Results 91 to 100 of about 4,376,990 (279)
On global (strong) defensive alliances in some product graphs
A defensive alliance in a graph is a set $S$ of vertices with the property that every vertex in $S$ has at most one more neighbor outside of $S$ than it has inside of $S$. A defensive alliance $S$ is called global if it forms a dominating set. The
Ismael Gonz\'alez Yero +2 more
doaj +1 more source
The strong converse theorem for the product-state capacity of quantum channels with ergodic Markovian memory [PDF]
Establishing the strong converse theorem for a communication channel confirms that the capacity of that channel, that is, the maximum achievable rate of reliable information communication, is the ultimate limit of communication over that channel. Indeed,
Dorlas, Tony, Morgan, Ciara
core +1 more source
Structural biology of ferritin nanocages
Ferritin is a conserved iron‐storage protein that sequesters iron as a ferric mineral core within a nanocage, protecting cells from oxidative damage and maintaining iron homeostasis. This review discusses ferritin biology, structure, and function, and highlights recent cryo‐EM studies revealing mechanisms of ferritinophagy, cellular iron uptake, and ...
Eloise Mastrangelo, Flavio Di Pisa
wiley +1 more source
Closed Formulae for the Strong Metric Dimension of Lexicographic Product Graphs
Given a connected graph G, a vertex w ∈ V (G) strongly resolves two vertices u, v ∈ V (G) if there exists some shortest u − w path containing v or some shortest v − w path containing u. A set S of vertices is a strong metric generator for G if every pair
Kuziak Dorota +2 more
doaj +1 more source
We identified a systemic, progressive loss of protein S‐glutathionylation—detected by nonreducing western blotting—alongside dysregulation of glutathione‐cycle enzymes in both neuronal and peripheral tissues of Taiwanese SMA mice. These alterations were partially rescued by SMN antisense oligonucleotide therapy, revealing persistent redox imbalance as ...
Sofia Vrettou, Brunhilde Wirth
wiley +1 more source
On products of strong Skolem starters
AbstractIn 1991, Shalaby conjectured that any , where or , admits a strong Skolem starter. In 2018, the authors fully described and explicitly constructed the infinite “cardioidal” family of strong Skolem starters. No other infinite family of these combinatorial designs was known to date.
Oleg Ogandzhanyants +2 more
openaire +3 more sources
In this study, we found that human cervical‐derived adipocytes maintain intracellular iron level by regulating the expression of iron transport‐related proteins during adrenergic stimulation. Melanotransferrin is predicted to interact with transferrin receptor 1 based on in silico analysis.
Rahaf Alrifai +9 more
wiley +1 more source
Bounding the Open k-Monopoly Number of Strong Product Graphs
Let G = (V, E) be a simple graph without isolated vertices and minimum degree δ, and let k ∈ {1 − ⌈δ/2⌉, . . . , ⌊δ/2⌋} be an integer. Given a set M ⊂ V, a vertex v of G is said to be k-controlled by M if δM(v)≥δG(v)2+k$\delta _M (v) \ge {{\delta _G (v)}
Kuziak Dorota +2 more
doaj +1 more source
Solving Strong-Substitutes Product-Mix Auctions
This paper develops algorithms to solve strong-substitutes product-mix auctions: it finds competitive equilibrium prices and quantities for agents who use this auction’s bidding language to truthfully express their strong-substitutes preferences over an arbitrary number of goods, each of which is available in multiple discrete units.
Elizabeth Baldwin +3 more
openaire +4 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

