نتایج جستجو برای: myh9 gene

تعداد نتایج: 1141526  

Journal: :Bratislavske lekarske listy 2013
M Gresikova

This paper reviews the most common causes of thrombocytopenia in the newborn. It mentions few classification schemes that clearly characterize the most common causes, diagnosis and treatment approaches for neonatal thrombocytopenia. Particular attention is paid to inborn macrothrombocytopenia without congenital anomalies. They represent a rare group of diseases, often captured randomly or durin...

2013
Chen Yu Li Xu Lii-fang Chen Ying-jie Guan Minsoo Kim Walter L. Biffl Y. Eugene Chin

CONTEXT Neutrophils are the primary effector cells in the pathogenesis of transfusion-related acute lung injury or multiple organ failure after blood transfusion. OBJECTIVE We aimed to investigate the effect of fresh (1 day preparation) and aged (42 day preparation) PRBC-derived plasma on neutrophil morphology, migration and phagocytosis. MATERIALS AND METHODS We evaluated the production of...

2007
Jean-Pierre Cazenave Francois Lanza Radek Skoda Christelle Nonne Josiane Weber Ralph Tiedt Marie-Pierre Gratacap Sonia Severin Catherine Leon Anita Eckly Beatrice Hechler Boris Aleil Monique Freund Catherine Ravanat Béatrice Hechler Marie Jourdain François Lanza Christian Gachet

Mutations in the MYH9 gene encoding the non-muscle myosin heavy chain-IIA result in bleeding disorders characterized by a macrothrombocytopenia. To understand the role of myosin in normal platelet functions and in pathology, we generated mice with disruption of MYH9 in megakaryocytes. MYH9Δ mice displayed macrothrombocytopenia with a strong increase in bleeding time and absence of clot retracti...

Journal: :Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2016
Jessica Cooke Bailey Sarah Wilson Kristin Brown-Gentry Robert J. Goodloe Dana C. Crawford

Kidney disease is a well-known health disparity in the United States where African Americans are affected at higher rates compared with other groups such as European Americans and Mexican Americans. Common genetic variants in the myosin, heavy chain 9, non-muscle (MYH9) gene were initially identified as associated with non-diabetic end-stage renal disease in African Americans, and it is now und...

Journal: :Seminars in Thrombosis and Hemostasis 2009

Journal: :The Journal of Experimental Medicine 2008
Nicole A. Morin Patrick W. Oakes Young-Min Hyun Dooyoung Lee Y. Eugene Chin Michael R. King Timothy A. Springer Motomu Shimaoka Jay X. Tang Jonathan S. Reichner Minsoo Kim

Precise spatial and temporal regulation of cell adhesion and de-adhesion is critical for dynamic lymphocyte migration. Although a great deal of information has been learned about integrin lymphocyte function-associated antigen (LFA)-1 adhesion, the mechanism that regulates efficient LFA-1 de-adhesion from intercellular adhesion molecule (ICAM)-1 during T lymphocyte migration is unknown. Here, w...

Journal: :Blood 2007
Catherine Léon Anita Eckly Béatrice Hechler Boris Aleil Monique Freund Catherine Ravanat Marie Jourdain Christelle Nonne Josiane Weber Ralph Tiedt Marie-Pierre Gratacap Sonia Severin Jean-Pierre Cazenave François Lanza Radek Skoda Christian Gachet

Mutations in the MYH9 gene encoding the nonmuscle myosin heavy chain IIA result in bleeding disorders characterized by a macrothrombocytopenia. To understand the role of myosin in normal platelet functions and in pathology, we generated mice with disruption of MYH9 in megakaryocytes. MYH9Delta mice displayed macrothrombocytopenia with a strong increase in bleeding time and absence of clot retra...

ژورنال: :فصلنامه علوم پزشکی دانشگاه آزاد اسلامی واحد پزشکی تهران 0
پوپک بهزاد poopak b faculty of medicine, islamic azad university, tehran medical unitدانشکده پزشکی، دانشگاه آزاد اسلامی، واحد پزشکی تهران یحیوی سیدحسین yahyavi sh faculty of medicine, islamic azad university, tehran medical unitدانشکده پزشکی، دانشگاه آزاد اسلامی، واحد پزشکی تهران حق نژاددوشانلو فریبا haghnejad doshanlo f faculty of medicine, islamic azad university, tehran medical unitدانشکده پزشکی، دانشگاه آزاد اسلامی، واحد پزشکی تهران رضوانی حمید rezvani h departmen t of hematology-oncology, taleghani hospital, shaheed beheshti university of medical sciencesبخش هماتولوژی، بیمارستان آیت ا... طالقانی، دانشگاه علوم پزشکی شهید بهشتی مارتیگتی جان martignetti j departments of human genetics , mount sinai school of medicine, new york, usaگروه ژنتیک انسانی، دانشکده پزشکی mount siani، نیویورک، آمریکا دیفئو آنالیزا difeo a departments of human genetics , mount sinai school of medicine, new york, usaگروه ژنتیک انسانی، دانشکده پزشکی mount siani، نیویورک، آمریکا خسروی پور گلاره

آنومالی may-hegglin یک اختلال نادر اتوزومال غالب است که با تریاد کاهش پلاکت، پلاکت های بزرگ و اجسام شبیه دوهل در گرانولوسیتها مشخص می گردد. .هدف از این بررسی گزارش اولین مورد نارسایی در ایران و تعیین نوع موتاسیون مربوطه است. در این بررسی آزمایش cbc و گستره خون محیطی دو بیمار از یک خانواده (پدر و پسر) که به ترتیب 51 و 15 ساله بودند با دو ضدانعقاد edta و سیترات تری سدیم با شمارنده خودکار و بررسی ...

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