Results 41 to 50 of about 70,010 (263)
Bi-parameter Potential theory and Carleson measures for the Dirichlet space on the bidisc
Bi-parameter potential theory and Carleson measures for the Dirichlet space on the bidisc, Discrete Analysis 2023:22, 58 pp. Carleson measures arise naturally when considering harmonic or holomorphic extensions from the boundary of a domain to the ...
Nicola Arcozzi +3 more
doaj +1 more source
Functions of bounded (φ, p) mean oscillation
In this paper we extend a result of Garnett and Jones to the case of spaces of homogeneous type.
CASTILLO, RENÉ ERLÍN +2 more
openaire +3 more sources
On the L_p-solvability of higher order parabolic and elliptic systems with BMO coefficients
We prove the solvability in Sobolev spaces for both divergence and non-divergence form higher order parabolic and elliptic systems in the whole space, on a half space, and on a bounded domain.
A. Friedman +29 more
core +1 more source
This perspective highlights emerging insights into how the circadian transcription factor CLOCK:BMAL1 regulates chromatin architecture, cooperates with other transcription factors, and coordinates enhancer dynamics. We propose an updated framework for how circadian transcription factors operate within dynamic and multifactorial chromatin landscapes ...
Xinyu Y. Nie, Jerome S. Menet
wiley +1 more source
LIPSCHITZ SPACES AND BOUNDED MEAN OSCILLATION OF HARMONIC MAPPINGS [PDF]
AbstractWe first study the bounded mean oscillation of planar harmonic mappings. Then we establish a relationship between Lipschitz-type spaces and equivalent modulus of real harmonic mappings. Finally, we obtain sharp estimates on the Lipschitz number of planar harmonic mappings in terms of the bounded mean oscillation norm, which shows that the ...
Chen, Shaolin +3 more
openaire +3 more sources
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
In this note, we define p-adic mixed Lebesgue space and mixed λ-central Morrey-type spaces and characterize p-adic mixed λ-central bounded mean oscillation space via the boundedness of commutators of p-adic Hardy-type operators on p-adic mixed Lebesgue ...
Naqash Sarfraz +3 more
doaj +1 more source
In this article, we consider the Laplace-Bessel differential operatorΔBk,n=∑i=1k∂2∂xi2+γixi∂∂xi+∑i=k+1n∂2∂xi2,γ1>0,…,γk>0.{\Delta }_{{B}_{k,n}}=\mathop{\sum }\limits_{i=1}^{k}\left(\frac{{\partial }^{2}}{\partial {x}_{i}^{2}}+\frac{{\gamma }_{i}}{{x}_{i}}
Hasanov Javanshir J. +2 more
doaj +1 more source
Gelfer Functions, Integral Means, Bounded Mean Oscillation, and Univalency [PDF]
A Gelfer function f f is a holomorphic function in D = { | z | > 1 } D = \{ \left | z \right | > 1\} such that f ( 0 ) = 1 f(0) = 1 and f ( z
openaire +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

