نتایج جستجو برای: mohsenin of abd al

تعداد نتایج: 21252692  

ژورنال: مطالعات عرفانی 2014

Monastic commands of St. Benedict (480- 547 BC.) to his monk disciples and mystic commands of Khājeh ‘Abd Allah Ansāri (481-396 A.H.) with an emphasis on “The Rule of St. Benedict” and “Manāzil al-Sāyerin” is compared in this article. This comparison has done in a descriptive –analytic way, in order to reveal convergence between these two figures. Considering that impressive place of these two...

ژورنال: حدیث پژوهی 2009
فتاحی‌زاده, فتحیه,

Abd- o al- ‘Ala Moosavi Sabzevari is one of the famous contemporary narrators of traditions and scholars. He has precious works in different religious sciences. Amongst these works, Mawahib Al- Rahman fi Tafseer-i- Al- Quran has special status for in this book we can see Allamah’s views about traditions very well. Allamah believes that traditions interpret the Quran and for this reason he has r...

Journal: :Clinical & Experimental Hepatology 2023

AMA Gawish E, Abdelsameea Shaban Osheba I, Mohsen Y, El-Abd M. Epidermal growth factor rs4444903 polymorphism and risk of cholangiocarcinoma. A case control study. Clinical Experimental Hepatology. 2023;9(2):138-145. doi:10.5114/ceh.2023.128131. APA Gawish, E., Abdelsameea, Osheba, I., Mohsen, Y., & El-Abd, (2023). Hepatology, 9(2), 138-145. https://doi.org/10.5114/ceh.2023.128131 Chicago Eman ...

Journal: :Mechanisms of Development 2004
Tony DeFalco Stéphanie Le Bras Mark Van Doren

Sexual dimorphism requires the integration of positional information in the embryo with the sex determination pathway. Homeotic genes are a major source of positional information responsible for patterning along the anterior-posterior axis in embryonic development, and are likely to play a critical role in sexual dimorphism. Here, we investigate the role of homeotic genes in the sexually dimorp...

Journal: :Proteins 2012
Surinder M Singh Justine F Molas Narsimulu Kongari Swati Bandi Geoffrey S Armstrong Steve J Winder Krishna M G Mallela

Muscular dystrophy (MD) is the most common genetic lethal disorder in children. Mutations in dystrophin trigger the most common form of MD, Duchenne, and its allelic variant Becker MD. Utrophin is the closest homologue and has been shown to compensate for the loss of dystrophin in human disease animal models. However, the structural and functional similarities and differences between utrophin a...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید