نتایج جستجو برای: پروبیوتیک abt 10

تعداد نتایج: 1019339  

Journal: :The international journal of neuropsychopharmacology 2010
Ariel Graff-Guerrero Laura Redden Walid Abi-Saab David A Katz Sylvain Houle Penny Barsoum Anahita Bhathena Ramesh Palaparthy Mario D Saltarelli Shitij Kapur

Dopamine D3 receptors are preferentially localized in the limbic system and midbrain, and thus may be involved in the pathophysiology of neuropsychiatry disorders. [11C](+)-PHNO is the first preferential D3 receptor radioligand in humans, yet there are no blockade studies with a D3 receptor antagonist in humans. This study characterized the blockade of [11C](+)-PHNO binding by ABT-925, a D3 rec...

2016
Juliana Velez Rongqing Pan Jason T.C. Lee Leonardo Enciso Marta Suarez Jorge Eduardo Duque Daniel Jaramillo Catalina Lopez Ludis Morales William Bornmann Marina Konopleva Gerald Krystal Michael Andreeff Ismael Samudio

Metformin displays antileukemic effects partly due to activation of AMPK and subsequent inhibition of mTOR signaling. Nevertheless, Metformin also inhibits mitochondrial electron transport at complex I in an AMPK-independent manner, Here we report that Metformin and rotenone inhibit mitochondrial electron transport and increase triglyceride levels in leukemia cell lines, suggesting impairment o...

Journal: : 2021

Topicality: The problem of diagnosis and treatment otitis externa (OE) has been posed to doctors for a long time, until the discovery antibiotics (AB) antifungal drugs (AFD) remained unresolved. OE can affect up 10% people at different periods their lives, manifesting itself in form acute (AOE) 95% cases after age 2 years. There is reduction number patients admittance ENT specialist with onset ...

2017
Xiaoyan Wu Lin Wang Yining Qiu Bingyu Zhang Zhenhua Hu Runming Jin

T cell acute lymphoblastic leukemia (T-ALL) is caused by clonal expansion of variant T cell progenitors and is considered as a high risk leukemia. Contemporary single chemotherapy has a limited effect due to dynamic and versatile properties of T-ALL. Here IRAK1/4 inhibitor and ABT-737 were co-encapsulated into polyethylene glycol modified poly (lactic-co-glycolic acid) nanoparticles (IRAK/ABT-N...

2017
Hongqin Yang Peixiao Tang Bin Tang Yanmei Huang Hui Li

Veliparib (ABT-888), which can inhibit cancer growth by blocking DNA base excision repair, is one of several recently developed oral inhibitors of poly(ADP-ribose) polymerases, which are currently used in clinical trials. In this work, interaction of calf thymus DNA (ctDNA) with ABT-888 was first investigated following UV-visible absorption, nuclear magnetic resonance (NMR) spectroscopy, steady...

2013
Lei Liu Zhiwei Wang Songqi Jiang Bingfeng Shao Jibing Liu Suqing Zhang Yilong Zhou Yuan Zhou Yixin Zhang

BACKGROUND AND OBJECTIVE The impact of perioperative allogenenic blood transfusion (ABT) on clinical outcomes for hepatocellular carcinoma (HCC) is conflicting and unclear. The aim of this meta-analysis is to evaluate the association between ABT and HCC clinical outcomes. Outcomes evaluated were all-cause death, tumor recurrence and postoperative complications. METHODS Relevant articles were ...

2008
Shengbing Huang Frank A. Sinicrope

Tumor necrosis factor–related apoptosis-inducing ligand (TRAIL) has been shown to induce mitochondrial apoptotic signaling that can be negatively regulated by prosurvival Bcl-2 proteins. ABT-737 is a small-molecule BH3 mimetic that binds to and antagonizes Bcl-2/Bcl-xL but not Mcl-1. We show that ABT-737 can synergistically enhance TRAIL-mediated cytotoxicity in human pancreatic cancer cell lin...

Journal: :Blood 2013
Cassandra J Vandenberg Suzanne Cory

BH3-only proteins trigger the stress apoptosis pathway and chemical mimetics have great potential for cancer therapy. BH3-only proteins inhibit antiapoptotic members of the Bcl-2 family. Promising BH3 mimetic ABT-737 and the related orally available compound ABT-263 (navitoclax) bind avidly to antiapoptotic Bcl-2, Bcl-xL, and Bcl-w. However, their interaction with Bcl-xL provokes thrombocytopen...

Journal: :British journal of pharmacology 1997
R L Papke J S Thinschmidt B A Moulton E M Meyer A Poirier

1. ABT-418 appeared to function as a relatively broad spectrum activator of neuronal nicotinic receptors, expressed in Xenopus oocytes, with little cross reactivity to the mammalian muscle receptor subtype. However, the relative potencies of ABT-418 at the various subtypes differed from those acetylcholine (ACh). For example, ACh was most potent at alpha 3 beta 2 (EC50 approximately 30 microM) ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2015
Anthony C Faber Anna F Farago Carlotta Costa Anahita Dastur Maria Gomez-Caraballo Rebecca Robbins Bethany L Wagner William M Rideout Charles T Jakubik Jungoh Ham Elena J Edelman Hiromichi Ebi Alan T Yeo Aaron N Hata Youngchul Song Neha U Patel Ryan J March Ah Ting Tam Randy J Milano Jessica L Boisvert Mark A Hicks Sarah Elmiligy Scott E Malstrom Miguel N Rivera Hisashi Harada Brad E Windle Sridhar Ramaswamy Cyril H Benes Tyler Jacks Jeffrey A Engelman

BH3 mimetics such as ABT-263 induce apoptosis in a subset of cancer models. However, these drugs have shown limited clinical efficacy as single agents in small-cell lung cancer (SCLC) and other solid tumor malignancies, and rational combination strategies remain underexplored. To develop a novel therapeutic approach, we examined the efficacy of ABT-263 across >500 cancer cell lines, including 3...

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