نتایج جستجو برای: jam and etc

تعداد نتایج: 16833138  

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2009
Erdenechimeg Shagdarsuren Yassin Djalali-Talab Michel Aurrand-Lions Kiril Bidzhekov Elisa A Liehn Beat A Imhof Christian Weber Alma Zernecke

OBJECTIVE Although junctional adhesion molecule (JAM)-C has been implicated in the control of inflammatory leukocyte recruitment, its role in neointima formation after arterial injury has not been elucidated. METHODS AND RESULTS In apolipoprotein E-deficient (Apoe(-/-)) mice fed an atherogenic diet, antibody blockade of JAM-C significantly reduced neointimal hyperplasia after wire injury of c...

2013
Sharmila Chatterjee Yan Wang Melinda K. Duncan Ulhas P. Naik

Inflammation and angiogenesis are integral parts of wound healing. However, excessive and persistent wound-induced inflammation and angiogenesis in an avascular tissue such as the cornea may be associated with scarring and visual impairment. Junctional adhesion molecule A (Jam-A) is a tight junction protein that regulates leukocyte transmigration as well as fibroblast growth factor-2 (FGF-2)-in...

2013
Ana C. Monteiro Ronen Sumagin Carl R. Rankin Giovanna Leoni Michael J. Mina Dirk M. Reiter Thilo Stehle Terence S. Dermody Stacy A. Schaefer Randy A. Hall Asma Nusrat Charles A. Parkos

Intestinal barrier function is regulated by epithelial tight junctions (TJs), structures that control paracellular permeability. Junctional adhesion molecule-A (JAM-A) is a TJ-associated protein that regulates barrier; however, mechanisms linking JAM-A to epithelial permeability are poorly understood. Here we report that JAM-A associates directly with ZO-2 and indirectly with afadin, and this c...

2012
Sandra Iden Steve Misselwitz Swetha S.D. Peddibhotla Hüseyin Tuncay Daniela Rehder Volker Gerke Horst Robenek Atsushi Suzuki Klaus Ebnet

The PAR-3-atypical protein kinase C (aPKC)-PAR-6 complex has been implicated in the development of apicobasal polarity and the formation of tight junctions (TJs) in vertebrate epithelial cells. It is recruited by junctional adhesion molecule A (JAM-A) to primordial junctions where aPKC is activated by Rho family small guanosine triphosphatases. In this paper, we show that aPKC can interact dire...

Journal: :Cancer research 2005
Chrystelle Lamagna Kairbaan M Hodivala-Dilke Beat A Imhof Michel Aurrand-Lions

The junctional adhesion molecule-C (JAM-C) was recently described as an adhesion molecule localized at interendothelial contacts and involved in leukocyte transendothelial migration. The protein JAM-C interacts with polarity complex molecules and regulates the activity of the small GTPase Cdc42. The angiogenesis process involves rearrangement of endothelial junctions and implicates modulation o...

1997
Salvatore J. Stolfo Andreas L. Prodromidis Shelley Tselepis Wenke Lee Dave W. Fan Philip K. Chan

In this paper, we describe the JAM system, a distributed, scalable and portable agent-based data mining system that employs a general approach to scaling data mining applications that we call meta-learning. JAM provides a set of learning programs, implemented either as JAVA applets or applications, that compute models over data stored locally at a site. JAM also provides a set of meta-learning ...

Journal: :Bulletin of the Society for Near Eastern Studies in Japan 1974

Journal: :Arthritis and rheumatism 2008
Bradley J Rabquer Angela Pakozdi James E Michel Bansari S Gujar G Kenneth Haines Beat A Imhof Alisa E Koch

OBJECTIVE Leukocyte infiltration into the rheumatoid arthritis (RA) synovium is a multistep process in which leukocytes leave the bloodstream and invade the synovial tissue (ST). Leukocyte transendothelial migration and adhesion to RA ST requires adhesion molecules on the surface of endothelial cells and RA ST fibroblasts. This study was undertaken to investigate the role of junctional adhesion...

2008
Meghna U. Naik Tejal U. Naik Arthur T. Suckow Melinda K. Duncan Ulhas P. Naik

The metastatic potential of cancer cells is directly attributed to their ability to invade through the extracellular matrix. The mechanisms regulating this cellular invasiveness are poorly understood. Here, we show that junctional adhesion molecule A (JAM-A), a tight junction protein, is a key negative regulator of cell migration and invasion. JAM-A is robustly expressed in normal human mammary...

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