Results 21 to 30 of about 3,579,879 (270)
On a Higher-Order Difference Equation
We describe in an elegant and short way the behaviour of positive solutions of the higher-order difference equation xn=cxn−pxn−p−q/xn−q, n∈ℕ0, where p,q∈ℕ and c>0, extending some recent results in the literature.
Bratislav D. Iričanin, Wanping Liu
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ON SOLVABILITY OF ONE DIFFERENCE EQUATION
We consider a system of difference equation similar to those that appear as description of cumulative sums. Using Hamel bases, we construct pathological solutions to this system for constant right-hand sides.
I. A. Chernov
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On an Exponential-Type Fuzzy Difference Equation
Our goal is to investigate the existence of the positive solutions, the existence of a nonnegative equilibrium, and the convergence of a positive solution to a nonnegative equilibrium of the fuzzy difference equation , , , where and the initial values
Stefanidou G +2 more
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ABSTRACT Introduction Adult‐onset Still's disease (AOSD) complicated by macrophage activation syndrome (MAS) carries substantial mortality. The role of therapeutic plasma exchange (TPE) remains uncertain. Methods We retrospectively analyzed patients with AOSD‐MAS treated with TPE at a single‐center.
Masataka Ueda +15 more
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Differential-difference equations reducible to difference and q-difference equations
Asymptotic properties of solutions of the differential-difference equation \[ x'(qt+1)=h(x(t))x'(t), \quad t\geq 0,\;q\geq 1 \tag{*} \] are investigated. Let \(\varphi\in C^1([0,1];\mathbf R)\) satisfies \(\varphi'(1)=h(\varphi(0))\varphi'(0)\). A solution \(x\) of (*) satisfying \(x(t)=\varphi(t)\), \(t\in [0,1)\), is denoted by \(x_{\varphi}\).
openaire +1 more source
Mapping the evolution of mitochondrial complex I through structural variation
Respiratory complex I (CI) is crucial for bioenergetic metabolism in many prokaryotes and eukaryotes. It is composed of a conserved set of core subunits and additional accessory subunits that vary depending on the organism. Here, we categorize CI subunits from available structures to map the evolution of CI across eukaryotes. Respiratory complex I (CI)
Dong‐Woo Shin +2 more
wiley +1 more source
Difference equation for a population model
In this paper we consider a difference equation of the form u(t+2)=αu(t+1)+βu(t+1)−αu(t)αu(t), for t>−∞, seems to be a general statement of a relative socio-spatial dynamics. Indeed this equation is one of “population model”.
Mami Suzuki
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An integrable discretization of KdV at large times
An "exact discretization" of the Schroedinger operator is considered and its direct and inverse scattering problems are solved. It is shown that a differential-difference nonlinear evolution equation depending on two arbitrary constants can be solved by ...
A Spire +18 more
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By dawn or dusk—how circadian timing rewrites bacterial infection outcomes
The circadian clock shapes immune function, yet its influence on infection outcomes is only beginning to be understood. This review highlights how circadian timing alters host responses to the bacterial pathogens Salmonella enterica, Listeria monocytogenes, and Streptococcus pneumoniae revealing that the effectiveness of immune defense depends not only
Devons Mo +2 more
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The role and implications of mammalian cellular circadian entrainment
At their most fundamental level, mammalian circadian rhythms occur inside every individual cell. To tell the correct time, cells must align (or ‘entrain’) their circadian rhythm to the external environment. In this review, we highlight how cells entrain to the major circadian cues of light, feeding and temperature, and the implications this has for our
Priya Crosby
wiley +1 more source

