نتایج جستجو برای: serine375

تعداد نتایج: 3  

Journal: :iranian journal of pharmaceutical sciences 0
mohammad rabbani department of pharmacology and toxcicology,isfahan pharmaceutical sciences research centre hamid mir mohammad sadeghi department of pharmaceutical biotechnology, faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran ali omidsalary department of pharmaceutical biotechnology, faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran jahangir langari department of pharmaceutical biotechnology, faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran fatemeh moazen department of pharmaceutical biotechnology, faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran

the aim of this study was to use site directed mutagenesis technique to construct a vector in which serine363 and serine375 residues of the cooh-terminal portion of the μ-opioid receptor (mor) were substituted by alanine. these constructs are essential in studying g-protein coupled receptor kinase-mediated mor desensiti-zation. the nested pcr carried out for conversion of serine363 and serine37...

Journal: :Cancer research 2009
Run-Qiang Chen Qing-Kai Yang Bing-Wen Lu Wei Yi Greg Cantin Yan-Ling Chen Colleen Fearns John R Yates Jiing-Dwan Lee

Because the mammalian target of rapamycin (mTOR) pathway is commonly deregulated in human cancer, mTOR inhibitors, rapamycin and its derivatives, are being actively tested in cancer clinical trials. Clinical updates indicate that the anticancer effect of these drugs is limited, perhaps due to rapamycin-dependent induction of oncogenic cascades by an as yet unclear mechanism. As such, we investi...

Ali Omidsalary Fatemeh Moazen Hamid Mir Mohammad Sadeghi Jahangir Langari Mohammad Rabbani,

     The aim of this study was to use site directed mutagenesis technique to construct a vector in which serine363 and serine375 residues of the COOH-terminal portion of the μ-opioid receptor (MOR) were substituted by alanine. These constructs are essential in studying G-protein coupled receptor kinase-mediated MOR desensiti-zation. The nested PCR carried out for conversio...

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