Quantitative Analysis of Errors in On-Wafer S-Parameter De-embedding Techniques for High Frequency Device Modeling

Author(s):  
Rob Groves ◽  
Jing Wang ◽  
Lawrence Wagner ◽  
Ava Wan
2018 ◽  
Vol 746 ◽  
pp. 532-539 ◽  
Author(s):  
Rohit Sharma ◽  
Prashant Thakur ◽  
Manoj Kumar ◽  
Pankaj Sharma ◽  
Vineet Sharma

2007 ◽  
Vol 305 (2) ◽  
pp. 403-407 ◽  
Author(s):  
J.A. Freitas ◽  
J.G. Tischler ◽  
J.-H. Kim ◽  
Y. Kumagai ◽  
A. Koukitu

Author(s):  
Potereau Manuel ◽  
Sebastien Fregonese ◽  
Arnaud Curutchet ◽  
Peter Baureis ◽  
Thomas Zimmer

2020 ◽  
Vol 27 (3) ◽  
pp. 280-306
Author(s):  
Elena Martínez Caro ◽  
Jorge Arús-Hita

Abstract Light Verb Constructions (LVCs) have received widespread attention. Research on these constructions, however, has for the most part focused exclusively on their syntactic and lexical-semantic properties. Additionally, studies devoted to specific LVCs tend to neglect the phrasal-semantic and pragmatic variation brought about by the combination of a light verb with different nominal complements. This paper tries to fill those gaps by means of a quantitative and qualitative corpus-based study of Light give Constructions (LgiveCs). The quantitative analysis investigates frequencies of LgiveCs in British English and compares them across spoken and written (fiction) discourse, which reveals a high frequency of this construction in speech, especially in combinations of give with a ring, a kiss and an answer. When these combinations are excluded, LgiveCs are significantly more frequent in writing. In a complementary qualitative approach, we highlight the structural and discursive features of the construction and attempt to explore the factors that motivate the frequent use of the LgiveC in British English.


2014 ◽  
Vol 25 (22) ◽  
pp. 3569-3580 ◽  
Author(s):  
Kyoko Chiba ◽  
Masahiko Araseki ◽  
Keisuke Nozawa ◽  
Keiko Furukori ◽  
Yoichi Araki ◽  
...  

Alzheimer's β-amyloid precursor protein (APP) associates with kinesin-1 via JNK-interacting protein 1 (JIP1); however, the role of JIP1 in APP transport by kinesin-1 in neurons remains unclear. We performed a quantitative analysis to understand the role of JIP1 in APP axonal transport. In JIP1-deficient neurons, we find that both the fast velocity (∼2.7 μm/s) and high frequency (66%) of anterograde transport of APP cargo are impaired to a reduced velocity (∼1.83 μm/s) and a lower frequency (45%). We identified two novel elements linked to JIP1 function, located in the central region of JIP1b, that interact with the coiled-coil domain of kinesin light chain 1 (KLC1), in addition to the conventional interaction of the JIP1b 11–amino acid C-terminal (C11) region with the tetratricopeptide repeat of KLC1. High frequency of APP anterograde transport is dependent on one of the novel elements in JIP1b. Fast velocity of APP cargo transport requires the C11 domain, which is regulated by the second novel region of JIP1b. Furthermore, efficient APP axonal transport is not influenced by phosphorylation of APP at Thr-668, a site known to be phosphorylated by JNK. Our quantitative analysis indicates that enhanced fast-velocity and efficient high-frequency APP anterograde transport observed in neurons are mediated by novel roles of JIP1b.


2019 ◽  
Vol 11 (6) ◽  
pp. 445-460
Author(s):  
Frank Schwierz

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