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Patologicheskaia Fiziologiia I Eksperimental'Naia Terapiia|January 18, 2006
[Influence of cell therapy and alimentary correction on the condition of microcirculatory system in experimental dyslipidemia]L P Kobozeva, A B Michunskaia, O S Kulikova, et al.Zhurnal Nevrologii I Psikhiatrii Imeni S.S. Korsakova|February 28, 2020
[Daytime sleepiness and cognitive disorders in elderly patients]G V Kovrov, A V Medvedeva, A V Aronson, et al.Pharmaceutics|June 28, 2023
Polymorphism of Carbamazepine Pharmaceutical Cocrystal: Structural Analysis and Solubility PerformanceArtem O Surov, Ksenia V Drozd, Anna G Ramazanova, et al.Stem Cell Research|June 10, 2021
Generation of an induced pluripotent stem cell line HPCASRi002-A from a patient with neonatal severe primary hyperparathyroidism caused by a compound heterozygous mutation in the CASR geneAlexandra V Panova, Kristina S Kulikova, Natalia V Klementieva, et al.Physical Chemistry Chemical Physics : PCCP|April 17, 2024
Effect of photoconversion conditions on the spectral and cytotoxic properties of photoconvertible fluorescent polymer markersPolina A Demina, Oleg V Grishin, Sergey N Malakhov, et al.Eksperimental'Naia I Klinicheskaia Farmakologiia|January 1, 1996
[The biochemical and rheological properties of the blood during the performance of angiography using Ultravist]Iu A Poliaev, V V Lazarev, I S Kulikova, et al.Antibiotiki I Khimioterapiia = Antibiotics and Chemoterapy [Sic]|May 25, 2013
[Experimental study on chemotherapy of acute glanders]V I Iliukhin, K A Rotov, T V Senina, et al.Problemy Endokrinologii|June 2, 2026
[Complications of Pseudohypoparathyroidism and Congenital Forms of Hypoparathyroidism in Children]A A Dzhamaludinova, L S Sozaeva, N V Makazan, et al.Inorganic Chemistry|December 13, 2023
Formation of Neptunium(V) Carbonates: Examining the Forceful Influence of Alkali and Alkaline Earth CationsAnastasiia S Kuzenkova, Tatiana V Plakhova, Iurii M Nevolin, et al.Human Cell|October 24, 2024
Generation of CRISPR/Cas9 modified human iPSC line with correction of heterozygous mutation in exon 6 of the CaSR geneP I Semenova, A V Panova, J V Sopova, et al.Pageof 5