Zobrazeno 1 - 10
of 22
pro vyhledávání: '"V P, Shirinskiĭ"'
Publikováno v:
Терапевтический архив, Vol 80, Iss 8, Pp 63-65 (2008)
Aim. To study activity of rheumatoid arthritis (RA) and cholesterol content in subfractions of blood serum lipoproteins in the course of simvastatin treatment. Material and methods. The pilot study enrolled 16 patients with active rheumatoid arthriti
Externí odkaz:
https://doaj.org/article/b2ccefef48e9437b94f258a7bc31a6d3
Autor:
A Iu, Khapchaev, M V, Samsonov, O A, Kazakova, E L, Vilitkevich, M V, Sidorova, A A, Az'muko, A S, Molokoedov, Zh D, Bespalova, V P, Shirinskiĭ
Publikováno v:
Biofizika. 57(5)
Novel peptides originating from the peptide inhibitor of myosin light chain kinase, L-PIK (Arg-Lys-Lys-Tyr-Lys-Tyr-Arg-Arg-Lys), have been studied for ability to attenuate the thrombin-induced hyperpermeability of endothelial cell monolayer in cultur
Autor:
E V, Shreĭder, E V, Bazaeva, O V, Stukalova, M A, Saidova, A V, Chadin, V P, Shirinskiĭ, A N, Meshkov, A N, Samko, E P, Mazygula, S A, Boĭtsov
Publikováno v:
Kardiologiia. 52(1)
Autor:
A V, Marchenko, E O, Stepanova, A V, Sekridova, M V, Sidorova, V N, Bushuev, Zh D, Bespalova, V P, Shirinskiĭ
Publikováno v:
Biofizika. 55(6)
The ability of novel cell-permeating peptide molecules derived from the peptide inhibitor of the myosin light chain kinase (MLCK) L-PIK (Arg-Lys-Lys-Tyr-Lys-Tyr-Arg-Arg-Lys) to inhibit this kinase in vitro and attenuate the thrombin-induced hyperperm
Autor:
O V, Stepanova, A V, Chadin, A G, Masiutin, T G, Kulikova, Ia V, Gurin, I A, Sergeeva, V P, Shirinskiĭ
Publikováno v:
Biofizika. 55(5)
It has been shown that Y-27632, an inhibitor of Rho-associated kinase, delays sarcomere assembly in rat neonatal cardiomyocytes pretreated with angiotensin II. Y-27632 affects the beat rate of cardiomyocytes; however, this effect is only observed at
Autor:
A V, Sekridova, M V, Sidorova, A A, Az'muko, A S, Molokoedov, V N, Bushuev, A V, Marchenko, O V, Shcherbakova, V P, Shirinskiĭ, Zh D, Bespalova
Publikováno v:
Bioorganicheskaia khimiia. 36(4)
Myosin light chain kinase (MLCK) is the key regulator of various forms of cell motility including endothelial and epithelial permeability in particular. One of the potential MLCK inhibitors to be used in humans is a membrane permeable peptide H-RKKYK
Autor:
A V, Vorotnikov, O V, Shchrbakova, T V, Kudriashova, O S, Tarasova, V P, Shirinskiĭ, G, Pfitzer, V A, Tkachuk
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 95(10)
Rho-kinase is a key enzyme of the receptor-dependent signal cascades and is regarded today as the most prospective target for pharmacological therapy of smooth muscle contractility disorders.
Autor:
A V, Marchenko, M V, Sidorova, A V, Sekridova, V N, Bushuev, V L, Lakomkin, Ts R, Orlova, O V, Stepanova, V I, Kapel'ko, D M, Watterson, L J, Van Eldik, Zh D, Bespalova, V P, Shirinskiĭ
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 95(5)
Nonapeptide H-Arg-Lys-Lys-Tyr-Lys-Tyr-Arg-Arg-Lys-NH2 corresponding to a modified sequence of autoinhibitory region of myosin light chain kinase (MLCK) was synthesized from L-amino acids and from D-amino acids. Using nuclear magnetic resonance spectr
Publikováno v:
Molekuliarnaia biologiia. 42(5)
This review analyzes the current state in investigations of molecular, genetic and cellular mechanisms of cardiac development as well as perspectives to use this knowledge for treatment of cardiac failure by means of replenishing cardiomyocytes in da
Publikováno v:
Biofizika. 51(5)
The skeletal myosin light chain kinase (skMLCK) was identified in human and chicken embryo myocardium but not in embryo and adult rat heart using western blotting. The content of skMLCK and myosin-activating protein kinases: RhaA-activated protein ki