نتایج جستجو برای: heterojunction gaa nw tfet

تعداد نتایج: 18213  

2016
G. SANKARAIAH CH. SATHYANARAYANA

--In today’s technological environment, there is a huge demand for devices with low power and low cost storage space. Memories with low power are driving the entire VLSI industry as most of the devices work on remote power supply. Demand of low power becomes the key of VLSI designs rather than high speed, particularly in embedded SRAM’s and caches. The tunneling field effect transistor uses the...

2014
Mingxing Feng Juan Zhao Jiwen Zhang Zhaonong Hu Wenjun Wu

Periplocoside NW (PSNW) is a novel insecticidal compound isolated from the root bark of Periploca sepium Bunge and has potent stomach toxicity against some insect pests. Previous studies showed that the Mythimna separata larva is sensitive to PSNW, but the Agrotis ispilon larva is insensitive. In this study, preliminary target localization on the midgut of M. separata larvae was conducted via a...

2010
Christian Philipp Sandow

Over the last decades, the continuous down-scaling of metal-oxide-semiconductor field-effect transistors (MOSFETs) enabled faster and more complex chips while at the same time the space and power-consumption was kept under control. However, in the future, the further reduction of the power consumption per unit area will be restricted by a fundamental limit of the inverse subthreshold swing of M...

2015
Irina G. Adonina Nikolay P. Goncharov Ekaterina D. Badaeva Ekaterina M. Sergeeva Nadezhda V. Petrash Elena A. Salina

Although the wheat A genomes have been intensively studied over past decades, many questions concerning the mechanisms of their divergence and evolution still remain unsolved. In the present study we performed comparative analysis of the A genome chromosomes in diploid (Triticum urartu Tumanian ex Gandilyan, 1972, Triticum boeoticum Boissier, 1874 and Triticum monococcum Linnaeus, 1753) and pol...

2010
Miriam Mancuso Mimi C. Sammarco Ed Grabczyk

BACKGROUND Expansion of an unstable GAA*TTC repeat in the first intron of the FXN gene causes Friedreich ataxia by reducing frataxin expression. Structure formation by the repeat has been implicated in both frataxin repression and GAA*TTC instability. The GAA*TTC sequence is capable of adopting multiple non-B DNA structures including Y*R*Y and R*R*Y triplexes. Lower pH promotes the formation of...

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2014
Benjamin L Farah Lauran Madden Songtao Li Sierra Nance Andrew Bird Nenad Bursac Paul M Yen Sarah P Young Dwight D Koeberl

Enzyme or gene replacement therapy with acid α-glucosidase (GAA) has achieved only partial efficacy in Pompe disease. We evaluated the effect of adjunctive clenbuterol treatment on cation-independent mannose-6-phosphate receptor (CI-MPR)-mediated uptake and intracellular trafficking of GAA during muscle-specific GAA expression with an adeno-associated virus (AAV) vector in GAA-knockout (KO) mic...

1999
Shin'ichi Wakabayashi Tetsushi Koide Naoyoshi Toshine Mutsuaki Goto Yoshikatsu Nakayama Koichi Hatta

This paper describes an LSI implementation of a genetic algorithm (GA), called the Genetic Algorithm Accelerator (GAA) chip. The GAA chip is an LSI implementation of a GA, in which two types of crossover operators are supported, and the operator to be actually used in the algorithm is not fixed in advance, but dynamically selected for each pair of chromosomes in the algorithm execution. The GAA...

2017
Erik van der Wal Atze J. Bergsma Joon M. Pijnenburg Ans T. van der Ploeg W.W.M. Pim Pijnappel

The most common variant causing Pompe disease is c.-32-13T>G (IVS1) in the acid α-glucosidase (GAA) gene, which weakens the splice acceptor of GAA exon 2 and induces partial and complete exon 2 skipping. It also allows a low level of leaky wild-type splicing, leading to a childhood/adult phenotype. We hypothesized that cis-acting splicing motifs may exist that could be blocked using antisense o...

Journal: :Molecular therapy : the journal of the American Society of Gene Therapy 2010
Baodong Sun Michael D Kulis Sarah P Young Amy C Hobeika Songtao Li Andrew Bird Haoyue Zhang Yifan Li Timothy M Clay Wesley Burks Priya S Kishnani Dwight D Koeberl

Infantile Pompe disease progresses to a lethal cardiomyopathy in absence of effective treatment. Enzyme-replacement therapy (ERT) with recombinant human acid alpha-glucosidase (rhGAA) has been effective in most patients with Pompe disease, but efficacy was reduced by high-titer antibody responses. Immunomodulatory gene therapy with a low dose adeno-associated virus (AAV) vector (2 x 10(10) part...

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