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237 results for “Antifungals”

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ClinicalTrials.gov32/100

Antifungal Prophylaxis in Pediatric Acute Leukemia

ClinicalTrials.gov study NCT00624143. IPD Sharing: Not stated. Countries: 1. Publications: 2.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Beta-Glucan Driven vs. Empirical Antifungal Therapy in Critically Ill Patients

ClinicalTrials.gov study NCT03117439. IPD Sharing: NO. Countries: 1. Publications: 1.

closedIPD-NOFeb 2026View details →
ClinicalTrials.gov32/100

Study of EL219 vs Standard of Care for Early Antifungal Therapy of Suspected Invasive Mould Infections

ClinicalTrials.gov study NCT07215273. IPD Sharing: UNDECIDED. Countries: 1. Publications: 38.

restrictedIPD-UNDECIDEDFeb 2026View details →
ClinicalTrials.gov32/100

Evaluation of Antifungal Prophylaxis on Graft-versus-host Disease (GVHD) Patients

ClinicalTrials.gov study NCT01282879. IPD Sharing: Not stated. Countries: 1. Publications: 3.

restrictedIPD-UNDECIDEDFeb 2026View details →
dryad32/100

Data from: Effectiveness of antifungal treatments during chytridiomycosis epizootics in populations of an endangered frog

Open the record for dataset details and reuse information.

publicDec 2021View details →
dryad32/100

Structure-guided discovery of potent antifungals that prevent Ras signaling by inhibiting protein farnesyltransferase

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publicOct 2022View details →
dryad32/100

Data from: Phase-dependent differential in vitro and ex vivo susceptibility of Aspergillus flavus and Fusarium keratoplasticum to azole antifungals

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publicAug 2023View details →
dryad32/100

Data from: Antifungal activity of water-stable copper-containing metal–organic frameworks

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publicSep 2017View details →
dryad32/100

Data from: Young but not defenseless: antifungal activity during embryonic development of a social insect

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publicJul 2020View details →
dryad28/100

Young but not defenseless: Antifungal activity during embryonic development of a social insect

<p>      Termites live in environments heavily colonized by diverse microbial communities, including pathogens. Eggs laid within the nest likely experience similar pathogenic pressures as their older nestmates. Consequently, they may have also been under selective pressures to be immune-competent. Through <i>in vitro</i> experiments, we tested the ontogeny, location and strength of embryos' antifungal activity against the fungus <i>Metarhizium brunneum</i>. Extraembryonic washes and intraembryonic components were incubated with fungal conidia, which was then scored for viability. Fungistatic activity was location- and stage-dependent. Extraembryonic washes had relatively weak antifungal activity. Conversely, intraembryonic contents were highly antifungal, exhibiting increased potency through development. Boiling both embryonic washes and intraembryonic contents rescued conidia viability, indicating the antifungal agent(s) is (are) heat-sensitive, and likely proteinaceous. Embryonic protein profiles shifted from putative vitellogenins in young embryos to multiple proteins in subsequent stages, suggesting that the increase in fungistatic activity may be due to the expression of endogenous proteins during embryogenesis. This study is the first to address embryonic antifungal activity in a hemimetabolous, eusocial taxon. Our results support the hypothesis that microbes have been significant agents of selection, fostering the evolution of antifungal properties in termite eggs, the most immature and supposed, most vulnerable stage of development.</p>

opencc-zeroAug 2020View details →
zenodo28/100

Figure 1 from: Hrytsyk RA, Kutsyk RV, Yurchyshyn OI, Struk ОА, Kireev IV, Grytsyk AR (2021) The investigation of antimicrobial and antifungal activity of some Artemisia L. species. Pharmacia 68(1): 93-100. https://doi.org/10.3897/pharmacia.68.e47521

Figure 1 Antimicrobial activity of Artemisia absinthium L., Artemisia vulgaris L., Artemisia abrotanum L. extracts in relation to the test cultures of microorganisms: АEsherichia coli, BStaphylococcus epidermidis, CCandida tropicalis, DAspergillus niger, EEnterococcus faecalis, FStaphylococcus aureus

opencc-by-4.0Jan 2021View details →
dryad28/100

Data from: Identification and evaluation of novel acetolactate synthase inhibitors as antifungal agents

High-throughput phenotypic screening against yeast Saccharomyces cerevisiae revealed a series of triazolo-pyrimidine-sulfonamide compounds with broad-spectrum antifungal activity, no significant cytotoxicity, and low protein binding. To elucidate the target of this series we have applied a chemogenomic profiling approach using the S. cerevisiae deletion collection. All compounds of the series yielded highly similar profiles that suggested acetolactate synthase (Ilv2p, catalyzes the first common step in branched chain amino acid biosynthesis) as a possible target. High correlation to profiles of known Ilv2p inhibitors like chlorimuron-ethyl provided further evidence for a similar mechanism of action. Genome-wide mutagenesis in S. cerevisiae identified 13 resistant clones with 3 different mutations in the catalytic subunit of acetolactate synthase that also conferred cross-resistance to established Ilv2p inhibitors. Mapping the mutations into the published Ilv2p crystal structure outlined the chlorimuron-ethyl binding cavity and it was possible to dock the triazolo-pyrimidine-sulfonamide compound into this pocket in silico. However, fungal growth inhibition could be bypassed through supplementation with exogenous branched chain amino acids, or by the addition of serum to the medium in all of the fungal organisms tested except for Aspergillus fumigatus. Thus, these data support the identification of triazolo-pyrimidine-sulfonamide as inhibitors of acetolactate synthase but suggest that targeting may be compromised due to the possibility of nutrient bypass in vivo.

opencc-zeroDec 2012View details →
zenodo28/100

Data for / Comparison of Antifungal Activity of Thymus Vulgaris Essential Oil and Triple Antibiotic Paste Against Candida Albicans Isolated from Root Canal (In Vitro Study)

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opencc-by-4.0Mar 2023View details →
zenodo28/100

Figure 1 from: Fadhilah QG, Santoso I, Maryanto AE, Abdullah S, Yasman Y (2021) Evaluation of the antifungal activity of marine actinomycetes isolates against the phytopathogenic fungi Colletotrichum siamense KA: A preliminary study for new antifungal compound discovery. Pharmacia 68(4): 837-843. https://doi.org/10.3897/pharmacia.68.e72817

Figure 1 Results of the antibiosis assay of SM14 isolate in PDA filtrate medium. A. control, B. 6 days, C. 9 days, D. 12 days.

opencc-by-4.0Nov 2021View details →
zenodo28/100

Figure 3 from: Fadhilah QG, Santoso I, Maryanto AE, Abdullah S, Yasman Y (2021) Evaluation of the antifungal activity of marine actinomycetes isolates against the phytopathogenic fungi Colletotrichum siamense KA: A preliminary study for new antifungal compound discovery. Pharmacia 68(4): 837-843. https://doi.org/10.3897/pharmacia.68.e72817

Figure 3 Phylogenetic analysis of marine actinomycetes isolates. The neighbor-joining tree of the three marine actinomycetes isolates (SM11, SM14, and SM15) was based on the 16S rRNA gene sequences. Streptomyces albus subsp. albus DSM 40313T is represented as an outgroup. The bootstrap values, based on 1,000 replications, are shown at the nodes; only values above 50% are given. The scale bar indicates 0.0050 substitutions per nucleotide position.

opencc-by-4.0Nov 2021View details →
zenodo28/100

Figure 5 from: Santoso I, Fadhilah QG, Safitri SD, Handayani S, Maryanto AE, Yasman Y (2022) Inhibition of the phytopathogenic fungi Curvularia lunata BM and Ganoderma sp. TB4 by antifungal compounds produced by Bacillus siamensis LDR grown on hanjeli (Coix lacryma-jobi L.) starch. Pharmacia 69(1): 203-210. https://doi.org/10.3897/pharmacia.69.e80180

Figure 5 The chromatogram profile of the crude extract of Bacillus siamensis LDR : A. C14 iturin A; B. C14 bacillomycin F; C. C15 bacillomycin F; D. C16 bacillomycin F; E. C12 surfactin; F. C13 surfactin.

opencc-by-4.0Mar 2022View details →
zenodo28/100

Figure 4 from: Santoso I, Fadhilah QG, Safitri SD, Handayani S, Maryanto AE, Yasman Y (2022) Inhibition of the phytopathogenic fungi Curvularia lunata BM and Ganoderma sp. TB4 by antifungal compounds produced by Bacillus siamensis LDR grown on hanjeli (Coix lacryma-jobi L.) starch. Pharmacia 69(1): 203-210. https://doi.org/10.3897/pharmacia.69.e80180

Figure 4 Thin layer chromatography of crude extract Bacillus siamensis LDR : A. lipid moiety; B. protein moiety.

opencc-by-4.0Mar 2022View details →
zenodo28/100

Figure 6 from: Santoso I, Fadhilah QG, Safitri SD, Handayani S, Maryanto AE, Yasman Y (2022) Inhibition of the phytopathogenic fungi Curvularia lunata BM and Ganoderma sp. TB4 by antifungal compounds produced by Bacillus siamensis LDR grown on hanjeli (Coix lacryma-jobi L.) starch. Pharmacia 69(1): 203-210. https://doi.org/10.3897/pharmacia.69.e80180

Figure 6 The results of mass spectrometry analysis: A. C14 iturin A (m/z 1043.5526); B. C14 iturin A (m/z 1044.5375); C. C14 bacillomycin F (m/z 1057.5688); D. C15 bacillomycin F (m/z 1071.5848); E. C16 bacillomycin F (m/z 1085.6011); F. C12 surfactin (m/z 994.6440); and G. C13 surfactin (m/z 1008.6606)

opencc-by-4.0Mar 2022View details →
zenodo28/100

Figure 2 from: Santoso I, Fadhilah QG, Safitri SD, Handayani S, Maryanto AE, Yasman Y (2022) Inhibition of the phytopathogenic fungi Curvularia lunata BM and Ganoderma sp. TB4 by antifungal compounds produced by Bacillus siamensis LDR grown on hanjeli (Coix lacryma-jobi L.) starch. Pharmacia 69(1): 203-210. https://doi.org/10.3897/pharmacia.69.e80180

Figure 2 Growth inhibition of Ganoderma sp. TB4 on potato dextrose agar (PDA)-filtrate medium: A. control, B. 12 days, C. 14 days, D. 16 days.

opencc-by-4.0Mar 2022View details →
zenodo28/100

Figure 3 from: Santoso I, Fadhilah QG, Safitri SD, Handayani S, Maryanto AE, Yasman Y (2022) Inhibition of the phytopathogenic fungi Curvularia lunata BM and Ganoderma sp. TB4 by antifungal compounds produced by Bacillus siamensis LDR grown on hanjeli (Coix lacryma-jobi L.) starch. Pharmacia 69(1): 203-210. https://doi.org/10.3897/pharmacia.69.e80180

Figure 3 Growth inhibition of Curvularia lunata BM: A. control, B. treatment; Ganoderma sp. TB4 : C. control; D. treatment caused by the crude extract of Bacillus siamensis LDR.

opencc-by-4.0Mar 2022View details →

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Allen Brain Atlas

Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

Annotated Behaviour and Observability Dataset (ABODe)

ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record