Results 31 to 40 of about 86,062 (223)
Foulkes modules and decomposition numbers of the symmetric group [PDF]
, 2014 The decomposition matrix of a finite group in prime characteristic p records the multiplicities of its p-modular irreducible representations as composition factors of the reductions modulo p of its irreducible representations in characteristic zero.
Giannelli, Eugenio, Wildon, Mark
core
FEBS Letters, EarlyView.Three‐dimensional (3D) biological systems have become key tools in lymphoma research, offering reliable in vitro and ex vivo platforms to explore pathogenesis and support precision medicine. This review highlights current 3D non‐Hodgkin lymphoma models, detailing their features, advantages, and limitations, and provides a broad perspective on future ...
Carla Faria +3 more
wiley +1 more source
FEBS Letters, EarlyView.Tuberculosis remains a global health challenge and new therapeutic targets are required. Here, we characterized SseA, a sulfurtransferase from Mycobacterium tuberculosis involved in macrophage infection, and its interaction with the newly identified protein SufEMtb that activates SseA enzymatic activity.
Giulia Di Napoli +10 more
wiley +1 more source
Young module multiplicities and classifying the indecomposable Young permutation modules [PDF]
, 2015 We study the multiplicities of Young modules as direct summands of permutation modules on cosets of Young subgroups. Such multiplicities have become known as the p-Kostka numbers.
Gill, Christopher C.
core
, 2008 One of the most central and long-standing open questions in combinatorial design theory concerns the existence of Steiner t-designs for large values of t. Although in his classical 1987 paper, L.
A. Betten +40 more
core +2 more sources
FEBS Letters, EarlyView.In this work, we reveal how different enzyme binding configurations influence the fluorescence decay of NAD(P)H in live cells using time‐resolved anisotropy imaging and fluorescence lifetime imaging microscopy (FLIM). Mathematical modelling shows that the redox states of the NAD and NADP pools govern these configurations, shaping their fluorescence ...
Thomas S. Blacker +8 more
wiley +1 more source
The number of inversions of permutations with fixed shape
, 2017 The Robinson-Schensted correspondence can be viewed as a map from permutations to partitions. In this work, we study the number of inversions of permutations corresponding to a fixed partition $\lambda$ under this map.
Ayyer, Arvind, Bhatnagar, Nayantara
core +1 more source
Neutrophil deficiency increases T cell numbers at the site of tissue injury in mice
FEBS Letters, EarlyView.In wild‐type mice, injury or acute inflammation induces neutrophil influx followed by macrophage accumulation. Mcl1ΔMyelo (neutrophil‐deficient) mice lack neutrophils, and in response to muscle injury show fewer macrophages and exhibit strikingly elevated T‐cell numbers, primarily non‐conventional “double‐negative” (DN) αβ and γδ T cells.
Hajnalka Halász +6 more
wiley +1 more source
Algebraic properties of generalized Rijndael-like ciphers [PDF]
, 2012 We provide conditions under which the set of Rijndael functions considered as permutations of the state space and based on operations of the finite field $\GF (p^k)$ ($p\geq 2$ a prime number) is not closed under functional composition.
B. Scott +5 more
core
Exploring lipid diversity and minimalism to define membrane requirements for synthetic cells
FEBS Letters, EarlyView.Designing the lipid membrane of synthetic cells is a complex task, in which its various roles (among them solute transport, membrane protein support, and self‐replication) should all be integrated. In this review, we report the latest top‐down and bottom‐up advances and discuss compatibility and complexity issues of current engineering approaches ...
Sergiy Gan +2 more
wiley +1 more source