Results 71 to 80 of about 156,468 (326)

Young's integral inequality with upper and lower bounds

open access: yesElectronic Journal of Differential Equations, 2011
Young's integral inequality is reformulated with upper and lower bounds for the remainder. The new inequalities improve Young's integral inequality on all time scales, such that the case where equality holds becomes particularly transparent in this ...
Douglas R. Anderson   +2 more
doaj  

On the Achievable Stabilization Delay Margin for Linear Plants with Time-Varying Delays

open access: yesMathematics, 2017
The paper contributes to stabilization problems of linear systems subject to time-varying delays. Drawing upon small gain criteria and robust analysis techniques, upper and lower bounds on the largest allowable time-varying delay are developed by using ...
Jing Zhu
doaj   +1 more source

Circulating microRNA signatures of cachexia and cancer in Canis familiaris as a comparative oncology model for human disease

open access: yesMolecular Oncology, EarlyView.
Circulating microRNAs as biomarkers of cachexia and sex‐specific cancer in senior dogs. In 25 client‐owned dogs, four circulating miRNAs (miR‐15a, miR‐15b, miR‐16, miR‐140) were downregulated in cachexia, with miR‐16 the strongest individual biomarker (AUC = 0.899).
Soon‐Seok Park   +6 more
wiley   +1 more source

Upper and Lower Bounds on Black-Box Steganography [PDF]

open access: yesJournal of Cryptology, 2005
We study the limitations of steganography when the sender is not using any properties of the underlying channel beyond its entropy and the ability to sample from it. On the negative side, we show that the number of samples the sender must obtain from the channel is exponential in the rate of the stegosystem.
Nenad Dedic   +3 more
openaire   +6 more sources

Translating whole‐genome doubling into precision medicine in cancer

open access: yesMolecular Oncology, EarlyView.
Whole‐genome doubling creates a WGD‐positive tumor state characterized by persistent chromosomal instability, karyotypic diversification, and cellular stress. These same biological pressures drive aggressive tumor evolution while exposing therapeutic vulnerabilities, providing a rationale for WGD‐informed precision medicine. Whole‐genome doubling (WGD)
Sejung Lee, Junghyeok Lim, Jinhyuk Bhin
wiley   +1 more source

Independence number in graphs and its upper bounds [PDF]

open access: yesJournal of Mahani Mathematical Research
‎In this paper, we use the double counting method to find some upper bounds for the independence number of a simple graph in terms of its order, size and  maximum degree.   Moreover,  we determine extremal graphs attaining equality in upper bounds.
Farzad Shaveisi
doaj   +1 more source

CEACAM1 participation in breast cancer progression

open access: yesMolecular Oncology, EarlyView.
In invasive breast cancer (BC), CEACAM1 shifts from an apical to a uniform membranous/cytoplasmic pattern, or is lost, as tumors dedifferentiate, inversely tracking the Ki‐67 proliferative index. In MCF‐7 cells, only CEACAM1‐4L suppresses proliferation, repressing cell cycle and growth factor genes.
Mykola Lyndin   +3 more
wiley   +1 more source

Upper and Lower Bounds for Ranks of the Matrix Expression X-XAX

open access: yesAbstract and Applied Analysis, 2013
We consider the question of how to take X such that the nonlinear matrix expression X-XAX attains its maximal and minimal possible ranks.
Zhiping Xiong
doaj   +1 more source

An upper and lower bound for clock synchronization

open access: yesInformation and Control, 1984
Summary: The problem of synchronizing clocks of processes in a fully connected network is considered. It is proved that, even if the clocks all run at the same rate as real time and there are no failures, an uncertainty of \(\epsilon\) in the message delivery time makes it impossible to synchronize the clocks of n processes any more closely than ...
Jennifer Lundelius, Nancy A. Lynch
openaire   +3 more sources

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