نتایج جستجو برای: مدل محاسبه تلفات sma
تعداد نتایج: 183767 فیلتر نتایج به سال:
linear low density polyethylene (lldpe) was blended with esterified styrene-maleic anhydride (esma) and its physical and mechanical properties were studied. styrene-maleic anhydride (sma) copolymer was synthesized by precipitation reaction. then, sma was esterified by 1-decanol in methylethyl ketone solvent. from the ftir spectrum of esma it is evident that the corresponding peaks of anhydride ...
نیتروژن یکی از نهاده‌های کلیدی در کشاورزی است که بخش قابل توجهی از آن تلف شده و باعث آلودگی محیط‌زیست می‌شود. در این تحقیق با کمک مدل SUNDIAL به کمی‌سازی چرخه نیتروژن و تلفات آن در سیستمهای مختلف تولید چغندرقند در شرق ایران پرداخته شد. بهاین منظور داده‌های مربوط به تولید چغندرقند در سه سیستم تولید سنتی، نیمه‌مکانیزه و مکانیزه در 26 منطقه از 10 ناحیه جغرافیایی در خراسان (استان‌های خراسان شمالی...
Expression of alpha-smooth muscle actin (alpha-SMA) defines the phenotype of activated (myofibroblastic) hepatic stellate cells. These cells, but not quiescent stellate cells, have a high level of alpha-SMA and c-Myb expression, as well as increased c-Myb-binding activities to the proximal alpha-SMA E box. Therefore, we analyzed the role of c-Myb in alpha-SMA transcription and stellate cell act...
Spinal muscular atrophy (SMA) is an autosomal recessive disorder, which is the leading genetic cause of infantile death. SMA is the most common inherited motor neuron disease and occurs in approximately 1:6000 live births. The gene responsible for SMA is called Survival Motor Neuron-1 (SMN1). Interestingly, a human-specific copy gene is present on the same region of chromosome 5q, called SMN2. ...
The autosomal recessive neurodegenerative disease spinal muscular atrophy (SMA) results from low levels of survival motor neuron (SMN) protein; however, it is unclear how reduced SMN promotes SMA development. Here, we determined that ubiquitin-dependent pathways regulate neuromuscular pathology in SMA. Using mouse models of SMA, we observed widespread perturbations in ubiquitin homeostasis, inc...
Most patients with spinal muscular atrophy (SMA) have been reported to show homozygous deletion of the gene responsible for SMA, SMN1. However, whether SMA patients homozygous for the SMN1 deletion exist in Southeast Asian countries, including Vietnam, remains to be determined, because molecular genetic analyses of SMA patients from these countries have not been reported. In this preliminary st...
دراین مطالعه، رفتار لرزه¬ای سیستم¬های فولادی مجهز به مهاربندهای شورن که با یک عضو پیوند قائم به تیر قاب متصل شده اند، مورد بررسی قرار گرفته است. برای صحت سنجی مدل ساخته شده نیز، پاسخ مدل با مدل آزمایشگاهی دکتر زهرایی مقایسه شده است. در این تحقیق، عضو پیوند از جنس آلیاژهای حافظه دار شکلی(sma) می باشد. به همین منظور، ابتدا قاب¬های مهاربندی 3 و 6 و 9 و12 طبقه به صورت دوبعدی، با دهانه¬های 3، 5/4 و ...
Human fibrotic bone marrow (BM) stroma has been shown to contain alpha-smooth muscle actin (alpha-SMA)-positive cells. These closely resemble myofibroblasts that were described in other fibrotic tissues. We studied the expression of alpha-SMA in a series of murine BM-derived stromal cell lines to investigate the cellular origin and functional significance of myofibroblast-like cells in hematopo...
The ability to assess temporal structure is crucial in order to adapt to an ever-changing environment. Increasing evidence suggests that the supplementary motor area (SMA) is involved in both sensory and sensorimotor processing of temporal structure. However, it is not entirely clear whether the structural differentiation of the SMA translates into functional specialization, and how the SMA rel...
Spinal muscular atrophy (SMA) is a neuromuscular disorder characterized by motor neuron degeneration, although defects in multiple cell types and tissues have also been implicated. Three independent laboratories recently identified immune organ defects in SMA. We therefore propose a novel pathogenic mechanism contributory to SMA, resulting in higher susceptibility to infection and exacerbated d...
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