Results 61 to 70 of about 379,757 (307)
Enzymatic degradation of biopolymers in amorphous and molten states: mechanisms and applications
This review explains how polymer morphology and thermal state shape enzymatic degradation pathways, comparing amorphous and molten biopolymer structures. By integrating structure–reactivity principles with insights from thermodynamics and enzyme engineering, it highlights mechanisms that enable efficient polymer breakdown.
Anđela Pustak, Aleksandra Maršavelski
wiley +1 more source
In this work, we introduce and study a class of Langevin equation with nonlocal boundary conditions governed by a Caputo fractional order proportional derivatives of an unknown function with respect to another function. The qualitative results concerning
Zaid Laadjal, Fahd Jarad
doaj +1 more source
Some considerations in connection with Kurepa's function [PDF]
In this paper we consider the functional equation for factorial sum and its particular solutions (Kurepa's function $K(z)$ \cite{Kurepa_71} and function $K_{1}(z)$).
Branko J. Malešević +1 more
core
Luminosity Functions of Gamma-Ray Burst Afterglows
Aims: Use the standard fireball model to create virtual populations of gamma-ray burst afterglows and study their luminosity functions. Methods: We randomly vary the parameters of the standard fireball model to create virtual populations of afterglows.
Costa +15 more
core +1 more source
Functional inequalities for the incomplete gamma function
Let \(f_a(x)= \Gamma(a,x)/\Gamma(a,0)\), where \(\Gamma(a,x)\) denotes the incomplete gamma function \((a,x> 0)\). The authors prove various new functional inequalities for \(f_a(x)\). For example, they study the double inequality \[ f_a(S_p(x_1,\dots, x_n))\leq f_a(x_1)\cdots f_a(x_n)\leq f_a(S_q(x_1,\dots, x_n)), \] where \(S_t\) is the power sum of ...
Alzer, Horst, Baricz, Árpád
openaire +2 more sources
Chemoresistance in bladder cancer: Macrophage recruitment associated with CXCL1, CXCL5 and CXCL8 expression is characteristic of Gemcitabine/Cisplatin (Gem/Cis) Non‐Responder tumors (right side) while Responder tumors did not show substantial tumor‐stromal crosstalk (left side). All biological icons are attributed to Bioicons: carcinoma, cancerous‐cell‐
Sophie Leypold +11 more
wiley +1 more source
New upper and lower bounds for the upper incomplete gamma function
Some new upper and lower bounds for the upper incomplete gamma function Γ(a,x) are presented. Some of the bounds are given for all real x>0 and some are for only certain combinations of a and x.
Steven G. From, Suthakaran Ratnasingam
doaj +1 more source
Enzymes of the 2‐hydroxyacyl‐CoA lyase group catalyze the condensation of formyl‐CoA with aldehydes or ketones. Thus, by structural adaptation of active sites, practically any pharmaceutically and industrially important 2‐hydroxyacid could be biotechnologically synthesized. Combining crystal structure analysis, active site mutations and kinetic assays,
Michael Zahn +4 more
wiley +1 more source
Inequalities for the incomplete gamma function [PDF]
The incomplete gamma function \(\Gamma(a,x)\) is given by \(\Gamma (a,x)= \int^\infty_0e^{-t}t^{a-1}dt\) with \(a>0\), \(t>0\). The authors prove the following result: Let \(a\) be a positive parameter, and let \(q(x)\) be a function differentiable on \((0,\infty)\) such that \(\lim_{x\to\infty} x^ae ^{-x}q(x)=0\). If we put \(T(x)=1+(a-x)q(x)+xq'(x)\)
NATALINI, PIERPAOLO, PALUMBO, Biagio
openaire +2 more sources
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source

