Results 91 to 100 of about 9,407,399 (300)
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
Average distance and independence number
For a connected graph \(G\) of order \(n\), the average distance \(\mu(G)\) is defined as \[ \mu(G)= \left({n\atop 2}\right)^{-1} \sum_{u,v\in V(G)} d(u,v), \] where \(d(u,v)\) denotes the length of a shortest path joining the vertices \(u\) and \(v\).
openaire +2 more sources
Bounds on the Clique and the Independence Number for Certain Classes of Graphs
In this paper, we study the class of graphs Gm,n that have the same degree sequence as two disjoint cliques Km and Kn, as well as the class G¯m,n of the complements of such graphs.
Valentin E. Brimkov, Reneta P. Barneva
doaj +1 more source
Hyperosmotic stress induces PARP1‐mediated HPF1‐dependent mono(ADP‐ribosyl)ation
Sorbitol‐induced hyperosmotic stress rapidly induces reversible mono(ADP‐ribosyl)ation (MARylation) on PARP1 without the signs of genotoxic signaling. We show that PARP1 autoMARylation is HPF1 dependent and forms hydroxylamine‐resistant O‐glycosidic linkages.
Anna Georgina Kopasz +11 more
wiley +1 more source
On the number of maximum independent sets of graphs [PDF]
Let $G$ be a simple graph. An independent set is a set of pairwise non-adjacent vertices. The number of vertices in a maximum independent set of $G$ is denoted by $alpha(G)$. In this paper, we characterize graphs $G$ with $n$ vertices and with maximum
Tajedin Derikvand, Mohammad Reza Oboudi
doaj
Buskirk\u27s Independence Nurseries, Independence, Ohio [nursery stock catalog]
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Henry G. Gilbert Nursery and Seed Trade Catalog Collection. +1 more
core +1 more source
An isoform of 14‐3‐3 protein regulates transbilayer lipid movement at the plasma membrane
Loss of 14‐3‐3ζ in CHO cells confers resistance to exogenous phosphatidylserine (PS) and impairs endocytosis‐independent inward flip‐flop of fluorescent PS at the plasma membrane. RNAi‐mediated knockdown reproduces this defect, while no additive effect is seen in ATP11C‐deficient cells.
Akiko Yamaji‐Hasegawa +3 more
wiley +1 more source
Plasma membranes contain dynamic nanoscale domains that organize lipids and receptors. Because viruses operate at similar scales, this architecture shapes early infection steps, including attachment, receptor engagement, and entry. Using influenza A virus and HIV‐1 as examples, we highlight how receptor nanoclusters, multivalent glycan interactions ...
Jan Schlegel, Christian Sieben
wiley +1 more source
Independence numbers of polyhedral graphs
A polyhedral graph is a $3$-connected planar graph. We find the least possible order $p(k,a)$ of a polyhedral graph containing a $k$-independent set of size $a$ for all positive integers $k$ and $a$. In the case $k = 1$ and $a$ even, we prove that the extremal graphs are exactly the vertex-face (radial) graphs of maximal planar graphs.
Gaspoz S., Maffucci R. W.
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Independence Number of Graphs with a Prescribed Number of Cliques
We consider the following problem posed by Erdős in 1962. Suppose that $G$ is an $n$-vertex graph where the number of $s$-cliques in $G$ is $t$. How small can the independence number of $G$ be? Our main result suggests that for fixed $s$, the smallest possible independence number undergoes a transition at $t=n^{s/2+o(1)}$. In the case of triangles ($s=
Tom Bohman, Dhruv Mubayi
openaire +4 more sources

