M. Varra

发表

Solid phase synthesis of a thrombin binding aptamer on macroporous silica for label free optical quantification of thrombin

Principia Dardano, Gennaro Piccialli, Nicola Borbone, 2016 .

Synthesis and characterization of DNA quadruplexes containing T‐tetrads formed by bunch‐oligonucleotides

G. Piccialli, Jussara Amato, L. Mayol, 2006, Biopolymers.

Synthesis and characterization of a bunchy oligonucleotide forming a monomolecular parallel quadruplex structure in solution

G. Piccialli, L. Mayol, A. Galeone, 2004 .

Combating Actions of Green 2D-Materials on Gram Positive and Negative Bacteria and Enveloped Viruses

A. Vergara, L. Altucci, C. Altucci, 2020, Frontiers in Bioengineering and Biotechnology.

Targeting G-quadruplex structure in the human c-Kit promoter with short PNA sequences.

G. Piccialli, E. Pauw, B. Pagano, 2011, Bioconjugate chemistry.

Backbone modified TBA analogues endowed with antiproliferative activity.

A. Russo, G. Russo, A. Galeone, 2017, Biochimica et biophysica acta. General subjects.

Spectroscopic Properties of Two 5′-(4-Dimethylamino)Azobenzene Conjugated G-Quadruplex Forming Oligonucleotides

S. d'Auria, A. Varriale, C. Altucci, 2020, International journal of molecular sciences.

Aptamer-Based Biosensors for the Analytical Determination of Bisphenol A in Foodstuffs

S. Albrizio, M. Varra, Marica Erminia Schiano, 2022, Applied Sciences.

A straightforward modification in the thrombin binding aptamer improving the stability, affinity to thrombin and nuclease resistance.

L. Mayol, A. Galeone, A. Virgilio, 2014, Organic & biomolecular chemistry.

Unusual Chair-Like G-Quadruplex Structures: Heterochiral TBA Analogues Containing Inversion of Polarity Sites

L. Mayol, A. Galeone, A. Virgilio, 2015 .

Structural study of four-stranded quadruplex structures containing 2'-deoxy-8-(propyn-1-yl)adenosine.

L. Mayol, A. Randazzo, A. Galeone, 2004, Bioorganic & medicinal chemistry.

New anticancer agents mimicking protein recognition motifs.

E. Novellino, D. Brancaccio, A. Carotenuto, 2013, Journal of medicinal chemistry.

Solid-phase synthesis of oligonucleotides containing a bipyridine ligand at the 3'-3' inversion of polarity site.

L. Mayol, A. Galeone, G. Oliviero, 2001, Bioorganic & medicinal chemistry letters.

Reaction of 3′,5′-di-O-acetyl-2′-deoxyinosine with the chlorinating agent PPh3–CCl4: synthesis of the 6-chloroderivative and of a new base linked dimer, useful intermediate to 15N-1-labelled 2′-deoxyinosine

G. Piccialli, D. Montesarchio, A. Messere, 1994 .

Synthesis of New Acadesine (AICA-riboside) Analogues Having Acyclic d-ribityl or 4-Hydroxybutyl Chains in Place of the Ribose

G. Piccialli, L. Mayol, N. Borbone, 2013, Molecules.

Photo-control of cancer cell growth by benzodiazo N-substituted pyrrole derivatives

C. Altucci, A. Russo, G. Russo, 2019, Journal of Photochemistry and Photobiology A: Chemistry.

Effect of gamma-hydroxypropano deoxyguanosine, the major acrolein-derived adduct, on monomolecular quadruplex structure of telomeric repeat d(TTAGGG)(4).

G. Piccialli, L. Mayol, A. Galeone, 2004, Bioorganic & medicinal chemistry letters.

A new ferrocenemethyl-thymidine nucleoside: Synthesis, incorporation into oligonucleotides and optical spectroscopic studies on the resulting single strand, duplex and triplex structures

G. Piccialli, A. Romanelli, E. Bucci, 1999 .

Solid-Phase Synthesis of a New Diphosphate 5-Aminoimidazole-4-carboxamide Riboside (AICAR) Derivative and Studies toward Cyclic AICAR Diphosphate Ribose

G. Piccialli, L. Mayol, N. Borbone, 2011, Molecules.

A solid-phase approach to the synthesis of N-1-alkyl analogues of cyclic inosine-diphosphate-ribose (cIDPR)

G. Piccialli, Jussara Amato, L. Mayol, 2010 .

Synthetic studies on the glycosylation of the base residues of inosine and uridine

G. Piccialli, D. Montesarchio, A. Messere, 1999 .

1-Substituted 2′-deoxyinosine analogues

G. Piccialli, D. Montesarchio, A. Messere, 1997 .

Synthesis of a New N1‐Pentyl Analogue of Cyclic Inosine Diphosphate Ribose (cIDPR) as a Stable Potential Mimic of Cyclic ADP Ribose (cADPR)

G. Piccialli, L. Mayol, A. Galeone, 2002 .

INTERACTION OF DISTAMYCIN A AND NETROPSIN WITH QUADRUPLEX AND DUPLEX STRUCTURES: A COMPARATIVE 1H-NMR STUDY

L. Mayol, A. Randazzo, A. Galeone, 2002, Nucleosides, nucleotides & nucleic acids.

Site specific replacements of a single loop nucleoside with a dibenzyl linker may switch the activity of TBA from anticoagulant to antiproliferative

Nicola Borbone, Giuseppe Cirino, Elisa Rivieccio, 2015, Nucleic acids research.

Dereplication of Gambierdiscus balechii extract by LC-HRMS and in vitro assay: First description of a putative ciguatoxin and confirmation of 44-methylgambierone.

A. Penna, C. Dell’Aversano, S. Capellacci, 2023, Chemosphere.

5‐Hydroxymethyl‐2′‐Deoxyuridine Residues in the Thrombin Binding Aptamer: Investigating Anticoagulant Activity by Making a Tiny Chemical Modification

L. Mayol, A. Galeone, A. Virgilio, 2014, Chembiochem : a European journal of chemical biology.

A Facile Solid‐Phase Synthesis of Oligonucleotides Containing a 3′−3′ Phosphodiester Bond for Alternate Strand Triple‐Helix Formation

G. Piccialli, D. Montesarchio, A. Messere, 1998 .

Improved synthesis of isoguanosine and 6-substituted xanthosine derivatives

G. Piccialli, D. Montesarchio, M. Varra, 1995 .

SYNTHESIS OF 5-METHYLAMINO-2′-DEOXYURIDINE DERIVATIVES

B. Catalanotti, L. Mayol, A. Galeone, 2001, Nucleosides, nucleotides & nucleic acids.

Syntheses of [1-15N]-2′-Deoxyinosine, [4-15N]-2′-DeoxyAICAR, and [1-15N]-2′-Deoxyguanosine

G. Piccialli, B. Catalanotti, L. Mayol, 1999 .

Synthesis and Triple Helix Formation by Alternate Strand Recognition of Oligonucleotides Containing 3‘-3‘ Phosphodiester Bonds

A. Pepe, D. Montesarchio, A. Messere, 1997 .

6-Chloroxanthosine, a Useful Intermediate for the Efficient Syntheses of [6-15N]-Isoguanosine, Isoinosine and Other Purine Nucleoside Analogues

G. Piccialli, D. Montesarchio, A. Messere, 1997 .

Synthesis of a novel N-1 carbocyclic, N-9 butyl analogue of cyclic ADP ribose (cADPR)

G. Piccialli, L. Mayol, A. Galeone, 2002 .

Syntheses of [1-15N]-2′-Deoxyinosine, [4-15N]-2′-DeoxyAICAR, and [1-15N]-2′-Deoxyguanosine.

G. Piccialli, B. Catalanotti, L. Mayol, 1999 .

Synthesis of thymidine dimers containing a new internucleosidic amide linkage and their incorporation into oligodeoxyribonucleotides

G. Piccialli, D. Montesarchio, M. Varra, 1995 .

A model for triple helix formation on human telomerase reverse transcriptase (hTERT) promoter and stabilization by specific interactions with the water soluble perylene derivative, DAPER.

L. Mayol, M. Varra, M. Savino, 2007, Biophysical chemistry.

Oligonucleotides Containing an Acridine Group Covalently Bonded to the Nucleotide Flanking the 3′-3′ Phosphodiester Junction for Alternate Strand Triple Helix Formation

G. Piccialli, B. Catalanotti, L. Mayol, 2003, Nucleosides, nucleotides & nucleic acids.

6-Chloroxanthosine (I), a Useful Intermediate for Efficient Syntheses of (6-15N)-Isoguanosine (IV), Isoinosine (VII), and Other Purine Nucleoside Analogues (IX).

G. Piccialli, D. Montesarchio, A. Messere, 2010 .

Synthesis of A New Ribose Modified Analogue of Cyclic Inosine Diphosphate Ribose

G. Piccialli, Jussara Amato, L. Mayol, 2007, Nucleosides, nucleotides & nucleic acids.

SYNTHESIS OF A NEW N-9 RIBITYL ANALOGUE OF CYCLIC INOSINE DIPHOSPHATE RIBOSE (cIDPR) AS A MIMIC OF CYCLIC ADP RIBOSE (cADPR)

G. Piccialli, L. Mayol, G. Oliviero, 2005, Nucleosides, nucleotides & nucleic acids.

Improved Synthesis of Isoguanosine (V) and 6‐Substituted Xanthosine Derivatives.

G. Piccialli, D. Montesarchio, M. Varra, 1995 .

A new synthesis of oxanosine and 2′-deoxyoxanosine

G. Piccialli, D. Montesarchio, A. Messere, 1998 .

Spectroscopic Properties of Two 5 (cid:48) -(4-Dimethylamino)Azobenzene Conjugated G-Quadruplex Forming Oligonucleotides

S. d'Auria, A. Varriale, C. Altucci, 2020 .

Investigating the role of T7 and T12 residues on the biological properties of thrombin-binding aptamer: enhancement of anticoagulant activity by a single nucleobase modification.

Gennaro Piccialli, Nicola Borbone, Marco Persico, 2012, Journal of medicinal chemistry.

Synthesis of quadruplex‐forming tetra‐end‐linked oligonucleotides: Effects of the linker size on quadruplex topology and stability

G. Piccialli, Jussara Amato, L. Mayol, 2009, Biopolymers.

Exploring the Photodynamic Properties of Two Antiproliferative Benzodiazopyrrole Derivatives

C. Altucci, C. Dell’Aversano, L. Tartaglione, 2020, International journal of molecular sciences.

Structural studies and biological evaluation of T30695 variants modified with single chiral glycerol-T reveal the importance of LEDGF/p75 for the aptamer anti-HIV-integrase activities.

C. Dell’Aversano, L. Tartaglione, L. Mayol, 2019, Biochimica et biophysica acta. General subjects.

Site-specific replacement of the thymine methyl group by fluorine in thrombin binding aptamer significantly improves structural stability and anticoagulant activity

L. Mayol, A. Pepe, A. Galeone, 2015, Nucleic acids research.

Outstanding effects on antithrombin activity of modified TBA diastereomers containing an optically pure acyclic nucleotide analogue.

E. Novellino, G. Piccialli, L. Mayol, 2014, Organic & biomolecular chemistry.

Synthesis of a dibromoperylene phosphoramidite building block and its incorporation at the 5' end of a G-quadruplex forming oligonucleotide: spectroscopic properties and structural studies of the resulting dibromoperylene conjugate.

G. Ortaggi, Jussara Amato, L. Mayol, 2011, Bioconjugate chemistry.

Synthesis, structural studies and biological properties of new TBA analogues containing an acyclic nucleotide.

Nicola Borbone, Giuseppe Cirino, Giorgia Oliviero, 2008, Bioorganic & medicinal chemistry.

Toward Isolation of Palytoxins: Liquid Chromatography Coupled to Low- or High-Resolution Mass Spectrometry for the Study on the Impact of Drying Techniques, Solvents and Materials

P. Hess, C. Dell’Aversano, P. Ciminiello, 2021, Toxins.

EFFECTS OF ACROLEIN ON THE QUADRUPLEX FORMING d(TTAGGG)4 TELOMERIC REPEAT SEQUENCE

G. Piccialli, L. Mayol, N. Borbone, 2005, Nucleosides, nucleotides & nucleic acids.

UNUSUAL MONOMOLECULAR DNA QUADRUPLEX STRUCTURES USING BUNCH-OLIGONUCLEOTIDES

G. Piccialli, L. Mayol, A. Galeone, 2005, Nucleosides, Nucleotides & Nucleic Acids.

A BUNCH-OLIGONUCLEOTIDE FORMING STABLE MONOMOLECULAR QUADRUPLEX CONTAINING A T-TETRAD

G. Piccialli, L. Mayol, A. Galeone, 2005, Nucleosides, Nucleotides & Nucleic Acids.

Synthesis and characterization of monomolecular DNA G-quadruplexes formed by tetra-end-linked oligonucleotides.

G. Piccialli, Jussara Amato, L. Mayol, 2006, Bioconjugate chemistry.

Tetrasubstituted Pyrrole Derivative Mimetics of Protein–Protein Interaction Hot-Spot Residues: A Promising Class of Anticancer Agents Targeting Melanoma Cells

P. Campiglia, C. Fattorusso, M. Persico, 2023, Molecules.

Improved thrombin binding aptamer analogues containing inversion of polarity sites: structural effects of extra-residues at the ends.

L. Mayol, R. Filosa, A. Galeone, 2016, Organic & biomolecular chemistry.

Superstructural self-assembly of the G-quadruplex structure formed by the homopurine strand in a DNA tract of human telomerase gene promoter.

L. Mayol, S. Pisano, M. Varra, 2008, Biophysical Chemistry.

The Effectiveness of Cyrene as a Solvent in Exfoliating 2D TMDs Nanosheets

C. Altucci, A. Sasso, G. Rusciano, 2023, International journal of molecular sciences.

Targeting G-quadruplex structure in the human c-Kit promoter with short PNA sequences.

G. Piccialli, E. Pauw, Jussara Amato, 2011, Bioconjugate chemistry.