Results 41 to 50 of about 15,309,834 (359)
A survey on groups with some restrictions on normalizers or centralizers [PDF]
We consider conditions on normalizers or centralizers in a group and we collect results showing how such conditions influence the structure of the group.
Leire Legarreta, Maria Tota
doaj +1 more source
Saturation rank for finite group schemes: Finite groups and infinitesimal group schemes [PDF]
Abstract We investigate the saturation rank of a finite group scheme defined over an algebraically closed field đ {\Bbbk} of positive characteristic ...
openaire +3 more sources
Sylow multiplicities in finite groups [PDF]
Let $G$ be a finite group and let $mathcal{P}=P_{1},ldots,P_{m}$ be a sequenceâ âof Sylow $p_{i}$-subgroups of $G$â, âwhere $p_{1},ldots,p_{m}$ are the distinctâ âprime divisors of $leftvert Grightvert $â. âThe Sylow multiplicity of $ginâ âG$ in $mathcal{
Dan Levy
doaj +1 more source
Signless Laplacian spectrum of power graphs of finite cyclic groups
In this paper, we have studied the Signless Laplacian spectrum of the power graph of finite cyclic groups. We have shown that is an eigen value of Signless Laplacian of the power graph of with multiplicity at least In particular, using the theory of ...
Subarsha Banerjee, Avishek Adhikari
doaj +1 more source
Finite rank and pseudofinite groups
It is proven that an infinite finitely generated group cannot be elementarily equivalent to an ultraproduct of finite groups of a given Pr\"ufer rank.
PalacĂn, Daniel
core +1 more source
Finitely generated -groups [PDF]
This paper is taken from the author's doctoral dissertation at New York University; the work was supported by the National Science Foundation, Grant G19674. The author would like to thank Professor Gilbert Baumslag for suggesting the questions treated in this paper, and for his very helpful guidance.
openaire +1 more source
The newfound relationship between extrachromosomal DNAs and excised signal circles
Extrachromosomal DNAs (ecDNAs) contribute to the progression of many human cancers. In addition, circular DNA byâproducts of V(D)J recombination, excised signal circles (ESCs), have roles in cancer progression but have largely been overlooked. In this Review, we explore the roles of ecDNAs and ESCs in cancer development, and highlight why these ...
Dylan Casey, Zeqian Gao, Joan Boyes
wiley +1 more source
Finite group with some c#-normal and S-quasinormally embedded subgroups
Let pp be a prime that divides the order of a finite group GG, and let PP be a Sylow pp-subgroup of GG. Assume that dd is the smallest number of generators of PP and define âłd(P)={P1,P2,âŚ,Pd}{{\mathcal{ {\mathcal M} }}}_{d}\left(P)=\left\{{P}_{1},{P}_{2},
Li Ning, Jiang Jing, Liu Jianjun
doaj +1 more source
Overview of molecular signatures of senescence and associated resources: pros and cons
Cells can enter a stress response state termed cellular senescence that is involved in various diseases and aging. Detecting these cells is challenging due to the lack of universal biomarkers. This review presents the current state of senescence identification, from biomarkers to molecular signatures, compares tools and approaches, and highlights ...
Orestis A. Ntintas +6 more
wiley +1 more source
Unramified Brauer groups of finite and infinite groups
The Bogomolov multiplier is a group theoretical invariant isomorphic to the unramified Brauer group of a given quotient space. We derive a homological version of the Bogomolov multiplier, prove a Hopf-type formula, find a five term exact sequence ...
Moravec, Primoz
core +1 more source

