نتایج جستجو برای: tyrosine kinase inhibitors

تعداد نتایج: 417183  

Journal: :The Cancer Journal 2019

Journal: :Mediterranean Journal of Hematology and Infectious Diseases 2014

Journal: :Indian Journal of Pharmaceutical Education and Research 2023

Abstract: Aim: LK (B-lymphocyte kinase) is a protein from the family SRC (Proto-oncogene tyrosine-protein kinase), an important cell signaling molecule that influences cellular response. The BLK kinase has been potential target for cancer therapy. As result, this could be initial step toward development of novel inhibitors to fight cancer. Materials and Methods: A homology model human tyrosine ...

Journal: :Memo – Magazine of European Medical Oncology 2021

Summary Chronic myeloid leukemia is nowadays associated with a good prognosis and an excellent life expectancy. However, certain levels of responses have to be achieved the various available tyrosine kinase inhibitors at time points during treatment otherwise adequate diagnostic therapeutic actions initiated. This paper will focus on these issues.

Journal: :iranian journal of pharmaceutical sciences 0
ajay gaur l.b.s. college of pharmacy, jaipur-302004, rajasthan, india arvind lal bhatia radiation biology laboratory, center for advanced studies, department of zoology, university of rajasthan, jaipur-302004, rajasthan, india.

genistein is a soya isoflavone, which is found naturally in legumes, such as soybeans and chickpeas. the intraperitoneal administration of the optimum dose (200 mg/kg) of genistein 24 h and 15 minbefore irradiation (8 gy at a dose rate of 1.02 gy/min) recovered the deficit in protein content (28.63±1.44%) and the dna content (21.61±8.19%) if an average of 5 intervals of autopsies 1st, 3rd, 7th,...

Journal: :Science-Business eXchange 2008

Journal: :Mediterranean Journal of Hematology and Infectious Diseases 2014

Journal: :Journal of Thoracic Disease 2023

Background: The transformation of epidermal growth factor receptor (EGFR)-mutant lung adenocarcinoma (LUAD) into small cell cancer (SCLC) accounts for 3–14% the resistance mechanism to EGFR tyrosine kinase inhibitors (TKIs). At present, there is no relevant research explore dynamic expression EGFR-mutant proteins and genomic evolution in transformed SCLC/neuroendocrine carcinoma (NEC).

Journal: :World journal of clinical oncology 2011
Fleur Broekman Elisa Giovannetti Godefridus J Peters

Since in most tumors multiple signaling pathways are involved, many of the inhibitors in clinical development are designed to affect a wide range of targeted kinases. The most important tyrosine kinase families in the development of tyrosine kinase inhibitors are the ABL, SCR, platelet derived growth factor, vascular endothelial growth factor receptor and epidermal growth factor receptor famili...

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