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1 ion in the lungs of naive mice infected with Histoplasma capsulatum.
2 ith class 5 or 6 organisms than with class 2 Histoplasma capsulatum.
3 omoters of two yeast phase-specific genes in Histoplasma capsulatum.
4 nt of heat shock protein 60 from the fungus, Histoplasma capsulatum.
5 e during primary infection with the pathogen Histoplasma capsulatum.
6 of both primary and secondary infection with Histoplasma capsulatum.
7 ular genetic studies of the dimorphic fungus Histoplasma capsulatum.
8 sponse against Mycobacterium tuberculosis or Histoplasma capsulatum.
9 are essential for controlling infection with Histoplasma capsulatum.
10 lution of infection with the fungal pathogen Histoplasma capsulatum.
11 inst many intracellular infections including Histoplasma capsulatum.
12 fungal nitric oxide reductase (P450nor) from Histoplasma capsulatum.
13 ell as to the natural CR3 ligands, iC3b, and Histoplasma capsulatum.
14 laboratory evidence of recent infection with Histoplasma capsulatum.
15 recombinant (r) hsp60 protects mice against Histoplasma capsulatum.
16 ochondria of the pathogenic dimorphic fungus Histoplasma capsulatum.
17 TNF-alpha in CCR5(-/)(-) mice infected with Histoplasma capsulatum.
18 is) infected with the intracellular pathogen Histoplasma capsulatum.
19 charomyces cerevisiae, Candida albicans, and Histoplasma capsulatum.
20 tope in Blastomyces dermatitidis and also in Histoplasma capsulatum.
21 R5 during infection with the fungal pathogen Histoplasma capsulatum.
22 eople harbor latent infections of the fungus Histoplasma capsulatum.
23 control of infection by the dimorphic fungus Histoplasma capsulatum.
24 e human pathogens Coccidioides posadasii and Histoplasma capsulatum.
25 tective immunity in an Ag-specific manner to Histoplasma capsulatum.
26 ith recognition of the worldwide presence of Histoplasma capsulatum.
27 elevated in the lungs of mice infected with Histoplasma capsulatum.
28 sis influenced host resistance to the fungus Histoplasma capsulatum.
29 role of these agents in host defense against Histoplasma capsulatum.
30 influenced protective and memory immunity to Histoplasma capsulatum.
31 these genes in vivo, mice were infected with Histoplasma capsulatum.
32 ve domain (F3) of heat-shock protein 60 from Histoplasma capsulatum.
33 A monoclonal antibody (MAb) raised against a Histoplasma capsulatum 80-kDa hsp showed cross-reactivit
34 dermatitidis an extracellular pathogen, and Histoplasma capsulatum a facultative intracellular patho
36 D-1 in a mouse model of acute infection with Histoplasma capsulatum, a major human pathogenic fungus.
37 CBP is the most abundant protein secreted by Histoplasma capsulatum, a pathogenic fungus that causes
40 ffers from the epitopes that are shared with Histoplasma capsulatum and Blastomyces dermatitidis.
41 it exerts potent antifungal activity against Histoplasma capsulatum and Cryptococcus neoformans by di
42 f microarrays built with genomic elements of Histoplasma capsulatum and ESTs of Paracoccidioides bras
43 oplasmosis; it has in vitro activity against Histoplasma capsulatum and has shown success in case rep
44 oplasmosis; it has in-vitro activity against Histoplasma capsulatum and has shown success in case rep
45 ular evidence suggests a direct link between Histoplasma capsulatum and presumed ocular histoplasmosi
46 nsformation system for the pathogenic fungus Histoplasma capsulatum and used it to examine the effect
47 nt Candida species, Cryptococcus neoformans, Histoplasma capsulatum, and Blastomyces dermatitidis fro
48 ns in North America (Coccidioides posadasii, Histoplasma capsulatum, and Blastomyces dermatitidis), h
50 DCs) with Leishmania donovani promastigotes, Histoplasma capsulatum, and Mycobacterium kansasii impai
52 s in the lungs of C57BL/6 mice infected with Histoplasma capsulatum, and the elimination of these cel
57 rmally dimorphic fungal pathogens, including Histoplasma capsulatum, are soil fungi that undergo dram
58 fungi, including the subject of this study, Histoplasma capsulatum, are temperature-responsive organ
60 nction of HIF-1alpha in the host response to Histoplasma capsulatum because granulomas induced by thi
61 ribosomal DNA, were used to amplify DNA from Histoplasma capsulatum, Blastomyces dermatitidis, Coccid
63 r to a triglycosyl IPC (Hc-VI) reported from Histoplasma capsulatum, but differing in the anomeric co
64 nses against intracellular pathogens such as Histoplasma capsulatum, but its mode of action remains e
67 molecular cloning and characterization of a Histoplasma capsulatum cDNA (GH17) that encodes an antig
69 y significant episodes, the isolated fungus (Histoplasma capsulatum, Coccidioides immitis/posadasii,
71 esented with a Mycobacterium haemophilum and Histoplasma capsulatum coinfection occurring 21 years af
72 ported that immunization with H antigen from Histoplasma capsulatum did not protect mice against an i
74 dentified a secreted proteolytic activity in Histoplasma capsulatum effective toward DppIV-specific s
79 1990 through 1994, we fortuitously isolated Histoplasma capsulatum from six patients with AIDS whose
81 library representing 10-fold coverage of the Histoplasma capsulatum G217B genome was used to construc
87 human fungal pathogens Candida albicans and Histoplasma capsulatum have been reported to protect aga
93 rimary and secondary infection by the fungus Histoplasma capsulatum (HC) is multifactorial, requiring
96 genic fungi Cryptococcus neoformans (CN) and Histoplasma capsulatum (HC) to external gamma-radiation
97 ix proteins, and the intracellular growth of Histoplasma capsulatum (Hc) yeasts were quantified and c
98 e deficient in their capacity to phagocytose Histoplasma capsulatum (Hc) yeasts, and are more permiss
102 ), Cryptococcus neoformans (cryptococcosis), Histoplasma capsulatum (histoplasmosis), and Talaromyces
105 e examined the immunobiological responses to Histoplasma capsulatum in lungs of gamma interferon (IFN
106 n-4 impairs clearance of the fungal pathogen Histoplasma capsulatum in mice lacking the chemokine rec
110 tion with heat shock protein 60 (Hsp60) from Histoplasma capsulatum induces a protective immune respo
111 tigated whether Blastomyces dermatitidis and Histoplasma capsulatum-infected canine and feline lungs
113 emonstrate that CCR5 controls the outcome of Histoplasma capsulatum infection by dictating thymic and
114 mmalian host specifically limits iron during Histoplasma capsulatum infection, and fungal acquisition
129 cell-depleted mice infected with the fungus Histoplasma capsulatum is associated with impairment of
130 A fundamental feature of the fungal pathogen Histoplasma capsulatum is its ability to shift from a my
132 the pathogenesis of the respiratory pathogen Histoplasma capsulatum is the conversion from the mold f
136 The phylogeny of 46 geographically diverse Histoplasma capsulatum isolates representing the three v
139 ients with deficient cell-mediated immunity, Histoplasma capsulatum may disseminate throughout the bo
140 uconazole (Flu) and amphotericin B (AmB) for Histoplasma capsulatum meningitis, MICs were determined
142 ronment in which the primary fungal pathogen Histoplasma capsulatum multiplies and disseminates from
144 ve with IS only (three Candida albicans, one Histoplasma capsulatum, one Candida glabrata, and one Fu
145 tion of mice with heat shock protein 60 from Histoplasma capsulatum or a polypeptide from the protein
146 ombinant heat shock protein 60 (rHsp60) from Histoplasma capsulatum or a region of the protein design
147 statistically significantly more isolates of Histoplasma capsulatum (P = 0.004), but all of these iso
148 ntiana, Fusarium oxysporum, Fusarium solani, Histoplasma capsulatum, Phialophora spp., Pseudallescher
149 sis, a systemic mycosis caused by the fungus Histoplasma capsulatum, primarily affects immune-suppres
156 bility to bind calcium and its prevalence as Histoplasma capsulatum's most abundant secreted protein.
163 parasite of macrophages, the yeast phase of Histoplasma capsulatum, survives and proliferates within
165 FM) is a rare complication of infection with Histoplasma capsulatum that can lead to obstruction of p
166 are consequence of infection with the fungus Histoplasma capsulatum that can lead to occlusion of lar
167 tested a real-time LightCycler PCR assay for Histoplasma capsulatum that correctly identified the 34
168 ermatitidis, the agent of blastomycosis, and Histoplasma capsulatum, the agent of histoplasmosis, are
169 xpressed the gene encoding this protein from Histoplasma capsulatum to study its immunological activi
170 h chitin, in patterns ranging from circular (Histoplasma capsulatum) to punctate (Cryptococcus neofor
174 be of limited use, whereas the detection of Histoplasma capsulatum var. capsulatum antigens may prov
176 ther the thermally dimorphic fungal pathogen Histoplasma capsulatum var. capsulatum produced melanin
180 nd ploidy of the dimorphic pathogenic fungus Histoplasma capsulatum was determined by using DNA renat
181 e H antigen of the dimorphic fungal pathogen Histoplasma capsulatum was first described over 40 years
182 )-alpha after intranasal exposure of mice to Histoplasma capsulatum was necessary for control of prim
183 irulence mutants of Francisella novicida and Histoplasma capsulatum, we confirmed the applicability o
184 yces dermatitidis, Sporothrix schenckii, and Histoplasma capsulatum were each ingested by amoebae and
187 esii; and a more diverged pathogenic fungus, Histoplasma capsulatum, were sequenced and compared with
188 t (Y) phase of the dimorphic fungal pathogen Histoplasma capsulatum which are transcriptionally silen
189 ts with disseminated Coccidioides immitis or Histoplasma capsulatum with heterozygous missense mutati
190 can is present in the outermost layer of the Histoplasma capsulatum yeast cell wall and contributes t
191 potent and long-lasting fungistasis against Histoplasma capsulatum yeasts and that all of the fungis