Results 21 to 30 of about 86,062 (223)
Splendid and perverse equivalences [PDF]
, 2014 Inspired by the works of Rickard on splendid equivalences and of Chuang and Rouquier on perverse equivalences, we are here interested in the combination of both, a splendid perverse equivalence.
Dreyfus-Schmidt, Léo
core +1 more source
Social context prevents heat hormetic effects against mutagens during fish development
FEBS Letters, EarlyView.This study shows that sublethal heat stress protects fish embryos against ultraviolet radiation, a concept known as ‘hormesis’. However, chemical stress transmission between fish embryos negates this protective effect. By providing evidence for the mechanistic molecular basis of heat stress hormesis and interindividual stress communication, this study ...
Lauric Feugere +5 more
wiley +1 more source
Enhanced Recursive Reed-Muller Erasure Decoding [PDF]
, 2016 Recent work have shown that Reed-Muller (RM) codes achieve the erasure channel capacity. However, this performance is obtained with maximum-likelihood decoding which can be costly for practical applications. In this paper, we propose an encoding/decoding
Cunche, Mathieu +4 more
core +5 more sources
A stepwise emergence of evolution in the RNA world
FEBS Letters, EarlyView.How did biological evolution emerge from chemical reactions? This perspective proposes a gradual scenario of self‐organization among RNA molecules, where catalytic feedback on random mixtures plays the central role. Short oligomers cross‐ligate, and self‐assembly enables heritable variations. An event of template‐externalization marks the transition to
Philippe Nghe
wiley +1 more source
Evolutionary interplay between viruses and R‐loops
FEBS Letters, EarlyView.Viruses interact with specialized nucleic acid structures called R‐loops to influence host transcription, epigenetic states, latency, and immune evasion. This Perspective examines the roles of R‐loops in viral replication, integration, and silencing, and how viruses co‐opt or avoid these structures.
Zsolt Karányi +4 more
wiley +1 more source
Equivalences between blocks of p-local Mackey algebras [PDF]
, 2014 Let $G$ be a finite group and $(K,\mathcal{O},k)$ be a $p$-modular system. Let $R=\mathcal{O}$ or $k$. There is a bijection between the blocks of the group algebra and the blocks of the so-called $p$-local Mackey algebra $\mu_{R}^{1}(G)$.
Rognerud, Baptiste
core +2 more sources
Journal of Combinatorial Theory, 1998 An imprimitive permutation group of order 4200 is used for the construction of a 2-(175, 7, 1) design. The design yields also a group divisible design 7?GDDand a generalized Bhaskar Rao designGBRD(25, 100, 28, 7, 7; Z7).
Z. Janko, V. Tonchev
semanticscholar +1 more source
Disruption of SETD3‐mediated histidine‐73 methylation by the BWCFF‐associated β‐actin G74S mutation
FEBS Letters, EarlyView.The β‐actin G74S mutation causes altered interaction of actin with SETD3, reducing histidine‐73 methylation efficiency and forming two distinct actin variants. The variable ratio of these variants across cell types and developmental stages contributes to tissue‐specific phenotypical changes. This imbalance may impair actin dynamics and mechanosensitive
Anja Marquardt +8 more
wiley +1 more source
FEBS Letters, EarlyView.This study reveals how prime editing guide RNA (pegRNA) secondary structure and reverse transcriptase template length affect prime editing efficiency in correcting the phospholamban R14del cardiomyopathy‐associated mutation. Insights support the design of structurally optimized enhanced pegRNAs for precise gene therapy.
Bing Yao +7 more
wiley +1 more source
FEBS Letters, EarlyView.Exposure to common noxious agents (1), including allergens, pollutants, and micro‐nanoplastics, can cause epithelial barrier damage (2) in our body's protective linings. This may trigger an immune response to our microbiome (3). The epithelial barrier theory explains how this process can lead to chronic noncommunicable diseases (4) affecting organs ...
Can Zeyneloglu +17 more
wiley +1 more source