Results 51 to 60 of about 1,241,136 (285)

The group reduction for bounded cosine functions on UMD spaces

open access: yes, 2007
It is shown that if A generates a bounded cosine operator function on a UMD space X, then i(-A)^{1/2} generates a bounded C_0-group.
Haase, Markus
core   +1 more source

Personalized Selumetinib Dosing in Pediatric Neurofibromatosis Type 1: Insights From a Pilot Therapeutic Drug Monitoring Study

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Objective To evaluate selumetinib exposure using therapeutic drug monitoring (TDM) in pediatric patients with neurofibromatosis type 1 (NF1) and plexiform neurofibromas (PN), assess interpatient pharmacokinetic variability, and explore the relationship between drug exposure, clinical response, and adverse effects.
Janka Kovács   +8 more
wiley   +1 more source

A universal bound on the variations of bounded convex functions [PDF]

open access: yes, 2015
Given a convex set $C$ in a real vector space $E$ and two points $x,y\in C$, we investivate which are the possible values for the variation $f(y)-f(x)$, where $f:C\longrightarrow [m,M]$ is a bounded convex function. We then rewrite the bounds in terms of
Kwon, Joon
core  

Effects of the Fluid Replacement Method During Online Hemodiafiltration on the Solute Removal Performance and Biocompatibility Using the Asymmetric Cellulose Triacetate Membrane

open access: yesTherapeutic Apheresis and Dialysis, EarlyView.
ABSTRACT Introduction Pre‐dilution online hemodiafiltration (Pre‐HDF) is predominantly used in Japan, whereas post‐dilution online HDF (Post‐HDF) is more common in Europe. An asymmetric cellulose triacetate (ATA) membrane may improve biocompatibility.
Kenji Sakurai   +4 more
wiley   +1 more source

Integral Representation of Functions of Bounded Variation

open access: yesJournal of Mathematics, 2019
Functions of bounded variations form important transition between absolute continuous and singular functions. With Bainov’s introduction of impulsive differential equations having solutions of bounded variation, this class of functions had eventually ...
Z. Lipcsey   +3 more
doaj   +1 more source

Small values of the Euler function and the Riemann hypothesis

open access: yes, 2012
Let $\vfi$ be Euler's function, $\ga$ be Euler's constant and $N_k$ be the product of the first $k$ primes. In this article, we consider the function $c(n) =(n/\vfi(n)-e^\ga\log\log n)\sqrt{\log n}$. Under Riemann's hypothesis, it is proved that $c(N_k)$
Nicolas, Jean-Louis
core   +4 more sources

Revealing the structure of land plant photosystem II: the journey from negative‐stain EM to cryo‐EM

open access: yesFEBS Letters, EarlyView.
Advances in cryo‐EM have revealed the detailed structure of Photosystem II, a key protein complex driving photosynthesis. This review traces the journey from early low‐resolution images to high‐resolution models, highlighting how these discoveries deepen our understanding of light harvesting and energy conversion in plants.
Roman Kouřil
wiley   +1 more source

Slice Holomorphic Functions in the Unit Ball Having a Bounded L-Index in Direction

open access: yesAxioms, 2020
Let b∈Cn\{0} be a fixed direction. We consider slice holomorphic functions of several complex variables in the unit ball, i.e., we study functions that are analytic in the intersection of every slice {z0+tb:t∈C} with the unit ball Bn={z∈C:|z|:=|z|12 ...
Andriy Bandura   +2 more
doaj   +1 more source

AN EXISTENCE AND UNIQUENESS OF THE SOLUTION OF SEMILINEAR MONOTONE ELLIPTIC EQUATION WITH THE DATA IN STUMMEL CLASSES

open access: yesBarekeng, 2023
Let  be a bounded open subset of , ,  be a function in Stummel classes , where , and be a semilinear monotone elliptic equation, where  is  symmetric matrix, elliptic, bounded, and  is non decreasing and Lipschitz. By proving a weighted estimation for
Nicky Kurnia Tumalun
doaj   +1 more source

Mapping the evolution of mitochondrial complex I through structural variation

open access: yesFEBS Letters, EarlyView.
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

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