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A Routine Coronary Angiography before Carotid Endarterectomy as an Example of Interdisciplinary Work: The Immediate Results of the Surgery.
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- Journal of Clinical Medicine, 2024, v. 13, n. 18, p. 5495, doi. 10.3390/jcm13185495
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- Article
Pelvic Electric Potential as a Marker of Autonomic Dysfunctions and Risk Factor of Neurogenic Arrhythmias in Humans.
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- Bulletin of Experimental Biology & Medicine, 2019, v. 166, n. 6, p. 404, doi. 10.1007/s10517-019-04360-z
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- Article
Pelvic Electric Potential as a Marker of Autonomic Dysfunctions and Risk Factor of Neurogenic Arrhythmias in Humans.
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- Bulletin of Experimental Biology & Medicine, 2019, v. 166, n. 3, p. 404, doi. 10.1007/s10517-019-04360-z
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- Article
Synthesis of Substituted 2-Oxo-2,3-dihydro-1H-imidazo-[1,2-a]indole-6,7-dicarbonitriles.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 3, p. 287, doi. 10.1134/S1070428019030011
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- Article
Polypeptide Modulators of TRPV1 Produce Analgesia without Hyperthermia.
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- Marine Drugs, 2013, v. 11, n. 12, p. 5100, doi. 10.3390/md11125100
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A Condensation of Biginelli Products with 1,3- Benzenediols: a Facile Access to Diastereomerically Pure Hexahydro-5H-chromeno[4,3-d]pyrimidin-5-ones.
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- ChemistrySelect, 2019, v. 4, n. 33, p. 9550, doi. 10.1002/slct.201901997
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- Article
Taste Cells of the Type III Employ CASR to Maintain Steady Serotonin Exocytosis at Variable Ca 2+ in the Extracellular Medium.
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- Cells (2073-4409), 2022, v. 11, n. 8, p. 1369, doi. 10.3390/cells11081369
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- Article
Synthesis and physicochemical evaluation of a new carrier based on an interpolyelectrolyte complex formed by Eudragit® EPO and Carbomer 940.
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- Pharmaceutical Chemistry Journal, 2010, v. 44, n. 5, p. 271, doi. 10.1007/s11094-010-0447-0
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- Article
Diffusion Transport Properties of Polymeric Complex Matrix Systems Based on Eudragit E100 and L100 Copolymers.
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- Pharmaceutical Chemistry Journal, 2005, v. 39, n. 2, p. 89, doi. 10.1007/s11094-005-0090-3
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- Article
Synthesis and characterization of an interpolyelectrolyte complex based on Eudragit E100 and L100 copolymers.
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- Pharmaceutical Chemistry Journal, 2004, v. 38, n. 11, p. 625, doi. 10.1007/s11094-005-0044-9
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- Article
Novel nucleophilic rearrangement of 1-substituted isoquinolines using an alcoholic sodium hydroxide solution.
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- Chemistry of Heterocyclic Compounds, 2011, v. 47, n. 1, p. 74, doi. 10.1007/s10593-011-0722-3
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- Article
Synthesis and Properties of Electroconductive Polymeric Composite Material Based on Polypyrrole.
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- ISRN Polymer Science, 2012, p. 1, doi. 10.5402/2012/320316
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- Article
Contribution of TRPC3-mediated Ca<sup>2+</sup> entry to taste transduction.
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- Pflügers Archiv: European Journal of Physiology, 2023, v. 475, n. 8, p. 1009, doi. 10.1007/s00424-023-02834-8
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- Article
Electrodeposition of thin films of polypyrrole-polyelectrolyte complexes and their ammonia-sensing properties.
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- Journal of Solid State Electrochemistry, 2020, v. 24, n. 11/12, p. 3091, doi. 10.1007/s10008-020-04766-0
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- Article
Ink-Jet Printing of Polyaniline Layers for Perovskite Solar Cells.
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- Technical Physics Letters, 2019, v. 45, n. 9, p. 858, doi. 10.1134/S1063785019090050
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- Article
Unusual recyclization of 2-methyl-1-phenyliso- quinolinium iodide to 1-phenyl-1,4-dihydro- 3h-isochroman-3-one.
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- Chemistry of Heterocyclic Compounds, 2010, v. 46, n. 3, p. 361, doi. 10.1007/s10593-010-0516-z
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- Article
Unexpected tandem condensation of 2-furonitriles with diethylenetriamine.
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- Chemistry of Heterocyclic Compounds, 2010, v. 46, n. 3, p. 351, doi. 10.1007/s10593-010-0512-3
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- Article
Formylation of pyrrolo-[1,2- a]pyrazines.
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- Chemistry of Heterocyclic Compounds, 2008, v. 44, n. 1, p. 73, doi. 10.1007/s10593-008-0010-z
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Acylation of 3,4-Dihydropyrrolo[1,2-a]pyrazines.
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- Chemistry of Heterocyclic Compounds, 2004, v. 40, n. 3, p. 351, doi. 10.1023/B:COHC.0000028632.61226.cd
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Dipyrrolo[1,2-a;2':,1'-c]pyrazines. 7. Electrophilic Substitution of Dipyrrolo[1,2-a;2',1'-c]pyrazines and 5,6-Dihydrodipyrrolo[1,2-a;2',1'-c]pyrazines via Formylation of Dipyrrolo[1,2-a;2':,1'-c]pyrazines.
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- Chemistry of Heterocyclic Compounds, 2003, v. 39, n. 11, p. 1487, doi. 10.1023/B:COHC.0000014413.07428.a1
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DIPYRROLO[1,2-a;2',1'-c]PYRAZINES. 6*. ELECTROPHILIC SUBSTITUTION IN A SERIES OF DIPYRROLO[1,2-a;2',1'-c]PYRAZINE AND 5,6-DIHYDRODIPYRROLO[1,2-a;2',1'-c]PYRAZINE DERIVATIVES. PHOSPHORYLATION OF DIPYRROLO[1,2-a;2',1'-c]PYRAZINES.
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- Chemistry of Heterocyclic Compounds, 2003, v. 39, n. 7, p. 943, doi. 10.1023/A:1026158724018
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- Article
Agonist-Induced Ca 2+ Signaling in HEK-293-Derived Cells Expressing a Single IP 3 Receptor Isoform.
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- Cells (2073-4409), 2024, v. 13, n. 7, p. 562, doi. 10.3390/cells13070562
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- Article
Terahertz Time-Domain Spectroscopy of Blood Serum for Differentiation of Glioblastoma and Traumatic Brain Injury.
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- Applied Sciences (2076-3417), 2024, v. 14, n. 7, p. 2872, doi. 10.3390/app14072872
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- Article
Optimization of pyrrolo[3,4‐f]indole‐5,7‐dione and indole‐5,6‐dicarbonitrile derivatives as inhibitors of monoamine oxidase.
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- Drug Development Research, 2019, v. 80, n. 7, p. 970, doi. 10.1002/ddr.21576
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An investigation of the monoamine oxidase inhibition properties of pyrrolo[3,4‐<italic>f</italic>]indole‐5,7‐dione and indole‐5,6‐dicarbonitrile derivatives.
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- Drug Development Research, 2018, v. 79, n. 2, p. 81, doi. 10.1002/ddr.21425
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Synthesis of Functional Derivatives of 3-Acyl-1-hydroxyindole-5,6-dicarboxylic Acids.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 3, p. 626, doi. 10.1134/S1070363219030447
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- Article