Results 31 to 40 of about 1,573,587 (265)
Inverse M-matrix inequalities and generalized ultrametric matrices
The authors introduce a class of matrices called generalized ultrametric matrices. That class is defined in terms of triangles in the weighted graph of the matrix, and it contains the ultrametric matrices as well as some unsymmetric matrices. The authors show that a generalized ultrametric matrix is the inverse of a row diagonally dominant \(M\)-matrix
McDonald, J.J. +3 more
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Mapping the evolution of mitochondrial complex I through structural variation
Respiratory complex I (CI) is crucial for bioenergetic metabolism in many prokaryotes and eukaryotes. It is composed of a conserved set of core subunits and additional accessory subunits that vary depending on the organism. Here, we categorize CI subunits from available structures to map the evolution of CI across eukaryotes. Respiratory complex I (CI)
Dong‐Woo Shin +2 more
wiley +1 more source
Some determinantal inequalities for Hadamard and Fan products of matrices
In this note, we generalize some determinantal inequalities which are due to Lynn (Proc. Camb. Philos. 60:425-431, 1964), Chen (Linear Algebra Appl. 368:99-106, 2003) and Ando (Linear Multilinear Algebra 8:291-316, 1980).
Xiaohui Fu, Yang Liu
doaj +1 more source
Organoids in pediatric cancer research
Organoid technology has revolutionized cancer research, yet its application in pediatric oncology remains limited. Recent advances have enabled the development of pediatric tumor organoids, offering new insights into disease biology, treatment response, and interactions with the tumor microenvironment.
Carla Ríos Arceo, Jarno Drost
wiley +1 more source
ON CONDITIONS FOR MATRICES T SUCH THAT T-I AND I-T^(-1) ARE INVERSE H-MATRICES*
In this article, we study an analogue of a classical result for M-matrices: if T - I is an invertible M-matrix, then both T and I - T-1 are also invertible M-matrices. We extend this implication to a broader class—inverse H-matrices.
Jeriko Gormantara +3 more
doaj +1 more source
Teorema Pohon Matriks Untuk Menentukan Banyaknya Pohon Rentangan Graf Bipartisi Komplit (Km,n)
This research aims to observes panning tree number of complete bipartite graph (Km,n) by matrix-tree theorem.This research was using library research method which the step are:(1)Drawing complete bipartite graph (Km,n) where m= 1,2,3,4,and; (2)Determinin
Novia Rahmawati
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Reciprocal control of viral infection and phosphoinositide dynamics
Phosphoinositides, although scarce, regulate key cellular processes, including membrane dynamics and signaling. Viruses exploit these lipids to support their entry, replication, assembly, and egress. The central role of phosphoinositides in infection highlights phosphoinositide metabolism as a promising antiviral target.
Marie Déborah Bancilhon, Bruno Mesmin
wiley +1 more source
M-matrix characterizations.I—nonsingular M-matrices
AbstractThe purpose of this survey is to classify systematically a widely ranging list of characterizations of nonsingular M-matrices from the economics and mathematics literatures. These characterizations are grouped together in terms of their relations to the properties of (1) positivity of principal minors, (2) inverse-positivity and splittings, (3)
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ALGORITHMS FOR THE RICCATI EQUATION WITH A NONSINGULAR M-MATRIX
We consider different algorithms with linear rate of convergence for computing the minimal nonnegative solution of M-matrix algebraic Riccati equation. The performance of the considered algorithms are illustrated on numerical examples.
Ivanov, Ivelin, Baeva, Neli
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Fluorescent probes allow dynamic visualization of phosphoinositides in living cells (left), whereas mass spectrometry provides high‐sensitivity, isomer‐resolved quantitation (right). Their synergistic use captures complementary aspects of lipid signaling. This review illustrates how these approaches reveal the spatiotemporal regulation and quantitative
Hiroaki Kajiho +3 more
wiley +1 more source

