The STE12alpha homolog is required for haploid filamentation but largely dispensable for mating and virulence in Cryptococcus neoformans.
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Cryptococcus gattii infectionsTranscription factors Mat2 and Znf2 operate cellular circuits orchestrating opposite- and same-sex mating in Cryptococcus neoformansCryptococcus neoformans STE12alpha regulates virulence but is not essential for mating.Regulatory roles of phosphorylation in model and pathogenic fungiCalcineurin is required for hyphal elongation during mating and haploid fruiting in Cryptococcus neoformansSte50 adaptor protein governs sexual differentiation of Cryptococcus neoformans via the pheromone-response MAPK signaling pathwayCalcineurin governs thermotolerance and virulence of Cryptococcus gattii.Mating-type locus of Cryptococcus neoformans: a step in the evolution of sex chromosomes.Adenylyl cyclase-associated protein Aca1 regulates virulence and differentiation of Cryptococcus neoformans via the cyclic AMP-protein kinase A cascadeThe DEAD-box RNA helicase Vad1 regulates multiple virulence-associated genes in Cryptococcus neoformans.Specialization of the HOG pathway and its impact on differentiation and virulence of Cryptococcus neoformansSte12 and Ste12-like proteins, fungal transcription factors regulating development and pathogenicityMating-type-specific and nonspecific PAK kinases play shared and divergent roles in Cryptococcus neoformans.Cyclic AMP-dependent protein kinase controls virulence of the fungal pathogen Cryptococcus neoformansMapping of the Cryptococcus neoformans MATalpha locus: presence of mating type-specific mitogen-activated protein kinase cascade homologs.Serotype AD strains of Cryptococcus neoformans are diploid or aneuploid and are heterozygous at the mating-type locusSignal transduction cascades regulating fungal development and virulence.The homeodomain transcription factor Ste12: Connecting fungal MAPK signalling to plant pathogenicity.Cryptococcus neoformans capsule structure evolution in vitro and during murine infectionRegulatory circuitry governing fungal development, drug resistance, and disease.Interaction between genetic background and the mating-type locus in Cryptococcus neoformans virulence potential.A STE12 homolog is required for mating but dispensable for filamentation in candida lusitaniaeAn STE12 homolog from the asexual, dimorphic fungus Penicillium marneffei complements the defect in sexual development of an Aspergillus nidulans steA mutant.The second STE12 homologue of Cryptococcus neoformans is MATa-specific and plays an important role in virulenceA novel specificity protein 1 (SP1)-like gene regulating protein kinase C-1 (Pkc1)-dependent cell wall integrity and virulence factors in Cryptococcus neoformansRoles for inositol-phosphoryl ceramide synthase 1 (IPC1) in pathogenesis of C. neoformans.A yeast under cover: the capsule of Cryptococcus neoformans.Cryptococcus gattii: a resurgent fungal pathogenSte12 transcription factor homologue CpST12 is down-regulated by hypovirus infection and required for virulence and female fertility of the chestnut blight fungus Cryphonectria parasitica.Cyclic AMP-dependent protein kinase catalytic subunits have divergent roles in virulence factor production in two varieties of the fungal pathogen Cryptococcus neoformans.Identification of the MATa mating-type locus of Cryptococcus neoformans reveals a serotype A MATa strain thought to have been extinctAnalysis of Cryptococcus neoformans sexual development reveals rewiring of the pheromone-response network by a change in transcription factor identityMitogen-activated protein kinase pathways and fungal pathogenesis.Amt2 permease is required to induce ammonium-responsive invasive growth and mating in Cryptococcus neoformansImpact of mating type, serotype, and ploidy on the virulence of Cryptococcus neoformansCongenic strains for genetic analysis of virulence traits in Cryptococcus gattiiMutation of the regulator of G protein signaling Crg1 increases virulence in Cryptococcus neoformans.Identification of QTLs Associated with Virulence Related Traits and Drug Resistance in Cryptococcus neoformans.Signalling pathways in the pathogenesis of Cryptococcus.Regulatory diversity of TUP1 in Cryptococcus neoformans.
P2860
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P2860
The STE12alpha homolog is required for haploid filamentation but largely dispensable for mating and virulence in Cryptococcus neoformans.
description
1999 nî lūn-bûn
@nan
1999 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@ast
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@en
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@nl
type
label
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@ast
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@en
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@nl
prefLabel
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@ast
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@en
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@nl
P2093
P2860
P1433
P1476
The STE12alpha homolog is requ ...... ce in Cryptococcus neoformans.
@en
P2093
J A Alspaugh
J R Perfect
L M Cavallo
P2860
P304
P407
P577
1999-12-01T00:00:00Z