نتایج جستجو برای: 453

تعداد نتایج: 3022  

Journal: :Oncology letters 2011
Semir Vranic Zoran Gatalica Zhao-Yi Wang

Apocrine carcinoma of the breast has recently been refined through gene expression profiling. Due to various pathological studies, we compared the results with the MDA-MB-453 breast cancer cell line, a proposed model for apocrine breast carcinoma. The MDA-MB-453 cell line is androgen receptor-positive and `triple-negative' in respect to estrogen receptor-α, progesterone receptor and the Her-2/n...

Journal: :Cancer 2005
Ryungsa Kim Kazuaki Tanabe Manabu Emi Yoko Uchida Tetsuya Toge

BACKGROUND Because the overexpression of HER-2 and Bcl-2 is associated with resistance to tamoxifen (TAM), the authors examined the effect of antisense (AS) Bcl-2 on sensitivity to TAM compared with the effect of trastuzumab on sensitivity to TAM in breast carcinoma cell lines. METHODS Drug sensitivity was assessed in vitro using a [3-4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide ...

2017
Mojgan Naghitorabi Hamid Mir Mohammad Sadeghi Javad Mohammadi Asl Mohammad Rabbani Abbas Jafarian-Dehkordi

Promoter methylation is one of the main epigenetic mechanisms that leads to the inactivation of tumor suppressor genes during carcinogenesis. Due to the reversible nature of DNA methylation, many studies have been performed to correct theses epigenetic defects by inhibiting DNA methyltransferases (DNMTs). In this case novel therapeutics especially siRNA oligonucleotides have been used to specif...

2017
Viera Tischlerova Martin Kello Mariana Budovska Jan Mojzis

AIM To investigate the mechanism of the antiproliferative effect of synthetic indole phytoalexin derivatives on human colorectal cancer cell lines. METHODS Changes in cell proliferation and the cytotoxic effect of the tested compounds on human colorectal cancer cell lines and human fibroblasts were evaluated using MTS and BrdU assay, allowing us to choose the most potent substance. Cell cycle...

2013
Hongguang ZHANG

Attached you find an SWG report on a possible new area of standardization activity: Web Collaboration At its June 2013 meeting SWG-P adopted this report, recognizing that it might still be too early to start standardization work right away. Instead we would like to get some feedback from the SC Chairmen on this report. In section 11 of the report SWG on Planning has identified a number of possi...

2013
XIAO-CHUN ZHAO XIAO-CHENG CAO FEI LIU MEI-FANG QUAN KAI-QUN REN JIAN-GUO CAO

We previously demonstrated that 5,7-dihydroxy-8-nitrochrysin (NOC), a novel synthetic chrysin analog, preferentially inhibits HER-2/neu-overexpressing MDA-MB-453 breast cancer cell growth by inducing apoptosis; however, the precise molecular mechanism was unclear. In this study, we demonstrated that NOC significantly induces apoptosis of MDA-MB-453 cells and that this is primarily mediated thro...

Promoter methylation is one of the main epigenetic mechanisms that lead to the inactivation of tumor suppressor genes during carcinogenesis. Due to the reversible nature of DNA methylation, many studies have been performed to correct theses epigenetic defects by inhibiting DNA methyltransferases (DNMTs). In this case novel therapeutics especially siRNA oligonucleotides have been used to specifi...

Journal: :Alfinge 2022

Reseña de García Gallarín, Consuelo, Diccionario histórico la morfología del español. Madrid: Escolar y Mayo, 2018. ISBN 978-84-1713-453-2. 701 pp.

Journal: :The Biochemical journal 2003
Amro A Amara Bernd H A Rehm

The class II PHA (polyhydroxyalkanoate) synthases [PHA(MCL) synthases (medium-chain-length PHA synthases)] are mainly found in pseudomonads and catalyse synthesis of PHA(MCL)s using CoA thioesters of medium-chain-length 3-hydroxy fatty acids (C6-C14) as a substrate. Only recently PHA(MCL) synthases from Pseudomonas oleovorans and Pseudomonas aeruginosa were purified and in vitro activity was ac...

Journal: :Molecular cancer therapeutics 2009
Rong Deng Jun Tang Liang-Ping Xia Dan-Dan Li Wen-Jun Zhou Lin-Lin Wang Gong-Kan Feng Yi-Xin Zeng You-Heng Gao Xiao-Feng Zhu

Isodon diterpenoids have received considerable phytochemical and biological attention for their strong antitumor activity with low toxicity. In this study, ExcisaninA, a diterpenoid compound purified from Isodon MacrocalyxinD, was tested on human Hep3B and MDA-MB-453 cell lines and Hep3B xenograft models. The results showed ExcisaninA could inhibit the proliferation of Hep3B and MDA-MB-453 cell...

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