نتایج جستجو برای: 468

تعداد نتایج: 3255  

Journal: :Journal of nuclear medicine : official publication, Society of Nuclear Medicine 2008
Zhongli Cai Zhuo Chen Kristy E Bailey Deborah A Scollard Raymond M Reilly Katherine A Vallis

UNLABELLED The Auger electron-emitting radiopharmaceutical 111In-diethylenetriaminepentaacetic acid human epidermal growth factor (111In-DTPA-hEGF) binds the epidermal growth factor receptor (EGFR), is internalized, and translocates to the nucleus. The purpose of this study was to investigate the relationship between EGFR expression, DNA damage, and cytotoxicity in cells exposed to 111In-DTPA-h...

Journal: :iranian journal of pharmaceutical research 0
mina mirian isfahan pharmaceutical research center, school of pharmacy, isfahan university of medical sciences, isfahan, iran. afshin zarghi school of pharmacy, shahid beheshti university of medical sciences (m. c), tehran, iran. sedighe sadeghi isfahan pharmaceutical research center, school of pharmacy, isfahan university of medical sciences, isfahan, iran. parisa tabaraki school of pharmacy, azad university, tehran, iran. mojdeh tavallaee school of pharmacy, azad university, tehran, iran. orkideh dadrass school of pharmacy, azad university, tehran, iran.

sulfonamides are the first effective chemotherapeutic agents used for several years to cure or prevent systemic bacterial infections. in addition, this agents showed anti-carbonic anhydrase and cause cell cycle perturbation in the g1 phase, disruption of microtubule assembly, suppression of the transcription activator nf-y, angiogenesis and matrix metalloproteinase (mmp). in recent years, novel...

Journal: :Cancer research 1994
D K Armstrong S H Kaufmann Y L Ottaviano Y Furuya J A Buckley J T Isaacs N E Davidson

MDA-MB-468 human breast cancer cells lack estrogen receptors, overexpress epidermal growth factor (EGF) receptors, and are growth inhibited by EGF. We show that treatment of MDA-MB-468 cells with EGF leads to inhibition of cell proliferation, fragmentation of DNA into nucleosomal oligomers, and the development of apoptotic morphology. This treatment is associated with increased expression of c-...

Journal: :Journal of clinical microbiology 2010
Hongxiu Wang Jun Yue Min Han Jinghui Yang Yanlin Zhao

A multiplex method using the SNaPshot technique was developed to screen for six common mycobacterial species: Mycobacteria tuberculosis, M. avium, M. intracellulare, M. chelonae, M. kansasii, and M. gordonae. A total of 468 mycobacterial clinical isolates were subjected to analysis for the presence of the six mycobacterial species by the multiplex SNaPshot method. Of the 468 mycobacterial isola...

Journal: :Bioorganic & medicinal chemistry letters 2013
Narva Suresh Hunsur Nagendra Nagesh Kondapalli Venkata Gowri Sekhar Anil Kumar Amir N Shirazi Keykavous Parang

A series of twenty two novel 1-cyclopropyl-6-fluoro-4-oxo-7-(4-substituted piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid analogues have been synthesized, characterized ((1)H NMR, (13)C NMR and LCMS) and evaluated for their inhibitory activity on the proliferation of human caucasian acute lymphoblastic leukemia cells (CCRF-CEM), breast adenocarcinoma cells (MDA-MB-468) and human colon c...

2014
Yanjie Kong Jianchao Chen Zhongmei Zhou Houjun Xia Ming-Hua Qiu Ceshi Chen

Triple negative breast cancer (TNBC) is a highly aggressive form of breast cancer resistant to many common treatments. In this study, we compared the effects of 12 phytochemical drugs on four cancer cell lines, and noticed that Cucurbitacin E (CuE) significantly inhibited TNBC cell growth by inducing cell cycle G2/M phase arrest and apoptosis. CuE reduced expression of Cyclin D1, Survivin, XIAP...

Sulfonamides are the first effective chemotherapeutic agents used for several years to cure or prevent systemic bacterial infections. In addition, this agents showed anti-carbonic anhydrase and cause cell cycle perturbation in the G1 phase, disruption of microtubule assembly, suppression of the transcription activator Nf-Y, angiogenesis and matrix metalloproteinase (MMP). In recent years, novel...

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