₈Stefano Moro

Summary for 2004 [at-glance overview of Stefano Moro work for the selected year as suggested by data mining algorithms]

This is an Authoratory overview of author Stefano Moro. According to available data, in 2004 Stefano Moro published at least 8 articles. This work was completed in collaboration with several authors including Palumbo, Manlio and Capranico, Giovanni. Many other authors have collaborated with Stefano Moro as well. There is no information about the funding or the grants awarded to support this work.

Stefano Moro is a key opinion leader in the specific area of Intercalating Agents. This author's rank is 4 when compared to all other authors using the same keyword. Analysis of the article abstracts and the titles suggests that Stefano Moro professional interests are focused around "water-soluble fullerene derivatives", "dna topoisomerase ii" and "moiety attractive scaffold". These might also be referred to as "topoisomerase ii", "model anthracycline" or "dna topoisomerase". Statistical analysis shows that Stefano Moro's writing is likely to contains terms "dna", "ii", "studies", "activity", "derivatives" and "molecular".

Unfortunately, there is not enough information to establish Stefano Moro affiliation. Luckily, several email addresses are on file.

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Alternative names (1) [other authors with names similar to Stefano Moro]

₃₁Moro, S

Year 2004 Charts [Stefano Moro frequent coauthors and the most common unique vocabulary terms for the selected year]

Historical Performance Charts [graphical overview of Stefano Moro publication and funding history for the range of years]

Emails (3) [email addresses extracted from Stefano Moro affiliations]

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Stefano Moro Coauthors (44) [all coauthors with the number of joint publications]

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₆Trincavelli, Letizia

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₅Catarzi, Daniela

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₅Colotta, Vittoria

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₅Dall'Acqua, Francesco

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₄Veronese, Francesco M

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₃Beretta, Giovanni L

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₃Sarno, Stefania

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₂Dolmella, Alessandro

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₁Deflorian, Francesca

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Affiliations (7) [condensed summary of the Stefano Moro affiliations, the leading number and the color conveys importance]

₂Department of Pharmaceutical Sciences, University of Padova, Via Marzolo 5, 35131 Padova, Italy.
₁Dipartimento di Scienze Farmaceutiche, Università di Trieste, Piazzale Europa, 1-34127 Trieste, Italy.
₁Dipartimento di Chimica Biologica, Istituto di Neuroscienze del CNR, Università di Padova, Padova, Italy.
₁Dipartimento di Science Farmaceutiche, Via Marzolo, 5, 35131 Padova, Italy.
₁Dipartimento di Scienze Farmaceutiche, Università degli Studi di Firenze, Polo Scientifico, Via Ugo Schiff 6, 50019 Sesto Fiorentino, Florence, Italy.
₁Dipartimento di Scienze Chimiche e Istituto CNR Tecnologia delle Membrane-Sezione di Padova, Università di Padova, via Marzolo 1, I-35131 Padua, Italy.
₁Department of Pharmaceutical Sciences, University of Pada Via F. Marzolo 5, Padua 35131, Italy.

Key Opinion Leader In [Stefano Moro is considered a key opinion leader in any keyword where the rank of 5 is achieved, the leading number before the keyword shows the author's rank as compared to all other authors]

₄Intercalating Agents | ₃₅₇Models, Molecular | ₃₉₆DNA

Keywords (32) [keywords assigned to Stefano Moro articles by PubMed, the leading number and the color conveys importance]

₅Models, Molecular | ₄Humans | ₃Intercalating Agents | ₃DNA | ₂Structure-Activity Relationship | ₂Animals | ₂Binding Sites | ₂Molecular Conformation | ₂DNA Topoisomerases, Type II | ₂Anthracyclines | ₂Mutation | ₁Cyclohexanes | ₁Organometallic Compounds | ₁Triazoles | ₁Phenols | ₁Crystallography, X-Ray | ₁Casein Kinase II | ₁Radioligand Assay | ₁Cattle | ₁Computational Biology | ₁Tumor Cells, Cultured | ₁Cricetinae | ₁Circular Dichroism | ₁Flavonoids | ₁Mice, Inbred BALB C | ₁Yeasts | ₁Lysine | ₁Protein Structure, Tertiary | ₁Psoralens | ₁Solubility | ₁Quinoxalines | ₁Sulfur

Stefano Moro Unique Vocabulary (96) [single words, word pairs and phrases obtained by analysis of abstracts and titles, the leading number and the color conveys importance; Stefano Moro might be a good expert witness on these terms]

₁₄dna | ₈ii | ₈studies | ₈activity | ₇derivatives | ₇molecular | ₇drug | ₆anthracycline | ₆top2 | ₆ck2 | ₆compounds | ₆properties | ₅receptor | ₅cleavage | ₅protein | ₅hydrolysis | ₅topoisomerase | ₅inhibition | ₅different | ₅group | ₄specific | ₄9-aza | ₄several | ₄may | ₃scaffold | ₃length | ₃compound | ₃human | ₃series | ₃synthesis | ₃investigated | ₃effects
₅topoisomerase ii | ₃model anthracycline | ₃dna topoisomerase | ₃water-soluble fullerene | ₃fullerene derivatives | ₃ic values | ₃branched pegs | ₂attractive scaffold | ₂adenosine receptor | ₂4-triazolo 3-a | ₂interaction model | ₂hemolytic properties | ₂develop potent | ₂intercalate dna | ₂effects water-soluble | ₂cap-like domain | ₂vitro vivo | ₂scaffold develop | ₂pharmacological ligand-receptor | ₂moiety attractive | ₂antagonists synthesis | ₂receptor antagonists | ₂drug molecule | ₂hemolytic effects | ₂modeling studies | ₂quinoxalin-1-one moiety | ₂anthracycline activity | ₂synthesis pharmacological | ₂selective human | ₂ligand-receptor modeling | ₂human a3 | ₂vivo study
₃water-soluble fullerene derivatives | ₃dna topoisomerase ii | ₂moiety attractive scaffold | ₂quinoxalin-1-one moiety attractive | ₂a3 adenosine receptor | ₂receptor antagonists synthesis | ₂selective human a3 | ₂antagonists synthesis pharmacological | ₂interaction model anthracycline | ₂human a3 adenosine | ₂hemolytic effects water-soluble | ₂vitro vivo study | ₂activity dna topoisomerase | ₂3-a quinoxalin-1-one moiety | ₂adenosine receptor antagonists | ₂4-triazolo 3-a quinoxalin-1-one | ₂model anthracycline activity | ₂potent selective human | ₂ligand-receptor modeling studies | ₂develop potent selective | ₂effects water-soluble fullerene | ₂anthracycline activity dna | ₂scaffold develop potent | ₂synthesis pharmacological ligand-receptor | ₂attractive scaffold develop | ₂pharmacological ligand-receptor modeling | ₂efficient zn ii | ₂studies 9-aza regioisomers | ₂structure computer-aided studies | ₂aza-anthrapyrazoles biophysical biochemical | ₂1-thioangelicin crystal structure | ₂based artificial nucleases

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