Results 51 to 60 of about 5,737,630 (301)
The Shewanella oneidensis Fic enzyme SoFic targets the switch‐I region of EF‐Tu for AMPylation
FEBS Letters, EarlyView.Fic enzymes mediate diverse post‐translational modifications across all domains of life, including AMPylation. Prokaryotic EF‐Tu can be AMPylated and deAMPylated by the conserved Fic enzyme SoFic. Structural and biochemical approaches were used to characterize the effect of AMPylation on EF‐Tu, SoFic's enzymatic activities, and the enzyme‐target ...
Svenja Runge +6 more
wiley +1 more source
Cross-Validation, Support Vector Machines and Slice Models [PDF]
, 2001 We show how to implement the cross-validation technique used in ma- chine learning as a slice model. We describe the formulation in terms of support vector machines and extend the GAMS/DEA interface to allow for e cient solu- tions of linear, mixed ...
Ferris, Michael, Voelker, Meta
core
Mathematical Formulation for the Network Slice Design Problem
, 2020 In this document, we provide a Mixed Integer Linear Program to the Network Slice Design problem, which includes novel mapping decision points rising with new 5G radio and core function placement policies.
Secci, Stefano +3 more
core +3 more sources
Slicing Functional Programs by Calculation
, 2006 Program slicing is a well known family of techniques used to identify code fragments which depend on or are depended upon specific program entities. They are particularly useful in the areas of reverse engineering, program understanding, testing and software maintenance.
F. Rodrigues, Nuno, Barbosa, Luís S.
openaire +4 more sources
Slice Starlike Functions Over Quaternions [PDF]
The Journal of Geometric Analysis, 2018 25 ...
Xu, Zhenghua, Ren, Guangbin
openaire +3 more sources
Metastatic niche shaped by host factors influences disseminated cancer cell fate
FEBS Letters, EarlyView.Metastasis is shaped not only by cancer cells but also by the environments they encounter. This review explores how factors such as aging, diet, the microbiome, lifestyle, and environmental exposures remodel organ‐specific niches in the lung, liver, bone, and brain, influencing where metastatic cells survive, remain dormant, or grow, and ultimately ...
Gwennan Delyth Ward +2 more
wiley +1 more source
The complexity of central slice functions
Theoretical Computer Science, 1986 The k-slice of a Boolean function \(f(x_ 1,...,x_ n)\) is the function \(f_ k=(f\wedge T^ n_ k)\vee T^ n_{k+1}\), where \(T^ n_ k\) is the k-th threshold function. Berkowitz has shown that the nonmonotone combinational and monotone circuit complexities of any k-slice function differ by at most an additive term of O(n log\({}^ 2 n)\).
openaire +1 more source
The Bohr Theorem for slice regular functions [PDF]
Mathematische Nachrichten, 2012 AbstractIn this paper we prove the Bohr Theorem for slice regular functions. Following the historical path that led to the proof of the classical Bohr Theorem, we also extend the Borel‐Carathéodory Theorem to the new setting.
Della Rocchetta, Chiara +2 more
openaire +2 more sources
Molecular Oncology, EarlyView.Matched spatial transcriptomics and single‐nuclei RNA‐seq were generated for anaplastic and BRAFV600E papillary thyroid cancers revealing generic and tumor‐specific states occurring in cancer cells and in the tumor microenvironment. In this context, cancer dedifferentiation mirrored organoid maturation through ordered thyroid marker gain/loss ...
Adrien Tourneur +11 more
wiley +1 more source
Variation of mean and maximum esophageal motion as a function of CT slice number.
, 2014 Variation of mean and maximum esophageal motion as a function of CT slice number.
Tinsu Pan (207479) +3 more
core +1 more source