Results 41 to 50 of about 317,601 (325)
Disordered but rhythmic—the role of intrinsic protein disorder in eukaryotic circadian timing
Unstructured domains known as intrinsically disordered regions (IDRs) are present in nearly every part of the eukaryotic core circadian oscillator. IDRs enable many diverse inter‐ and intramolecular interactions that support clock function. IDR conformations are highly tunable by post‐translational modifications and environmental conditions, which ...
Emery T. Usher, Jacqueline F. Pelham
wiley +1 more source
Nonexistence of positive radial solutions for a problem with singular potential
This article completes the picture in the study of positive radial solutions in the function space 𝒟1,2(ℝN)∩L2(ℝN,|x|-αdx)∩Lp(ℝN)${{\mathcal {D}^{1,2}({\mathbb {R}^N}) \cap L^2({{\mathbb {R}^N}, | x |^{-\alpha } dx})\cap L^p({\mathbb {R}^N})}}$ for the ...
Catrina Florin
doaj +1 more source
We study the effects of higher order transversal modes in a model of a singly-resonant OPO, using both numerical solutions and mode expansions including up to two radial modes.
Ashby +11 more
core +1 more source
Time after time – circadian clocks through the lens of oscillator theory
Oscillator theory bridges physics and circadian biology. Damped oscillators require external drivers, while limit cycles emerge from delayed feedback and nonlinearities. Coupling enables tissue‐level coherence, and entrainment aligns internal clocks with environmental cues.
Marta del Olmo +2 more
wiley +1 more source
Strongly increasing solutions of cyclic systems of second order differential equations with power-type nonlinearities [PDF]
We consider \(n\)-dimensional cyclic systems of second order differential equations \[(p_i(t)|x_{i}'|^{\alpha_i -1}x_{i}')' = q_{i}(t)|x_{i+1}|^{\beta_i-1}x_{i+1},\] \[\quad i = 1,\ldots,n, \quad (x_{n+1} = x_1) \tag{\(\ast\)}\] under the assumption that
Jaroslav Jaroš, Kusano Takaŝi
doaj +1 more source
Non-radial multipeak positive solutions for the Schrödinger–Poisson problem
zbMATH Open Web Interface contents unavailable due to conflicting licenses.
Long, Wei, Xiong, Zhiwei
openaire +2 more sources
Existence results for fully nonlinear equations in radial domains
We consider the fully nonlinear problem \begin{equation*} \begin{cases} -F(x,D^2u)=|u|^{p-1}u & \text{in $\Omega$}\\ u=0 & \text{on $\partial\Omega$} \end{cases} \end{equation*} where $F$ is uniformly elliptic, $p>1$ and $\Omega$ is either an annulus or ...
Galise, Giulio +2 more
core +1 more source
Structural biology of ferritin nanocages
Ferritin is a conserved iron‐storage protein that sequesters iron as a ferric mineral core within a nanocage, protecting cells from oxidative damage and maintaining iron homeostasis. This review discusses ferritin biology, structure, and function, and highlights recent cryo‐EM studies revealing mechanisms of ferritinophagy, cellular iron uptake, and ...
Eloise Mastrangelo, Flavio Di Pisa
wiley +1 more source
Radial Symmetry of Positive Solutions of Nonlinear Elliptic Equations
Three results concerning the radial symmetry and asymptotic behaviour at \(x=\infty\) of positive solutions of \[ \Delta u = \varphi(\mid x\mid)u^{\lambda}, \quad x\in \mathbb{R}^n \] and \(|x|\) large are presented. Here \(\lambda>1\) and \(\varphi(r)\) is positive and continuous for \(r\) large. There are three cases which are separately analysed: (I)
openaire +1 more source
Structural insights into an engineered feruloyl esterase with improved MHET degrading properties
A feruloyl esterase was engineered to mimic key features of MHETase, enhancing the degradation of PET oligomers. Structural and computational analysis reveal how a point mutation stabilizes the active site and reshapes the binding cleft, expading substrate scope.
Panagiota Karampa +5 more
wiley +1 more source

