human | Q5 |
P496 | ORCID iD | 0000-0002-8850-6975 |
P1053 | ResearcherID | A-4212-2019 |
P69 | educated at | University of Debrecen | Q903092 |
P108 | employer | University of Debrecen | Q903092 |
P106 | occupation | researcher | Q1650915 |
Q55280636 | Additional oxidative stress reroutes the global response of Aspergillus fumigatus to iron depletion. |
Q39525768 | Antifungal activity of extracellular hydrolases produced by autolysing Aspergillus nidulans cultures |
Q33836555 | Antifungal protein PAF severely affects the integrity of the plasma membrane of Aspergillus nidulans and induces an apoptosis-like phenotype |
Q43174154 | AtfA bZIP-type transcription factor regulates oxidative and osmotic stress responses in Aspergillus nidulans |
Q33963137 | Autolysis and aging of Penicillium chrysogenum cultures under carbon starvation: Chitinase production and antifungal effect of allosamidin |
Q48368914 | Autolytic enzymes are responsible for increased melanization of carbon stressed Aspergillus nidulans cultures. |
Q88229508 | Autolytic hydrolases affect sexual and asexual development of Aspergillus nidulans |
Q39036231 | Betamethasone augments the antifungal effect of menadione--towards a novel anti-Candida albicans combination therapy |
Q36548620 | Characterization of the aodA, dnmA, mnSOD and pimA genes in Aspergillus nidulans |
Q44223017 | Chromate sensitivity in fission yeast is caused by increased glutathione reductase activity and peroxide overproduction |
Q44441045 | Chromate tolerance caused by reduced hydroxyl radical production and decreased glutathione reductase activity in Schizosaccharomyces pombe |
Q25257237 | Comparison of gene expression signatures of diamide, H2O2 and menadione exposed Aspergillus nidulans cultures--linking genome-wide transcriptional changes to cellular physiology |
Q62641476 | Comparison of transcriptional and translational changes caused by long-term menadione exposure in Aspergillus nidulans |
Q35676014 | Core oxidative stress response in Aspergillus nidulans |
Q85390924 | Degradation of glutathione in Aspergillus nidulans - Short communication |
Q91342559 | Deletion of the fungus specific protein phosphatase Z1 exaggerates the oxidative stress response in Candida albicans |
Q61428000 | Development of oxidative stress tolerance resulted in reduced ability to undergo morphologic transitions and decreased pathogenicity in at-butylhydroperoxide-tolerant mutant ofCandida albicans |
Q44519620 | Does the detoxification of penicillin side-chain precursors depend on microsomal monooxygenase and glutathione S-transferase in Penicillium chrysogenum? |
Q38086769 | Echinocandins: production and applications |
Q45834078 | Effect of cell wall integrity stress and RlmA transcription factor on asexual development and autolysis in Aspergillus nidulans. |
Q45325495 | Effect of high relative humidity on dried Plantago lanceolata L. leaves during long-term storage: effects on chemical composition, colour and microbiological quality. |
Q62662653 | Effect of vitamin E on autolysis and sporulation of Aspergillus nidulans |
Q51019437 | Effects of hemin, CO2, and pH on the branching of Candida albicans filamentous forms. |
Q52000374 | Effects of mutations in the GanB/RgsA G protein mediated signalling on the autolysis of Aspergillus nidulans. |
Q55154084 | Endophytic fungi from the roots of horseradish (Armoracia rusticana) and their interactions with the defensive metabolites of the glucosinolate - myrosinase - isothiocyanate system. |
Q51852606 | Extracellular proteinase formation in carbon starving Aspergillus nidulans cultures--physiological function and regulation. |
Q85494286 | Filamentous fungi from Plantago lanceolata L. leaves: contribution to the pattern and stability of bioactive metabolites |
Q61423648 | Fungal siderophores function as protective agents of LDL oxidation and are promising anti-atherosclerotic metabolites in functional food |
Q102329292 | FvmnSOD is involved in oxidative stress defence, mitochondrial stability and apoptosis prevention in Fusarium verticillioides |
Q94600064 | General stress response or adaptation to rapid growth in Aspergillus nidulans? |
Q54578251 | Glucose-mediated repression of autolysis and conidiogenesis in Emericella nidulans. |
Q87610109 | Glutathione protects Candida albicans against horseradish volatile oil |
Q46506599 | Heterotrimeric G protein mediated regulation of proteinase production in Aspergillus nidulans |
Q44628611 | High-dose methylprednisolone influences the physiology and virulence of Candida albicans ambiguously and enhances the candidacidal activity of the polyene antibiotic amphotericin B and the superoxide-generating agent menadione |
Q95658538 | Increased Cd2+ biosorption capability of Aspergillus nidulans elicited by crpA deletion |
Q87194125 | Increased oxidative stress tolerance results in general stress tolerance in Candida albicans independently of stress-elicited morphological transitions |
Q45013981 | Influence of fadAG203R and deltaflbA mutations on morphology and physiology of submerged Aspergillus nidulans cultures |
Q79419990 | Lovastatin possesses a fungistatic effect against Candida albicans, but does not trigger apoptosis in this opportunistic human pathogen |
Q42327065 | MeaB-dependent nutrition sensing regulates autolysis in carbon starved Aspergillus nidulans cultures |
Q36235930 | Optimization of desferrioxamine E production by Streptomyces parvulus |
Q53522999 | Optimization of triacetylfusarinine C and ferricrocin productions in Aspergillus fumigatus. |
Q85643680 | Penicillium antifungal protein (PAF) is involved in the apoptotic and autophagic processes of the producer Penicillium chrysogenum |
Q92533115 | Physiological and Transcriptional Responses of Candida parapsilosis to Exogenous Tyrosol |
Q46374315 | Physiological and morphological characterization of tert -butylhydroperoxide tolerant Candida albicans mutants |
Q91247644 | Physiological background of the remarkably high Cd2+ tolerance of the Aspergillus fumigatus Af293 strain |
Q54352816 | Polyphasic characterization of "Aspergillus nidulans var. roseus" ATCC 58397. |
Q46848581 | Regulation of autolysis in Aspergillus nidulans |
Q124853304 | Stress Responses Elicited by Glucose Withdrawal in Aspergillus fumigatus |
Q38750212 | Study on the glutathione metabolism of the filamentous fungus Aspergillus nidulans |
Q96221302 | Supplementation of Aspergillus glaucus with gfdB gene encoding a glycerol 3-phosphate dehydrogenase in Aspergillus nidulans |
Q84699304 | The abc1-/coq8- respiratory-deficient mutant of Schizosaccharomyces pombe suffers from glutathione underproduction and hyperaccumulates Cd2+ |
Q46705654 | The appearances of autolytic and apoptotic markers are concomitant but differently regulated in carbon-starving Aspergillus nidulans cultures |
Q47812501 | The echinocandin B producer fungus Aspergillus nidulans var. roseus ATCC 58397 does not possess innate resistance against its lipopeptide antimycotic |
Q46668474 | The fluG-BrlA pathway contributes to the initialisation of autolysis in submerged Aspergillus nidulans cultures. |
Q37903792 | The small molecular mass antifungal protein of Penicillium chrysogenum--a mechanism of action oriented review |
Q39204957 | Towards high-siderophore-content foods: optimisation of coprogen production in submerged cultures of Penicillium nalgiovense |
Q54283577 | Transcriptome changes initiated by carbon starvation in Aspergillus nidulans. |
Q38645342 | Transcriptome-Based Modeling Reveals that Oxidative Stress Induces Modulation of the AtfA-Dependent Signaling Networks in Aspergillus nidulans |
Q39748880 | Trehalose overproduction affects the stress tolerance of Kluyveromyces marxianus ambiguously |
Q46797375 | γ-Glutamyl transpeptidase (GgtA) of Aspergillus nidulans is not necessary for bulk degradation of glutathione |
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