Results 31 to 40 of about 2,731,359 (291)
Certain spaces of X-valued sequences are introduced and some of their properties are investigated. Köthe- Toeplitz duals of these spaces are examined.
S. Pehlivan
doaj +1 more source
Delay Differential Equations in Sequence Spaces
The standard delay equations are newly studied in the context of classical separable Banach Sequence Spaces. As a classical solution is shown to exist, the associated semigroup and its infinitesimal generator are found, and some important properties of
Luis Gerardo Mármol +1 more
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Maximal ideals in the algebra of operators on certain Banach spaces. [PDF]
For a Banach space $\mathfrak{X}$, let $\mathcal{B}(\mathfrak{X})$ denote the Banach algebra of all continuous linear operators on $\mathfrak{X}$. First, we study the lattice of closed ideals in $\mathcal{B}(\mathfrak{J}_p)$, where $1 < p < \infty$ and $\
Laustsen, Niels Jakob +1 more
core +4 more sources
Structural and biochemical characterisations show that the planar cell polarity (PCP) protein Inturned harbours a unique PDZ‐like domain that does not bind canonical PDZ‐binding motifs (PBMs) like that of another PCP protein Vangl2. In contrast, the apical‐basal polarity protein Scribble contains four PDZ domains that bind Vangl2, but one PDZ domain ...
Stephan Wilmes +4 more
wiley +1 more source
Diversity and complexity in neural organoids
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
On New Banach Sequence Spaces Involving Leonardo Numbers and the Associated Mapping Ideal
In the present study, we have constructed new Banach sequence spaces ℓpL,c0L,cL, and ℓ∞L, where L=lv,k is a regular matrix defined by lv,k=lk/lv+2−v+2, 0≤k≤v,0, k>v, for all v,k=0,1,2,⋯, where l=lk is a sequence of Leonardo numbers.
Taja Yaying +3 more
doaj +1 more source
Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai +4 more
wiley +1 more source
The continuity of superposition operators on some sequence spaces defined by moduli [PDF]
summary:Let $\lambda $ and $\mu $ be solid sequence spaces. For a sequence of modulus functions $\Phi =(\varphi _{k})$ let $ \lambda (\Phi )= \lbrace x=(x_{k}) \: (\varphi _{k}(|x_{k}|))\in \lambda \rbrace $. Given another sequence of modulus functions $
Kolk, Enno, Raidjõe, Annemai
core +1 more source
The Polya algorithm in sequence spaces
Let \(K\) be a finite-dimensional linear subspace of the sequence space \({l_1}\). Let \({h\in l_p}\) and \({h\notin K}\). Let \(h_p\) denote the best \(l_p\)-approximation of \(h\) from \(K\). It is well known that \(h_p\) exists and is unique. In general, the unicity of the best uniform approximation of \(h\) is not guarantied.
José M. Quesada +3 more
openaire +2 more sources
From mice to humans—divergent strategies for intestinal homeostasis and regeneration
Recent advances such as organoid genome editing, xenotransplantation, imaging, and whole‐genome sequencing have enabled direct studies of human intestinal stem cells (ISCs). These studies reveal species‐specific features, including slower ISC proliferation, distinct injury responses, slower somatic mutation accumulation in humans, and an inverse ...
Keiko Ishikawa +2 more
wiley +1 more source

