergillus niger.

36 atory bacterial disease in a Sahel region of Niger.

37 that drives colonization of wheat bran in A. niger.

38 1.4%), A. flavus (0.8%, 5.1%, and 1.7%), A. niger (17.3%, 3.7%, and 0.6%), A. terreus (0.0%, 1.6%, a

39 /30 min), followed by those from Aspergillus niger (2.4 nmol/1.0 x 10(6) AMs/30 min) and Eurotium ams

40 [7.6-9.7] in Jordan to 51.1% [49.1-53.1] in Niger), 22.7% (22.5-22.9) were underweight (ranging from

41 d in 93% of Aspergillus fumigatus, 75% of A. niger, 25% of A. terreus, and 4% of A. flavus cultures.

42 ed 181 Aspergillus fumigatus, 28 Aspergillus niger, 27 Aspergillus flavus, 22 Aspergillus terreus, se

43 31 to 143 for A. nidulans, 366 to 520 for A. niger, 330 to 462 for A. terreus, and 45 to 84 for A. ve

44 ogram (553 A. fumigatus, 76 A. flavus, 59 A. niger, 35 A. terreus, and 24 A. versicolor isolates and

45 igatus, 235 of A. flavus, 162 of Aspergillus niger, 64 of Aspergillus terreus, and 15 of Aspergillus

46 ved using the free form of inulinase from A. niger (77.19% of GF2; 14.03% of GF3 and 0.07% of GF4) us

47 isk factors in the poorest countries (eg, in Niger, 82% of the population among the poorest billion)

48 ed countries were Nigeria (17 375 cases) and Niger (9343 cases).

49 ent was observed for isolates of Aspergillus niger (95%), which were particularly susceptible to casp

50 lly, the brain of the Black Skimmer Rynchops niger, a taxon with a unique feeding ecology that involv

51 migatus isolates, and 10 isolates each of A. niger, A. nidulans, and A. terreus to voriconazole, posa

52 es (A. flavus, A. fumigatus, A. nidulans, A. niger, A. terreus, A. ustus, and A. versicolor) was also

53 ates of Aspergillus fumigatus, A. flavus, A. niger, A. terreus, A. ustus, and A. versicolor.

54 solates included A. fumigatus, A. flavus, A. niger, A. terreus, A. versicolor, A. glaucus, A. nidulan

55 Compared with A. niger A1 and L2, A. niger H915-1 contained 92 mutated ge

56 World primates (Cebus apella, Saguinus midas niger, Alouatta caraya, Aotus azarae, and Callicebus mol

57 Cebus apella, Saimiri ustius, Saguinus midas niger, Alouatta caraya, Aotus azarae, and Callicebus mol

58 Aspergillus niger also precipitated lead oxalate during growth in th

59 lead us to conclude that the cofactor in A. niger amine oxidase AO-I has been misidentified.

60 has been reported to exist in an Aspergillus niger amine oxidase AO-I.

61 e of a prolyl endopeptidase from Aspergillus niger (An-PEP) for HDX-MS.

62 A. niger and A. carbonarius samples were relatively higher

63 cans, Aspergillus fumigatus, and Aspergillus niger and antibacterial activity against Escherichia col

64 e obtained in Neurospora crassa, Aspergillus niger and Aspergillus awamori by codon optimization of t

65 early indicate that oxalate production in A. niger and B. cinerea is solely dependent on the hydrolyt

66 erium, Bacillus subtilis (including Bacillus niger and Bacillus globigii), Bacillus sphaericus, and B

67 Members of the A. niger and C. humicola species complexes may play unexpec

68 (MAO) was recently isolated from Aspergillus niger and cloned.

69 break response vaccination campaign in urban Niger and compare campaign estimates to measurements fro

70 port identification of tigA from Aspergillus niger and erp38 from Neurospora crassa, two novel member

71 ors of glucose oxidase (GO) from Aspergillus niger and horseradish peroxidase (HRP).

72 FINDINGS: In all pilots except Niger and Madagascar, there were large increases in QAAC

73 herichia coli, Candida albicans, Aspergillus niger and Microsporum gypseum with minimal inhibitory co

74 Both the A. niger and N. crassa proteins show homology with a stress

75 suspected and laboratory-confirmed cases in Niger and Nigeria from 2013 to 2017.

76 ntly caused large epidemics of meningitis in Niger and Nigeria.

77 In 2010, Niger and other meningitis belt countries introduced a m

78 s, and lead oxalate (PbC2O4), produced by A. niger and P. javanicus.

79 Aspergillus niger and Paecilomyces javanicus grew in 5 mM Pb(NO3)2-c

80 Aspergillus niger and Paecilomyces javanicus were grown on modified

81 a albicans, Rhizopus stolonifer, Aspergillus niger and Penicillium notatum when compared with standar

82 f two typical filamentous fungi, Aspergillus niger and Penicillium oxalicum.

83 nuclear genome of N. tabacum, plastome of H. niger and recombinant mitochondria.

84 nd brandy distillery wastes with Aspergillus niger and Rhizopus oligosporus were investigated.

85 the test manganese oxides after growth of A. niger and S. himantioides at 25 degrees C.

86 Manganese oxides were of low toxicity and A. niger and S. himantioides were able to grow on 0.5% (w/v

87 Aspergillus niger and S. himantioides were capable of solubilizing a

88 The ability of the soil fungi Aspergillus niger and Serpula himantioides to tolerate and solubiliz

89 s of NADPH eukNR from the fungus Aspergillus niger and the (15)epsilon for NADH eukNR from cell homog

90 h (Aspergillus fumigatus, A. flavus, and A. niger), and 48 h (other species); and (iii) the posacona

91 lipsiprymnus), a sable antelope (Hippotragus niger), and a white-tailed deer (Odocoileus virginianus)

92 kina Faso, 2.7 in Chad, 0.4 in Mali, 14.7 in Niger, and 12.5 in Togo.

93 spp. (64 A. flavus, 391 A. fumigatus, 46 A. niger, and 25 A. terreus isolates) collected from over 6

94 Conditioned media (CM) from A. fumigatus, A. niger, and A. flavus cultures also reduced CBF by ~10% a

95 gillus fumigatus, A. flavus, A. nidulans, A. niger, and A. terreus to caspofungin (MICs and minimum e

96 pecies (Aspergillus fumigatus, A. flavus, A. niger, and A. terreus).

97 ive aspergillosis (IA), with A. nidulans, A. niger, and A. ustus being rare causes of IA.

98 weight in rural areas of Timor-Leste, India, Niger, and Bangladesh.

99 programs in 3 West African countries (Mali, Niger, and Burkina Faso), covering the period 2009-2012.

100 ulous regions for three countries (DR Congo, Niger, and Nigeria).

101 i, P. aeruginosa, S. aureus, C. albicans, A. niger, and S. cerevisiae.

102 untries-Cameroon, Cote d'Ivoire, Madagascar, Niger, and Senegal--collected specimens from patients pr

103 cid-producing fungi, for example Aspergillus niger, and that plants grown with pyromorphite as sole p

104 mmercial enzyme preparation from Aspergillus niger, and the encoding gene was identified.

105 ite Plasmodium vivax, the fungus Aspergillus niger, and the TEM-family of beta-lactamase associated w

106 n 5 key countries: Burkina Faso, Chad, Mali, Niger, and Togo.

107 n meningitis belt: Burkina Faso, Chad, Mali, Niger, and Togo.

108 ub-Saharan Africa: Burkina Faso, Chad, Mali, Niger, and Togo.

109 4 African countries of Burkina Faso, Ghana, Niger, and Uganda.

110 oth experimentally, using colonies of Lasius niger, and with an agent-based simulation model, that ne

111 cose dehydrogenase, derived from Aspergillus niger (AnGDH), was characterized.

112 , however, we show that measles epidemics in Niger are highly episodic, particularly in the capital N

113 lygalacturonase II (EPG-II) from Aspergillus niger as it binds to an oligosaccharide substrate.

114 pergillus (Emericella) nidulans, Aspergillus niger, Aspergillus restrictus, Aspergillus sydowii, Aspe

115 fumigatus, Aspergillus nidulans, Aspergillus niger, Aspergillus terreus, Aspergillus ustus, and Asper

116 s flavus, Aspergillus fumigatus, Aspergillus niger, Aspergillus terreus, Fusarium spp., Pseudallesche

117 s fumigatus, Aspergillus flavus, Aspergillus niger, Aspergillus terreus, Scedosporium prolificans, Sc

118 predict seasonal incidence of meningitis in Niger at both the national and district levels.

119 aromyces bailii (ATCC 42476) and Aspergillus niger (ATCC 6275 (M68)).

120 reak occurred within a single watershed, the Niger basin, rather than between watersheds.

121 geoactive properties, including Aspergillus niger, Beauveria caledonica and Serpula himantioides, we

122 Here, we purified an A. niger beta-glucosidase (AnBgl1) and conducted its bioche

123 In the present work Aspergillus niger beta-glucosidase is immobilized within nanoscale p

124 cant spatial clustering in MM in Nigeria and Niger between 2013 and 2017, there is no strong evidence

125 e was used to capture Bacillus subtilis var. niger (BG) bacterial spores driven to the surface.

126 ydrogen uranyl phosphate were detected on A. niger biomass.

127 uatemala); in some African countries such as Niger, Burundi, and Burkina Faso; and in Vietnam and Chi

128 cacy against Penicillium sp. and Aspergillus niger but low effective against Rhizopus sp.

129 The orthologous transcript of Aspergillus niger can be alternatively spliced; the exon downstream

130 Trichoderma and Aspergillus niger cellulases activities were determined in a 5 min a

131 ing a multi-omics approach, adaptation of A. niger colonies to spatially separated and compositionall

132 OH)2 ) and bioaccumulated within Aspergillus niger colonies when grown on different inorganic nitroge

133 ered cybrids Nicotiana tabacum (+ Hyoscyamus niger) combining the nuclear genome of N. tabacum, plast

134 In the Niger component of the MORDOR I trial, we randomly assig

135 on average across the species in the Amazon, Niger, Congo, Salween, and Mekong basins.

136 ulations (Bini and Kanuri Nigerians, who are Niger-Congo [Bantu] and Nilo-Saharan speakers, respectiv

137 rghum population is distributed across early Niger-Congo and Afro-Asiatic language family areas with

138 two of the four major linguistic groups, the Niger-Congo and Afro-Asiatic, leaving the Nilo-Saharan a

139 population and between the Nilo-Saharan and Niger-Congo and Afro-Asiatic, we sequenced 50 genomes fr

140 umuz contributed a genetic component to most Niger-Congo B populations whereas Lugabara did not.

141 s associated with the Bantu languages of the Niger-Congo language family, in agreement with the farmi

142 lations than between any two Afro-Asiatic or Niger-Congo populations.

143 nd 250 genomes from 6 previously unsequenced Niger-Congo populations.

144 st 7000 years, and that Eastern and Southern Niger-Congo speaking groups share ancestry with Central

145 vity alleles were observed in equatorial and Niger-Congo speaking populations.

146 The San and Niger-Congo, Afroasiatic, and Nilo-Saharan lineages were

147 Niger-Congo, Nilo-Saharan, and Afroasiatic lineages dive

148 One involved populations related to Niger-Congo-speaking African populations, and the other

149 e of an over-producing strain of Aspergillus niger containing multiple copies of the encoding aglA ge

150 re, ferulic acid esterase A from Aspergillus niger contributes to total plant cell wall degradation b

151 It was found that A. niger could grow in the presence of monazite and mediate

152 For infections caused by A. terreus and A. niger, culture and PCR amplification from BAL fluid yiel

153 including those in the areas surrounding the Niger Delta or north western Amazon oil operations; thos

154 torial Atlantic (EEA) sediment core from the Niger Delta.

155 alpha-casein (alphas-CN) with an Aspergillus niger derived prolyl endoproteinase (An-PEP) for 1, 2, 3

156 ut also chimeric, two-parent derived, and H. niger-derived genes in a tobacco nuclear background.

157 specific endoglucanase (CEG from Aspergillus niger) did not cause cell wall creep, either by itself o

158 The crystal structure of A. niger DMML (in complex with Mg(2+) and in complex with M

159 Lower Cretaceous fossils from central Niger document the succession of sauropod dinosaurs on A

160 This and the finding that A. niger does not thrive on nicotinamide as a sole carbon s

161 Lead oxalate was precipitated by Aspergillus niger during bioleaching of natural and synthetic vanadi

162 me PGC is produced by the fungus Aspergillus niger during invasion of plant cell walls.

163 e production of lead oxalate dihydrate by A. niger during pyromorphite transformation, which is the f

164 consists of glucose oxidase from Aspergillus niger electrically "wired" by polymer I, having a redox

165 Finally, our results demonstrate that A. niger employs different enzymatic tools to adapt its met

166 of the eroA and ervA genes from Aspergillus niger, encoding functional orthologues of S. cerevisiae

167 chia coli expressing recombinant Aspergillus niger epoxide hydrolase as the model enzyme for various

168 In contrast to Ero1p in S. cerevisiae, A. niger EroA appears to be retained in the ER lumen by a C

169 ts show that the specificities of the two A. niger esterases are complementary.

170 Using Aspergillus niger Fdc1 as a model system, we reveal that isomerizati

171 from a community-based cohort of children in Niger followed from August 2006 to March 2007.

172 ampled in four regions of Senegal, Mali, and Niger from 1983-2012, using satellite-derived vegetation

173 ing data from hospital-based surveillance in Niger from 2010 through 2016.

174 the epidemiology of bacterial meningitis in Niger from 2010 to 2018.

175 e Arabidopsis thaliana plant and Aspergillus niger fungal species are presented.

176 The Aspergillus niger genome contains four genes that encode proteins ex

177 BLAST analysis of the A. niger genome for the presence of a similar pathway revea

178 ns assays were conducted against Aspergillus niger given its strong resistance and its relevance in s

179 e starch-binding domain (SBD) of Aspergillus niger glucoamylase 1 (GA-I) with substrate has been inve

180 and bread improver, similarly to Aspergillus niger glucose oxidase (GOX).

181 Saprobic fungi, such as Aspergillus niger, grow as colonies consisting of a network of branc

182 binofuranosidases within the secretome of A. niger grown on arabinan.

183 ological samples, the culture filtrate of A. niger grown on wheat straw.

184 V-1-infected people in Ivory Coast, Nigeria, Niger, Guinea Bissau, Benin, and Equatorial Guinea.

185 ysis of citrate-producing strains-namely, A. niger H915-1 (citrate titer: 157 g L(-1)), A1 (117 g L(-

186 Compared with A. niger A1 and L2, A. niger H915-1 contained 92 mutated genes, including a suc

187 Furthermore, transcriptome analysis of A. niger H915-1 revealed that the transcription levels of 4

188 The 2012 Countdown profile shows that Niger has achieved far greater reductions in child morta

189 It was confirmed that A. niger has the higher Pb tolerance (up to 1500 mg l(-1) P

190 nigerensis, from the Middle (?) Jurassic of Niger, has revealed several previously unknown osteologi

191 e inotocin from the black garden ant (Lasius niger), identified and cloned its cognate receptor and d

192 Several outbreaks occurred: NmC in Niger in 2015-2017, NmC in Mali in 2016, and NmW in Togo

193 Tambuwal, Nigeria in 2013 and 2014, Niamey, Niger in 2016, and in Sokoto and Zamfara States in Niger

194 omyces marxianus NRRL Y 7571 and Aspergillus niger in an aqueous-organic system.

195 first used widely in Burkina Faso, Mali, and Niger in December 2010 with great success.

196 ne was introduced in Burkina Faso, Mali, and Niger in December 2010.

197 n x-ray structures of a PME from Aspergillus niger in deglycosylated and Asn-linked N-acetylglucosami

198 Aspergillus niger is known to secrete large amounts of beta-glucosid

199 n-linked sulfhydryl oxidase from Aspergillus niger is related to the pyridine nucleotide-dependent di

200 d a superior performance against Aspergillus niger, isolated from spoiled pomegranate, compared with

201 zole, 1 (97.7%); voriconazole, 2 (99.3%); A. niger, itraconazole, 2 (100%); posaconazole, 0.5 (96.9%)

202 a, DR Congo; Ethiopia; Ghana; Kenya; Niamey, Niger; Kaduna, Nigeria; Lagos, Nigeria; and Uganda).

203 y of African Americans is predominantly from Niger-Kordofanian (approximately 71%), European (approxi

204 frican ancestry is most similar to non-Bantu Niger-Kordofanian-speaking populations, consistent with

205 ungal protein expression system (Aspergillus niger) leads to significantly enhanced specific growth r

206 The MORDOR I trial(1), conducted in Niger, Malawi and Tanzania, demonstrated that mass azith

207 Monoamine oxidase from Aspergillus niger (MAO-N) is a flavoenzyme that catalyses the oxidat

208 monoamine oxidase variants from Aspergillus niger (MAO-N) which display remarkable substrate scope a

209 ec un Oeil sur la Resistance) showed that in Niger, mass administration of azithromycin twice a year

210 atic (endopolygalacturonase from Aspergillus niger) methods.

211 n vaccination campaigns was collected by the Niger Ministry of Health and WHO.

212 estores oxalate production in an Aspergillus niger mutant strain, lacking a functional oahA gene.

213 also found to influence the morphology of A. niger mycelial pellets.

214 The present work showed that A. niger NaR lost 99.2% of soluble activity on vacuum-dryin

215 kina Faso, Chad, Cote d'Ivoire, Ghana, Mali, Niger, Nigeria, and Togo) collected and curated by the W

216 ublic of the Congo, Ethiopia, Guinea, Kenya, Niger, Nigeria, Sierra Leone, and Uganda.

217 public of Congo, Ghana, Cote d'Ivoire, Mali, Niger, Nigeria, Togo).

218 subsidised ACTs in Ghana, Kenya, Madagascar, Niger, Nigeria, Uganda, and Tanzania (including Zanzibar

219 DNA array analysis showed that unlike the A. niger oah gene, the DMML encoding gene is subject to cat

220 ative top predator, the chain pickerel (Esox niger), on contemporary timescales.

221 s cinerea, Penicillium expansum, Aspergillus niger or A. carbonarius.

222 m A. candidus, whereas spores from either A. niger or E. amstelodami activated p56(Hck), p72(Syk), an

223 inetic constants of starch hydrolysis for A. niger parent and mutant GAs calculated on the basis of m

224 e three-dimensional structure of Aspergillus niger pectin lyase B (PLB) has been determined by crysta

225 recombinant proteins: the fungal Aspergillus niger PhyA or the bacterial Escherichia coli AppA phytas

226 evant recombinant glycoproteins (Aspergillus niger phytase and anti-HIV antibody 2G12) produced in di

227 lding of the protein; and a heat-resistant A.niger phytase may be achieved by mutating certain critic

228 Aspergillus niger phytase shares 66% sequence identity, however, it

229 of either the expression of the Aspergillus niger polygalacturonase II (AnPGII; 35S:AnPGII plants) o

230 a-rhamnosidase from a commercial Aspergillus niger preparation, were immobilized onto acrylic beads.

231 However, Malcosteus niger produces far-red bioluminescence and its longwave

232 The hydrolytic specificity of Aspergillus niger prolyl endoproteinase (An-PEP) on purified beta-ca

233 upplementation with enzymes like Aspergillus niger propyl-endoprotease (AN-PEP), which can hydrolyse

234 e Upper Permian Moradi Formation of northern Niger provide an insight into the faunas that inhabited

235 ptian) rocks in the Tenere Desert of central Niger provide new information about spinosaurids, a pecu

236 Cdc42, Rac1 and Rho function in Aspergillus niger provides the first global perspective on their res

237 All but one country program (Niger) reached the disease-control target by two treatme

238 mmunities (n=40 375 children at baseline) in Niger received mass azithromycin and 291 communities (n=

239 hromycin to children younger than 5 years in Niger reduced the primary outcome of all-cause mortality

240 tion and degradation of wheat bran by the A. niger reference strain CBS 137562 and araR/xlnR regulato

241 e, ferulic acid esterase A, from Aspergillus niger releases ferulic acid and 5-5- and 8-O-4-dehydrodi

242 fied as Penicillium oxalicum and Aspergillus niger respectively in this study.

243 m has a restricted distribution by the upper Niger River and its tributaries that is associated with

244 as domesticated in a single region along the Niger river as opposed to noncentric domestication event

245 ctor of dispersal toward the west across the Niger River, through Anambra, Kogi, Delta, and Edo into

246 inea, Kenya, Lesotho, Liberia, Malawi, Mali, Niger, Rwanda, Sierra Leone, Tanzania, Zambia, and Zimba

247 Niger's dynamic Nm serogroup distribution highlights the

248 gar, in conjunction with urea hydrolysis and Niger seed agar, or D2 LSU sequencing can be reliably us

249 We report the first meningitis epidemic in Niger since the nationwide introduction of MACV.

250 In the Niger site of the MORDOR trial, we enrolled 30 villages

251 Aspergillus tubingensis, a member of the A. niger species complex, is described from clinical specim

252 lus tubingensis, a member of the Aspergillus niger species complex, was most prevalent from bronchosc

253 erichia coli O157:H7, Bacillus subtilis var. niger spores, and Staphylococcal enterotoxin type B from

254 Previous studies have shown that a mutant A. niger strain lacking the OAH gene does not produce oxala

255 We report a pseudo-outbreak of Aspergillus niger that followed building construction in our clinica

256 ed a candidate fungal extract of Aspergillus niger that inhibited the interaction between FREP1 and P

257 en in rural areas of Burundi, Guatemala, and Niger the shortest, with the tallest and shortest more t

258 history of citrate production in Aspergillus niger, the molecular mechanism of citrate accumulation i

259 ke the native OxDC isolated from Aspergillus niger, the recombinant, bacterial OxDC from Bacillus sub

260 In Aspergillus niger, the target protein is normally fused downstream o

261 ability of the geoactive fungus Aspergillus niger to colonize and transform manganese nodules from t

262 decentralised nutrition programmes permitted Niger to decrease child mortality at a pace that exceeds

263 Countdown therefore invited Niger to do an in-depth analysis of their child survival

264 ed a randomized, placebo-controlled trial in Niger to evaluate the efficacy of a live, oral bovine ro

265 large simple trial randomized communities in Niger to receive biannual distributions of azithromycin

266 sequently enhanced microbial functions of A. niger to resist Pb toxicity.

267 biquitous geoactive soil fungus, Aspergillus niger, to affect the mobility of REE in monazite and ide

268 y 1, 2003, and December 31, 2010, in Niamey, Niger, to determine risk factors for bacterial meningiti

269 pathogens, Penicillium italicum, Aspergillus niger, Trichoderma harzianum and Botrytis cinerea.

270 In A. niger, two transcription factors, AraR and XlnR, regulat

271 of glaA was attenuated in that strain of A. niger, UPR was not evident, suggesting that the transcri

272 of ferulic acid esterase A from Aspergillus niger using a range of synthetic ethyl esterified dehydr

273 on of azithromycin on childhood mortality in Niger waned in the third year of treatment.

274 Aspergillus niger was able to colonize and penetrate manganese nodul

275 also occurred in a liquid medium in which A. niger was able to remove the fine particles from suspens

276 In liquid media, A. niger was able to solubilize natural and synthetic struv

277 as observed, but binding to A. flavus and A. niger was calcium dependent.

278 Aspergillus niger was capable of solubilizing natural (fragments and

279 kotanin biosynthetic pathway of Aspergillus niger was expressed in Saccharomyces cerevisiae.

280 The phytase gene from Aspergillus niger was inserted into soybean transformation plasmids

281 this work, the geoactive fungus Aspergillus niger was investigated for struvite transformation on so

282 dren aged 1-60 months in the Dosso region of Niger was randomized to receive a single dose of either

283 ocess, and beta-glucosidase from Aspergillus niger was selected.

284 meningococcal meningitis (MM) in Nigeria and Niger, we aimed to re-evaluate the vaccination policy us

285 a reesei (Hypocrea jecorina) and Aspergillus niger, we identified the genes lxr4 and xhrA, respective

286 a double-blind, placebo-controlled trial in Niger, we randomly assigned children who were 6 to 59 mo

287 r fungal pigments extracted from Aspergillus niger were analyzed by MALDI-TOF and MALDI-qTOF (quadrup

288 t and hyphal negative control extracts of A. niger were not inhibited.

289 cterial endospores of Bacillus subtilis var. niger were obtained in a bipolar aerosol time-of-flight

290 ant mutant of a locally isolated Aspergillus niger were purified to apparent homogeneity.

291 until 31 July 2017, 30 rural communities in Niger were randomized to 2 years of biannual mass distri

292 controlled trial, 594 community clusters in Niger were randomly allocated (1:1 ratio) to receive bia

293 ioral audiograms of 2 fox squirrels (Sciurus niger) were determined with a conditioned avoidance proc

294 atrophaeus, formerly Bacillus subtilis var. niger, were analyzed using bioaerosol mass spectrometry.

295 Forty-eight communities in Matameye, Niger, were randomized to annual oral azithromycin treat

296 ctase glucose oxidase (GOx) from Aspergillus niger, which is the most frequently applied enzyme in el

297 1) partially stimulate the bioactivity of A. niger, which was confirmed by its elevated respiration (

298 el, the child-based HDI ranged from 0.140 in Niger (with mean across first-level administrative units

299 rage of four heterogeneous countries: Nepal, Niger, Yemen, and Zambia.

300 ering FOS synthesis using the enzyme from A. niger, yields of 26.62% of GF2 (kestose), 30.62% of GF3