نتایج جستجو برای: ado wn

تعداد نتایج: 3291  

2013
Lei Zhang Peian Lou Yanan Zhu Peipei Chen Pan Zhang Jiaxi Yu Ning Zhang Na Chen Hongmin Wu Jing Zhao

BACKGROUND Patients with chronic obstructive pulmonary disease (COPD) often have organ dysfunction and resulting poor quality of life; however, in China little information is available regarding factors that affect their health. Here, the relationship between risk factors, activities and psychological disorders and health of patients with COPD in rural areas of Xuzhou, China was assessed. MET...

Journal: :The Biochemical journal 2006
Rupak Datta Ishita Das Banibrata Sen Anutosh Chakraborty Subrata Adak Chhabinath Mandal Alok K Datta

Despite designating catalytic roles of Asp299 and Arg131 during the transfer of gamma-phosphate from ATP to Ado (adenosine) [R. Datta, Das, Sen, Chakraborty, Adak, Mandal and A. K. Datta (2005) Biochem. J. 387, 591-600], the mechanisms that determine binding of substrate and cause product inhibition of adenosine kinase from Leishmania donovani remained unclear. In the present study, employing h...

2012
Alla Polotskaia Sandy Hoffman Nancy L. Krett Mala Shanmugam Steven T. Rosen Jill Bargonetti

8-Amino-adenosine (8-NH2-Ado) is a ribose sugar nucleoside analogue that reduces cellular ATP levels and inhibits mRNA synthesis. Estrogen receptor-negative (ER ) metastatic breast cancers often contain mutant p53; therefore, we asked if 8-NH2-Ado could kill breast cancer cells without activating the p53-pathway. Regardless of the breast cancer subtype tested or the p53 status of the cells, 8-N...

Journal: :The Journal of general virology 1989
D M Hunt

Other workers have reported that vesicular stomatitis virus makes aberrantly long polyadenylic acid [poly(A)] tracts in the presence of S-adenosylhomocysteine (S-Ado-Hcy). In the work reported in this paper, the effects of various analogues of S-adenosylmethionine (S-Ado-Met) and ATP on polyadenylation in an in vitro transcription system were examined to determine whether S-Ado-Hcy exerted its ...

Journal: :The Journal of biological chemistry 2010
Jennifer B Dennison Mary L Ayres Kumar Kaluarachchi William Plunkett Varsha Gandhi

8-Chloroadenosine (8-Cl-Ado) is a ribosyl nucleoside analog currently in phase I testing for the treatment of chronic lymphocytic leukemia (CLL). 8-Cl-Ado activity is dependent on adenosine kinase and requires intracellular accumulation of 8-Cl-Ado as mono-, di-, and tri-phosphates. In the current study with four mantle cell lymphoma cell lines, we report a new major metabolic pathway for 8-Cl-...

Journal: :Filomat 2022

In this paper, we prove that each of the following functions is convex on R: f(t) = wN(AtXA1?t ? A1?tXAt), g(t) wN(AtXA1?t), and h(t) wN(AtXAt) where A > 0, X Mn N(.) a unitarily invariant norm onMn. Consequently, answer positively question concerning convexity function t w(AtXAt) proposed by in (2018). We provide some generalizations extensions wN(.) using Kwong functions. More precisely, w...

2016
Miriam Fernandez-Gallardo Ricardo González-Ramírez Alejandro Sandoval Ricardo Felix Eduardo Monjaraz

Emerging evidence suggests that the adenosine (Ado) receptors may play crucial roles in tumor progression. Here, we show that Ado increases proliferation and migration in a triple negative breast cancer model, the MDA-MB 231 cell line. The use of specific agonists and antagonists evidenced that these effects depend on the activation of the A2B receptor, which then triggers an intracellular resp...

Journal: :Sen-ito Kogyo 1970

2009
Daniel R. Cavagnaro Mark A. Pitt Jay I. Myung

In cognitive science, empirical data collected from participants are the arbiters in model selection. Model discrimination thus depends on designing maximally informative experiments. It has been shown that adaptive design optimization (ADO) allows one to discriminate models as efficiently as possible in simulation experiments. In this paper we use ADO in a series of experiments with people to ...

2005
Igor Stojanov Kenneth G. Proctor

To characterize adenosine-mediated vascular responses, synthetic A, and A2 receptor agonists (JV-ethyl carboxamido adenosine [NECA], 2-chloro adenosine [2CA], or cyclohexyl adenosine [CHA]), the parent compound (adenosine [ADO]), an uptake inhibitor (dipyridamole [DIPYRID]) or a nonselective, competitive antagonist (8-phenyl theophylline [8pTHEO]) were topically applied to 20-60 /*m arterioles ...

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