نتایج جستجو برای: روش sma

تعداد نتایج: 388424  

2009
Monica STAVARACHI Mihai TOMA Pompilia APOSTOL Danut CIMPONERIU Irina RADU Nicolae Mircea PANDURU Niculina BUTOIANU Lucian GAVRILA

Spinal muscular atrophy (SMA) is a frequent neuromuscular disorder caused by motoneuronal apoptosis, as a result of SMN (Survival Motor Neuron) protein deficiency. Although the SMA determining gene was identified, the molecular mechanism of the disease is not clearly understood, due to the heterogeneity of clinical manifestations. Trying to complete the molecular describing SMA picture, by iden...

Journal: :Circulation research 2008
Yuefeng Tang Sumithra Urs Lucy Liaw

Notch signaling regulates smooth muscle cell phenotype and is critical for vascular development. One Notch target is smooth muscle alpha-actin (SMA), a differentiated smooth muscle cell marker. The Notch intracellular domain (NotchICD) forms a complex with CBF-1 (C-promoter-binding factor-1) and directly induces SMA expression. Using primary human smooth muscle cells, we show that expression of...

Journal: :Neurosurgery 2002
Denys Fontaine Laurent Capelle Hugues Duffau

OBJECTIVE This study, which aimed to confirm or invalidate the somatotopic organization of the supplementary motor area (SMA), correlates the pattern of clinical symptoms observed after SMA removal with the extent of resection. METHODS Eleven patients with medial precentral glioma underwent partial or complete tumoral resection of the SMA. Seven patients underwent preoperative functional magn...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
J G Chang H M Hsieh-Li Y J Jong N M Wang C H Tsai H Li

Spinal muscular atrophy (SMA) is an autosomal recessive disease characterized by degeneration of the anterior horn cells of the spinal cord, leading to muscular paralysis with muscular atrophy. No effective treatment of this disorder is presently available. Studies of the correlation between disease severity and the amount of survival motor neuron (SMN) protein have shown an inverse relationshi...

2014
Miho Maeda Ashlee W. Harris Brewster F. Kingham Casey J. Lumpkin Lynn M. Opdenaker Suzanne M. McCahan Wenlan Wang Matthew E. R. Butchbach

Proximal spinal muscular atrophy (SMA) is an early onset, autosomal recessive motor neuron disease caused by loss of or mutation in SMN1 (survival motor neuron 1). Despite understanding the genetic basis underlying this disease, it is still not known why motor neurons (MNs) are selectively affected by the loss of the ubiquitously expressed SMN protein. Using a mouse embryonic stem cell (mESC) m...

2011
Vicenç Torra Antonio Carlota Auguet Guillem Carreras Fabio Casciati Francisco C. Lovey Patrick Terriault

Guaranteeing the use of Shape Memory Alloys (SMA) in mitigation of extreme load effects requires a deep study of the SMA behavior according to the specific requirements of the applications in damping. The damper was defined according the expected requirements (length of SMA and number of SMA wires). It is applied to two types of alloys (CuAlBe and NiTi) in the diagonals of a realistic steel por...

2000
Bernd Schneider

Since the 1960s, Stone Mastic Asphalt (SMA) pavement surfaces have been used successfully in Germany on heavily trafficked roads. Because of its excellent performance characteristics, road authorities in Germany as well as major European Countries quickly adopted SMA as a standard wearing course. As a consequence of an asphalt study tour in Europe of an American delegation in 1990, SMA test sec...

2011

Superelastic Shape Memory Alloy (SMA) is accepted when it used as connection in steel structures. The seismic behaviour of steel frames with SMA is being assessed in this study. Three eightstorey steel frames with different SMA systems are suggested, the first one of which is braced with diagonal bracing system, the second one is braced with nee bracing system while the last one is which the SM...

ژورنال: بینا 2008
آزادبخت, فرنوش, اسدی‌آملی, فهیمه, اکبرزاده جهرمی, مژگان, جهانزاد, عیسی, صادقی‌طاری, علی,

هدف: تعیین منشا میوفیبروبلاستی سودوتومورهای التهابی (IPT: inflammatory pseudotumor) ایدیوپاتیک اربیت با بررسی نشانگرهای ایمونوهیستوشیمی موجود در یاخته‌های دوکی‌شکل این تومورها. روش پژوهش: در این مطالـعه، نمونه‌های آسیب‌شناسی 32 بیـمار با تشخیص IPT ایـدیـوپاتیـک اربیت از نظر نشانگرهای SMA (smooth muscle actin)، ویمنتین (Vimentin)، دسمین (Desmin) و ALK (anaplastic lymphokinase) تحت بررسی ایمو...

Journal: : 2022

هدف: هدف از این پژوهش بررسی واسطه‌­ای راهبردهای سازش نایافته تنظیم شناختی هیجان در رابطه باورهای فراشناختی با اضطراب امتحان بود. روش: روش حاضر توصیفی و نوع همبستگی جامعه آماری را کلیه دانش‌­آموزان پسر دوره دوم متوسطه شهر تهران سال تحصیلی 1401-1400 تشکیل دادند که تعداد 456 نفر به نمونه‏‌گیری دسترس انتخاب شرکت کردند. ابزارها شامل سیاهه ابوالقاسمی همکاران (1375)، پرسشنامه باکو دیگران (2009)، فرم ک...

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