nioch.ru

Федеральное государственное бюджетное учреждение науки
Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук


Warning: Creating default object from empty value in /disk2/www/nioch/tmp/sourcerer_php_c7c7d1397fb1b551c86204f82febc354 on line 21

(2006 - 2023 )

  1. E.G. Bagryanskaya, S.R. A. Marque
    Scavenging of Organic C-Centered Radicals by Nitroxides
    Chem. Rev., 2014, 114 (9), pp 5011-5056. doi:10.1021/cr4000946, IF=45.66
     
  2. M. Slota, A. Keerthi, W.K. Myers, E. Tretyakov, M. Baumgarten, A. Ardavan, H. Sadeghi, C.J. Lambert, A. Narita, K. Müllen, L. Bogani
    Magnetic edge states and coherent manipulation of graphene nanoribbons
    Nature, 2018, V. 557, N 7707, pp. 691-695 doi:10.1038/s41586-018-0154-7, IF=41.577
     
  3. I.P. Koskin, Ch.S. Becker, A.A. Sonina, V.A. Trukhanov, N.A. Shumilov, A.D. Kuimov, Yu.S. Zhuravleva, Yu.O. Kiseleva, I.K. Shundrina, P.S. Sherin, D.Yu. Paraschuk, M.S. Kazantsev
    Selectively Fluorinated Furan-Phenylene Co-Oligomers Pave the Way to Bright Ambipolar Light-Emitting Electronic Devices
    Advanced Functional Materials, 2021, V.31, N 48, ArtNum.2104638 doi:10.1002/adfm.202104638, IF=18.808
     
  4. E.V. Tretyakov, P.V. Petunin, S. Zhivetyeva, D.E. Gorbunov, N.P. Gritsan, M.V. Fedin, D.V. Stass, R.I. Samoilova, I.Yu. Bagryanskaya, I.K. Shundrina, A.S. Bogomyakov, M.S. Kazantsev, P.S. Postnikov M. E. Trusova, V.I. Ovcharenko
    Platform for High-Spin Molecules: A Verdazyl-Nitronyl Nitroxide Triradical with Quartet Ground State
    Journal of the American Chemical Society, 2021, 143, 21, 8164-8176 doi:10.1021/jacs.1c02938, IF=15.419
     
  5. O. Schieman, C.A. Heubach, D. Abdullin, K. Ackermann, M. Azarkh, E.G. Bagryanskaya, M. Drescher, B. Endeward, J.H. Freed, L. Galazzo, D. Goldfarb, T. Hett, L.E. Hofer, L.F. Ibanez, E.J. Hustedt, S. Kucher, I. Kuprov, J.E. Lovett, A. Meyer, Sh. Ruthstein, S. Saxena, S. Stoll, Ch.R. Timmel, M.D. Valentin, H.S. Mchaourab, T.F. Prisner, B.E. t Bode, E. Bordignon, M. Bennati, G. Jeschke
    Benchmark Test and Guidelines for DEER/PELDOR Experiments on Nitroxide-Labeled Biomolecules
    Journal of the American Chemical Society, Journal of the American Chemical Society, 2021, 143, 43, 17875-17890 doi:10.1021/jacs.1c07371, IF=15.418
     
  6. A.V. Artem'ev, M.P. Davydova, A.S. Berezin, D.G. Samsonenko, I.Yu. Bagryanskaya, V.K. Brel, Xi. Hei, K.A. Brylev, O.I. Artyushin, L.E. Zelenkov, I.I. Shishkin, Jing. Li
    New Approach toward Dual-Emissive Organic-Inorganic Hybrids by Integrating Mn(II) and Cu(I) Emission Centers in Ionic Crystals
    ACS Applied Materials & Interfaces, Articles ASAP (Functional Inorganic Materials and Devices), 2022, 14, 27, 31000-31009 doi:10.1021/acsami.2c06438, IF=14.4
     
  7. M. Kruchinina, A. Gromov, V. Kruchinin, M. Shashkov, A. Sokolova, I. Yakovina, A. Shestov
    P-15 Diagnostic potential of erythrocyte and serum fatty acids in spotting adenomatous polyps and identifying the early stages of colorectal cancer depending on tumor localization
    Annals of Oncology, 2021, V. 32, Suppl. 3, . P.S101 doi:10.1016/j.annonc.2021.05.070, IF=14.196
     
  8. M.V. Kruchinina, A.A. Gromov, Ya.I. Prudnikova, M.V. Shashkov, A.S. Sokolova, V.N. Kruchinin, I.N. Yakovina, N.A. Bannova
    Perturbation of fatty acids of erythrocyte membranes and blood serum in patients with colorectal cancer: new opportunities for diagnostics
    Annals of Oncology. 2019. Т. 30. № S4. С. 109. Аннотация к встрече: P - 003 doi:10.1093/annonc/mdz155, IF=14.196
     
  9. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, 2020, V. 59, N 46, Pp 20704-20710 doi:10.1002/anie.202010041, IF=12.959
     
  10. D. Polyukhov, A.S. Poryvaev, S.A. Gromilov, M.V. Fedin
    Precise Measurement and Controlled Tuning of Effective Window Sizes in ZIF-8 Framework for Efficient Separation of Xylenes
    Nano Letters, 2019, V. 19, N 9, Pp 6506-6510 doi:10.1021/acs.nanolett.9b02730, IF=12.279
     
  11. M. l Froba, E. Gjuzi, F. Hoffmann, A.S. Poryvaev, M.V. Fedin, D.M. Polyukhov
    Blatter Radical-Grafted Mesoporous Silica as Prospective Nanoplatform for Spin Manipulation at Ambient Conditions
    Angewandte Chemie International Edition, First published: 24 January 2021 doi:10.1002/anie.202015058, IF=12.256
     
  12. O.A. Krumkacheva, I.O. Timofeev, L.V. Politanskaya, Yu.F. Polienko, E.V. Tretyakov, O.Yu. Rogozhnikova, D.V. Trukhin, V.M. Tormyshev, A.S. Chubarov, E.G. Bagryanskaya, M.V. Fedin
    Triplet Fullerenes as Prospective Spin Labels for Nanoscale Distance Measurements by Pulsed Dipolar EPR
    Angewandte Chemie International Edition, 2019, V. 58, N 38, Pp 13271-13275 doi:10.1002/anie.201904152, IF=12.256
     
  13. M.V. Fedin, S.L. Veber, E.G. Bagryanskaya, V.I. Ovcharenko
    Electron paramagnetic resonance of switchable copper-nitroxide-based molecular magnets: An indispensable tool for intriguing systems
    Coordination Chemistry Reviews, 2015, V. 289–290, Pp 341-356, Special Issue: SI doi:10.1016/j.ccr.2014.11.015, IF=12.239
     
  14. E.S. Stoyanov, I.V. Stoyanova
    Features of protonation of the simplest weakly basic molecules, SO2, CO, N2O, CO2, and others, by solid carborane superacids
    Angewandte Chemie International Edition, 2018, V. 57, N 17, Pp 4516-4520 doi:10.1002/anie.201704645, IF=12.102
     
  15. B. Joseph, V.M. Tormyshev, O.Yu. Rogozhnikova, D. Akhmetzyanov, E.G. Bagryanskaya, T.F. Prisner
    Selective High-Resolution Detection of Membrane Protein–Ligand Interaction in Native Membranes using Trityl-Nitroxide PELDOR
    Angewandte Chemie International Edition, 2016, V, 55, N 38, Pp 11538-11542 doi:10.1002/anie.201606335, IF=11.709
     
  16. A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, I.O. Timofeev, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Structural rearrangements in mRNA upon its binding to human 80S ribosomes revealed by EPR spectroscopy
    Nucleic Acids Research, Volume 46, Issue 2, 25 January 2018, Pp 897-904 doi:10.1093/nar/gkx1136, IF=11.561
     
  17. D.R. Gruber, J.J. Toner, H.L. Miears, A.V. Shernyukov, A.S. Kiryutin, A.A. Lomzov, A.V. Endutkin, I.R. Grin, D.V. Petrova, M.S. Kupryushkin, A.V. Yurkovskaya, E.C. Johnson, M. Okon, Е.G. Bagryanskaya, D.O. Zharkov, S.L. Smirnov
    Oxidative damage to epigenetically methylated sites affects DNA stability, dynamics and enzymatic demethylation
    Nucleic Acids Research, 2018, V.46,N 20, Pp 10827-10839 doi:10.1093/nar/gky893, IF=11.56
     
  18. I. Yu. Barskaya, E. V. Tretyakov, R. Z. Sagdeev, V. I. Ovcharenko, E. G. Bagryanskaya, K. Yu. Maryunina, T. Takui, K. Sato, M. V. Fedin
    Photoswitching of a Thermally Unswitchable Molecular Magnet Cu(hfac)2Li-Pr Evidenced by Steady-State and Time-Resolved Electron Paramagnetic Resonance
    J. Am. Chem. Soc., 2014, 136 (28), pp 10132-10138. doi:10.1021/ja504774q, IF=11.444
     
  19. G.Yu. Shevelev, O.A. Krumkacheva, A.A. Kuzhelev, A.A. Lomzov, O.Yu. Rogozhnikova, D.V. Trukhin, T.I. Troitskaya, V.M. Tormyshev, M.V. Fedin, D.V. Pyshnyi, E.G. Bagryanskaya
    Physiological- Temperature Distance Measurement in Nucleic Acid using Triarylmethyl-Based Spin Labels and Pulsed Dipolar EPR Spectroscopy.
    J. Am. Chem. Soc., 2014, 136 (28), pp 9874-9877. doi:10.1021/ja505122n, IF=11.444
     
  20. W. Kaszub, A. Marino, M. Lorenc, E. Collet, E.G. Bagryanskaya, E.V. Tretyakov, V.I. Ovcharenko, M.V. Fedin
    Ultrafast Photoswitching in a Copper-Nitroxide-Based Molecular Magnet
    Angewandte Chemie International Edition, 2014, V. 53, N 40, Pp 10636-10640. doi:10.1002/anie.201403672, IF=11.336
     
  21. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
     
  22. A.A. Malygin, O.A. Krumkacheva, D.M. Graifer, I.O. Timofeev, A.S. Ochkasova, M.I. Meschaninova, A.G. Venyaminova, M.V. Fedin, M. Bowman, G.G. Karpova, E.G. Bagryanskaya
    Exploring the interactions of short RNAs with the human 40S ribosomal subunit near the mRNA entry site by EPR spectroscopy
    Nucleic Acids Research, 2019, V. 47, N 22, Pp 11850-11860 doi:10.1093/nar/gkz1039, IF=11.147
     
  23. O. Guselnikova, S.R-A. Marque, E.V. Tretyakov, D. Mares, V. Jerabek, G. Audran, J-P. Joly, M. Trusova, V. Svorcik, O. Lyutakov, P. Postnikov
    Unprecedented plasmon-induced nitroxide-mediated polymerization (PI-NMP): a method for preparation of functional surfaces
    J. Mater. Chem. A, 2019, 2019, V. 7, N 2, Pp 12414-12419 , 2019 Journal of Materials Chemistry A HOT Papers doi:10.1039/C9TA01630A, IF=10.733
     
  24. I. Dhimitruka, A.A. Bobko, T.D. Eubank, D.A. Komarov, V.V. Khramtsov
    Phosphonated Trityl Probes for Concurrent in Vivo Tissue Oxygen and pH Monitoring Using Electron Paramagnetic Resonance-Based Techniques
    Journal of the American Chemical Society, 2013, V. 135, N 15, P. 5904-5910. doi:10.1021/ja401572r, IF=10.677
     
  25. M.V. Fedin, E.G. Bagryanskaya, H. Matsuoka, S. Yamauchi, S.L. Veber, K.Yu. Maryunina, E.V. Tretyakov, V.I. Ovcharenko, R.Z. Sagdeev
    W-Band Time-Resolved Electron Paramagnetic Resonance Study of Light-Induced Spin Dynamics in Copper–Nitroxide-Based Switchable Molecular Magnets
    J. Am. Chem. Soc., 2012, 134 (39), 16319–16326. doi:10.1021/ja306467e, IF=9.906
     
  26. A.V. Artem’ev, M.P. Davydova, Xi. Hei, M.I. Rakhmanova, D.G. Samsonenko, I.Yu. Bagryanskaya, K.A. Brylev, V.P. Fedin, Jia-Shiang. Chen, M. Cotlet, Ji. Li
    Family of Robust and Strongly Luminescent CuI-Based Hybrid Networks Made of Ionic and Dative Bonds
    Chemistry of Materials, 2020, 32, 24, 10708-10718 doi:10.1021/acs.chemmater.0c03984, IF=9.567
     
  27. C. Gmeiner, D. Klose, E. Mileo, V. Belle, S.R-A. Marque, G. Dorn, F.H-T. Allain, B. Guigliarelli, G. Jeschke, M. Yulikov
    Orthogonal Tyrosine and Cysteine Site-Directed Spin Labeling for Dipolar Pulse EPR Spectroscopy on Proteins
    J. Phys. Chem. Lett., 2017, 8(19), pp 4852-4857 doi:10.1021/acs.jpclett.7b02220, IF=9.352
     
  28. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    lsoinversion Behavior in the Enantioselective Oxidations of Pyridylmethylthiobenzimidazoles to Chiral Proton Pump Inhibitors on Titanium Salalen Complexes
    ACS Catal., 2015, 5 (8), pp 4673-4679 doi:10.1021/acscatal.5b01212, IF=9.312
     
  29. O. Mallow, M.A. Khanfar, M. Malischewski, P. Finke, M. Hesse, E. Lork, T. Augenstein, F. Breher, J.R. Harmer, N.V. Vasilieva, A.V. Zibarev, A.S. Bogomyakov, K. Seppelt, J. Beckmann
    Diaryldichalcogenide radical cations
    Chem. Sci., 2015,6(1), 497-504. doi:10.1039/C4SC02964J, IF=9.211
     
  30. E.S. Babaylova, A.A. Malygin, A.A. Lomzov, D.V. Pyshnyi, M. Yulikov, G. Jeschke, O.A. Krumkacheva, M.V. Fedin, G.G. Karpova, E.G. Bagryanskaya
    Complementary-addressed site-directed spin labeling of long natural RNAs
    Nucl. Acids Res. (19 September 2016), 44(16): 7935-7943. doi:10.1093/nar/gkw516, IF=9.201
     
  31. V.V. Chernyshov, I.I. Popadyuk, O.I. Yarovaya, N.F. Salakhutdinov
    Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
    Topics in Current Chemistry, 2022, V. 380, Art. number: 42 doi:10.1007/s41061-022-00399-1, IF=8.904
     
  32. A.S. Poryvaev, D.M. Polyukhov, M.V. Fedin
    Mitigation of Pressure-Induced Amorphization in Metal–Organic Framework ZIF-8 upon EPR Control
    ACS Appl. Mater. Interfaces 2020, V. 12, N 14, Pp 16655-16661 doi:10.1021/acsami.0c03462, IF=8.758
     
  33. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
     
  34. M.Yu. Ivanov, S.A. Prikhod'ko, N. Yu. Adonin, I.A. Kirilyuk, S.V. Adichtchev, N.V. Surovtsev, S.A. Dzuba, M.V. Fedin
    Structural Anomalies in Ionic Liquids near the Glass Transition Revealed by Pulse EPR
    J. Phys. Chem. Lett., Publication Date (Web): July 27, 2018 (Chemical and Dynamical Processes in Solution; Polymers, Glasses, and Soft Matter) doi:10.1021/acs.jpclett.8b02097, IF=8.708
     
  35. A.D. Kuimov, Ch.S. Becker, N.A. Shumilov, I.P. Koskin, A.A. Sonina, V.Yu. Komarov, I.K. Shundrina, M.S. Kazantsev
    Synthetic approach for the control of self-doping in luminescent organic semiconductors
    Mater. Chem. Front., 2022, V. 6, N 16, Pp. 2244-2255 doi:10.1039/D2QM00345G, IF=8.683
     
  36. A.A. Kuzhelev, G. Yu. Shevelev, O.A. Krumkacheva, V.M. Tormyshev, D.V. Pyshnyi, M.V. Fedin, E.G. Bagryanskaya
    Saccharides as Prospective Immobilizers of Nucleic Acids for Room-Temperature Structural EPR Studies
    J. Phys. Chem. Lett., 2016, V. 7, N 12, pp 2544-2548 doi:10.1021/acs.jpclett.6b01024, IF=8.538
     
  37. I.S. Merenkov, M.S. Myshenkov, Yu.M. Zhukov, Yo. Sato, T.S. Frolova, D.V. Danilov, I.A. Kasatkin, O.S. Medvedev, R.V. Pushkarev, O.I. Sinitsyna, M. Terauchi, I.A. Zvereva, M.L. Kosinova, K. Ostrikov
    Orientation-controlled, low-temperature plasma growth and applications of h-BN nanosheets
    Nano Research, 2019, V. 12, N 1, pp 91-99 doi:10.1007/s12274-018-2185-7, IF=8.515
     
  38. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, K.P. Bryliakov
    Direct Regio- and Stereoselective Mono- and Polyoxyfunctionalization of Estrone Derivatives at C(sp3)-H Bonds
    Journal of Catalysis, Available online 30 September 2022 doi:10.1016/j.jcat.2022.09.020, IF=8.46
     
  39. R.V. Ottenbacher, D.G. Samsonenko, A.A. Nefedov, E.P. Talsi, K.P. Bryliakov
    Mn Aminopyridine Oxidase Mimics: Switching Between Biosynthetic-like and Xenobiotic Regioselectivity in C-H Oxidation of (-)-Ambroxide
    Journal of Catalysis, 2021, V.399, July 2021, Pp 224-229 doi:10.1016/j.jcat.2021.05.014, IF=7.92
     
  40. Z. Tang, E. Chulanova, M. Kullmer, A. Winter, J. Picker, Ch. Neumann, K. Schreyer, F. Herrmann-Westendorf, A. Arnlind, B. Dietzek, U.S. Schubert, A. Turchanin
    Photoactive ultrathin molecular nanosheets with reversible lanthanide binding terpyridine centers† Check for updates
    Nanoscale, 2021,13(48), 20583-20591 doi:10.1039/D1NR05430A, IF=7.789
     
  41. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
     
  42. A.Yu.Sidorenko, A.V.Kravtsova, A.Aho, I.Heinmaa, J.Warna, H.Pazniak, K.P.Volcho, N.F.Salakhutdinov, D.Yu.Murzin, V.E.Agabekov
    Highly selective Prins reaction over acid-modified halloysite nanotubes for synthesis of isopulegol-derived 2H-chromene compounds
    Journal of Catalysis, 2019, V. 374, Pp 360-377 doi:10.1016/j.jcat.2019.05.009, IF=7.723
     
  43. R.S. Fedorenko, A.V. Kuevda, V.A. Trukhanov, V.G. Konstantinov, A.Yu. Sosorev, A.A. Sonina, M.S. Kazantsev, N.M. Surin, S. Grigorian, O.V. Borshchev, S.A. Ponomarenko, D.Yu. Paraschuk
    Luminescent High-Mobility 2D Organic Semiconductor Single Crystals
    Advanced Electronic Materials, 2022, V. 8, N 7, July 2022, 2101281 doi:10.1002/aelm.202101281, IF=7.633
     
  44. E.A. Pronina, Yu.A. Vorotnikov, T.N. Pozmogova, A. O. Solovieva, S.M. Miroshnichenko, P. E. Plyusnin, D. P. Pishchur, I. V. Eltsov, M.V. Edeleva, M.A. Shestopalov, O.A. Efremova
    No catalyst added hydrogen peroxide oxidation of dextran: an environment-friendly route to multifunctional polymers
    ACS Sustainable Chem. Eng. 2020, V. 8, N 13, Pp 5371-5379 doi:10.1021/acssuschemeng.0c01030, IF=7.632
     
  45. Е.В. Третьяков, В.И. Овчаренко, А.О. Терентьев, И.Б. Крылов, Т.В. Магдесиева, Д.Г. Мажукин, Н.П. Грицан
    Сопряженные нитроксильные радикалы
    Успехи химии, 2022, 91 (2), RCR5025 (Conjugated nitroxide radicals/ E V Tretyakov, V I Ovcharenko, A O Terent'ev, I B Krylov, T V Magdesieva, D G Mazhukin, N P Gritsan// Russian Chemical Reviews, 2022, 91 (2), RCR5025 doi:10.1070/RCR5025), IF=7.46
     
  46. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=7.328
     
  47. K.N. Bulygin, I.O. Timofeev, A.A. Malygin, D.M. Graifer, M.I. Meschaninova, A.G. Venyaminova, O.A. Krumkacheva, M.V. Fedin, L.Yu. Frolova, G.G. Karpova, E.G. Bagryanskaya
    Two alternative conformations of mRNA in the human ribosome during elongation and termination of translation as revealed by EPR spectroscopy
    Computational and Structural Biotechnology Journal, 2021, V. 19, Pp 4702-4710 doi:10.1016/j.csbj.2021.08.024, IF=7.27
     
  48. R. Nazarewicz, A. Dikalova, A. Bikineyeva, S. Ivanov, I.A. Kirilyuk, I.A. Grigor'ev, S.I. Dikalov
    Does Scavenging of Mitochondrial Superoxide Attenuate Cancer Prosurvival Signaling Pathways?
    Antioxidants & Redox Signaling, 2013, V.19, N 4, pp 344-349. doi:10.1089/ars.2013.5185, IF=7.189
     
  49. E.G. Kovaleva, L.S. Molochnikov, D. Tambasova, A. Marek, M. Chestnut, V.A. Osipova, D.O. Antonov, I.A. Kirilyuk, A. Smirnov
    Electrostatic Properties of Inner Nanopore Surfaces of Anodic Aluminum Oxide Membranes upon High Temperature Annealing Revealed by EPR of pH-sensitive Spin Probes and Labels
    Journal of Membrane Science, V. 604, 1 June 2020, 118084 doi:10.1016/j.memsci.2020.118084, IF=7.183
     
  50. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144
     
  51. O.N. Fedyaeva, S.V. Morozov, A.A. Vostrikova
    Supercritical water oxidation of chlorinated waste from pulp and paper mill
    Chemosphere, 2021, V. 238, 131239 doi:10.1016/j.chemosphere.2021.131239, IF=7
     
  52. E.V. Sokol, O.A. Kozmenko, H.N. Khoury, S.N. Kokh, S.A. Novikova, A.A. Nefedov, I.A. Sokol, P. Zaikin
    Calcareous sediments of the Muwaqqar Chalk Marl Formation, Jordan: Mineralogical and geochemical evidences for Zn and Cd enrichment
    Gondwana Research, 2017, V. 46, Pp 204-226 doi:10.1016/j.gr.2017.03.008, IF=6.959
     
  53. И.С. Антипин, М.В. Алфимов, В.В. Арсланов, В.А. Бурилов, С.З. Вацадзе, Я.З. Волошин, К.П. Волчо, В.В. Горбачук, Ю.Г. Горбунова, С.П. Громов, С.В. Дудкин, С.Ю. Зайцев, Л.Я. Захарова, М.А. Зиганшин, А.В. Золотухина, М.А. Калинина, Э.А. Караханов, Р.Р. Кашапов, О.И. Койфман, А.И. Коновалов, В.С. Коренев, А.Л. Максимов, Н.Ж. Мамардашвили, Г.М. Мамардашвили, А.Г. Мартынов, А.Р. Мустафина, Р.И. Нугманов, А.С. Овсянников, П.Л. Падня, А.С. Потапов, С.Л. Селектор, М.Н. Соколов, С.Е. Соловьева, И.И. Стойков, П.А. Стужин, Е.В. Суслов, Е.Н. Ушаков, В.П. Федин, С.В. Федоренко, О.А. Федорова, Ю.В. Федоров, С.Н. Чвалун, А.Ю. Цивадзе, С.Н. Штыков, Д.Н. Шурпик, М.А. Щербина, Л.С. Якимова
    Функциональные супрамолекулярные системы: дизайн и области применения
    Успехи химии. 2021. Т. 90. № 8. С. 895-1107. (Functional supramolecular systems: design and applications/ I S Antipin, M V Alfimov, V V Arslanov, V A Burilov, S Z Vatsadze, Ya Z Voloshin, K P Volcho, V V Gorbatchuk, Yu G Gorbunova, S P Gromov, S V Dudkin, S Yu Zaitsev, L Ya Zakharova, M A Ziganshin, A V Zolotukhina, M A Kalinina, E A Karakhanov, R R Kashapov, O I Koifman, A I Konovalov, V S Korenev, A L Maksimov, N Zh Mamardashvili, G M Mamardashvili, A G Martynov, A R Mustafina, R I Nugmanov, A S Ovsyannikov, P L Padnya, A S Potapov, S L Selektor, M N Sokolov, S E Solovieva, I I Stoikov, P A Stuzhin, E V Suslov, E N Ushakov, V P Fedin, S V Fedorenko, O A Fedorova, Yu V Fedorov, S N Chvalun, A Yu Tsivadze, S N Shtykov, D N Shurpik, M A Shcherbina, L S Yakimova// Russian Chemical Reviews, 2021, 90 (8), 895-1107 doi:10.1070/RCR5011?locatt=label:RUSSIAN), IF=6.926
     
  54. О.И. Яровая, Н.Ф. Салахутдинов
    Моно- и сесквитерпены в качестве стартовой платформы для создания противовирусных средств
    Успехи химии, 2021, Т. 90, N 4, Сc 488-510 (Mono- and sesquiterpenes as a starting platform for the development of antiviral drugs/ O I Yarovaya, N F Salakhutdinov// RUSS CHEM REV, 2021, 90 (4), 488-510 doi:10.1070/RCR4969), IF=6.926
     
  55. M. Yu. Ivanov, A. S. Poryvaev, D. M. Polyukhov, S. A. Prikhod'ko, N.Yu. Adonin, M. V. Fedin
    Nanoconfinement effects on structural anomalies in imidazolium ionic liquids
    Nanoscale, 2020,12 (46), 23480-23487 doi:10.1039/D0NR06961B, IF=6.894
     
  56. Yu.S. Demidova, E.V. Suslov, I.L. Simakova, E.S. Mozhajcev, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, D.Yu. Murzin
    One-pot monoterpene alcohol amination over Au/ZrO2 catalyst: Effect of the substrate structure
    Journal of Catalysis, 2018, V. 360, Pages 127-134 doi:10.1016/j.jcat.2018.01.020, IF=6.759
     
  57. M.N. Timofeeva, V.N. Panchenko, A.A. Abel, N.A. Khan, I. Ahmed, A.B. Ayupov, K.P. Volcho, S.H. Jhung
    Rearrangement of α-pinene oxide to campholenic aldehyde over the trimesate metal-organic frameworks MIL-100, MIL-110 and MIL-96
    Journal of Catalysis, 2014, V. 311, Pp 114-120. doi:10.1016/j.jcat.2013.11.006, IF=6.72
     
  58. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
     
  59. D.M. Polyukhov, S. Krause, V. Bon, A.S. Poryvaev, S. Kaskel, M.V. Fedin
    Structural Transitions of the Metal-Organic Framework DUT-49(Cu) upon Physi- and Chemisorption Studied by in Situ Electron Paramagnetic Resonance Spectroscopy
    J. Phys. Chem. Lett. 2020, 11, 15, 5856-5862 doi:10.1021/acs.jpclett.0c01705, IF=6.71
     
  60. A.M. Sheveleva, D.I. Kolokolov, A.A. Gabrienko, A.G. Stepanov, S.A. Gromilov, I.K. Shundrina, R.Z. Sagdeev, M.V. Feedin, E.G. Bagryanskaya
    Structural Dynamics in a “Breathing” Metal–Organic Framework Studied by Electron Paramagnetic Resonance of Nitroxide Spin Probes
    J. Phys. Chem. Lett., 2014, 5 (1), pp 20-24. doi:10.1021/jz402357v, IF=6.686
     
  61. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641
     
  62. A.Y. Glagoleva, A.V. Vikhorev, N.A. Shmakov, S.V. Morozov, E.I. Chernyak, G.V. Vasiliev, N.V. Shatskaya, E.K. Khlestkina, O.Y. Shoeva
    Features of Activity of the Phenylpropanoid Biosynthesis Pathway in Melanin-Accumulating Barley Grains
    Frontiers in Plant Science, 2022, V.1311, Art.Num. 923717 doi:10.3389/fpls.2022.923717, IF=6.626
     
  63. Yu.B. Borozdina, E. Mostovich, V. Enkelmann, B. Wolf, P.T. Cong, U. Tutsch, M. Langc, M. Baumgarten
    Interacting networks of purely organic spin-1/2 dimers
    J. Mater. Chem. C, 2014,2 (48), 6618-6629 doi:10.1039/c4tc00399c, IF=6.625
     
  64. A.M. Genaev, G.E. Salnikov, A.V. Shernyukov, Z. Zhu, K.Yu. Koltunov
    Protonation Behavior of 1,1'-Bi-2-naphthol and Insights into Its Acid-Catalyzed Atropisomerization
    Org. Lett., 2017, 19 (3), pp 532-535 doi:10.1021/acs.orglett.6b03696, IF=6.578
     
  65. A.V. Artem'ev, M. P.Davydova, M.I. Rakhmanova, I.Yu. Bagryanskaya, D.P. Pishchur
    A family of Mn(ii) complexes exhibiting strong photo- and triboluminescence as well as polymorphic luminescence
    Inorg. Chem. Front., 2021, V. 8, N 15, Pp 3767-3774 doi:10.1039/D1QI00556A, IF=6.569
     
  66. K. Suzuki, Y. Takemoto, S. Takaoka, K.Taguchi. Y. Uchida, D.G. Mazhukin, I.A. Grigor'ev, R. Tamura
    Chiral all-organic nitroxide biradical liquid crystals showing remarkably large positive magneto-LC effects
    Chem. Commun., 2016,52(20), 3935-3938 doi:10.1039/C5CC09202G, IF=6.566
     
  67. S. Dikalov, Yu.F. Polienko, I. Kirilyuk
    Electron Paramagnetic Resonance Measurements of Reactive Oxygen Species by Cyclic Hydroxylamine Spin Probes
    Antioxidants & Redox Signaling, 2018, V. 28, N 15, Pp 1433-1444 doi:10.1089/ars.2017.7396, IF=6.53
     
  68. N. Polyakov, T. Leshina, L. Fedenok, I. Slepneva, I. Kirilyuk, J. Furso, M. Olchawa, T. Sarna, M. Elas, I. Bilkis, L. Weiner
    Redox-Active Quinone Chelators: Properties, Mechanisms of Action, Cell Delivery, and Cell Toxicity
    Antioxidants & Redox Signaling, 2018, V.28, N 15, Pp 1394-1403 doi:10.1089/ars.2017.7406, IF=6.53
     
  69. V.S. Moskaliuk, R.V. Kozhemyakina, D.V. Bazovkina, E. Terenina, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov, A.V. Kulikov, V.S. Naumenko, E. Kulikova
    On an association between fear-induced aggression and striatal-enriched protein tyrosine phosphatase (STEP) in the brain of Norway rats
    Biomedicine & Pharmacotherapy, V. 147, March 2022, 112667 doi:10.1016/j.biopha.2022.112667, IF=6.528
     
  70. A.G. Ogienko, S.A. Myz, A.A. Nefedov, A.A. Ogienko, T.P. Adamova, O.M. Voronkova, S.V. Amosova, B.A. Trofimov, V.V. Boldyrev, E.V. Boldyreva
    Clathrate Hydrates of Organic Solvents as Auxiliary Intermediates in Pharmaceutical Research and Development: Improving Dissolution Behaviour of a New Anti-Tuberculosis Drug, Perchlozon
    Pharmaceutics 2022, 14(3), 495 doi:10.3390/pharmaceutics14030495, IF=6.525
     
  71. I.V. Beregovaya, I.S. Tretyakova, V.I. Borovkov
    An Updated View of Primary Ionization Processes in Polar Liquids
    The Journal of Physical Chemistry Letters, 2021, 12, 47, 11573-11577 doi:10.1021/acs.jpclett.1c03388, IF=6.475
     
  72. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
     
  73. E.Yu. Schmidt, B.A. Trofimov, I.A. Bidusenko, N.A. Cherimichkina, I.A. Ushakov, N.I. Protzuk, Yu.V. Gatilov
    Base-Catalyzed Domino Cyclization of Acetylenes with Ketones to Functionalized Cyclopentenes
    Org. Lett., 2014, 16 (15), pp 4040-4043. doi:10.1021/ol501881e, IF=6.323
     
  74. M.V. Khvostov, E.D. Gladkova, S.A. Borisov, N.A. Zhukova, M.K. Marenina, Yu.V. Meshkova, O.A. Luzina, T.G. Tolstikova, N.F. Salakhutdinov
    Discovery of the First in Class 9-N-Berberine Derivative as Hypoglycemic Agent with Extra-Strong Action
    Pharmaceutics 2021, 13(12), 2138 doi:10.3390/pharmaceutics13122138, IF=6.321
     
  75. M. Neganova, Yu. Aleksandrova, E. Suslov, E. Mozhaitsev, A. Munkuev, D. Tsypyshev, M. Chicheva, A. Rogachev, O. Sukocheva, K. Volcho, S. Klochkov
    Novel Multitarget Hydroxamic Acids with a Natural Origin CAP Group against Alzheimer’s Disease: Synthesis, Docking and Biological Evaluation
    Pharmaceutics, 2021, 13(11), 1893 doi:10.3390/pharmaceutics13111893, IF=6.321
     
  76. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
     
  77. E.S. Stoyanov, I.V. Stoyanova
    The Chloronium Cation [(C2H3)2Cl+] and Unsaturated C4-Carbocations with C=C and C=C Bonds in Their Solid Salts and in Solutions: An H1/C13 NMR and Infrared Spectroscopic Study
    Int. J. Mol. Sci. 2022, 23(16), 9111 doi:10.3390/ijms23169111, IF=6.208
     
  78. O.V. Salomatina, A.V. Sen'kova, A.D. Moralev, I.A. Savin, N.I. Komarova, N.F. Salakhutdinov, M.A. Zenkova, A.V. Markov
    Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo
    Int. J. Mol. Sci. 2022, 23(11), 6214; doi:10.3390/ijms23116214, IF=6.208
     
  79. B. Epel, M.C. Maggio, E.D. Barth, R.C. Miller, C.A. Pelizzari, M. Krzykawska-Serda, S.V. Sundramoorthy, B. Aydogan, R.R. Weichselbaum, V.M. Tormyshev, H.J. Halpern
    Oxygen-guided radiation therapy
    International Journal of Radiation Oncology Biology Physics, 2019, V. 103, N 4, Pp 977-984 doi:10.1016/j.ijrobp.2018.10.041, IF=6.203
     
  80. N. Jugniot, I. Duttagupta, A. Rivot, P. Massot, C. Cardiet, A. Pizzoccaro, M. Jean, N. Vanthuyne, Jean-Michel Franconi, P. Voisin, G. Devouassoux, E. Parzy, E. Thiaudiere, S.R.A. Marque, A. Bentaher, G. Audran, P. Mellet
    An Elastase Activity Reporter for Electronic Paramagnetic Resonance (EPR) and Overhauser-enhanced Magnetic Resonance Imaging (OMRI) as a Line-Shifting Nitroxide
    Free Radical Biology and Medicine, 2018, V. 126, Pp 101-112 doi:10.1016/j.freeradbiomed.2018.08.006, IF=6.19
     
  81. M. Edeleva, D. Morozov, D. Parkhomenko, Yu. Polienko, A. Iurchenkova, I. Kirilyuk, E. Bagryanskaya
    Versatile approach to activation of alkoxyamine homolysis by 1,3-dipolar cycloaddition for efficient and safe nitroxide mediated polymerization
    Chem. Commun., 2019,V. 55, N 2, Pp 190-193 doi:10.1039/C8CC08541B, IF=6.164
     
  82. A.E. Grazhdannikov, L.M. Kornaukhova, V.I. Rodionov, N.A. Pankrushina, E.E. Shults, A.S. Fabiano-Tixier, S.A. Popov, F. Chemat
    Selecting a green strategy on extraction of birch bark and isolation of pure betulin using monoterpenes
    ACS Sustainable Chem. Eng., , 2018, 6 (5), pp 6281-6288 doi:10.1021/acssuschemeng.8b00086, IF=6.14
     
  83. D.A. Komarov, Yu. Ichikawa, K. Yamamoto, N.J. Stewart, S. Matsumoto, H. Yasui, I.A. Kirilyuk, V.V. Khramtsov, O. Inanami, H. Hirata
    In vivo extracellular pH mapping of tumors using electron paramagnetic resonance
    Anal. Chem., 90 (23), pp 13938-13945 doi:10.1021/acs.analchem.8b03328, IF=6.042
     
  84. A.Yu. Vorobev, A.E. Moskalensky
    Long-wavelength photoremovable protecting groups: On the way to in vivo application
    Computational and Structural Biotechnology Journal, 2020, V. 18, Pp 27-34 doi:10.1016/j.csbj.2019.11.007, IF=6.018
     
  85. B. Sharma, V.A. Tran, T. Pongratz, L. Galazzo, I. Zhurko, E. Bordignon, S.M. Kast, F. Neese, D. Marx
    A Joint Venture of Ab Initio Molecular Dynamics, Coupled Cluster Electronic Structure Methods, and Liquid-State Theory to Compute Accurate Isotropic Hyperfine Constants of Nitroxide Probes in Water
    Journal of Chemical Theory and Computation, 2021, V. 17, N 10, Pp 6366-6386 doi:10.1021/acs.jctc.1c00582, IF=6.006
     
  86. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
     
  87. N.A. Puskarevsky, A.I. Smolentsev, A.A. Dmitriev, I. Vargas-Baca, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Bis(2,1,3-benzotelluradiazolidyl)2,1,3-benzotelluradiazole: a pair of radical anions coupled by Te⋯N chalcogen bonding
    Chem. Commun., 2020, V. 56, N 7, Pp 1113-1116 doi:10.1039/C9CC08110K, IF=5.996
     
  88. N.A. Shekhovtsov, K.A. Vinogradova, A.S. Berezin, T.S. Sukhikh, V.P. Krivopalov, E.B. Nikolaenkova, M. B. Bushuev
    Excitation wavelength dependent emission of silver(i) complexes with a pyrimidine ligand†
    Inorg. Chem. Front., 2020, Advance Article doi:10.1039/D0QI00254B, IF=5.958
     
  89. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
     
  90. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
     
  91. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
     
  92. A.V. Artem'ev, E.P. Doronina, M.I. Rakhmanova, O.A. Tarasova, I.Yu. Bagryanskaya, N.A. Nedolya
    Chemoselective mechanochemical route toward a bright TADF-emitting CuI-based coordination polymer
    Inorg. Chem. Front., 2019, V. 6, N 3, Pp 671-679 doi:10.1039/C8QI01302K, IF=5.934
     
  93. M.V. Bermeshev, B.A. Bulgakov, A.M. Genaev, Ju.V. Kostina, G.N. Bondarenko, E.S. Finkelshtein
    Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes
    Macromolecules, 2014, V. 47, N 16, Pp. 5470-5483. doi:10.1021/ma5010919, IF=5.927
     
  94. S.S. Khutsishvili, A.I. Perfileva, O.A. Nozhkina, T.V. Ganenko, K.V. Krutovsky
    Novel Nanobiocomposites Based on Natural Polysaccharides as Universal Trophic Low-Dose Micronutrients
    International Journal of Molecular Sciences, 2021, 22(21), 12006 doi:10.3390/ijms222112006, IF=5.923
     
  95. M.Yu. Ivanov, Yu.F. Polienko, I.A. Kirilyuk, S.A. Prikhod'ko, N
    Peek Inside the Water Mixtures of Ionic Liquids at Molecular Level: Microscopic Properties Probed by EPR Spectroscopy
    Int. J. Mol. Sci. 2021, 22(21), 11900 doi:10.3390/ijms222111900, IF=5.923
     
  96. N.S. Dyrkheeva, A.S. Filimonov, O.A. Luzina, K.A. Orlova, I.A. Chernyshova, T.E. Kornienko, A.A. Malakhova, S.P. Medvedev, A.L. Zakharenko, E.S. Ilina, R.O. Anarbaev, K.N. Naumenko, K.V. Klabenkova, E.A. Burakova, D.A. Stetsenko, S.M. Zakian, N.F. Salakhutdinov, O.I. Lavrik
    New Hybrid Compounds Combining Fragments of Usnic Acid and Thioether Are Inhibitors of Human Enzymes TDP1, TDP2 and PARP1
    Int. J. Mol. Sci. 2021, 22(21), 11336 doi:10.3390/ijms222111336, IF=5.922
     
  97. V.A. Demina, S.V. Krasheninnikov, A.I. Buzin, R.A. Kamyshinsky, N.V. Sadovskaya, E.N.Goncharov, N.A. Zhukova, M.V. Khvostov, A.V. Pavlova, T.G. Tolstikova, N.G. Sedush, S.N. Chvalun
    Biodegradable poly(l-lactide)/calcium phosphate composites with improved properties for orthopedics: Effect of filler and polymer crystallinity
    Materials Science and Engineering: C, 2020, V. 112, 110813 doi:10.1016/j.msec.2020.110813, IF=5.88
     
  98. S.V. Valiulin, A.A. Onischuk, A.M. Baklanov, S.N. Dubtsov, S.V. An'kov, N.N. Shkil, E.V. Nefedova, M.E. Plokhotnichenko, T.G. Tolstikova, A.M. Dolgov, G.G. Dultseva
    Aerosol Inhalation Delivery of Cefazolin in Mice: Pharmacokinetic Measurements and Antibacterial Effect
    International Journal of Pharmaceutics, V. 607, 25 September 2021, 121013 doi:10.1016/j.ijpharm.2021.121013, IF=5.875
     
  99. D.F. Avgustinovich, M.K. Marenina, S.Ya. Zhanaeva, M.V. Tenditnik, A.V. Katokhin, K.S. Pavlov, A.Yu. Sivkov, G.B. Vishnivetskaya, M.N. Lvova, T.G. Tolstikova, V.A. Mordvinov
    Combined effects of social stress and liver fluke infection in a mouse model
    Brain, Behavior, and Immunity, 2016, V. 53, Pp 262-272 doi:10.1016/j.bbi.2016.01.012, IF=5.874
     
  100. E. Avdeeva, E. Porokhova, I. Khlusov, T. Rybalova, E. Shults, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Sukhodol, M. Belousov
    Calcium Chelidonate: Semi-Synthesis, Crystallography, and Osteoinductive Activity In Vitro and In Vivo
    Pharmaceuticals 2021, 14(6), 579 doi:10.3390/ph14060579, IF=5.863