about
UV-induced electron transfer between triethylamine and 5-bromo-2'-deoxyuridine. A puzzle concerning the photochemical debromination of labeled DNA.An ESR and DFT study of hydration of the 2'-deoxyuridine-5-yl radical: a possible hydroxyl radical intermediate.Photoelectron spectroscopic studies of 5-halouracil anions.5-Thiocyanato-2'-deoxyuridine as a possible radiosensitizer: electron-induced formation of uracil-C5-thiyl radical and its dimerization.Mechanisms of Damage to DNA Labeled with Electrophilic Nucleobases Induced by Ionizing or UV Radiation.Quantitative assay of photoinduced DNA strand breaks by real-time PCR.Presolvated low energy electron attachment to peptide methyl esters in aqueous solution: C-O bond cleavage at 77 KElectrophilic 5-Substituted Uracils as Potential Radiosensitizers: A Density Functional Theory Study.The anionic (9-methyladenine)-(1-methylthymine) base pair solvated by formic acid. A computational and photoelectron spectroscopy study.Stabilization of very rare tautomers of uracil by an excess electron.DHPLC and MS studies of a photoinduced intrastrand cross-link in DNA labeled with 5-bromo-2'-deoxyuridine.Calculation of quantum-mechanical descriptors for QSPR at the DFT level: is it necessary?Photoelectron spectroscopic and density functional theoretical studies of the 2'-deoxycytidine homodimer radical anion.Barrier-free intermolecular proton transfer induced by excess electron attachment to the complex of alanine with uracil.Interaction with glycine increases stability of a mutagenic tautomer of uracil. A density functional theory study.Benign decay vs. photolysis in the photophysics and photochemistry of 5-bromouracil. A computational study.Valence anions of 9-methylguanine-1-methylcytosine complexes. Computational and photoelectron spectroscopy studies.Dominant Pathways of Adenosyl Radical-Induced DNA Damage Revealed by QM/MM Metadynamics.Valence anion of thymine in the DNA pi-stack.AT base pair anions versus (9-methyl-A)(1-methyl-T) base pair anions.5-Bromo-2'-deoxycytidine-a potential DNA photosensitizer.Reactivity pattern of bromonucleosides induced by 2-hydroxypropyl radicals: photochemical, radiation chemical, and computational studies.Barrier-free proton transfer in the valence anion of 2'-deoxyadenosine-5'-monophosphate. II. A computational study.Stabilization of very rare tautomers of 1-methylcytosine by an excess electron.Photoelectron spectroscopy of adiabatically bound valence anions of rare tautomers of the nucleic acid bases.5-Selenocyanatouracil: A Potential Hypoxic Radiosensitizer. Electron Attachment Induced Formation of Selenium Centered Radical.The Sequence Dependence of Photoinduced Single Strand Break in 5-Bromo-2'-deoxyuridine Labeled DNA Supports That Electron Transfer Is Responsible for the Damage.Photoinduced single strand breaks and intrastrand cross-links in an oligonucleotide labeled with 5-bromouracil.Electron induced single strand break and cyclization: a DFT study on the radiosensitization mechanism of the nucleotide of 8-bromoguanine.Chemically-enzymatic synthesis of photosensitive DNA.The Transformation Mechanism of 3,4,6-Tri-O-acetyl-1,5-anhydro-2-deoxy-D-arabino-hex-1-enitol in Water.PCR synthesis of double stranded DNA labeled with 5-bromouridine. A step towards finding a bromonucleoside for clinical trials.Low-energy electron-induced decomposition of 5-trifluoromethanesulfonyl-uracil: A potential radiosensitizerPhotoinduced electron transfer in 5-bromouracil labeled DNA. A contrathermodynamic mechanism revisited by electron transfer theoriesLocal Excitation of the 5-Bromouracil Chromophore in DNA. Computational and UV Spectroscopic StudiesTheoretical studies on interactions between low energy electrons and protein–DNA fragments: valence anions of AT-amino acids side chain complexesBarrier-free proton transfer induced by electron attachment to the complexes between 1‐methylcytosine and formic acidCan an excess electron localize on a purine moiety in the adenine-thymine Watson-Crick base pair? A computational studyIntermolecular proton transfer induced by excess electron attachment to adenine(formic acid)n (n=2, 3) hydrogen-bonded complexesEffect of Hydrogen Bonding on Barrier-Free Proton Transfer in Anionic Complexes of Uracil with Weak Acids: (U…HCN)−versus (U…H2S)−
P50
Q33365441-AF7A0566-3AC1-4533-BD18-09D1B3A6902BQ34422134-211CDED1-BDF9-4C51-90AE-A448B4BFD106Q35284155-6E43A5DA-5F65-4E4C-929B-86F16520708BQ35783000-7D7682D6-F71C-4D18-8495-2E7328B7E01CQ38523819-E20268A8-1F5E-4F0A-AD48-8C269C86AE9EQ38846003-7838EEDA-7438-4CCE-A08C-BEE5054251A8Q39620865-59BB6365-E6F6-4B4A-976D-0C9B75D0AF48Q39785770-72E1C01A-DD8D-4DDE-85A3-E7F6FC86E17AQ42940734-9B73C874-0F5A-483C-9CEA-5B124F0C71CBQ43269292-585AE43D-DD6F-447B-B9BE-8405C309A43CQ43507323-C14967FD-CA03-4F9B-A743-22025E87828EQ43657482-13641647-FC10-453B-BB5C-361722543A33Q43663098-E1C2B7C5-25E9-4924-A2FA-F5B8B576D1CAQ44988513-AB9291E0-3056-4788-9C36-80125264564BQ45266594-71054DFD-5924-40FA-8B45-BF334C378906Q46047111-EB4A1B4A-E85A-4FDA-830B-5001212F53F8Q46146485-6CA98D31-23EF-44BE-9B8A-C0C1D4C9CB88Q46265596-EF7964BD-3F22-46D9-B923-4E762AB0CB0CQ46293346-E055D5EC-C1B4-4606-BB62-0DAA76877041Q46456740-3D798F2F-61FC-4C0B-905D-852F1A45A4C0Q46480749-C7EE46BE-A89C-483D-BEAA-69514B00C3B0Q46729095-3623097A-9A78-4AB8-8209-1CC5F5530618Q46773440-C3F4265D-34AD-4D5B-88B7-9C90C70876C6Q46850806-65C2E489-70B6-4FC4-BD50-9686A855F09CQ46906045-4973BAD6-FC09-4101-97DC-EBBA32CE6E8BQ48060374-974211CC-58FD-4A0A-BCE1-2AA800187AB5Q48092465-7294B8D5-D65C-47DE-AAC6-3645D6A9A8D8Q53055566-165FFACC-6BDF-40D9-9DC5-77F8BE9D3657Q53064895-A5A8067E-4E01-498F-B9BF-8E1E579C6162Q53705038-E66B4105-2241-41E9-A1EC-A5071E12C209Q53987528-4A57B6E2-F0ED-4DBC-9905-BB549670C628Q54567937-AF8E0983-FD95-4295-913E-E7C03E62CE82Q58600881-3691CFB2-4861-4495-85DF-59AFF2F4D427Q62110541-DE035399-617F-42C8-9C3F-0D0FA6C5DE63Q62514058-5223E810-5FC0-4B0B-BDBF-34F325865F5CQ63284230-1EFE8A4B-3571-402F-A0B5-B8B9DA86AADEQ63927560-9CFCCE98-0041-45F6-BD75-D3CA81609BE3Q63927562-B4336519-1FEA-42CE-81A0-C8C6CB65AAC2Q63927564-85BC8058-D0DA-4779-A2B9-A3EF8A35EAA7Q63927565-1102F85E-FC7E-4329-BA0F-21133AD44DCC
P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Janusz Rak
@ast
Janusz Rak
@en
Janusz Rak
@es
Janusz Rak
@nl
type
label
Janusz Rak
@ast
Janusz Rak
@en
Janusz Rak
@es
Janusz Rak
@nl
prefLabel
Janusz Rak
@ast
Janusz Rak
@en
Janusz Rak
@es
Janusz Rak
@nl
P106
P1153
35227887600
P31
P496
0000-0003-3036-0536