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Author
4
Garoufis, A.
4
Sakarellos, C.
3
Gerothanassis, I. P.
3
Hadjiliadis, N.
2
Karidi, K.
2
Malina, J.
2
Myari, A.
2
Sakarellos-Daitsiotis, M.
2
Troganis, A.
2
Tsikaris, V.
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3
nmr
2
amino-acids
2
conformation
2
crystal-structure
2
deoxynucleotide duplex
2
DNA
2
enantioselective binding
2
h-1-nmr
2
ligands
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magnetic-resonance
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12
journalArticle
Date
1
2010 - 2013
9
2000 - 2009
2
1996 - 1999
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
Σχολή Θετικών Επιστημών
Τμήμα Χημείας
Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά). ΧΗΜ
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Immunoreactivity and conformation of the P-P-G-M-R-P-P repetitive epitope of the Sm autoantigen (Journal article)
Models of oxovanadium(IV)-protein interactions: The first oxovanadium(IV) complexes with dipeptides (Journal article)
Investigation of the role of adjacent amino acids to the 313-320 sequence of the alpha(IIb) subunit on platelet activation and fibrinogen binding to alpha(IIb)beta(3) (Journal article)
Sequential oligopeptide carriers: from thermal polymerization to the construction of reconstituted antigenic and immunogenic conjugates (Journal article)
On the molecular basis of the recognition of angiotensin II (AII) - NMR structure of AII in solution compared with the X-ray structure of AII bound to the mAb Fab131 (Journal article)
Oligopyridine-ruthenium(II)-amino acid conjugates: synthesis, characterization, DNA binding properties and interactions with the oligonucleotide duplex d(5 '-CGCGCG-3 ')(2) (Journal article)
NMR analysis of duplex d(CGCGATCGCG)(2) modified by Lambda- and Delta-[Ru(bpy)(2)(m-GHK)]Cl-2 and DNA photocleavage study (Journal article)
Cu(II) and Ni(II) interactions with the terminally blocked hexapeptide Ac-Leu-Ala-His-Tyr-Asn-Lys-amide model of histone H2B (80-85) (Journal article)
Synthesis and characterization of ruthenium(II)-oligopyridine-peptide conjugates. Interactions of the diasteromeres Delta- and Lambda-[Ru(bpy)(2) (4-COY-4 '-Mebpy)]Cl-2 (Y = Gly-Lys(1)-Lys(2)CONH(2), Lys(1)-Gly-Lys(2)CONH(2), Lys(1)-Lys(2)-GlyCONH(2)) with the oligonucleotide d(5 '-CGCGAATTCGCG-3 ')(2) (Journal article)
Domain-selective ligand-binding modes and atomic level pharmacophore refinement in angiotensin I converting enzyme (ACE) inhibitors (Journal article)