نتایج جستجو برای: پروبیوتیک abt 10

تعداد نتایج: 1019339  

Journal: :The Journal of pharmacology and experimental therapeutics 1997
J P Sullivan D Donnelly-Roberts C A Briggs D J Anderson M Gopalakrishnan I C Xue M Piattoni-Kaplan E Molinari J E Campbell D G McKenna D E Gunn N H Lin K B Ryther Y He M W Holladay S Wonnacott M Williams S P Arneric

Accumulating preclinical and clinical evidence data suggests that compounds that selectively activate neuronal nicotinic acetylcholine receptor (nAChR) subtypes may have therapeutic utility for the treatment of several neurological disorders. In the present study, the in vitro pharmacological properties of the novel cholinergic channel modulator ABT-089 [2-methyl-3-(2-(S)-pyrrolidinylmethoxy)py...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2007
Cherrie K Donawho Yan Luo Yanping Luo Thomas D Penning Joy L Bauch Jennifer J Bouska Velitchka D Bontcheva-Diaz Bryan F Cox Theodore L DeWeese Larry E Dillehay Debra C Ferguson Nayereh S Ghoreishi-Haack David R Grimm Ran Guan Edward K Han Rhonda R Holley-Shanks Boris Hristov Kenneth B Idler Ken Jarvis Eric F Johnson Lawrence R Kleinberg Vered Klinghofer Loren M Lasko Xuesong Liu Kennan C Marsh Thomas P McGonigal Jonathan A Meulbroek Amanda M Olson Joann P Palma Luis E Rodriguez Yan Shi Jason A Stavropoulos Alan C Tsurutani Gui-Dong Zhu Saul H Rosenberg Vincent L Giranda David J Frost

PURPOSE To evaluate the preclinical pharmacokinetics and antitumor efficacy of a novel orally bioavailable poly(ADP-ribose) polymerase (PARP) inhibitor, ABT-888. EXPERIMENTAL DESIGN In vitro potency was determined in a PARP-1 and PARP-2 enzyme assay. In vivo efficacy was evaluated in syngeneic and xenograft models in combination with temozolomide, platinums, cyclophosphamide, and ionizing rad...

2011
Chong Zhang Tian-yu Cai Hong Zhu Liu-qing Yang Hai Jiang Xiao-wu Dong Yong-zhou Hu Neng-ming Lin Qiao-jun He Bo Yang

The Bcl-2 antagonist ABT-737 targets Bcl-2/Bcl-xL, but not Mcl-1, which may confer resistance to this agent in various cancers with high levels of Mcl-1. Here, we showed that the combination of gemcitabine and ABT737 exhibited synergistic cytotoxicity and induced significant apoptosis in multiple cancer types, including lung, renal, bladder, and prostate cancers. The enhanced apoptosis induced ...

Journal: :Gut 2001
N J Talley M Verlinden D J Geenen R B Hogan D Riff R W McCallum R J Mack

INTRODUCTION Erythromycin, a motilin agonist, is a potent prokinetic. ABT-229 is a specific motilin agonist that dose dependently accelerates gastric emptying. Dyspepsia and gastroparesis are common problems in type 1 diabetes mellitus. We aimed to evaluate the efficacy of ABT-229 in symptomatic diabetic patients with and without delayed gastric emptying. METHODS Patients with type 1 diabetes...

Journal: :Clinical chemistry 2006
Frank Giton Jean Fiet Jérôme Guéchot Fidaa Ibrahim Françoise Bronsard Dominique Chopin Jean-Pierre Raynaud

BACKGROUND Bioavailable testosterone (BT), circulating testosterone not bound to sex hormone-binding globulin (SHBG), is thought to easily penetrate cells. We compared BT measurements obtained by assays with those obtained by calculation with different testosterone association constants. METHODS We obtained sera from 2 groups of hypogonadal men [group 1 (G1), 1421 samples; group 2 (G2), 170 s...

2004
Shingo Ata Tetsuya Takine Masayuki Murata Hideo Miyahara

ATM Block Transfer (ABT) is promising for effectively transferring highly bursty data traffic in ATM networks. We develop an approximate analysis for two types of ABT (ABT/DT and ABT/IT) to discuss performance comparisons of ABT/IT and DT. Through numerical examples, we show that ABT/DT is quite sensitive to propagation delays while ABT/IT is not. We next investigate the performance improvement...

2015
Yu-lou Tian Fang Liu Hong-jing Sun Pin Lv Yu-ming Cao Mo Yu Yang Yue

OBJECTIVE To assess the labial and lingual alveolar bone thickness in adults with maxillary central incisors of different inclination by cone-beam computed tomography (CBCT). METHODS Ninety maxillary central incisors from 45 patients were divided into three groups based on the maxillary central incisors to palatal plane angle; lingual-inclined, normal, and labial-inclined. Reformatted CBCT im...

2011
Juan Camilo Barreto-Andrade Elena V. Efimova Helena J. Mauceri Michael A. Beckett Harold G. Sutton Thomas E. Darga Everett E. Vokes Mitchell C. Posner Stephen J. Kron Ralph R. Weichselbaum

Radiation therapy remains a promising modality for curative treatment of localized prostate cancer, but dose-limiting toxicities significantly limit its effectiveness. Agents that enhance efficacy at lower radiation dosesmight have considerable value in increasing tumor control without compromising organ function. Here, we tested the hypothesis that the PARP inhibitor ABT-888 (veliparib) can en...

Journal: :Molecular cancer therapeutics 2013
Esther P Jane Daniel R Premkumar Joseph D DiDomenico Bo Hu Shi-Yuan Cheng Ian F Pollack

Antiapoptotic proteins are commonly overexpressed in gliomas, contributing to therapeutic resistance. We recently reported that clinically achievable concentrations of the Bcl-2/Bcl-xL inhibitor ABT-737 failed to induce apoptosis in glioma cells, with persistent expression of survivin and Mcl-1. To address the role of these mediators in glioma apoptosis resistance, we analyzed the effects of YM...

Journal: :The Journal of pharmacology and experimental therapeutics 2000
V E Cowles H N Nellans T R Seifert L M Besecke J A Segreti K M Mohning R Faghih M H Verlinden C D Wegner

ABT-229 (8,9-anhydro-4"-deoxy-3'-N-desmethyl-3'-N-ethylerythromycin B-6,9-hemiacetal), a synthetic derivative of erythromycin (ERY) with no antibiotic activity, has been shown to bind to motilin receptors and stimulate contractile activity of the antrum and small intestine. The objective of this study was to determine the effect of ABT-229 on canine gastric emptying (GE) and contractile activit...

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