نتایج جستجو برای: مدل سهبعدی خرد 3d ws

تعداد نتایج: 320501  

2015
Francesca Foti Stefano Sdoia Deny Menghini Laura Mandolesi Stefano Vicari Fabio Ferlazzo Laura Petrosini

Williams syndrome (WS) is associated with a distinct profile of relatively proficient skills within the verbal domain compared to the severe impairment of visuo-spatial processing. Abnormalities in executive functions and deficits in planning ability and spatial working memory have been described. However, to date little is known about the influence of executive function deficits on navigationa...

Journal: :Bioscience trends 2013
M Goto Y Ishikawa M Sugimoto Y Furuichi

As ~75% of the Werner syndrome (WS) patients recognized between 1904 and 2008 all over the world are of Japanese origin, the most case reports and clinical studies on WS has been published in Japanese journals. Thus, the detailed English-written clinical review on the recent WS case reports has been warranted. Although WS has been characterized by a variety of clinical manifestations mimicking ...

Journal: :Science 1996
C E Yu J Oshima Y H Fu E M Wijsman F Hisama R Alisch S Matthews J Nakura T Miki S Ouais G M Martin J Mulligan G D Schellenberg

Werner's syndrome (WS) is an inherited disease with clinical symptoms resembling premature aging. Early susceptibility to a number of major age-related diseases is a key feature of this disorder. The gene responsible for WS (known as WRN) was identified by positional cloning. The predicted protein is 1432 amino acids in length and shows significant similarity to DNA helicases. Four mutations in...

2010
R. Ng

Introduction: Williams syndrome (WS) is a neurogenetic disorder associated with a mild to moderate cognitive impairment and a hypersocial personality, most notably an unusually high tendency to approach and interact with strangers (Järvinen-Pasley et al., 2008). Within the WS phenotype, increased sociability is accompanied by an interesting profile of music processing. Reports of increased emot...

Journal: :Pediatric blood & cancer 2014
Nelli Vanhapiha Sakari Knuutila Kim Vettenranta Olli Lohi

Williams syndrome (WS) is a relatively rare multisystem neurodevelopmental disorder caused by a hemizygous deletion of contiguous genes on chromosome 7q11.23. Although WS does not predispose carriers to cancers, alterations of chromosome 7 are common in several human neoplasms. We report here a patient with WS and two different cancers, Burkitt lymphoma and Ewing sarcoma. Array-CGH analysis of ...

Journal: : 2022

در این پژوهش سعی می‌­شود مدلی برای شبیه‌­سازی چرخه عمر صنعت برق با استفاده از شبیه‌سازی عامل­بنیان ارائه شود، مدل، 5 عامل استخراج شد و شبیه­‌سازی به کمک نرم‌افزار Anylogic صورت پذیرفت. بهینه‌­سازی مدل چهار سناریو نظر خبرگان شد. سناریوی نخست، جذابیت نیروگاه گازی سیکل ترکیبی کاهش یافت بر دو دیگر افزوده نتیجه افزایش تولید آبی است که توجه کمبود منابع کشور به‌صرفه نیست. دوم ورود یک فناوری جدید میزان...

2005
Kyriakos Kritikos

1 Main Theme of Thesis Web Services (WSs) are modular, self-describing, loosely-coupled, platform and programming language-agnostic software applications that can be advertised , located and used across the Internet. They are viewed as one of the promising technologies that could help business entities to automate their operations on the web on a large scale by automatic discovery and consumpti...

2007
Motoki TAKAGI Masanobu SUGIMOTO

causing symptoms of premature ageing. In 1996, the Werner syndrome gene (WRN) responsible for WS was identified. The gene product, WRN, acts as a DNA helicase (WRN helicase) with exonuclease activity. WRN greatly participates in DNA metabolism by facilitating cellular processes, including DNA replication, recombination, repair, and transcription in cooperation with other cellular proteins. WRN ...

2013
Masahiro Hirai Yukako Muramatsu Seiji Mizuno Naoko Kurahashi Hirokazu Kurahashi Miho Nakamura

Williams syndrome (WS) is a genetic disorder caused by the partial deletion of chromosome 7. Individuals with WS have atypical cognitive abilities, such as hypersociability and compromised visuospatial cognition, although the mechanisms underlying these deficits, as well as the relationship between them, remain unclear. Here, we assessed performance in mental rotation (MR) and level 2 visual pe...

Journal: :The Plant cell 1996
J E Parker E B Holub L N Frost A Falk N D Gunn M J Daniels

The interaction between Arabidopsis and the biotrophic oomycete Peronospora parasitica (downy mildew) provides an attractive model pathosystem to identify molecular components of the host that are required for genotype-specific recognition of the parasite. These components are the so-called RPP genes (for resistance to P. parasitica). Mutational analysis of the ecotype Wassilewskija (Ws-0) reve...

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