نتایج جستجو برای: gleevec

تعداد نتایج: 513  

Journal: :Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2011
Xabier Altuna Jay Patrick Lopez Michael Andrew Yu Maria Jesus Arandazi Jeffrey P Harris Jessica Wang-Rodriguez Yi An Robert Dobrow Joni K Doherty Weg M Ongkeko

HYPOTHESIS To determine the expression of the tyrosine kinases platelet-derived growth factor receptor (PDGFR) and c-Kit in vestibular schwannoma (VS) and to determine the potential role of imatinib mesylate (Gleevec) in regulating the growth and cell death of this tumor. BACKGROUND Protein tyrosine kinases are transmembrane tyrosine kinase receptors that transduce signals from inside and out...

Journal: :American journal of clinical pathology 2002
Jay L Hess

Gleevec (STI571, imatinib mesylate) is the first major success in the development of targeted anticancer therapies. This oral drug was designed “from the ground up” as an inhibitor of the ABL tyrosine kinase, which becomes constitutively expressed and activated as a result of its fusion to BCR in chronic myelogenous leukemia (CML). Early clinical studies were so promising that the US Food and D...

Journal: :Cancer research 2009
Joydeep Mukherjee Deepak Kamnasaran Anand Balasubramaniam Ivan Radovanovic Gelareh Zadeh Tim-Rasmus Kiehl Abhijit Guha

Schwannomas, although benign, can be fatal or give rise to significant morbidity due to an unpredictable growth rate. They can reoccur after surgery or radiation, current treatments each with significant inherent risks. These risks are further amplified in neurofibromatosis type 2 (NF2), a germ line predisposition syndrome characterized by multiple schwannomas, underlying the need for biologica...

Journal: :In vivo 2005
Xiang Li Na Qiao Denis Reynaud Mohamed Abdelhaleem Cecil R Pace-Asciak

PBT-3 is one of a family of stable chemical analogs of the hepoxilins, products derived from arachidonic acid. We previously showed that PBT-3 caused apoptosis in the chronic myelogenous leukemia (CML) cell line K-562 in vitro (Anti-cancer Res 23: 3617-3622, 2003). It was as effective as Gleevec, a novel agent that blocks tyrosine kinase activity during treatment of CML. We describe, herein, th...

Journal: :Journal of Infectious Diseases 2015

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
William J Netzer Karima Bettayeb Subhash C Sinha Marc Flajolet Paul Greengard Victor Bustos

Neurotoxic amyloid-β peptides (Aβ) are major drivers of Alzheimer's disease (AD) and are formed by sequential cleavage of the amyloid precursor protein (APP) by β-secretase (BACE) and γ-secretase. Our previous study showed that the anticancer drug Gleevec lowers Aβ levels through indirect inhibition of γ-secretase activity. Here we report that Gleevec also achieves its Aβ-lowering effects throu...

Journal: :JNCI Journal of the National Cancer Institute 2012

Journal: :The Keio journal of medicine 2010
Brian Druker

ژورنال: :فصلنامه پژوهشی خون 0
غلامرضا نویدی gh.r. navidi کارشناس ارشد هماتولوژی- آزمایشگاه بیمارستان دی، خیابان ولیعصر، نبش خیابان شهید عباسپور دکتر حوری رضوان h. rezvan استاد مرکز تحقیقات سازمان انتقال خون ایران دکتر سیامک سمیعی s. samiei آزمایشگاه بیمارستان دیسازمان اصلی تایید شده: سازمان انتقال خون ایران (blood transfusion research center) رامین تقی زاده r. naghizadeh دکتر عباس حاجی فتحعلی a. hajifathali دانشگاه علوم پزشکی شهید بهشتی دکتر فرامرز سلیمانلو f. soleimanlo آزمایشگاه بیمارستان دی دکتر رهی طاهرنیا

چکید ه سابقه و هدف   لوسمی میلوئید مزمن (cml) بیماری است که به دلیل موتاسیون اختصاصی در سلول های بنیادی چند قوه ای مغزاستخوان ایجاد می شود. وجود کروموزوم فیلادلفیا و عوامل ژنتیک در این بیماری برای نخستین بار در سال 1973 گزارش گردید. امروزه وجود محصول ژن اتصال یافته bcr-abl که دارای فعالیت غیرطبیعی تیروزین کینازی است و موجب بی نظمی در تکثیر سلول ها می شود در این بیماری ثابت شده است. در این بررسی...

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