Zobrazeno 1 - 5
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pro vyhledávání: '"Maryam Oladghaffari"'
Publikováno v:
Radiology Research and Practice, Vol 2020 (2020)
CT and its comprehensive usage have become one of the most indispensable components in medical field especially in the diagnosis of several diseases. SECT and DECT have developed CT diagnostic potentials in several means. In this review article we ha
Externí odkaz:
https://doaj.org/article/3ab93fb8a17d44cfa248a75597719190
Autor:
Maryam Oladghaffari, Alireza Farajollahi, Mohammad Asghari Jafar Abadi, Mohsen Mohammadi, Jalil Pirayesh Islamian, Behzad Baradaran, Dariush Shanehbandi, Ali Shabestani Monfared
Publikováno v:
International Journal of Radiation Biology. 93:590-599
Two-deoxy-D-glucose (2DG) causes cytotoxicity in the cancer cells by disrupting the thiol metabolism, and MLN4924 inactivates the SCF E3 ligase and so causes the accumulation of its substrates which trigger apoptosis and hence might enhance the effic
Autor:
Jalil Pirayesh Islamian, Kazem Nejati-Koshki, Alireza Farajollahi, Maryam Oladghaffari, Hadi Karami, Mohsen Mohammadi
Publikováno v:
International Journal of Cancer Management. 10
Background: Radio therapy plays an important role in controlling tumor growth in esophageal cancer patients. Objectives: Our study provided comprehensive information about radio-sensitivity of Hdm2 gene in esophageal cancer cells in cancer cells. Met
Autor:
Asghar Mesbahi, Maryam Oladghaffari
Publikováno v:
International Journal of Radiology & Radiation Therapy. 2
Analyzing the dose distribution inside target volumes of cancer patients before radiation delivery and then selection of the biologically optimal dose distribution has been one of the crucial steps in recent treatment planning developments Plan evalu
Autor:
Mohsen Mohammadi, Maryam Oladghaffari, Alireza Farajollahi, Dariush Shanehbandi, Jalil Pirayesh Islamian, Behzad Baradaran, Ali Shabestani Monfared
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 16(13)
2-deoxy-D-Glucose (2DG) causes cytotoxicity in cancer cells by disrupting thiol metabolism. It is an effective component in therapeutic strategies. It targets the metabolism of cancer cells with glycolysis inhibitory activity. On the other hand, MLN4