Results 81 to 90 of about 18,386,226 (307)
Study of the growth analysis of entire or meromorphic functions has generally been done through their Nevanlinna's characteristic function in comparison with those of exponential function.
T. Biswas
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Measurable Entire Functions II
Abstract Let $\mathcal{E}$ denote the space of entire functions with the topology of uniform convergence on compact sets. The action of $\mathbb{C}$ by translations on $\mathcal{E}$ is defined by $T_{z}f(w) = f(w+z)$. Let $\mathcal{U}$ denote the set of entire functions whose orbit under $T$ is dense.
Glücksam, Adi, Weiss, Benjamin
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Multiplicative functionals and entire functions, II [PDF]
[Part I, cf. Stud. Math. 119, No. 3, 289-297 (1996; Zbl 0868.46037).] The following result is proved in this very interesting paper: Let \(A\) be a complex Banach algebra with a unit \(e\), let \(F\) be a nonconstant entire function, and let \(T\) be a linear functional with \(T(e) = 1\) and such that \(T\circ F\) defined from \(A\) to the complex ...
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Molecular bases of circadian magnesium rhythms across eukaryotes
Circadian rhythms in intracellular [Mg2+] exist across eukaryotic kingdoms. Central roles for Mg2+ in metabolism suggest that Mg2+ rhythms could regulate daily cellular energy and metabolism. In this Perspective paper, we propose that ancestral prokaryotic transport proteins could be responsible for mediating Mg2+ rhythms and posit a feedback model ...
Helen K. Feord, Gerben van Ooijen
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Crosstalk between the ribosome quality control‐associated E3 ubiquitin ligases LTN1 and RNF10
Loss of the E3 ligase LTN1, the ubiquitin‐like modifier UFM1, or the deubiquitinating enzyme UFSP2 disrupts endoplasmic reticulum–ribosome quality control (ER‐RQC), a pathway that removes stalled ribosomes and faulty proteins. This disruption may trigger a compensatory response to ER‐RQC defects, including increased expression of the E3 ligase RNF10 ...
Yuxi Huang +8 more
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A new result for entire functions and their shifts with two shared values
Let ff be a transcendental entire function of hyperorder strictly less than 1, and let cc be a nonzero finite complex number. We prove that if f(z)f\left(z) and f(z+c)f\left(z+c) partially share 0, 1 ignoring multiplicity (i.e., E¯(0,f(z))⊆E¯(0,f(z+c ...
Xu Aizhu, Lin Peiqiang, Chen Shengjiang
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The work is devoted to the study of algebras of entire symmetric functions on Cartesian products of real and complex Banach spaces of Lebesgue integrable functions.
R.V. Ponomarov, T.V. Vasylyshyn
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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
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On entire solutions with a two-member recurrent formula for Taylor's coefficients of linear differential equations [PDF]
It is proved that the differential equation$$z^nw^{(n)}+(a_1^{(n-1)}z+a_2^{(n-1)})z^{n-1}w^{(n-1)}+ sum_{k=0}^{n-2}{(a_{n-1-k}^{(k)}z^2+a_{n-k}^{(k)}z+a_{n+1-k}^{(k)})z^kw^{(k)}}=0$$has an entire solution $f$ with a two-member recurrent formulafor its ...
Ya. S. Mahola
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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
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