شعراء أندلسیون مغمورون" غرناطة نموذجاً " ( 635 – 897 هـ)
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چکیده
منابع مشابه
#635 - Parkinson's
Parkinson's begins when a certain class of brain cells begins to die, cells that produce a chemical called dopamine, which your body needs. Dopamine serves as a chemical messenger helping to control muscle activities. Loss of dopamine leads to the progressive loss of muscular control, giving rise to a variety of symptoms: stiffness, tremor, slow movement, difficulty with balance, difficulty wal...
متن کاملDmd062935 889..897
We previously reported upregulation of UGT2B15 by 17b-estradiol in breast cancer MCF7 cells via binding of the estrogen receptor a (ERa) to an estrogen response unit (ERU) in the proximal UGT2B15 promoter. In the present study, we show that this ERa-mediated upregulation was significantly reduced by two ER antagonists (fulvestrant and raloxifene) but was not affected by a third ER antagonist, 4...
متن کاملDmd050054 897..905
Lipophilic (logP > 1) and amphiphilic drugs (also known as cationic amphiphilic drugs) with ionizable amines (pKa > 6) can accumulate in lysosomes, a process known as lysosomal trapping. This process contributes to presystemic extraction by lysosome-rich organs (such as liver and lung), which, together with the binding of lipophilic amines to phospholipids, contributes to the large volume of di...
متن کاملMss20666 886..897
Habitual physical activity reduces coronary heart disease events, but vigorous activity can also acutely and transiently increase the risk of sudden cardiac death and acute myocardial infarction in susceptible persons. This scientific statement discusses the potential cardiovascular complications of exercise, their pathological substrate, and their incidence and suggests strategies to reduce th...
متن کاملDmm019430 635..641
Nemaline myopathy (NM) is one of the most common forms of congenital myopathy, and affects either fast myofibers, slow myofibers, or both. However, an animal model for congenital myopathy with fast-myofiber-specific atrophy is not available. Furthermore, mutations in the leiomodin-3 (LMOD3) gene have recently been identified in a group of individuals with NM. However, it is not clear how loss o...
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ژورنال
عنوان ژورنال: مجلة الآداب والعلوم الإنسانیة
سال: 2018
ISSN: 1110-4341
DOI: 10.21608/fjhj.2018.93480