نتایج جستجو برای: rap1a

تعداد نتایج: 218  

Journal: :The Journal of Cell Biology 2006
Lawrence E. Goldfinger Celeste Ptak Erin D. Jeffery Jeffrey Shabanowitz Donald F. Hunt Mark H. Ginsberg

The Ras family of small GTPases regulates cell proliferation, spreading, migration and apoptosis, and malignant transformation by binding to several protein effectors. One such GTPase, R-Ras, plays distinct roles in each of these processes, but to date, identified R-Ras effectors were shared with other Ras family members (e.g., H-Ras). We utilized a new database of Ras-interacting proteins to i...

Journal: :Cancer research 2009
Candice L Bailey Patrick Kelly Patrick J Casey

Elucidating the mechanisms of prostate cancer (CaP) survival and metastasis are critical to the discovery of novel therapeutic targets. The monomeric G protein Rap1 has been implicated in cancer tumorigenesis. Rap1 signals to pathways involved in cell adhesion, migration, and survival, suggesting Rap1 may promote several processes associated with cancer cell metastasis. Examination of CaP cell ...

Journal: :The Biochemical journal 1999
A R Cross R W Erickson B A Ellis J T Curnutte

The role of magnesium ions in the activation of NADPH oxidase has been investigated using flavocytochrome b-245 and either neutrophil cytosol or mixtures of recombinant p40phox, p47phox, p67phox and Rac2. Purified flavocytochrome b-245 is highly active (turnover number 120-150 mol of O2(-)/s per mol of cytochrome haem) in the absence of Mg2+, in marked contrast to neutrophil membranes or deterg...

Journal: :Human molecular genetics 2002
Jon S Zawistowski Ilya G Serebriiskii Maximilian F Lee Erica A Golemis Douglas A Marchuk

Mutations in KRIT1, a protein initially identified based on a yeast two-hybrid interaction with the RAS-family GTPase RAP1A, are responsible for the development of the inherited vascular disorder cerebral cavernous malformations (CCM1). As the function of the KRIT1 protein and its role in CCM pathogenesis remain unknown, we performed yeast two-hybrid screens to identify additional protein bindi...

Journal: :Molecular pharmacology 2005
Douglas G Tilley Donald H Maurice

Sustained activation of adenylyl cyclase in vascular smooth muscle cells (VSMCs) results in the activation of a series of complex regulatory systems designed to desensitize these cells to further cAMP-mediated events. Although an increase in phosphodiesterase (PDE) 4-mediated hydrolysis of cAMP forms an integral part of this desensitization program in both "contractile/quiescent" and "synthetic...

Journal: :Journal of cell science 2017
Spencer A Freeman Sonja Christian Pamela Austin Irene Iu Marcia L Graves Lin Huang Shuo Tang Daniel Coombs Michael R Gold Calvin D Roskelley

Although it is known that a stiffening of the stroma and the rearrangement of collagen fibers within the extracellular matrix facilitate the movement of tumor cells away from the primary lesion, the underlying mechanisms responsible are not fully understood. We now show that this invasion, which can be initiated by applying tensional loads to a three-dimensional collagen gel matrix in culture, ...

Journal: :The Biochemical journal 2004
Grant G Kelley Sarah E Reks Alan V Smrcka

PLCepsilon (phospholipase Cepsilon) is a novel PLC that has a CDC25 guanine nucleotide exchange factor domain and two RA (Ras-association) domains of which the second (RA2) is critical for Ras activation of the enzyme. In the present studies, we examined hormonal stimulation to elucidate receptor-mediated pathways that functionally regulate PLCepsilon. We demonstrate that EGF (epidermal growth ...

Journal: :The Journal of clinical investigation 2015
Nina Bögershausen I-Chun Tsai Esther Pohl Pelin Özlem Simsek Kiper Filippo Beleggia E Ferda Percin Katharina Keupp Angela Matchan Esther Milz Yasemin Alanay Hülya Kayserili Yicheng Liu Siddharth Banka Andrea Kranz Martin Zenker Dagmar Wieczorek Nursel Elcioglu Paolo Prontera Stanislas Lyonnet Thomas Meitinger A Francis Stewart Dian Donnai Tim M Strom Koray Boduroglu Gökhan Yigit Yun Li Nicholas Katsanis Bernd Wollnik

The genetic disorder Kabuki syndrome (KS) is characterized by developmental delay and congenital anomalies. Dominant mutations in the chromatin regulators lysine (K)-specific methyltransferase 2D (KMT2D) (also known as MLL2) and lysine (K)-specific demethylase 6A (KDM6A) underlie the majority of cases. Although the functions of these chromatin-modifying proteins have been studied extensively, t...

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