Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans.
about
Histone Deacetylases and Their Inhibition in Candida SpeciesHOS2 and HDA1 encode histone deacetylases with opposing roles in Candida albicans morphogenesis.Piperazinyl quinolines as chemosensitizers to increase fluconazole susceptibility of Candida albicans clinical isolates.Regulatory circuitry governing fungal development, drug resistance, and disease.ML212: A small-molecule probe for investigating fluconazole resistance mechanisms in Candida albicansDirect effects of non-antifungal agents used in cancer chemotherapy and organ transplantation on the development and virulence of Candida and Aspergillus speciesOvercoming fluconazole resistance in Candida albicans clinical isolates with tetracyclic indolesFungal KATs/KDACs: A New Highway to Better Antifungal Drugs?The therapeutic uses of chromatin-modifying agents.Small-molecule chromatin-modifying agents: therapeutic applications.MC1568 inhibits HDAC6/8 activity and influenza A virus replication in lung epithelial cells: role of Hsp90 acetylation.tert-Butylcarbamate-containing histone deacetylase inhibitors: apoptosis induction, cytodifferentiation, and antiproliferative activities in cancer cells.Activity of MGCD290, a Hos2 histone deacetylase inhibitor, in combination with azole antifungals against opportunistic fungal pathogens.Novel hydroxamates potentiated in vitro activity of fluconazole against Candida albicans.A histone deacetylase-dependent screen in yeast.Synthesis, antifungal activity, and QSAR studies of 1,6-dihydropyrimidine derivatives.One pot synthesis, antimicrobial and antioxidant activities of fused uracils: pyrimidodiazepines, lumazines, triazolouracil and xanthines.Synthesis, anti-angiogenic and DNA cleavage studies of novel N-(4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)phenyl)piperidine-4-carboxamide derivatives.Anti-Candida Activity of Bursera morelensis Ramirez Essential Oil and Two Compounds, α-Pinene and γ-Terpinene-An In Vitro Study.Synthesis and antimicrobial evaluation of novel 4-amino-6-(1,3,4-oxadiazolo/1,3,4-thiadiazolo)-pyrimidine derivatives.The Rpd3/Hda1 family of histone deacetylases regulates azole resistance in Candida albicans.Developing novel non-hydroxamate histone deacetylase inhibitors: the chelidamic warhead
P2860
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P2860
Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans.
description
2006 nî lūn-bûn
@nan
2006 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@ast
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@en
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@nl
type
label
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@ast
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@en
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@nl
prefLabel
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@ast
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@en
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@nl
P2093
P50
P1476
Discovery of uracil-based hist ...... ng growth in Candida albicans.
@en
P2093
Claudio Passariello
Gerald Brosch
Silvio Massa
P304
P356
10.1016/J.BMCL.2006.12.028
P407
P577
2006-12-12T00:00:00Z