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1 nown whether such an association exists with Cryptococcus neoformans.
2 for virulence of the human pathogenic fungus Cryptococcus neoformans.
3 th a similar function in the related species Cryptococcus neoformans.
4 mall-RNA biogenesis in the pathogenic fungus Cryptococcus neoformans.
5 ual development of the human fungal pathogen Cryptococcus neoformans.
6 ntainment following pulmonary challenge with Cryptococcus neoformans.
7 C57BL/6 mice after pulmonary infection with Cryptococcus neoformans.
8 pC) and with the LPMO-like protein Bim1 from Cryptococcus neoformans.
9 hose for the pathogens, Candida albicans and Cryptococcus neoformans.
10 involved in polysaccharide O-acetylation in Cryptococcus neoformans.
11 haromyces cerevisiae, Malassezia furfur, and Cryptococcus neoformans.
12 illness caused by the opportunistic pathogen Cryptococcus neoformans.
13 ts (MC) arising from phenotypic switching of Cryptococcus neoformans.
14 transgene array in the human fungal pathogen Cryptococcus neoformans.
15 prolongs the survival of mice infected with Cryptococcus neoformans.
16 ghest prevalence of coinfection with HIV and Cryptococcus neoformans.
17 e host survival of the human fungal pathogen Cryptococcus neoformans.
18 al3b (CNAG_07348) from the pathogenic fungus Cryptococcus neoformans.
19 tic cells (DC) during their interaction with Cryptococcus neoformans.
20 ssociated trait by the human fungal pathogen Cryptococcus neoformans.
21 nt role in protection against infection with Cryptococcus neoformans.
22 osis induced by intratracheal inoculation of Cryptococcus neoformans.
23 T cell responses to the opportunistic fungus Cryptococcus neoformans.
24 l time of mice infected intracerebrally with Cryptococcus neoformans.
25 nt role in immunity to the pathogenic fungus Cryptococcus neoformans.
26 Candida species, Aspergillus fumigatus, and Cryptococcus neoformans.
27 sponse to infection with the fungal pathogen Cryptococcus neoformans.
28 nsing pathway in the human pathogenic fungus Cryptococcus neoformans.
29 t regulates virulence in the fungal pathogen Cryptococcus neoformans.
30 IP5/IP7, which is essential for virulence of Cryptococcus neoformans.
31 central role in regulating the virulence of Cryptococcus neoformans.
32 d with the distantly related fungal pathogen Cryptococcus neoformans.
33 of H3K27 methylation (H3K27me) in the yeast Cryptococcus neoformans.
36 a spp., 146 from 9 Aspergillus spp., 84 from Cryptococcus neoformans, 40 from 23 other mold species,
37 nfected with a moderately virulent strain of Cryptococcus neoformans (52D), which resulted in prolong
38 trophils have been shown to efficiently kill Cryptococcus neoformans, a causative agent of meningoenc
40 c functional analysis of the phosphatases in Cryptococcus neoformans, a fungal pathogen that causes l
47 es for melanization of the pathogenic fungus Cryptococcus neoformans also offers unique opportunities
48 ulates not only mating but also virulence in Cryptococcus neoformans, an opportunistic human pathogen
50 d specificity were as follows: 100% each for Cryptococcus neoformans and C. gattii, 98.6% and 100% fo
51 ally expressed by the four main serotypes of Cryptococcus neoformans and C. gattii, is heterogeneousl
52 Aspergillus fumigatus, Alternaria alternata, Cryptococcus neoformans and Candida albicans) proteins w
53 inent function in the capture of circulating Cryptococcus neoformans and Candida albicans, thereby re
54 e of macrophage autophagy in the response to Cryptococcus neoformans and Candida albicans, two import
55 ectivity for the Hsp90 isoforms expressed by Cryptococcus neoformans and Candida albicans, two pathog
62 ompare the molecular genotypes of strains of Cryptococcus neoformans and Cryptococcus gattii isolated
65 poxia-mimetic CoCl2 in the pathogenic fungus Cryptococcus neoformans and demonstrated that CoCl2 lead
66 rabidopsis thaliana, Caenorhabditis elegans, Cryptococcus neoformans and Drosophila melanogaster.
67 Rho-GDI homolog in the human fungal pathogen Cryptococcus neoformans and investigated its impact on p
68 erol endoperoxide, which were active against Cryptococcus neoformans and methicillin-resistance Staph
70 H)2) cell bias upon pulmonary infection with Cryptococcus neoformans and other non-T(H)2 stimuli.
71 in GM-CSF are susceptible to infections with Cryptococcus neoformans and other opportunistic fungi.
72 ons against Candida albicans, Candida auris, Cryptococcus neoformans, and Aspergillus fumigatus (Sigm
74 sential for virulence of the fungal pathogen Cryptococcus neoformans, and bacterial P5CDHs have been
75 heromone responses, mating, and virulence in Cryptococcus neoformans, and it also reiterates that the
76 hly active against a second fungal pathogen, Cryptococcus neoformans, and moderately active against a
77 ntamoeba histolytica, Trichomonas vaginalis, Cryptococcus neoformans, and Saccharomyces cerevisiae us
80 gh activity toward Aspergillus fumigatus and Cryptococcus neoformans at acidic pH, yet remained nonto
81 e infections with pathogenic species such as Cryptococcus neoformans Because the purine biosynthesis
83 se, and catalytically dead Tps2PD(D24N) from Cryptococcus neoformans bound to trehalose-6-phosphate (
84 can is a major component of the cell wall of Cryptococcus neoformans, but its function has not been i
88 rated that the opportunistic fungal pathogen Cryptococcus neoformans can synthesize authentic immunom
89 ificity of V region-identical IgE and IgA to Cryptococcus neoformans capsular polysaccharide and foun
95 xin, Srx1, in oxidative stress resistance of Cryptococcus neoformans causing fungal meningoencephalit
99 rain - is a recently described phenomenon in Cryptococcus neoformans (Cn) and Cryptococcus gattii (Cg
102 tudies, we showed that the pathogenic fungus Cryptococcus neoformans (Cn) produces a specific and uni
103 iodiomycete forming an induced DOPA-melanin, Cryptococcus neoformans (CN); and the slow-growing envir
106 D82 showed rapid and specific recruitment to Cryptococcus neoformans-containing phagosomes compared t
107 ith Pneumocystis jirovecii (pneumocystosis), Cryptococcus neoformans (cryptococcosis), Histoplasma ca
109 an parechovirus, varicella-zoster virus, and Cryptococcus neoformans/Cryptococcus gattii We describe
111 l-deficient mice have demonstrated increased Cryptococcus neoformans dissemination from lungs to brai
112 aride capsule of the human pathogenic fungus Cryptococcus neoformans elicit diverse effects on fungal
116 e expulsion of the lethal endosomal pathogen Cryptococcus neoformans from mammalian macrophages, also
118 he pathogenicity of a human fungal pathogen, Cryptococcus neoformans, GCS1 is not required for the pa
120 AfTOK1 (Aspergillus fumigatus), and H99TOK (Cryptococcus neoformans grubii) are K(+) -selective and
121 ed the role of a Th2 bias in pathogenesis of Cryptococcus neoformans H99 infection by comparing inhal
126 ot been studied in the human fungal pathogen Cryptococcus neoformans Here, we identified and characte
127 n of clinically significant Candida species, Cryptococcus neoformans, Histoplasma capsulatum, and Bla
128 nistic fungal pathogens Candida albicans and Cryptococcus neoformans However, the molecular mechanism
129 ction with the opportunistic fungal pathogen Cryptococcus neoformans; however, the role of plasmacyto
131 e mAbs to the capsule of the fungal pathogen Cryptococcus neoformans impaired yeast budding by trappi
134 he development of the protective response to Cryptococcus neoformans in mice with cryptococcal pneumo
135 ts for different levels of susceptibility to Cryptococcus neoformans in the mouse infection model.
138 e highly susceptible to intratracheal (i.t.) Cryptococcus neoformans infection relative to BALB/c mic
139 ing the risk of dissemination and outcome of Cryptococcus neoformans infection were assessed in 111 o
140 cterium tuberculosis, Toxoplasma gondii, and Cryptococcus neoformans infection, implicating inflammat
141 tes transmigration of the neurotropic fungus Cryptococcus neoformans into the brain parenchyma after
178 The SREBP ortholog in the pathogenic fungus Cryptococcus neoformans is also activated by high levels
199 ity to progressive infection with the fungus Cryptococcus neoformans is associated with an allergic p
200 pulmonary infection with the fungal pathogen Cryptococcus neoformans is associated with the accumulat
201 ulmonary clearance of the encapsulated yeast Cryptococcus neoformans is associated with the CCR2-medi
204 the disease (cryptococcal disease) caused by Cryptococcus neoformans is incontrovertible, but whether
209 d trait of the opportunistic fungal pathogen Cryptococcus neoformans is the production of melanin pig
210 The manifestation of virulence traits in Cryptococcus neoformans is thought to rely on intracellu
212 hannel from the model human fungal pathogen, Cryptococcus neoformans, is directly activated by the de
213 l pathogens of environmental origin, such as Cryptococcus neoformans, is their ability to adapt to ma
216 andida sp., 49 Aspergillus fumigatus, and 33 Cryptococcus neoformans isolates were obtained from infe
217 es, 15 isolates of the Zygomycetes order, 10 Cryptococcus neoformans isolates, 8 Rhodotorula isolates
218 C. glabrata, and 53 C. krusei isolates), 35 Cryptococcus neoformans isolates, and 191 other clinical
219 virulence factor laccase to the cell wall in Cryptococcus neoformans Laccase activity was perturbed,
221 e fungal pathogens Aspergillus fumigatus and Cryptococcus neoformans, little was known about their in
222 Pathogens included Balamuthia mandrillaris, Cryptococcus neoformans, lymphocytic choriomeningitis vi
224 Isavuconazole showed good activities against Cryptococcus neoformans (MIC90, 0.12 mug/ml) and other n
225 Numerous virulence factors expressed by Cryptococcus neoformans modulate host defenses by promot
226 rable to infection by the encapsulated yeast Cryptococcus neoformans Most commonly found in the envir
230 of 1201 signature-tagged deletion strains of Cryptococcus neoformans mutants to identify previously u
231 s presenting with P. marneffei (n = 719) and Cryptococcus neoformans (n = 1598) infection to the Hosp
235 seminated infections with the fungal species Cryptococcus neoformans or, less frequently, Cryptococcu
237 xylomannan (GXM), the major component of the Cryptococcus neoformans polysaccharide capsule, hydrolyz
238 b, and IgG3 with a 12-mer peptide mimetic of Cryptococcus neoformans polysaccharide revealed a stoich
242 aride capsule of the human pathogenic fungus Cryptococcus neoformans promotes opsonization but also i
244 gulatory networks in human pathogens such as Cryptococcus neoformans provides insights into host-path
245 The cell wall of pathogenic fungi such as Cryptococcus neoformans, provides a formidable barrier t
246 on and analysis of SRP in the human pathogen Cryptococcus neoformans, providing the first description
248 ulmonary clearance of the encapsulated yeast Cryptococcus neoformans requires a T1 adaptive immune re
249 ulmonary clearance of the encapsulated yeast Cryptococcus neoformans requires the development of T1-t
251 Candida albicans, Aspergillus fumigatus and Cryptococcus neoformans, result in more deaths annually
253 meningoencephalitis-causing fungal pathogen Cryptococcus neoformans, sexual development leads to the
256 of C57BL/6 mice with the moderately virulent Cryptococcus neoformans strain 52D models the complex ad
258 s in mice given a pulmonary infection with a Cryptococcus neoformans strain engineered to produce the
259 ential of these genes by comparing wild-type Cryptococcus neoformans strain H99 with deletant and com
260 of interferon-gamma transgene expression by Cryptococcus neoformans strain H99gamma in abrogating al
261 yptococcal meningitis patients infected with Cryptococcus neoformans strains with the same multilocus
262 oducibility strains (4 Candida species and 6 Cryptococcus neoformans strains), and 746 isolates of Ca
263 otective immune responses to highly virulent Cryptococcus neoformans strains, such as H99, are associ
264 etrotransposons in the human fungal pathogen Cryptococcus neoformans The resulting DSBs were repaired
266 pathogens Candida albicans, C. glabrata and Cryptococcus neoformans, the food spoilage organism Zygo
273 in plants and animals, but in fungi such as Cryptococcus neoformans they are also associated with vi
275 bilities of 110 isolates of Candida spp. and Cryptococcus neoformans to amphotericin B, caspofungin,
276 nase Ste20, allows the human fungal pathogen Cryptococcus neoformans to grow at high temperature.
278 ability of the opportunistic fungal pathogen Cryptococcus neoformans to resist oxidative stress is on
279 rcular (Histoplasma capsulatum) to punctate (Cryptococcus neoformans) to labeling at the bud sites (C
280 ignalling pathways to the basal tolerance of Cryptococcus neoformans towards fluconazole, the widely
281 that in the pathogenic basidiomycetous yeast Cryptococcus neoformans, two Galpha subunits (Gpa2, Gpa3
284 Most cases of cryptococcosis are caused by Cryptococcus neoformans var. grubii (serotype A), which
288 cies/organism groups were isolated, of which Cryptococcus neoformans was the most common (31.2% of al
289 the cell wall of the human pathogenic fungus Cryptococcus neoformans We observed that melanin is asse
293 r understanding Ab-mediated immunity against Cryptococcus neoformans, where the different isotypes ma
294 sis is important for virulence of the fungus Cryptococcus neoformans, which can cause lethal meningoe
295 ypic diversity in the human pathogenic yeast Cryptococcus neoformans, which is globally distributed a
296 fection with environmental organisms such as Cryptococcus neoformans, which require no host in their
297 ave directly correlated phenotypic traits of Cryptococcus neoformans with clinical outcome of infecte
299 of lipid droplets during the interaction of Cryptococcus neoformans with macrophages in the presence
300 vestigated the outcome of the interaction of Cryptococcus neoformans with murine macrophages using la