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Lyudmila V Sidorenko

Showing results (1-10 of 9) with videos related to

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Genetics|January 3, 2024
Transcribed enhancer sequences are required for maize p1 paramutationLyudmila V Sidorenko, Vicki L Chandler, Xiujuan Wang, et al.
Scientia Pharmaceutica|January 25, 2017
The Study of Structure-Analgesic Activity Relationships in a Series of 4-Hydroxy-2,2-dioxo-1H-2λ⁶,1-benzothiazine-3-carboxylic Acid Toluidides and XylididesIgor V Ukrainets, Lidiya A Petrushova, Lyudmila V Sidorenko, et al.
Scientia Pharmaceutica|January 25, 2017
Synthesis, Structure, and Analgesic Properties of Halogen-Substituted 4-Hydroxy-2,2-dioxo-1H-2λ⁶,1-benzothiazine-3-carboxanilidesIgor V Ukrainets, Lidiya A Petrushova, Svitlana V Shishkina, et al.
Scientia Pharmaceutica|April 13, 2018
N-Aryl-7-hydroxy-5-oxo-2,3-dihydro-1H,5H-pyrido-[3,2,1-ij]quinoline-6-carboxamides. The Synthesis and Effects on Urinary OutputIgor V Ukrainets, Lyudmila V Sidorenko, Mykola Y Golik, et al.
Acta Crystallographica. Section C, Structural Chemistry|December 6, 2018
Polymorphic modifications of a 1H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide possessing strong diuretic propertiesSvitlana V Shishkina, Igor A Levandovskiy, Igor V Ukrainets, et al.
Scientia Pharmaceutica|August 31, 2018
The Study of the Structure-Diuretic Activity Relationship in a Series of New <i>N</i>-(Arylalkyl)-6-hydroxy-2-methyl-4-oxo-2,4-dihydro-1<i>H</i>-pyrrolo-[3,2,1-<i>ij</i>]quinoline-5-carboxamidesIgor V Ukrainets, Mykola Y Golik, Lyudmila V Sidorenko, et al.
Scientia Pharmaceutica|June 1, 2018
Synthesis, Crystal Structure, and Biological Activity of Ethyl 4-Methyl-2,2-dioxo-1<i>H</i>-2λ⁶,1-benzothiazine-3-carboxylate Polymorphic FormsIgor V Ukrainets, Anna A Burian, Vyacheslav N Baumer, et al.
Nature Plants|November 1, 2017
GC-rich coding sequences reduce transposon-like, small RNA-mediated transgene silencingLyudmila V Sidorenko, Tzuu-Fen Lee, Aaron Woosley, et al.
Nature Biotechnology|July 12, 2016
Canola engineered with a microalgal polyketide synthase-like system produces oil enriched in docosahexaenoic acidTerence A Walsh, Scott A Bevan, Daniel J Gachotte, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Genetics|January 3, 2024
Transcribed enhancer sequences are required for maize p1 paramutationLyudmila V Sidorenko, Vicki L Chandler, Xiujuan Wang, et al.
Scientia Pharmaceutica|January 25, 2017
The Study of Structure-Analgesic Activity Relationships in a Series of 4-Hydroxy-2,2-dioxo-1H-2λ⁶,1-benzothiazine-3-carboxylic Acid Toluidides and XylididesIgor V Ukrainets, Lidiya A Petrushova, Lyudmila V Sidorenko, et al.
Scientia Pharmaceutica|January 25, 2017
Synthesis, Structure, and Analgesic Properties of Halogen-Substituted 4-Hydroxy-2,2-dioxo-1H-2λ⁶,1-benzothiazine-3-carboxanilidesIgor V Ukrainets, Lidiya A Petrushova, Svitlana V Shishkina, et al.
Scientia Pharmaceutica|April 13, 2018
N-Aryl-7-hydroxy-5-oxo-2,3-dihydro-1H,5H-pyrido-[3,2,1-ij]quinoline-6-carboxamides. The Synthesis and Effects on Urinary OutputIgor V Ukrainets, Lyudmila V Sidorenko, Mykola Y Golik, et al.
Acta Crystallographica. Section C, Structural Chemistry|December 6, 2018
Polymorphic modifications of a 1H-pyrrolo[3,2,1-ij]quinoline-5-carboxamide possessing strong diuretic propertiesSvitlana V Shishkina, Igor A Levandovskiy, Igor V Ukrainets, et al.
Scientia Pharmaceutica|August 31, 2018
The Study of the Structure-Diuretic Activity Relationship in a Series of New <i>N</i>-(Arylalkyl)-6-hydroxy-2-methyl-4-oxo-2,4-dihydro-1<i>H</i>-pyrrolo-[3,2,1-<i>ij</i>]quinoline-5-carboxamidesIgor V Ukrainets, Mykola Y Golik, Lyudmila V Sidorenko, et al.
Scientia Pharmaceutica|June 1, 2018
Synthesis, Crystal Structure, and Biological Activity of Ethyl 4-Methyl-2,2-dioxo-1<i>H</i>-2λ⁶,1-benzothiazine-3-carboxylate Polymorphic FormsIgor V Ukrainets, Anna A Burian, Vyacheslav N Baumer, et al.
Nature Plants|November 1, 2017
GC-rich coding sequences reduce transposon-like, small RNA-mediated transgene silencingLyudmila V Sidorenko, Tzuu-Fen Lee, Aaron Woosley, et al.
Nature Biotechnology|July 12, 2016
Canola engineered with a microalgal polyketide synthase-like system produces oil enriched in docosahexaenoic acidTerence A Walsh, Scott A Bevan, Daniel J Gachotte, et al.
Pageof 1