Results 61 to 70 of about 1,033,944 (257)
Some applications of minimal open sets
We characterize minimal open sets in topological spaces. We show that any nonempty subset of a minimal open set is pre-open. As an application of a theory of minimal open sets, we obtain a sufficient condition for a locally finite space to be a pre ...
Fumie Nakaoka, Nobuyuki Oda
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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
On Strong $(i,j)$-Semi$^{*}$-$\Gamma $-Open Sets in Ideal Bitopological Space
In this study, we introduce the concepts of $(i,j)$-semi$^{*}$-$\Gamma $-open sets within the context of ideal bitopological spaces. This concept is demonstrated to be weaker than the established the notion of $(i,j)$-semi-$\Gamma $-open sets ...
Sibel Demiralp, Ibtissam Bukhatwa
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Effectively approximating measurable sets by open sets
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openaire +2 more sources
Tau acetylation at K331 has limited impact on tau pathology in vivo
We mapped tau post‐translational modifications in humanized MAPT knock‐in mice and in amyloid‐bearing double knock‐in mice. Acetylation within the repeat domain, particularly around K331, showed modest increases under amyloid pathology. To test functional relevance, we generated MAPTK331Q knock‐in mice.
Shoko Hashimoto +3 more
wiley +1 more source
Asymmetric maximal and minimal open sets [PDF]
We introduce the notions of maximal and minimal open sets in bitopological spaces and obtain some properties of them. In contrary to maximal and minimal open sets in topological spaces, we observe that maximal and minimal open sets in bitopological ...
Mukharjee Ajoy +2 more
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Calpain small subunit homodimerization is robust and calcium‐independent
Calpains dimerize via penta‐EF‐hand (PEF) domains. Using single‐molecule force spectroscopy, we measured the strength and kinetics of PEF–PEF homodimer binding. The interaction is robust, shows a transient conformational step before dissociation, and remains largely insensitive to Ca2+.
Nesha May O. Andoy +4 more
wiley +1 more source
Some properties of maximal open sets
Some fundamental properties of maximal open sets are obtained, such as decomposition theorem for a maximal open set. Basic properties of intersections of maximal open sets are established, such as the law of radical closure.
Fumie Nakaoka, Nobuyuki Oda
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Structural insights into an engineered feruloyl esterase with improved MHET degrading properties
A feruloyl esterase was engineered to mimic key features of MHETase, enhancing the degradation of PET oligomers. Structural and computational analysis reveal how a point mutation stabilizes the active site and reshapes the binding cleft, expading substrate scope.
Panagiota Karampa +5 more
wiley +1 more source
In this paper we introduce new class of open sets called weak N-open sets and we study the relation between N-open sets , weak N-open sets and some other open sets. We prove several results about them.
Amer I. l Al-Saeed
doaj

