نتایج جستجو برای: tyrosine kinase

تعداد نتایج: 260379  

Journal: :Nature Biotechnology 2021

By targeting both arms of the immune system, not just B cells, brain-penetrant inhibitors Bruton’s tyrosine kinase could improve on anti-CD20 therapy for patients with multiple sclerosis.

Journal: :مجله پزشکی مولکولی 0
soheila moein , molecular medicine research center , faculty of medicine

introduction: atherosclerosis, hypertension, ischemic diseases, alzheimer’s disease, parkinson disease, cancer and inflammation emerge from imbalance between antioxidant and oxidants. cancer is a most important public health problem in both developed and developing countries. natural antioxidants such as polyphenols are being used for prevention and treatment cancer. polyphenols include phenoli...

Journal: :iranian journal of allergy, asthma and immunology 0
wei luo department of respiratory medicine, west china hospital, sichuan university, chengdu, sichuan 610041, pr china. chun-tao liu department of respiratory medicine, west china hospital, sichuan university, chengdu, sichuan 610041, pr china. qiu-hong yang department of respiratory medicine, the 7th people's hospital, chengdu, sichuan 610041, pr china. qi yu department of electroencephalogram, the people's hospital, leshan, sichuan 614000, pr china. tao wang laboratory of pulmonary disease, west china hospital, sichuan university, chengdu, sichuan 610041, pr china.

rho-kinase is an effector molecule of rhoa, a monomeric gtp-binding protein, and causes ca2+ sensitization through inactivation of myosin phosphatase. the major physiological functions of rho/rho-kinase cascade include contraction, proliferation and migration in cells.there are some excellent reviews about rho/rho-kinase signal pathway, most of which focus on the specific proteins of the pathwa...

Journal: :iranian journal of catalysis 2015
amit shivajirao waghmare tushar patil kailash kadam shivaji sandu pandit

an efficient synthesis of polyhydroquinoline derivatives is achieved via hantzsch condensation reaction between aldehydes, dimedone, ethyl acetoacetate and ammonium acetate in the presence of catalytic amount of sfhs in ethanol. this method gives remarkable advantages such as shorter reaction time, simple workup procedure and good to excellent yields. furthermore the catalyst can be recovered c...

An efficient synthesis of polyhydroquinoline derivatives is achieved via Hantzsch condensation reaction between aldehydes, dimedone, ethyl acetoacetate and ammonium acetate in the presence of catalytic amount of SFHS in ethanol. This method gives remarkable advantages such as shorter reaction time, simple workup procedure and good to excellent yields. Furthermore the catalyst can be recovered c...

An efficient synthesis of polyhydroquinoline derivatives is achieved via Hantzsch condensation reaction between aldehydes, dimedone, ethyl acetoacetate and ammonium acetate in the presence of catalytic amount of SFHS in ethanol. This method gives remarkable advantages such as shorter reaction time, simple workup procedure and good to excellent yields. Furthermore the catalyst can be recovered c...

Mohsen Beheshti, Reza Vali Robert Dudczak Shuren Li Werner Langsteger Wolfgang Schima

  Introduction: Gastrointestinal stromal tumors (GISTs) are the most common mesenchymal neoplasms of the gastrointestinal tract. GIST has been shown to over-express c-KIT (CD117), the receptor tyrosine kinase. Imatinib (STI571 or Glivec) is a new type of tyrosine kinase inhibitor that selectively inhibits various tyrosine kinases and has been successfully used to trea...

Lipid nanocapsules (LNCs) represent a stable, biocompatible and worthwhile drug delivery system, demonstrating significant potential as gene/drug delivery platforms for cancer therapy. Imatinib, a potent tyrosine kinase inhibitor, has revolutionized the therapy of malignancies resulting from abnormal tyrosine kinase activity. However, its Clinical effectiveness in cancer treatment is h...

Lipid nanocapsules (LNCs) represent a stable, biocompatible and worthwhile drug delivery system, demonstrating significant potential as gene/drug delivery platforms for cancer therapy. Imatinib, a potent tyrosine kinase inhibitor, has revolutionized the therapy of malignancies resulting from abnormal tyrosine kinase activity. However, its Clinical effectiveness in cancer treatment is h...

ژورنال: پیاورد سلامت 2019
Alizadeh Ghandfurosh, Nasrin , Chahardouli, Bahram , Ghadyaninejhad, Laya , Mohammadi, Saeed , Nikbakht, Mohsen, Rostami, Shahrbano , Yousefi, Peyman,

Background and Aim: Chronic myeloid leukemia(CML) is a clonal myeloproliferative disease, characterized by BCR/ABL translocation. Using tyrosine kinase inhibitors such as Imatinib, treatment for this disease has progressed remarkably. However, resistance to tyrosine kinase inhibitor is a major obstacle. Signal transducer and activator of transcription 3(STAT3) is an important transcription fact...

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