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تعداد نتایج: 193191  

ژورنال: :دوفصلنامه علمی پژوهشی تربیت اسلامی 2014
زهرا شعبانی

هدف این پژوهش تعیین مدل نوعدوستی خیِّرین و کشف روابط مشترک براساس تحلیل مسیر است. جامعه آماری آن تمام خیرین مدرسه ساز هستند که با روش نمونه گیری خوشه ای چند مرحله ای و براساس تعداد متغیرها و نمونه (15×22) و جدول کرجسی و مورگان، از میان آن ها 370 نفر به عنوان نمونه انتخاب شدند. برای اندازه گیری عوامل روان شناختی، اجتماعی و فرهنگی از سیزده آزمون شامل آزمون شخصیتی نئو، خوش بینی، خودکارآمدی عمومی، با...

Journal: :Sleep 2022

Abstract Introduction Circadian factors may contribute to sleep difficulties among chronic insomnia disorder (CID) patients who do not otherwise meet full criteria for a circadian rhythm sleep-wake disorder, particularly delayed and advanced phase disorders. Current nosology suggests that using preference measures can provide important diagnostic information aid in differential diagnosis. Howev...

Journal: :iranian journal of pediatric hematology and oncology 0
sima montazare lotfe elahi azam sadat hashemi shahid sadoughi university of medical sciences and health services, yazd, iran seid mostafa behjati department of pediatrics, hematology, oncology and genetics research center, shahid sadoughi university of medical scienسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) farideh zaolfaghari department of pediatrics, shahid sadoughi university of medical sciences and health services, yazd, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences) atefeh dehghani hematology, oncology and genetics research center, shahid sadoughi university of medical sciences and health services, y mahvash akhavane ghalibaf hematology, oncology and genetics research center, shahid sadoughi university of medical sciences and health services, yسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید صدوقی یزد (shahid sadooghi university of medical sciences)

abstract objective cardiac dysfunction is a major cause of death in patients with beta thalassemia. in these patients, repeated blood transfusion, ineffective erythropoiesis and increased gastrointestinal iron absorption lead to iron overload in the body and this induced heart failure. left ventricular ejection fraction was measured in major beta thalassemia (β-th) patients to detect the relati...

Journal: :iranian journal of pathology 2006
m.hossein ghaini t ghazanfari n fallah

objective: helicobacter pylori has a well-established role in the development of gastric cancer. in vitro studies reveal increased proliferation of the gastric mucosa in the presence of h. pylori infection. it has been also shown that production of some cytokines, such as interleukin-1 beta (il-1b) is increased in h. pylori infection. in addition, il-1b increases proliferation of gastric epithe...

Journal: :Materials 2023

Natural kaolinite was subjected to a successful exfoliation process into separated nanosheets (KNs), followed by hybridization with β-cyclodextrin biopolymer (β-CD), forming an advanced bio-nanocomposite (β-CD/KNs). The synthetic products were evaluated as enhanced delivery structures for oxaliplatin chemotherapy (OXAPN). of KNs β-CD polymer notably the loading capacity 355.3 mg/g (β-CD/KNs) co...

Journal: : 2022

Chi Weigela, thuộc họ Kim ngân (Caprifoliaceae) có vùng phân bố rộng trên thế giới, với hơn 200 loài đã được lai tạo phục vụ cho mục đích làm cảnh và dùng thuốc. W. florida “Jean’s Gold” là cây dạng bụi, trồng tại châu Âu do màu sắc hoa đẹp dễ phát triển. Từ cao chiết ethanol của phần rễ Florida Gold”, bằng các phương pháp ký khác nhau, kết hợp phổ hiện đại, nghiên cứu lập xác định cấu trúc 2 c...

Journal: :journal of agricultural science and technology 2014
m. sedaghati h. ezzatpanah m. mashhadi akbar boojar m. tajabadi ebrahimi

the presence of antibacterial activity in bovine β-lactoglobulin and in α-lactalbumin hydrolysates was investigated. the plasmin-digest of β-lactoglobulin (pdβ) and of α-lactalbumin (pdα) were fractionated, using reversed phase high performance liquid chromatography. the antibacterial activity of β-lactoglobulin, α-lactalbumin, nisin, plasmin, pdβ and pdα were in vitro tested against pathogenic...

Journal: :iranian journal of blood and cancer 0
sultan sadia irfan syed mohammad kaker jamal uddin zeeshan rozina kidwai asim

background: β-thalassemia is an autosomal hemoglobinopathy with inconsistent universal distribution. among patients with thalassemia diverse non-siderotic complications distinctly influence the attribute of life, including zinc deficiency due to varied etiologies. the objective of the present study was to determine zinc levels in patients with β-thalassemia major and its correlation with matern...

Journal: :international journal of hematology-oncology and stem cell research 0
majid farshdousti hagh division of laboratory hematology and blood banking, faculty of medicine, tabriz university of medical sciences, tabrez, iran ali dehghani fard department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran najmaldin saki research center of thalassemia and hemoglobinopathies, ahvaz jundishapur university of medical sciences, ahvaz, iran mohammad shahjahani department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran saied kaviani department of hematology and blood banking, faculty of medical sciences, tarbiat modares university,tehran, iran

hemoglobin f (hbf, α 2 γ 2 ) is a major contributor to the clinical heterogeneity and ameliorating agent observed in patients with the β-globin disorders including β-thalassemia and sickle cell disease (scd). during fetal life, hbf is the major hemoglobin but is largely substituted by adult hemoglobin (hba, α 2 β 2 ) following a globin expression switch after birth. increased γ-globin expressio...

Journal: :iranian biomedical journal 0
محمد حمید mohammad hamid فروزنده محجوبی frouzandeh mahjoubi محمدتقی اکبری mohammad taghi akbari حسین خان احمد hossein khanahmad فاطمه جمشیدی fatemeh jamshidi سیروس زینلی sirous zeinali مرتضی کریمی پور

background: in the previous study, we have shown that the presence of a allele at position -588 in aγ-globin gene was highly frequent and closely associated with fetal hemoglobin elevation among β-thalassemia intermedia patients. therefore, we decided to investigate whether this allele (a allele at -588) could result in an increase in aγ-globin gene expression to ameliorate the severity of the ...

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