| Org.No. |
Surname |
Name |
Title |
| P 01 |
Alexandrova |
Liudmila |
New 4-Modified cytidines: synthesis and evaluation as antimicrobial agents |
| P 02 |
Alibayov |
Babek |
Application of NAD captureSeq on viruses |
| P 03 |
Baszczyňski |
Ondřej |
Phosphonoacetate analogues of adenosine 5'-diphosphate ribose (ADPR): probes for the Transient Receptor Potential (TRP) cation channel TRPM2 |
| P 04 |
Benoni |
Roberto |
Mapping of m1A in the viral RNA |
| P 05 |
Berger |
Florence |
Fluorescent Modified Guanine Nucleotides to Probe Frameshift Mutations in DNA |
| P 06 |
Boháčová |
Soňa |
Nucleotides Bearing Photocleavable Groups for DNA Photocaging |
| P 07 |
Bood |
Mattias |
A highly emissive adenine analogue with promising properties for microscopy |
| P 08 |
Brehova |
Petra |
Synthesis of acyclic nucleoside phosphonates with unnatural heterocyclic bases bearing aryl substituents and their inhibitory activity towards bacterial and human adenylate cyclases |
| P 09 |
Brzezińska |
Jolanta |
Thermo-controlled Device in Orthogonal Protection Strategy for Bioconjugate Synthesis |
| P 10 |
Cechova |
Lucie |
5-Azopyrimidines: Synthesis and NMR study of their photochemical behavior |
| P 11 |
Cesnek |
Michal |
Synthesis and evaluation of novel acyclic nucleoside phosphonates with unnatural nucleobases as potent inhibitors of Bordetella pertussis adenylate cyclase toxin |
| P 12 |
Chmielewski |
Marcin |
Stereoselective Cyclisation and Diastereoisomeric Purification of 3-(Pyridin-2-yl)-1-phenyl-(1,3,2)oxazaphospholidine Formed from a Thermolabile Protecting Group |
| P 13 |
Croce |
Stefano |
EdU DetectPro |
| P 14 |
Debart |
Francoise |
2’-O-modified siRNA by disulfide-containing groups in a prodrug approach |
| P 15 |
Drenichev |
Mikhail S. |
Synthesis and antiviral activity of N6-substituted adenosine derivatives |
| P 16 |
Ebenryter-Olbinska |
Katarzyna |
Synthesis and physicochemical characterization of antisense oligonucleotides modified with boron clusters |
| P 17 |
Ermert |
Susanne |
Development of ATP-based Signaling Molecules |
| P 18 |
Esposito |
Anna |
Synthesis and Biological Evaluation of D- and L- Cyclohexenyl Nucleosides |
| P 19 |
Evéquoz |
Damien |
Exploring the backbone topology of DNA: the 7',5'-bicyclo-DNA system |
| P 20 |
Fantoni |
Nicolo |
Artificial Metallo-Nucleases for Gene Editing |
| P 21 |
Fignole |
Klavdja |
Synthesis and biophysical properties of C(6’)-modified tricyclo-DNA analogs |
| P 22 |
Fojta |
Miroslav |
Utilization of Catalytic Hydrogen Evolution in Electrochemical Analysis of Modified Nucleic Acids |
| P 23 |
Frei |
Sibylle |
Synthesis and Properties of Novel Fluorinated Bicyclic Nucleosides and Oligonucleotides |
| P 24 |
Gadakh |
Bharat |
Pharmacophoric importance of the adenine base in aminoacyl-sulfamoyl analogues (aaSAs) |
| P 25 |
Gasser |
Catherina |
Syntheses of S-adenosylmethionine (SAM) analogues – Towards alternative ligands for SAM riboswitches |
| P 26 |
Gołębiewska |
Justyna |
A new, efficient entry for the preparation of nucleoside 5'-phosphoramidates - as new substrates for the synthesis of biologically active nucleoside 5'-diphosphates |
| P 27 |
Güixens-Gallardo |
Pedro |
Synthesis of new fluorescent nucleosides through the Knoevenagel condensation and related reactions. |
| P 28 |
Hagiwara |
Kenta |
Reusable Enzymatic Production System for Artificial Nucleic Acids |
| P 29 |
Höbartner |
Claudia |
Fluorescence activating RNA aptamers |
| P 30 |
Hockova |
Dana |
Acyclic nucleoside phosphonates: Inhibition and structural investigations of Trypanosoma brucei 6-oxopurine phosphoribosyltranferases |
| P 31 |
Hudeček |
Oldřich |
Development of capturing technique for 5’-diphosphate RNA |
| P 32 |
Jankowska-Anyszka |
Marzena |
Synthesis and potential application of new double-functionalized dinucleotide mRNA cap analogues |
| P 33 |
Jastrzebska |
Katarzyna |
P-stereodefined homopurine chimeric [All-RP-PS]-DNA#LNA oligomers recruit Hoogsteen-paired DNA templates to form thermally stable parallel complexes |
| P 34 |
Jemielity |
Jacek |
5’ mRNA Cap Analogs for Efficient Translation and Specific Labeling of mRNA in Living Cells |
| P 35 |
Kaiser |
Martin Maxmilian |
Acyclic nucleoside phosphonates with (S)- and (R)-HPEP moiety as monomers for the synthesis of modified oligonucleotides |
| P 36 |
Kaniowski |
Damian |
Anti-EGFR silencing activity of antisense oligonucleotides labeled with boron clusters |
| P 37 |
Khandazhinskaya |
Anastasia |
Novel 5’-Norcarbocyclic Nucleoside Analogues As Antibacterial Agents |
| P 38 |
Kirillova |
Yuliya |
Synthesis of polyanionic ?-PNAs derived from L-Glu |
| P 39 |
Klejch |
Tomáš |
Acyclic nucleoside phosphonates bearing Favipiravir as a nucleobase: Potential inhibitors of hypoxanthine-guanine phosphoribosyltransferase |
| P 40 |
Koćmik |
Ilona |
Synthesis and biological evaluation of dinucleotide analogues of 5' end of the mRNA modified at the N2 and C2' (C3') positions of 7-methylguanosine |
| P 41 |
Kočišek |
Jaroslav |
DNA Binding Radiosensitizers and Low Energy Electrons |
| P 42 |
Kropp |
Heike |
Unraveling the interactions between a modified primer and KlenTaq DNA polymerase - on a structural level |
| P 43 |
Kryńska |
Paulina |
Reversible functionalization of sulfur containing guanosine derivatives |
| P 44 |
Lange |
Sandra |
Exploring Interaction Partners of Diadenosine Triphosphate |
| P 45 |
Lehner |
Maike |
Synthesis and Investigation of Cell-Permeable NAD+ Analogs |
| P 46 |
Leitner |
Kim |
DNA polymerase-based systems for site-specific sensing of the presence or absence of DNA modifications |
| P 47 |
Luo |
Min |
Expanding the Antiviral Spectrum of Fluorinated Acyclic Nucleoside Phosphonates (FPMPs): Diamyl Aspartate Amidate Prodrugs |
| P 48 |
Maciaszek |
Anna |
P-Diastereomers of the oxathiaphospholane derivatives of N6-methyl-2’-deoxyadenosine and N2,N2-dimethyl-2’-deoxyguanosine–discriminators of Watson-Crick interactions in parallel triplexes. |
| P 49 |
Mairhofer |
Elisabeth |
Towards the efficient synthesis of arginine-containing peptidyl-tRNA mimics |
| P 50 |
Manicardi |
Alex |
Crosslinking Peptide Nucleic Acids (PNAs) for DNA targeting |
| P 51 |
Matyašovský |
Ján |
2-Substituted dATP Derivatives as Building Blocks for Polymerase Catalyzed Synthesis of DNA Modified in the Minor Groove |
| P 52 |
Matyugina |
Elena |
Design and synthesis of novel fleximers |
| P 53 |
Mikhailov |
Sergey |
Synthesis of purines from nucleosides: ribose as a blocking group |
| P 54 |
Milisavljevic |
Nemanja |
Enzymatic synthesis of base-modified RNAs |
| P 55 |
Morvan |
Francois |
Double Oxime Ligation for the Synthesis of Circular Oligonucleotides |
| P 56 |
Muttach |
Fabian |
Novel AdoMet analogues as tools for enzymatic transfer of photo-crosslinkers and capturing RNA-protein interactions |
| P 57 |
Nautiyal |
Manesh |
Biological and structural analysis of base modified nucleosides as aminoacyl adenylate analogues inhibiting tRNA synthetases |
| P 58 |
Negrya |
Sergey |
Synthesis and biological properties of modified 2’-deoxyuridines with broad spectrum of antimicrobial activity |
| P 59 |
Olszewska |
Agata |
Development of reactive groups for DNA-protein cross-link information |
| P 60 |
Oslovsky |
Vladimir |
Synthesis and antiviral activity of new N6-benzyladenosine analogues with acetylene linker |
| P 61 |
Panattoni |
Alessandro |
Competitive primer extension of base-modified dNTPs in the presence of natural dNTPs. |
| P 62 |
Perlikova |
Pavla |
Mechanism of action of 7-(2-thienyl)-7-deazaadenosine (AB61), a potent cytostatic |
| P 63 |
Piecyk |
Karolina Ewa |
Synthesis and potencial application of new double-functionalized dinucleotide mRNA cap analogues |
| P 64 |
Ploschik |
Damian |
Enzymatic Synthesis and Copperfree Bioorthogonal Labeling of Cyclopropene-modified Oligonucleotides by the Use of Inverse Electron Demand Diels-Alder Cycloaddition |
| P 65 |
Pozmogova |
Galina |
A THF-based modification induces antiparallel to parallel conformational switches in G4 DNA |
| P 66 |
Promontorio |
Rossella |
Exploration of new chemical space through the synthesis of sp3-enriched bridged bicyclo compounds |
| P 67 |
Promontorio |
Rossella |
Crystal structure of an intramolecular telomeric DNA G-quadruplex-ligand complex |
| P 68 |
Rachwalak |
Marta |
Synthesis of nucleoside 5'-diphosphates and their tio- and seleno analogues using H-phosphonate chemistry |
| P 69 |
Rahimoff |
René |
A novel probe for the MS/MS-based detection and quantification of abasic site intermediates in genomic DNA |
| P 70 |
Ravn |
Jacob |
Conjugation and linker strategies for LNA SSO delivery |
| P 71 |
Räz |
Michael |
Torsional Constraints of DNA Substrates Impact Cas9 Cleavage |
| P 72 |
Reichle |
Valentin Frederik |
Biosynthetic isotope labeling reveals dynamics of the epitranscriptome and novel modified nucleosides |
| P 73 |
Reisacher |
Ulrike |
Copper-free, Bioorthogonal and Postsynthetic Labeling of Nucleic Acids |
| P 74 |
Richard |
Jean-Alexandre |
Synthesis of dihydroxanthene near-infrared emitting fluorophores and their water-soluble analogues |
| P 75 |
Romanowska |
Joanna |
Exploring new anti-HIV prodrugs – nucleoside 5’-diphosphates |
| P 76 |
Rydzik |
Anna |
Crosslinking strategies for capturing nucleic acid – protein interactions |
| P 77 |
Saha |
Subham |
Noncovalent Spin Labeling of Unmodified RNA: The Aptamer Approach |
| P 78 |
Schiffers |
Sarah |
Quantitative LC-MS provides no evidence for m6dA or m4dC in the genomes of mouse ESCs and tissues |
| P 79 |
Schmidt |
Olivia Paula |
A Fluorescent Base Analog Reveals High Kinetic Stabilities of T-HgII-T Base Pairs that Inhibit DNA Dynamics and Polymerase Activity |
| P 80 |
Schneider |
Christina |
Ubiquitous non-canonical RNA nucleosides are vestiges of the early Earth |
| P 81 |
Sherstyuk |
Yuliya |
ADP conjugates as potential PARP-1 inhibitors |
| P 82 |
Shin |
Dongwon |
Novel N1-Substituted Pseudouridine 5’-Triphosphates for the Synthesis of Modified mRNA and its Effect on mRNA Translation in THP-1 cells |
| P 83 |
Simonova |
Anna |
Phenothiazine as new oxidizable label for electrochemical detection of DNA |
| P 84 |
Skácel |
Jan |
Design and Synthesis of Potential HG(X)PRT Inhibitors Based on Polysubstituted Thiophenes: Utilization of Direct Metalation of Heterocycles. |
| P 85 |
Slator |
Creina |
Di-Copper Complexes Promote NCI-60 Chemotherapy by Intracellular Superoxide and Singlet Oxygen Facilitated DNA Damage |
| P 86 |
Slavíčková |
Michaela |
Synthesis of hydrophobic derivatives of 2'-deoxyadenosine and DNA |
| P 87 |
Soudah |
Terese |
PNA-peptide conjugates as splice switching oligonucleotides (SSO) of the MnK2 gene |
| P 88 |
Stazzoni |
Samuele |
Quantification of 5-formylcytosine in specific genomic sites |
| P 89 |
Šimonová |
Anna |
Studies of methylation of viral RNA |
| P 90 |
Špaček |
Petr |
Acyclic nucleoside bisphosphonates with asymmetric scaffold as inhibitors of Plasmodial and human 6-oxopurine phosphoribosyltransferases |
| P 91 |
Tichý |
Michal |
Synthesis and Biological Activities of Thieno-fused 7-Deazapurine Ribonucleosides |
| P 92 |
Varizhuk |
Anna |
New benzothiazole-derived dyes for staining of non-canonical DNA |
| P 93 |
Walczak |
Sylwia |
Triazole-modified dinucleotides as 5’ mRNA cap mimics and reagents for mRNA modification |
| P 94 |
Wanat |
Przemyslaw |
Nonhydrolyzable pyrene-excimer NTP-based molecular probes |
| P 95 |
Watanabe |
Yurika |
Water-Soluble Nucleotide Analogue (WSNA) with a Flexible Backbone-Containing Guanidinium Groups |
| P 96 |
Witkowska |
Agnieszka |
Chemical Switch in 2-Pyridinyl Thermolabile Protecting groups methodology |
| P 97 |
Zatsepin |
Timofey |
Specificity of SNP detection with molecular beacons is improved by stem and loop separation with spacers |