Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Mikhail V. Egorov"'
Autor:
Anna A. Lukianova, Mikhail M. Shneider, Peter V. Evseev, Mikhail V. Egorov, Anastasiya A. Kasimova, Anna M. Shpirt, Alexander S. Shashkov, Yuriy A. Knirel, Elena S. Kostryukova, Konstantin A. Miroshnikov
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 24, p 17288 (2023)
Klebsiella pneumoniae is a pathogen associated with various infection types, which often exhibits multiple antibiotic resistance. Phages, or bacterial viruses, have an ability to specifically target and destroy K. pneumoniae, offering a potential mea
Externí odkaz:
https://doaj.org/article/d7111cb44ea4451ca9e1de381cec7fa0
Autor:
Nikolai D Verveiko, Mikhail V Egorov
Publikováno v:
Vestnik Samarskogo Gosudarstvennogo Tehničeskogo Universiteta. Seriâ: Fiziko-Matematičeskie Nauki, Vol 22, Iss 2, Pp 325-343 (2018)
The paper presents a mathematical modeling of dynamic stress-strain state of the rotation of the shell elasto-viscoplastic material. We solve the modified system of S. P. Timoschenko’s partial differential equations by constructing a system of equa
Externí odkaz:
https://doaj.org/article/4297322c96234821b4541d5c9da95497
Autor:
Julia Fueller, Mikhail V Egorov, Kirstin A Walther, Ola Sabet, Jana Mallah, Markus Grabenbauer, Ali Kinkhabwala
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0154908 (2016)
[This corrects the article DOI: 10.1371/journal.pone.0139429.].
Externí odkaz:
https://doaj.org/article/d2e4c44b811f42d9a0cda671442f893f
Autor:
Julia Fueller, Mikhail V Egorov, Kirstin A Walther, Ola Sabet, Jana Mallah, Markus Grabenbauer, Ali Kinkhabwala
Publikováno v:
PLoS ONE, Vol 10, Iss 10, p e0139429 (2015)
The canonical protein tyrosine phosphatase PTP1B is an important regulator of diverse cellular signaling networks. PTP1B has long been thought to exert its influence solely from its perch on the endoplasmic reticulum (ER); however, an additional subp
Externí odkaz:
https://doaj.org/article/e1bc48e8f6d74a1d91f861b6c7b955aa
Autor:
Mikhail V. Egorov, Roman S. Polishchuk
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Loss of function mutations in the FGD1 gene cause a rare X-linked disease, faciogenital dysplasia (FGDY, also known as Aarskog-Skott syndrome), which is associated with bone and urogenital abnormalities. The FGD1 gene encodes a CDC42-specific guanine
Autor:
Jesús Sot, Britta Brügger, Roman S. Polishchuk, Carles Rentero, Juan M. Duran, Vivek Malhotra, Félix M. Goñi, Felix T. Wieland, Mikhail V. Egorov, Josse van Galen, Carlos Enrich, Timo Sachsenheimer, Felix Campelo
Publikováno v:
The EMBO Journal. 31:4535-4546
Sphingomyelin and cholesterol can assemble into domains and segregate from other lipids in the membranes. These domains are reported to function as platforms for protein transport and signalling. Do similar domains exist in the Golgi membranes and ar
Autor:
Mikhail V. Egorov, Roman S. Polishchuk
Publikováno v:
Tissuecell. 49(2 Pt)
It is widely accepted that the Golgi complex operates as a main sorting station in the biosynthetic pathway. On the other hand, the Golgi complex harbors numerous signaling molecules that generate the platform for the coordination of the transduction
Autor:
Anne-Marie Alleaume, Roman S. Polishchuk, Vivek Malhotra, Elena Forlanelli, Henrik Molina, Mikhail V. Egorov, Julia von Blume, Juan M. Duran
Publikováno v:
The Journal of Cell Biology
Sorting of both soluble and integral membrane proteins is disrupted by loss of ADF/cofilin, suggesting that actin severing controls expansion of a sorting domain within the TGN.
Knockdown of the actin-severing protein actin-depolymerizing factor
Knockdown of the actin-severing protein actin-depolymerizing factor
Autor:
Stefania Mariggiò, Jerome L. Gorski, Roman S. Polishchuk, Mariagrazia Capestrano, Alessio Di Pentima, Mikhail V. Egorov, Anastasia V. Egorova, Roberto Buccione, Stefano Tete, Olesya A. Vorontsova, Alberto Luini, M. Inmaculada Ayala
Publikováno v:
Molecular Biology of the Cell. 20:2413-2427
Mutations in the FGD1 gene are responsible for the X-linked disorder known as faciogenital dysplasia (FGDY). FGD1 encodes a guanine nucleotide exchange factor that specifically activates the GTPase Cdc42. In turn, Cdc42 is an important regulator of m
Autor:
Julia Fueller, Mikhail V Egorov, Kirstin A Walther, Ola Sabet, Jana Mallah, Markus Grabenbauer, Ali Kinkhabwala
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 10, p e0139429 (2015)
PLoS ONE, Vol 10, Iss 10, p e0139429 (2015)
The canonical protein tyrosine phosphatase PTP1B is an important regulator of diverse cellular signaling networks. PTP1B has long been thought to exert its influence solely from its perch on the endoplasmic reticulum (ER); however, an additional subp