A Sextuple Cross-Coupled Dual-Interlocked-Storage-Cell based Multiple-Node-Upset Self-Recoverable Latch

Author(s):  
Aibin Yan ◽  
Kuikui Qian ◽  
Jie Cui ◽  
Ningning Cui ◽  
Tianming Ni ◽  
...  
Keyword(s):  
2004 ◽  
Vol 39 (11) ◽  
pp. 1985-1996 ◽  
Author(s):  
M. O'Halloran ◽  
R. Sarpeshkar
Keyword(s):  

2015 ◽  
Vol 24 (5) ◽  
pp. 614-619 ◽  
Author(s):  
HyungKuk Ju ◽  
Jaeyoung Lee

1998 ◽  
Vol 72 (12) ◽  
pp. 1513-1515 ◽  
Author(s):  
Y. Chong ◽  
B. Ruck ◽  
R. Dittmann ◽  
C. Horstmann ◽  
A. Engelhardt ◽  
...  

2014 ◽  
Author(s):  
Daniel S Himmelstein ◽  
Sergio E Baranzini

The first decade of Genome Wide Association Studies (GWAS) has uncovered a wealth of disease-associated variants. Two important derivations will be the translation of this information into a multiscale understanding of pathogenic variants, and leveraging existing data to increase the power of existing and future studies through prioritization. We explore edge prediction on heterogeneous networks—graphs with multiple node and edge types—for accomplishing both tasks. First we constructed a network with 18 node types—genes, diseases, tissues, pathophysiologies, and 14 MSigDB (molecular signatures database)collections—and 19 edge types from high-throughput publicly-available resources. From this network composed of 40,343 nodes and 1,608,168 edges, we extracted features that describe the topology between specific genes and diseases. Next, we trained a model from GWAS associations and predicted the probability of association between each protein-coding gene and each of 29 well-studied complex diseases. The model, which achieved 132-fold enrichment in precision at 10% recall, outperformed any individual domain, highlighting the benefit of integrative approaches. We identified pleiotropy, transcriptional signatures of perturbations, pathways, and protein interactions as fundamental mechanisms explaining pathogenesis. Our method successfully predicted the results (with AUROC = 0.79) from a withheld multiple sclerosis (MS) GWAS despite starting with only 13 previously associated genes. Finally, we combined our network predictions with statistical evidence of association to propose four novel MS genes, three of which (JAK2, REL, RUNX3) validated on the masked GWAS. Furthermore, our predictions provide biological support highlighting REL as the causal gene within its gene-rich locus. Users can browse all predictions online (http://het.io). Heterogeneous network edge prediction effectively prioritized genetic associations and provides a powerful new approach for data integration across multiple domains.


2011 ◽  
Vol 25 (2) ◽  
pp. 262-267 ◽  
Author(s):  
Sunny L. Bottoms ◽  
Eric P. Webster ◽  
Justin B. Hensley ◽  
David C. Blouin

Studies were conducted to evaluate growth and reproductive capabilities of creeping rivergrass in response to rice herbicide programs. Creeping rivergrass grown from single-node stolon segments, multiple-node stolon segments, and rhizomes was treated with various herbicides to evaluate activity on subsequent growth and viability of nodes produced from treated plants. Comparison with the nontreated, cyhalofop, glyphosate, and imazethapyr reduced creeping rivergrass fresh weight by more than 84 to 96%. Glyphosate reduced sprouting of nodes from treated plants 93% compared with nontreated plants. Activity from these herbicides may decrease when applied to plants grown from rhizomes versus rhizome clusters. Plants treated with cyhalofop, glyphosate, and imazethapyr had reduced fresh weight of 36 to 46% when plants were grown from a rhizome cluster, and 69 to 90% when plants were grown from a single rhizome segment, compared with nontreated. Cyhalofop and glyphosate reduced node sprouting by 81 to 98% of nontreated, regardless of parent structure.


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