نتایج جستجو برای: u notch

تعداد نتایج: 183508  

Journal: :Cardiovascular research 2015
Ralph Klose Caroline Berger Iris Moll M Gordian Adam Frank Schwarz Kerstin Mohr Hellmut G Augustin Andreas Fischer

AIMS Notch signalling is essential for blood vessel formation. During angiogenesis, the Notch ligand DLL4 on the leading tip cell activates Notch receptors on the adjacent stalk cells. DLL4-Notch signalling is impaired by the Notch ligand JAG1 in endothelial cells. The Delta/Serrate/Lag2 (DSL) domain of the Notch ligands binds to the EGF-like repeats 11-13 of the Notch receptor. This study aime...

Journal: :Development 1999
P Beatus J Lundkvist C Oberg U Lendahl

The Notch signaling pathway is important for cellular differentiation. The current view is that the Notch receptor is cleaved intracellularly upon ligand activation. The intracellular Notch domain then translocates to the nucleus, binds to Suppressor of Hairless (RBP-Jk in mammals), and acts as a transactivator of Enhancer of Split (HES in mammals) gene expression. In this report we show that t...

Journal: :Mechanisms of Development 1995
R. Williams U. Lendahl M. Lardelli

The Drosophila Notch gene encodes a transmembrane receptor involved in the regulation of cell fate. It exerts its effect by lateral specification, inductive signaling and is also important for cell adhesion and axonal pathfinding. In this report we analyse the expression of the three mammalian Notch homologues during early mouse development by in situ hybridization. The Notch 1, 2 and 3 genes s...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Shaolin Shi Pamela Stanley

Notch receptor signaling regulates cell growth and differentiation, and core components of Notch signaling pathways are conserved from Drosophila to humans. Fringe glycosyltransferases are crucial modulators of Notch signaling that act on epidermal growth factor (EGF)-like repeats in the Notch receptor extracellular domain. The substrate of Fringe is EGF-O-fucose and the transfer of fucose to N...

Journal: :Anticancer research 2014
Shuji Tohda

NOTCH activation plays oncogenic roles in acute T-lymphoblastic leukaemia (T-ALL). However, whether NOTCH is oncogenic or tumor-suppressive in acute myeloid leukaemia (AML) is still controversial. Herein, the roles of NOTCH in AML are reviewed. AML cells express NOTCH and NOTCH ligands; however, cell-autonomous activation is not observed. Activating NOTCH1 mutations are rare in AML, unlike in T...

2005

T HE study of the U wave and of its clinical significance depends upon its accurate recognition. Accurate identification of the U wave is also needed for a correct determination of the Q-T duration. This identification is sometimes difficult because of superposition and fusion of the T and U waves. The term "superposition" is applied to patterns in which these waves are only partially merged an...

Journal: :Molecular cancer research : MCR 2011
Gang Chen Paritosh Ghosh Dan L Longo

There are multiple mechanisms by which cells evade TGF-β-mediated growth inhibitory effects. In this report, we describe a novel mechanism by which cells become resistant to TGF-β-mediated growth suppression. Although having all the components of the TGF-β signaling pathway, different cell lines, RL, HaCaT, and BJAB, have different sensitivities toward TGF-β-induced growth suppression. The TGF-...

2017
Tom V Lee Ashutosh Pandey Hamed Jafar-Nejad

The Drosophila glucoside xylosyltransferase Shams xylosylates Notch and inhibits Notch signaling in specific contexts including wing vein development. However, the molecular mechanisms underlying context-specificity of the shams phenotype is not known. Considering the role of Delta-Notch signaling in wing vein formation, we hypothesized that Shams might affect Delta-mediated Notch signaling in ...

Journal: :Science-Business eXchange 2011

Journal: :Blood 2009
Lynn M Schnapp

T -cell acute lymphoblastic leukemia (T-ALL) is an aggressive leukemia with a poor outcome. The majority of human T-ALL has gain-of-function (activating) mutations in Notch-1,1 implicating Notch-1 as a central component in the pathogenesis of T-ALL. Notch proteins are widely expressed transmembrane receptors involved in many cellular processes such as differentiation, proliferation, and apoptos...

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