Results 61 to 70 of about 3,568 (259)
Hyperosmotic stress induces PARP1‐mediated HPF1‐dependent mono(ADP‐ribosyl)ation
Sorbitol‐induced hyperosmotic stress rapidly induces reversible mono(ADP‐ribosyl)ation (MARylation) on PARP1 without the signs of genotoxic signaling. We show that PARP1 autoMARylation is HPF1 dependent and forms hydroxylamine‐resistant O‐glycosidic linkages.
Anna Georgina Kopasz +11 more
wiley +1 more source
Mixed-Criticality Scheduling to Minimize Makespan.
In the mixed-criticality job model, each job is characterized by two execution time parameters, representing a smaller (less conservative) estimate and a larger (more conservative) estimate on its actual, unknown, execution time. Each job is further classified as being either less critical or more critical.
Sanjoy K. Baruah +2 more
openaire +4 more sources
MultiPARTES: Multicore Virtualization for Mixed-Criticality Systems [PDF]
Modern embedded applications typically integrate a multitude of functionalities with potentially different criticality levels into a single system. Without appropriate preconditions, the integration of mixed-criticality subsystems can lead to a significant and potentially unacceptable increase of engineering and certification costs.
Salvador Trujillo +2 more
openaire +2 more sources
Plasma membranes contain dynamic nanoscale domains that organize lipids and receptors. Because viruses operate at similar scales, this architecture shapes early infection steps, including attachment, receptor engagement, and entry. Using influenza A virus and HIV‐1 as examples, we highlight how receptor nanoclusters, multivalent glycan interactions ...
Jan Schlegel, Christian Sieben
wiley +1 more source
Ascidian Ciona larvae initially show strong clockwise tail twisting, which is largely corrected during development. However, a small residual twist remains. This study shows that organized helical myofibrils in tail muscles mechanically stabilize this residual asymmetry, preventing complete restoration of bilateral symmetry and revealing how embryos ...
Yuki S. Kogure +3 more
wiley +1 more source
Component-Based Mixed-Criticality Real-Time Scheduling on a Single Processor System
This paper focuses on a two-level hierarchical system with dual-criticality components scheduled on a single processor. To address the independent scheduling of mixed-criticality (MC) components using fixed-priority (FP) servers, we introduce the mixed ...
Dandi Ma
doaj +1 more source
Risk-Aware Scheduling of Dual Criticality Job Systems Using Demand Distributions [PDF]
We pose the problem of scheduling Mixed Criticality (MC) job systems when there are only two criticality levels, Lo and Hi -referred to as Dual Criticality job systems- on a single processing platform, when job demands are probabilistic and their ...
Alahmad, Bader Naim +1 more
doaj +1 more source
The human gut microbiome across the life course
Despite significant individual variation and continuous change throughout life, the human gut microbiome follows some life stage‐specific trends. This article provides a brief overview of how gut microbiome composition shifts across different phases of life. Created in BioRender. Özkurt, E. (2026) https://BioRender.com/8q4nrnc.
Alise J. Ponsero +4 more
wiley +1 more source
This study reveals that the small GTPase Rab14 is necessary for human papillomavirus (HPV) infection and plays an essential role in the transport of virions to the trans‐Golgi network (TGN). HPV in the early endosome (EE), which harbors GTP‐bound Rab14, is transported to the TGN through the switch of Rab14 from its GTP‐bound to GDP‐bound form.
Yoshiyuki Ishii, Iwao Kukimoto
wiley +1 more source
Degradation mechanism of the von Willebrand factor A2 domain by nattokinase
Nattokinase, a natto‐derived protease, exhibits potent antithrombotic effects. This study demonstrates that nattokinase directly cleaves the von Willebrand factor (vWF) A2 domain in vitro. Unlike the native regulator ADAMTS13, nattokinase degrades folded vWF independently of shear stress.
Ryuichi Hyakumoto +3 more
wiley +1 more source

