Results 91 to 100 of about 36,261 (305)
Differential games through viability theory : old and recent results. [PDF]
This article is devoted to a survey of results for differential games obtained through Viability Theory. We recall the basic theory for differential games (obtained in the 1990s), but we also give an overview of recent advances in the following areas ...
Saint-Pierre, Patrick +2 more
core
Hazy Differential Inclusions [PDF]
, 1988 This paper is devoted to differential inclusions the right-hand sides of which are hazy subsets, which are fuzzy subsets whose membership functions are cost functions taking their values in [0,infinity] instead of [0,1].
Aubin, J.-P.
core
Structural insights into an engineered feruloyl esterase with improved MHET degrading properties
FEBS Letters, EarlyView.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
Existence of solutions to fractional differential inclusions with p-laplacian operator [PDF]
, 2014 In this article, we are prove the existence of solutions for three-point fractional differential inclusions with p-Laplacian operator. We use fixed point theory for set valued upper semi-continuous maps for obtaining the solutions.
Topal, F.S., Yantir, A.
core
Gut microbiome and aging—A dynamic interplay of microbes, metabolites, and the immune system
FEBS Letters, EarlyView.Age‐dependent shifts in microbial communities engender shifts in microbial metabolite profiles. These in turn drive shifts in barrier surface permeability of the gut and brain and induce immune activation. When paired with preexisting age‐related chronic inflammation this increases the risk of neuroinflammation and neurodegenerative diseases.
Aaron Mehl, Eran Blacher
wiley +1 more source
Impulsive differential inclusions with constrains
Electronic Journal of Differential Equations, 2006 In the paper, we study weak invariance of differential inclusions with non-fixed time impulses under compactness type assumptions. When the right-hand side is one sided Lipschitz an extension of the well known relaxation theorem is proved.
Tzanko Donchev
doaj
FEBS Letters, EarlyView.Biomolecular condensates formed by fused in sarcoma (FUS) are dissolved by high ATP concentrations yet persist in cells. Using a reconstituted system, we demonstrate that valosin‐containing protein (VCP), an AAA+ ATPase, counteracts ATP‐driven dissolution of FUS condensates through its D2 ATPase activity.
Hitomi Kimura +2 more
wiley +1 more source
Relaxation Problems Involving Second-Order Differential Inclusions
Abstract and Applied Analysis, 2013 We present relaxation problems in control theory for the second-order differential inclusions, with four boundary conditions, u¨(t)∈F(t,u(t),u˙(t)) a.e. on [0,1]; u(0)=0, u(η)=u(θ)=u(1) and, with m≥3 boundary conditions, u¨(t)∈F(t,u(t),u˙(t)) a.e. on [0,
Adel Mahmoud Gomaa
doaj +1 more source
A priori estimates for operational differential inclusions [PDF]
, 1990 We prove a set-valued Gronwall lemma and a relaxation theorem for the semilinear differential inclusion x′ ϵ Ax + F(t, x), x(0) = x0, where A is the infinitesimal generator of a C0-semigroup on a separable Banach space X and F: [0, T] × X ↦ X is a set ...
Frankowska, H. +2 more
core +1 more source
Diversity and complexity in neural organoids
FEBS Letters, EarlyView.Neural organoid research aims to expand genetic diversity on one side and increase tissue complexity on the other. Chimeroids integrate multiple donor genomes within single organoids. Self‐organising multi‐identity organoids, exogenous cell seeding, or enforced assembly of region‐specific organoids contribute to tissue complexity.
Ilaria Chiaradia, Madeline A. Lancaster
wiley +1 more source