Публикации за 2017 год
4 декабря 2018 г.
Kenyon, J.J., Shashkov, A.S., Senchenkova, S.N., Shneider, M.M., Liu, B., Popova, A.V., Arbatsky, N.P., Miroshnikov, K.A., Wang, L., Knirel, Y.A., Hall, R.M. Acinetobacter baumannii K11 and K83 capsular polysaccharides have the same 6-deoxy-L-talose-containing pentasaccharide K units but different linkages between the K units (2017) International Journal of Biological Macromolecules, 103, pp. 648-655. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019633409&doi=10.1016%2fj.ijbiomac.2017.05.082&partnerID=40&md5=42007f35366cf8722e542e562b591e49 DOI: 10.1016/j.ijbiomac.2017.05.082
Sigida, E.N., Fedonenko, Y.P., Shashkov, A.S., Zdorovenko, E.L., Ignatov, V.V., Knirel, Y.A. Structural studies of the O-specific polysaccharide from detergent degrading bacteria Pseudomonas putida TSh-18 (2017) Carbohydrate Research, 448, pp. 1-5. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019860162&doi=10.1016%2fj.carres.2017.05.013&partnerID=40&md5=b6f2e66d9ad5b8903c18659e525dcf43 DOI: 10.1016/j.carres.2017.05.013
Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Borodina, E.Y., Stonik, V.A., Nifantiev, N.E., Usov, A.I. A highly regular fucosylated chondroitin sulfate from the sea cucumber Massinium magnum: Structure and effects on coagulation (2017) Carbohydrate Polymers, 167, pp. 20-26. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015403404&doi=10.1016%2fj.carbpol.2017.02.101&partnerID=40&md5=1b7627e557728a1b80422f5122fb5f6d DOI: 10.1016/j.carbpol.2017.02.101
Zheng, H., Shashkov, A.S., Xiong, Y., Naumenko, O.I., Wang, H., Senchenkova, S.N., Wang, J., Knirel, Y.A. Structure and gene cluster of the O-antigen of Escherichia albertii O1 resembling the O-antigen of Pseudomonas aeruginosa O5 (2017) Carbohydrate Research, 446-447, pp. 28-31. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018783685&doi=10.1016%2fj.carres.2017.04.024&partnerID=40&md5=35b48f67819842ff56e1ef767c513c4f DOI: 10.1016/j.carres.2017.04.024
Baranov, V.V., Antonova, M.M., Karnoukhova, V.A., Kravchenko, A.N. Unexpected reductive transformation of 1-substituted 5-hydroxy-4,5-diphenyl-1H-imidazol-2(5H)-ones and their cyclic analogs by the reaction with thiourea and hydrochloric acid (2017) Tetrahedron Letters, 58 (23), pp. 2203-2205. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018430228&doi=10.1016%2fj.tetlet.2017.04.061&partnerID=40&md5=e55f9023e508c89ff04a702cfc0cc3a7 DOI: 10.1016/j.tetlet.2017.04.061
Sizova, O.V., Kondakova, A.N., Shashkov, A.S., Knirel, Y.A., Shaikhutdinova, R.Z., Ivanov, S.A., Platonov, M.E., Hurst, M.R.H., Dentovskaya, S.V. Structure and gene cluster of a tyvelose-containing O-polysaccharide of an entomopathogenic bacterium Yersinia entomophaga MH96T related to Yersinia pseudotuberculosis (2017) Carbohydrate Research, 445, pp. 93-97. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018330470&doi=10.1016%2fj.carres.2017.04.013&partnerID=40&md5=4b8b2f897efc606b33676948bd1a853c DOI: 10.1016/j.carres.2017.04.013
Mendkovich, A.S., Syroeshkin, M.A., Nasybullina, D.V., Mikhailov, M.N., Gultyai, V.P., Rusakov, A.I. Electroreduction mechanism of N-phenylhydroxylamines in aprotic solvents: N-(2-nitrophenyl)- and N-(3-nitrophenyl)hydroxylamines (2017) Electrochimica Acta, 238, pp. 9-20. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017470338&doi=10.1016%2fj.electacta.2017.03.174&partnerID=40&md5=f0e199fd849e61540987d00b53324c3a DOI: 10.1016/j.electacta.2017.03.174
Chizhkov, V.P., Boitsov, V.N. Method for performing a single act of the reversible separation of ideal solution components (2017) Russian Journal of Physical Chemistry A, 91 (6), pp. 1127-1131. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019660585&doi=10.1134%2fS0036024417060073&partnerID=40&md5=7c1691f7bf2c8ce18e7f7750446d6ff9 DOI: 10.1134/S0036024417060073
Zdorovenko, E.L., Kadykova, A.A., Shashkov, A.S., Varbanets, L.D., Bulyhina, T.V., Knirel, Y.A. Lipopolysaccharide of Pantoea agglomerans 7969: Chemical identification, function and biological activity (2017) Carbohydrate Polymers, 165, pp. 351-358. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85013847641&doi=10.1016%2fj.carbpol.2017.02.053&partnerID=40&md5=093db09d3abf1f4ba763b6bf272bdc38 DOI: 10.1016/j.carbpol.2017.02.053
Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Shashkov, A.S., Nifantiev, N.E., Usov, A.I. The structure of a fucosylated chondroitin sulfate from the sea cucumber Cucumaria frondosa (2017) Carbohydrate Polymers, 165, pp. 7-12. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85012307846&doi=10.1016%2fj.carbpol.2017.02.003&partnerID=40&md5=af5315b1338389676126d6a3e4b051fd DOI: 10.1016/j.carbpol.2017.02.003
Shvetsova, S.V., Shabalin, K.A., Bobrov, K.S., Ivanen, D.R., Ustyuzhanina, N.E., Krylov, V.B., Nifantiev, N.E., Naryzhny, S.N., Zgoda, V.G., Eneyskaya, E.V., Kulminskaya, A.A. Corrigendum to “Characterization of a new α-L-fucosidase isolated from Fusarium proliferatum LE1 that is regioselective to α-(1 → 4)-L-fucosidic linkage in the hydrolysis of α-L-fucobiosides” [Biochimie (2017) 132C (54–65)] (S0300908416303029) (10.1016/j.biochi.2016.10.014) (2017) Biochimie, 137, p. 198. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018899144&doi=10.1016%2fj.biochi.2017.04.007&partnerID=40&md5=c6e162583a61b1d5dcf12b5dd03029b4 DOI: 10.1016/j.biochi.2017.04.007
Egorova, K.S., Gordeev, E.G., Ananikov, V.P. Biological Activity of Ionic Liquids and Their Application in Pharmaceutics and Medicine (2017) Chemical Reviews, 117 (10), pp. 7132-7189. Cited 3 times. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017398702&doi=10.1021%2facs.chemrev.6b00562&partnerID=40&md5=a22814c48c489f59f30f601ab8d10558 DOI: 10.1021/acs.chemrev.6b00562
Volkova, Y., Gevorgyan, V. Synthesis of functionalyzed imidazo[1,2-a]pyridines via domino A3-coupling/cycloisomerization approach (2017) Chemistry of Heterocyclic Compounds, pp. 1-4. Article in Press. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019172895&doi=10.1007%2fs10593-017-2066-0&partnerID=40&md5=bd18b7caa30393d0a37a683b7f5673af DOI: 10.1007/s10593-017-2066-0
Ustyuzhanina, N.E., Bilan, M.I., Dmitrenok, A.S., Nifantiev, N.E., Usov, A.I. Two fucosylated chondroitin sulfates from the sea cucumber Eupentacta fraudatrix (2017) Carbohydrate Polymers, 164, pp. 8-12. Cited 1 time. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010818030&doi=10.1016%2fj.carbpol.2017.01.034&partnerID=40&md5=f912e930652f0aa6777ceff0928d64dc DOI: 10.1016/j.carbpol.2017.01.034
Ivanov, S.M., Mironovich, L.M., Rodinovskaya, L.A., Shestopalov, A.M. The first stable examples of compounds containing both diazonium and acyl azide, and synthesis of a new pyrazino[2′,3′:3,4]pyrazolo[5,1-c][1,2,4]triazin-4(6H)-one heterocyclic system (2017) Tetrahedron Letters, 58 (19), pp. 1851-1853. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017101688&doi=10.1016%2fj.tetlet.2017.03.083&partnerID=40&md5=11aca579be98eb485b23a17ffceb1389 DOI: 10.1016/j.tetlet.2017.03.083
Fershtat, L.L., Makhova, N.N. Molecular Hybridization Tools in the Development of Furoxan-Based NO-Donor Prodrugs (2017) ChemMedChem, 12 (9), pp. 622-638. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017469077&doi=10.1002%2fcmdc.201700113&partnerID=40&md5=c9b61c6704d64f4c78e13a9a6e0c007b DOI: 10.1002/cmdc.201700113
Medvedev, M.G., Bushmarinov, I.S., Sun, J., Perdew, J.P., Lyssenko, K.A. Response to comment on "Density functional theory is straying from the path toward the exact functional" (2017) Science, 356 (6337), p. 496c. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018422764&doi=10.1126%2fscience.aam9550&partnerID=40&md5=a8fb526cbab47697e90fd2cdf719f16f DOI: 10.1126/science.aam9550
Gerasimchuk, V.V., Kucherenko, A.S., Fakhrutdinov, A.N., Medvedev, M.G., Nelyubina, Y.V., Zlotin, S.G. Towards Sustainable Amino Acid Derived Organocatalysts for Asymmetric syn-Aldol Reactions (2017) European Journal of Organic Chemistry, 2017 (17), pp. 2540-2544. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019039251&doi=10.1002%2fejoc.201700166&partnerID=40&md5=c7d45889b73e9037fd3964a5042ed782 DOI: 10.1002/ejoc.201700166
Badikova, A.D., Kudasheva, F.K., Tsadkin, M.A., Mortikov, E.S., Yalalova, R.A. Complex Technological Solution for Recycling of Spent Sulfuric Acid from Alkylation of Isobutane by Olefins (2017) Chemistry and Technology of Fuels and Oils, pp. 1-9. Article in Press. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018364328&doi=10.1007%2fs10553-017-0778-6&partnerID=40&md5=09fa20aae55eac96ee88e83424dc5650 DOI: 10.1007/s10553-017-0778-6
Zaitsev, K.V., Kuchuk, E.A., Churakov, A.V., Navasardyan, M.A., Egorov, M.P., Zaitseva, G.S., Karlov, S.S. Synthesis and structural characterization of low-valent group 14 metal complexes based on aminobisphenol ligands (2017) Inorganica Chimica Acta, 461, pp. 213-220. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016720615&doi=10.1016%2fj.ica.2017.02.024&partnerID=40&md5=f623f77ba6ffcc893a091ebb71a3948a DOI: 10.1016/j.ica.2017.02.024
Medved'ko, A.V., Ivanov, V.K., Kiskin, M.A., Sadovnikov, A.A., Apostolova, E.S., Grinberg, V.A., Emets, V.V., Chizhov, A.O., Nikitin, O.M., Magdesieva, T.V., Kozyukhin, S.A. The design and synthesis of thiophene-based ruthenium(II) complexes as promising sensitizers for dye-sensitized solar cells (2017) Dyes and Pigments, 140, pp. 169-178. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010382995&doi=10.1016%2fj.dyepig.2017.01.030&partnerID=40&md5=bf5dec74b423b61c4afc7c1c11229d38 DOI: 10.1016/j.dyepig.2017.01.030
Asfandiarov, N.L., Pshenichnyuk, S.A., Vorob’ev, A.S., Nafikova, E.P., Mavrodiev, V.K., Furlei, I.I., Dokichev, V.A., Platonov, D.N., Belyy, A.Y. Estimating electron affinity from the lifetime of negative molecular ions: Cycloheptatriene derivatives (2017) Russian Journal of Physical Chemistry A, 91 (5), pp. 915-920. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85018485011&doi=10.1134%2fS0036024417050041&partnerID=40&md5=aa280cc706732cdc6114075fa424518a DOI: 10.1134/S0036024417050041
dos Passos Gomes, G., Yaremenko, I.A., Radulov, P.S., Novikov, R.A., Chernyshev, V.V., Korlyukov, A.A., Nikishin, G.I., Alabugin, I.V., Terent'ev, A.O. Stereoelectronic Control in the Ozone-Free Synthesis of Ozonides (2017) Angewandte Chemie — International Edition, 56 (18), pp. 4955-4959. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017375017&doi=10.1002%2fanie.201610699&partnerID=40&md5=efb363f1ae5d35e77f4570f109091504 DOI: 10.1002/anie.201610699
Gazieva, G.A., Karpova, T.B., Nechaeva, T.V., Nelyubina, Y.V., Zanin, I.E., Kravchenko, A.N. Synthesis of N-{ 5-Oxo-2-thioxo(2,5-dithioxo)hexahydroimidazo-[4,5-d]imidazol-1(2H)-yl}formamides (2017) Synlett, 28 (7), art. no. st-2016-d0667-l, pp. 858-862. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009357374&doi=10.1055%2fs-0036-1588388&partnerID=40&md5=c152e3aa9f51400fec419b37874f14cf DOI: 10.1055/s-0036-1588388
Samoilova, N.A., Krayukhina, M.A., Babushkina, T.A., Yamskov, I.A., Likhosherstov, L.M., Piskarev, V.E. Silver- and gold-labeled colloidal and crosslinked glycopolymers based on glycyl glycosynthons and maleic anhydride copolymers for lectin binding (2017) Journal of Applied Polymer Science, 134 (16), art. no. 44718, . Cited 1 time. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009816064&doi=10.1002%2fapp.44718&partnerID=40&md5=df060bc659821ae3c4988a3f87dc31ff DOI: 10.1002/app.44718
Chen, C., Hou, X., Utkina, N., Danilov, L., Zhou, D., Torgov, V., Veselovsky, V., Liu, B., Feng, L. Identification and biochemical characterization of a novel α-1,3-mannosyltransferase WfcD from Escherichia coli O141 (2017) Carbohydrate Research, 443-444, pp. 78-86. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017256670&doi=10.1016%2fj.carres.2017.04.003&partnerID=40&md5=b2dbfad233df9eb1ba12a125838da8e0 DOI: 10.1016/j.carres.2017.04.003
Abronina, P.I., Zinin, A.I., Malysheva, N.N., Stepanova, E.V., Chizhov, A.O., Torgov, V.I., Kononov, L.O. A Novel Glycosyl Donor with a Triisopropylsilyl Nonparticipating Group in Benzyl-Free Stereoselective 1,2-cis-Galactosylation (2017) Synlett, . Article in Press. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019158185&doi=10.1055%2fs-0036-1589028&partnerID=40&md5=62af308c20232abf2e359af881fb4d0c DOI: 10.1055/s-0036-1589028
Tukhvatshin, R.S., Kucherenko, A.S., Nelyubina, Y.V., Zlotin, S.G. Tertiary Amine-Derived Ionic Liquid-Supported Squaramide as a Recyclable Organocatalyst for Noncovalent "on Water" Catalysis (2017) ACS Catalysis, 7 (4), pp. 2981-2989. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85019688200&doi=10.1021%2facscatal.7b00562&partnerID=40&md5=9517a922b1279a648db5b18ffb0b2e31 DOI: 10.1021/acscatal.7b00562
Zhmurov, P.A., Khoroshutina, Y.A., Novikov, R.A., Golovanov, I.S., Sukhorukov, A.Y., Ioffe, S.L. Divergent Reactivity of In Situ Generated Metal Azides: Reaction with N,N-Bis(oxy)enamines as a Case Study (2017) Chemistry — A European Journal, 23 (19), pp. 4570-4578. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85012050440&doi=10.1002%2fchem.201605390&partnerID=40&md5=4adb829c9099994d9241424fa46e4d6a DOI: 10.1002/chem.201605390
Zhmurov, P.A., Khoroshutina, Y.A., Novikov, R.A., Golovanov, I.S., Sukhorukov, A.Y., Ioffe, S.L. Divergent Reactivity of In Situ Generated Metal Azides: Reaction with N,N-Bis(oxy)enamines as a Case Study (2017) Chemistry — A European Journal, 23 (19), p. 4466. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017173007&doi=10.1002%2fchem.201700193&partnerID=40&md5=1214975bfe065f90c4848e2694eb0767 DOI: 10.1002/chem.201700193
Kasimova, A.A., Shneider, M.M., Arbatsky, N.P., Popova, A.V., Shashkov, A.S., Miroshnikov, K.A., Balaji, V., Biswas, I., Knirel, Y.A. Structure and gene cluster of the K93 capsular polysaccharide of Acinetobacter baumannii B11911 containing 5-N-Acetyl-7-N-[(R)-3-hydroxybutanoyl]pseudaminic acid (2017) Biochemistry (Moscow), 82 (4), pp. 483-489. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017513953&doi=10.1134%2fS0006297917040101&partnerID=40&md5=4c86aed9e4b4cf341bda7eb7cd8d0108 DOI: 10.1134/S0006297917040101
Baranov, V.V., Antonova, M.M., Nelyubina, Y.V., Kolotyrkina, N.G., Kravchenko, A.N. New Method for the Synthesis of 1-Substituted (3a,6a)-Diarylglycolurils (2017) Synlett, 28 (6), art. no. st-2016-d0733-l, pp. 669-672. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009380828&doi=10.1055%2fs-0036-1588932&partnerID=40&md5=31e2d80b70005bd7bc1510bd2eb14e7f DOI: 10.1055/s-0036-1588932
Elinson, M.N., Vereshchagin, A.N., Korshunov, A.D., Ryzhkov, F.V., Egorov, M.P. Stereoselective cascade assembling of benzylidenecyanoacetates and 1,3-dimethylbarbituric acid into (1R∗,2S∗)-1-cyano-5,7-dialkyl-4,6,8-trioxo-2-aryl-5,7-diazaspiro[2.5]octane-1-carboxylates (2017) Heterocyclic Communications, 23 (2), pp. 85-90. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017288324&doi=10.1515%2fhc-2016-0190&partnerID=40&md5=1f19884b9d908d871cd055097dc00659 DOI: 10.1515/hc-2016-0190
Varizhuk, A., Ischenko, D., Tsvetkov, V., Novikov, R., Kulemin, N., Kaluzhny, D., Vlasenok, M., Naumov, V., Smirnov, I., Pozmogova, G. The expanding repertoire of G4 DNA structures (2017) Biochimie, 135, pp. 54-62. Cited 2 times. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85010662216&doi=10.1016%2fj.biochi.2017.01.003&partnerID=40&md5=42a790ff3b57b18936c8be24bcdda13d DOI: 10.1016/j.biochi.2017.01.003
Borisova, I.A., Zubarev, A.A., Rodinovskaya, L.A., Shestopalov, A.M. Synthesis and physicochemical properties of merocyanine dyes based on dihydropyridine and fragments of cyanoacetic acid derivatives (2017) Arkivoc, 2017 (3), pp. 73-86. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017303778&doi=10.3998%2fark.5550190.0018.300&partnerID=40&md5=2876966cc24f25a3fe058ef6721b49cf DOI: 10.3998/ark.5550190.0018.300
Shleeva, M.O., Trutneva, K.A., Demina, G.R., Zinin, A.I., Sorokoumova, G.M., Laptinskaya, P.K., Shumkova, E.S., Kaprelyants, A.S. Free trehalose accumulation in dormant Mycobacterium smegmatis cells and its breakdown in early resuscitation phase (2017) Frontiers in Microbiology, 8 (MAR), art. no. 524, . https://www.scopus.com/inward/record.uri?eid=2-s2.0-85016608640&doi=10.3389%2ffmicb.2017.00524&partnerID=40&md5=118a83db416fb37ea97f2f794b2d5c8e DOI: 10.3389/fmicb.2017.00524
Lyalin, B.V., Sigacheva, V.L., Kokorekin, V.A., Petrosyan, V.A. Oxidative conversion of N-substituted 3-Aminopyrazoles to azopyrazoles using electrogenerated NaOCl as the mediator (2017) Arkivoc, 2017 (3), pp. 55-62. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017322315&doi=10.3998%2fark.5550190.p010.030&partnerID=40&md5=6b841981bd2a7a9750a9be4fd9350b18 DOI: 10.3998/ark.5550190.p010.030
Baranov, V.V., Antonova, M.M., Karnoukhova, V.A., Kravchenko, A.N. Unusual formation of imidazooxazolone in the reaction of 1-[(2-Acetylamino)ethyl]imidazolone with KSCN in the presence of AcOH (2017) Arkivoc, 2017 (3), pp. 63-72. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017295243&doi=10.3998%2fark.5550190.p010.048&partnerID=40&md5=341418f56d5251aede8b1bc18782fbe8 DOI: 10.3998/ark.5550190.p010.048
Medvedev, M.G., Zeifman, A.A., Novikov, F.N., Bushmarinov, I.S., Stroganov, O.V., Titov, I.Yu., Chilov, G.G., Svitanko, I.V. Quantifying Possible Routes for SpnF-Catalyzed Formal Diels-Alder Cycloaddition (2017) Journal of the American Chemical Society, 139 (11), pp. 3942-3945. Cited 1 time. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015881878&doi=10.1021%2fjacs.6b13243&partnerID=40&md5=e30250666997710decc00b5960e97653 DOI: 10.1021/jacs.6b13243
Fedorov, O.V., Struchkova, M.I., Dilman, A.D. Synthesis of gem-Difluorinated Hydroxypyrrolidines (2017) Journal of Organic Chemistry, 82 (6), pp. 3270-3275. https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015677962&doi=10.1021%2facs.joc.6b03033&partnerID=40&md5=3cde7fc940df5fcd847682d649ac790f DOI: 10.1021/acs.joc.6b03033
Baranov, M.S., Kaskova, Z.M., Gritсenko, R., Postikova, S.G., Ivashkin, P.E., Kislukhin, A.A., Moskvin, D.I., Mineev, K.S., Arseniev, A.S., Labas, Y.A., Yampolsky, I.V. Synthesis of Panal Terpenoid Core (2017) Synlett, 28 (5), art. no. st-2016-b0575-l, pp. 583-588. https://www.scopus.com/inward/record.uri?eid=2-s2.0-84996939000&doi=10.1055%2fs-0036-1588104&partnerID=40&md5=404b9a305e60c487ae6a81c77fe38f54 DOI: 10.1055/s-0036-1588104
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