نتایج جستجو برای: p110α

تعداد نتایج: 322  

2013
Rabea Müller Catharina Fischer Thomas Wilmes Bernd Heimrich Vanessa Distel Norbert Klugbauer Dieter K. Meyer

In cells cultured from neocortex of newborn rats, phosphoinositide-3-kinases of class I regulate the DNA synthesis in a subgroup of astroglial cells. We have studied the location of these cells as well as the kinase isoforms which facilitate the S phase entry. Using dominant negative (dn) isoforms as well as selective pharmacological inhibitors we quantified S phase entry by nuclear labeling wi...

2011
Enrico Conte Mary Fruciano Evelina Fagone Elisa Gili Filippo Caraci Maria Iemmolo Nunzio Crimi Carlo Vancheri

Idiopathic pulmonary fibrosis (IPF) is a progressive fibroproliferative disease characterized by an accumulation of fibroblasts and myofibroblasts in the alveolar wall. Even though the pathogenesis of this fatal disorder remains unclear, transforming growth factor-β (TGF-β)-induced differentiation and proliferation of myofibroblasts is recognized as a primary event. The molecular pathways invol...

2016
Hua-Fu Zhao Jing Wang Hao-Ran Jiang Zhong-Ping Chen Shing-Shun Tony To

BACKGROUND Glioblastoma multiforme is the most aggressive malignant primary brain tumor, characterized by rapid growth and extensive infiltration to neighboring normal brain parenchyma. Both PI3K/Akt and JNK pathways are essential to glioblastoma cell survival, migration and invasion. Due to their hyperactivation in glioblastoma cells, PI3K and JNK are promising targets for glioblastoma treatme...

Journal: :JCI insight 2017
David Garcia-Galiano Beatriz C Borges Jose Donato Susan J Allen Nicole Bellefontaine Mengjie Wang Jean J Zhao Kenneth M Kozloff Jennifer W Hill Carol F Elias

The role of PI3K in leptin physiology has been difficult to determine due to its actions downstream of several metabolic cues, including insulin. Here, we used a series of mouse models to dissociate the roles of specific PI3K catalytic subunits and of insulin receptor (InsR) downstream of leptin signaling. We show that disruption of p110α and p110β subunits in leptin receptor cells (LRΔα+β) pro...

Journal: :Arteriosclerosis, Thrombosis, and Vascular Biology 2015

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