about
Unusual monomolecular DNA quadruplex structures using bunch-oligonucleotides.Synthesis and characterization of monomolecular DNA G-quadruplexes formed by tetra-end-linked oligonucleotides.Solid phase synthesis of nucleobase and ribose modified inosine nucleoside analogues.Targeting G-quadruplex structure in the human c-Kit promoter with short PNA sequences.New anti-HIV aptamers based on tetra-end-linked DNA G-quadruplexes: effect of the base sequence on anti-HIV activity.Synthesis, structural studies and biological properties of new TBA analogues containing an acyclic nucleotide.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.d(CGGTGGT) forms an octameric parallel G-quadruplex via stacking of unusual G(:C):G(:C):G(:C):G(:C) octadsPeptide Nucleic Acids as miRNA Target Protectors for the Treatment of Cystic Fibrosis.Solid-phase synthesis and pharmacological evaluation of novel nucleoside-tethered dinuclear platinum(II) complexes.Aminosilane functionalizations of mesoporous oxidized silicon for oligonucleotide synthesis and detection.Megastigmane and phenolic components from Laurus nobilis L. leaves and their inhibitory effects on nitric oxide production.Self-Assembly of G-Rich Oligonucleotides Incorporating a 3'-3' Inversion of Polarity Site: A New Route Towards G-Wire DNA Nanostructures.(3R,3aR,6R,6aR)-Hexa-hydro-furo[3,2-b]furan-3,6-diyl dibenzoate3β,6β-Diacet-oxy-5,9α-dihy-droxy-5α-cholest-7-en-11-one acetic acid 0.04-solvate5-Amino-1-(2',3'-O-iso-propyl-idene-d-ribit-yl)-1H-imidazole-4-carboxamide: a crystal structure with Z' = 4.Synthesis of new acadesine (AICA-riboside) analogues having acyclic D-ribityl or 4-hydroxybutyl chains in place of the ribose.3β,6α-Diacet-oxy-5,9α-dihy-droxy-5α-cholest-7-en-11-oneSynthesis of quadruplex-forming tetra-end-linked oligonucleotides: effects of the linker size on quadruplex topology and stability.Bioactive asterosaponins from the starfish Luidia quinaria and Psilaster cassiope. Isolation and structure characterization by two-dimensional NMR spectroscopy.New sesquiterpenes with intestinal relaxant effect from Celastrus paniculatus.PNA as a potential modulator of COL7A1 gene expression in dominant dystrophic epidermolysis bullosa: a physico-chemical study.Potent relaxant effect of a Celastrus paniculatus extract in the rat and human ileum.New sesquiterpene lactones from Laurus nobilis leaves as inhibitors of nitric oxide production.Effects of acrolein on the quadruplex forming d(TTAGGG)4 telomeric repeat sequence.Synthesis of a new ribose modified analogue of cyclic inosine diphosphate ribose.Synthesis and characterization of tetra-end linked oligonucleotides capable of forming monomolecular G-quadruplexes.Anti-HIV activity of new higher order G-quadruplex aptamers obtained from tetra-end-linked oligonucleotides.Synthesis and Biological Evaluation of a New Structural Simplified Analogue of cADPR, a Calcium-Mobilizing Secondary Messenger Firstly Isolated from Sea Urchin Eggs.Minor steroidal alkaloids from the marine sponge Corticium sp.Optical tweezers as a probe for oligodeoxyribonucleotide structurationDirect Synthesis of Oligonucleotides on Nanostructured Silica MultilayersIsolation of callipeltins A–C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltinsA facile synthesis of 5'-fluoro-5'-deoxyacadesine (5'-F-AICAR): a novel non-phosphorylable AICAR analogue.Synthesis and biological evaluation of unprecedented ring-expanded nucleosides (RENs) containing the imidazo[4,5-d][1,2,6]oxadiazepine ring systemLabel-Free Probing of G-Quadruplex Formation by Surface-Enhanced Raman ScatteringProbing the reactivity of nebularine N1-oxide. A novel approach to C-6 C-substituted purine nucleosidesSolid-Phase Synthesis of a New Diphosphate 5-Aminoimidazole-4-carboxamide Riboside (AICAR) Derivative and Studies toward Cyclic AICAR Diphosphate RiboseSynthesis 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 ConjugateA solid-phase approach to the synthesis of N-1-alkyl analogues of cyclic inosine-diphosphate-ribose (cIDPR)
P50
Q33225910-D95094C8-53BB-48FD-AB0B-2D86F80FAC5EQ33250530-53297E3C-CDDD-44A1-BFF6-34E4C1CAFDE6Q33309300-938F1DF9-AAB7-47A5-A559-B53A837F6B74Q33848293-E9B95017-37AE-4760-AEB8-5FFD14EF9638Q34382171-E9CAD6D9-9BD0-4133-80C6-B3C451BF648CQ38287971-30A13673-D8ED-4C93-A1B6-5D1815F43A01Q38320267-437D2CDF-2431-4E91-8C7A-7D70C779627DQ38535247-883D8C66-231F-4ADE-8AF7-FB59E709A961Q38683313-1624C7DA-9585-4D01-AAD1-97D79927454DQ39487759-CA9F5945-20A1-4956-A94D-87B0E1663193Q40434038-07F94828-373A-419C-AE8E-048A5139CF46Q40464700-D6B095BF-20DC-4D3D-B02B-55F592D8B9CEQ41239432-F8E2BDA7-2B80-47B0-9599-6BD649E781CEQ41857959-208DCCD9-0564-477D-8A0D-A54C96F699C6Q41863879-4C919FCA-69EF-4AE6-A4F3-87D19289F9A6Q42175035-76DB7E1B-6AE0-4F58-8A4E-6ACAC2CF2772Q42278323-31114207-6A17-429B-BC7E-B7AD3509ABD1Q42601378-60D778AC-015B-4929-9062-8AC3B6717E0AQ43475250-C0E30977-A63C-4843-BEC4-10471441C0EFQ44416181-B22E0887-21C7-441D-AC84-07A843A92242Q44979163-71119B4D-73CE-4EC9-9B3D-B596D2D08451Q45341469-396F0841-E333-499E-8B66-2735F7ECF7A0Q46017887-6C7B5C63-F213-4439-88B5-9804752842A1Q46687221-2B22D840-05B2-4723-90F2-F1771DC2161AQ46773162-DEE9BCF6-D425-4A79-BC0D-D75EF03DB599Q46860776-EBA49183-BB91-40C6-92A7-425E889FD111Q46860824-68785BE6-8CDF-46D0-8005-EAA060590ECCQ52654267-36B87884-715E-4EE7-927B-019B89C8A32AQ52657779-AF1E2F04-8896-4CAA-97AD-E9B282E03A68Q55473288-BC842B7A-075E-487F-96D3-6D7CA1BE8687Q56893853-A59FF7E0-E31D-4F6E-AB8E-7160D0092228Q57629896-5F991773-A063-4E22-816D-377D553F002AQ58043934-1C9480AD-F0A9-48B4-9E0E-C370A4F4E4D6Q59133291-CEAD5B4C-7BDE-4D25-9E56-CC870AE79C1EQ59133317-11280589-1407-4442-B1E4-B98A9A1BB672Q59133325-073C2F70-A7E9-46D5-B54E-3E346892E963Q59133327-0634844A-8AF3-424B-9E3F-C20D9DD2ED32Q59133335-9806551C-921F-4CA3-85B3-8C84020D88A7Q59133337-A84BE201-664B-4750-A469-D68D68809002Q59133343-2C7AD862-2B13-4A2F-B730-A7EA347B889A
P50
description
Italiaans biochemicus
@nl
Italian biochemist
@en
bioquímicu italianu
@ast
bithchemiceoir Iodálach
@ga
italienischer Biochemiker
@de
name
Nicola Borbone
@ast
Nicola Borbone
@ca
Nicola Borbone
@en
Nicola Borbone
@es
Nicola Borbone
@fr
Nicola Borbone
@ga
Nicola Borbone
@nl
Nicola Borbone
@sl
Nicola Borbone
@sq
type
label
Nicola Borbone
@ast
Nicola Borbone
@ca
Nicola Borbone
@en
Nicola Borbone
@es
Nicola Borbone
@fr
Nicola Borbone
@ga
Nicola Borbone
@nl
Nicola Borbone
@sl
Nicola Borbone
@sq
prefLabel
Nicola Borbone
@ast
Nicola Borbone
@ca
Nicola Borbone
@en
Nicola Borbone
@es
Nicola Borbone
@fr
Nicola Borbone
@ga
Nicola Borbone
@nl
Nicola Borbone
@sl
Nicola Borbone
@sq
P1053
A-6061-2009
P106
P1153
6507575589
P19
P21
P27
P31
P3829
P496
0000-0003-0216-9814
P569
1972-02-23T00:00:00Z