Results 31 to 40 of about 1,573,587 (265)

Inverse M-matrix inequalities and generalized ultrametric matrices

open access: yesLinear Algebra and its Applications, 1995
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
openaire   +1 more source

Mapping the evolution of mitochondrial complex I through structural variation

open access: yesFEBS Letters, EarlyView.
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

open access: yesJournal of Inequalities and Applications, 2016
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

open access: yesFEBS Letters, EarlyView.
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*

open access: yesBarekeng
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)

open access: yesFokus, 2016
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
doaj   +1 more source

Reciprocal control of viral infection and phosphoinositide dynamics

open access: yesFEBS Letters, EarlyView.
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

open access: yesLinear Algebra and its Applications, 1977
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)
openaire   +1 more source

ALGORITHMS FOR THE RICCATI EQUATION WITH A NONSINGULAR M-MATRIX

open access: yesAnnals of the Academy of Romanian Scientists Series on Mathematics and Its Application, 2023
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
openaire   +1 more source

Spatiotemporal and quantitative analyses of phosphoinositides – fluorescent probe—and mass spectrometry‐based approaches

open access: yesFEBS Letters, EarlyView.
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

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