Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Ararat J. Ablooglu"'
Autor:
Bart Weijts, Edgar Gutierrez, Semion K. Saikin, Ararat J. Ablooglu, David Traver, Alex Groisman, Eugene Tkachenko
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-11 (2018)
The mechanisms of sensing of blood flow and responses to it in vascular remodelling are poorly understood. Here, the authors show that in zebrafish blood flow controls both the fate determination of individual blood vessels and the arterial versus ve
Externí odkaz:
https://doaj.org/article/b1794bd622bc45d3a2fefd0e655fefd7
Autor:
Joseph M. Cantor, Ararat J. Ablooglu, Zhongji Liao, Mark H. Ginsberg, Manjula Pandey, Hisashi Kato, Sanford J. Shattil
Publikováno v:
Blood. 125:1995-2004
The bidirectional signaling and hemostatic functions of platelet αIIbβ3 are regulated by kindlin-3 through interactions with the β3 cytoplasmic tail. Little is known about kindlin regulation of the related "vitronectin receptor," αVβ3. These rel
Publikováno v:
Journal of Biological Chemistry. 289:11183-11193
Protein-protein interactions are driving forces in cellular processes. As a prime example, transmembrane integrins link extracellular matrix and intracellular proteins, resulting in bidirectional signaling that regulates cell migration, proliferation
Autor:
Alex Groisman, Eugene Tkachenko, Edgar Gutierrez, Semion K. Saikin, Bart Weijts, David Traver, Ararat J. Ablooglu
Arteries and veins are formed independently by different types of endothelial cells (ECs). In vascular remodeling, arteries and veins become connected and some arteries become veins. It is unclear how ECs in transforming vessels change their type and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af824940cf4127047f7b0177a8736538
https://doi.org/10.1101/095307
https://doi.org/10.1101/095307
Autor:
Rebecca A. Stockton, Mark H. Ginsberg, Andrey A. Bobkov, Ararat J. Ablooglu, Jian J. Liu, Alexandre R. Gingras, Jaewon Han
Publikováno v:
Molecular Biology of the Cell
Rap1 stabilizes cell–cell junctions by directly binding to KRIT1, displacing it from microtubules and enabling localization at the junctions.
Activation of Rap1 small GTPases stabilizes cell–cell junctions, and this activity requires Krev In
Activation of Rap1 small GTPases stabilizes cell–cell junctions, and this activity requires Krev In
Publikováno v:
Development. 137:3449-3458
Integrin αV can form heterodimers with several β subunits to mediate cell-cell and cell-extracellular matrix interactions. During zebrafish gastrulation, αV is expressed maternally and zygotically. Here, we used a morpholino-mediated αV knockdown
Publikováno v:
Developmental Dynamics. 236:2268-2276
alphaVbeta3 is a receptor for vitronectin and other extracellular matrix ligands, and it has been implicated in angiogenesis and osteoclast function in mammals. We have cloned full-length cDNAs of zebrafish integrin alphaV (itgalphaV), and two paralo
Autor:
Ronald A. Kohanski, John B. Alexander Ross, Mark Frankel, Ararat J. Ablooglu, Elena Rusinova, Robert L. Heinrikson, Joseph W. Leone
Publikováno v:
Molecular and Cellular Biology. 21:4197-4207
Receptor tyrosine kinases may use intrasteric inhibition to suppress autophosphorylation prior to growth factor stimulation. To test this hypothesis we made an Asp1161Ala mutant in the activation loop that relieved intrasteric inhibition of the unpho
Autor:
Mark Frankel, Ararat J. Ablooglu, Stevan R. Hubbard, Ronald A. Kohanski, Steven M. Bishop, Jeffrey H. Till
Publikováno v:
Journal of Biological Chemistry. 276:10049-10055
The tyrosine kinase domain of the insulin receptor is subject to autoinhibition in the unphosphorylated basal state via steric interactions involving the activation loop. A mutation in the activation loop designed to relieve autoinhibition, Asp-1161
Autor:
Jeffrey H. Till, Philip A. Cole, Ararat J. Ablooglu, Keykavous Parang, Ronald A. Kohanski, Stevan R. Hubbard
Publikováno v:
Nature Structural Biology. 8:37-41
Protein kinase inhibitors have applications as anticancer therapeutic agents and biological tools in cell signaling. Based on a phosphoryl transfer mechanism involving a dissociative transition state, a potent and selective bisubstrate inhibitor for