scholarly article | Q13442814 |
P50 | author | Ferry Hagen | Q41579860 |
Alfred Botha | Q56015824 | ||
P2093 | author name string | T Boekhout | |
J Swart | |||
A Botes | |||
H Vismer | |||
P2860 | cites work | The genome of the basidiomycetous yeast and human pathogen Cryptococcus neoformans | Q22065807 |
Sexual reproduction between partners of the same mating type in Cryptococcus neoformans | Q28246484 | ||
A new genus, filobasidiella, the perfect state of Cryptococcus neoformans | Q28296421 | ||
Cryptococcosis in the era of AIDS--100 years after the discovery of Cryptococcus neoformans. | Q30424017 | ||
Genetic relationship between Cryptococcus neoformans var. neoformans strains of serotypes A and D | Q33674974 | ||
Presence of alpha and a mating types in environmental and clinical collections of Cryptococcus neoformans var. gattii strains from Australia | Q33962499 | ||
Origin of Cryptococcus neoformans var. neoformans diploid strains | Q33973899 | ||
Serotype AD strains of Cryptococcus neoformans are diploid or aneuploid and are heterozygous at the mating-type locus | Q34005505 | ||
Laccase of Cryptococcus neoformans is a cell wall-associated virulence factor | Q34008955 | ||
Cryptococcus neoformans: size range of infectious particles from aerosolized soil | Q34414840 | ||
Multilocus sequence typing reveals three genetic subpopulations of Cryptococcus neoformans var. grubii (serotype A), including a unique population in Botswana | Q34588507 | ||
Clonal reproduction and limited dispersal in an environmental population of Cryptococcus neoformans var gattii isolates from Australia | Q34753071 | ||
Increasing the oxidative stress response allows Escherichia coli to overcome inhibitory effects of condensed tannins | Q35096188 | ||
'Ready made' virulence and 'dual use' virulence factors in pathogenic environmental fungi--the Cryptococcus neoformans paradigm | Q35206884 | ||
Uniqueness of the mating system in Cryptococcus neoformans | Q35761495 | ||
Cryptococcus neoformans mates on pigeon guano: implications for the realized ecological niche and globalization | Q35948250 | ||
Isolates of Cryptococcus neoformans from infected animals reveal genetic exchange in unisexual, alpha mating type populations | Q36939050 | ||
Natural habitat of Cryptococcus neoformans var. gattii | Q37186662 | ||
Dimorphism and haploid fruiting in Cryptococcus neoformans: association with the alpha-mating type | Q37502523 | ||
Ecology, life cycle, and infectious propagule of Cryptococcus neoformans | Q37600845 | ||
Molecular typing of Cryptococcus neoformans: taxonomic and epidemiological aspects | Q38558615 | ||
Epidemiologic differences between the two varieties of Cryptococcus neoformans | Q39154213 | ||
Natural habitat of Cryptococcus neoformans var. neoformans in decaying wood forming hollows in living trees | Q39426670 | ||
Transcription factor STE12alpha has distinct roles in morphogenesis, virulence, and ecological fitness of the primary pathogenic yeast Cryptococcus gattii | Q41487634 | ||
Evidence of recombination in mixed-mating-type and alpha-only populations of Cryptococcus gattii sourced from single eucalyptus tree hollows | Q42660028 | ||
Characterization of a novel laccase produced by the wood-rotting fungus Phellinus ribis | Q43697825 | ||
The use of Eucalyptus tereticornis Sm. (Myrtaceae) oil (leaf extract) as a natural larvicidal agent against the malaria vector Anopheles stephensi Liston (Diptera: Culicidae). | Q44170002 | ||
Long-distance dispersal and recombination in environmental populations of Cryptococcus neoformans var. grubii from India | Q45108087 | ||
The human fungal pathogen Cryptococcus can complete its sexual cycle during a pathogenic association with plants | Q46898402 | ||
Assessing nitrogen fixation in mixed- and single-species plantations of Eucalyptus globulus and Acacia mearnsii. | Q51102328 | ||
Ecology of Cryptococcus neoformans. | Q51207954 | ||
Same-sex mating and the origin of the Vancouver Island Cryptococcus gattii outbreak | Q57255677 | ||
Hybrid genotypes in the pathogenic yeast Cryptococcus neoformans | Q58035012 | ||
Infections with Cryptococcus neoformans in the acquired immunodeficiency syndrome | Q69532023 | ||
Haploid fruiting in Cryptococcus neoformans is not mating type alpha-specific | Q73738271 | ||
Decaying wood in tree trunk hollows as a natural substrate for Cryptococcus neoformans and other yeast-like fungi of clinical interest | Q74506658 | ||
Genetic characterization of environmental isolates of the Cryptococcus neoformans species complex from Brazil | Q79341217 | ||
P433 | issue | 4 | |
P921 | main subject | Cryptococcus neoformans | Q131924 |
P304 | page(s) | 757-765 | |
P577 | publication date | 2008-10-11 | |
P1433 | published in | Microbial Ecology | Q15766091 |
P1476 | title | Growth and mating of Cryptococcus neoformans var. grubii on woody debris | |
P478 | volume | 57 |
Q27002687 | Cryptococcus gattii infections |
Q33636108 | Cryptococcus gattii outbreak expands into the Northwestern United States with fatal consequences |
Q37937029 | Cryptococcus gattii: where do we go from here? |
Q34874531 | Development of an aerosol model of Cryptococcus reveals humidity as an important factor affecting the viability of Cryptococcus during aerosolization |
Q37672042 | Fungal sex and pathogenesis |
Q21284793 | Global Molecular Epidemiology of Cryptococcus neoformans and Cryptococcus gattii: An Atlas of the Molecular Types |
Q36284100 | Plants promote mating and dispersal of the human pathogenic fungus Cryptococcus |
Q84136113 | The lignicolous fungus Coniochaeta pulveracea and its interactions with syntrophic yeasts from the woody phylloplane |
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