Results 91 to 100 of about 15,537,269 (305)
A perfectoid duality between M-theory and F-theory
Nuclear Physics BWe present a non-singular, definition-level formulation of F-theory by replacing the traditional shrinking-fiber limit of M-theory with compactification on a tower-completed circle described using perfectoid geometry and condensed mathematics.
Arshid Shabir +2 more
doaj +1 more source
Degradation mechanism of the von Willebrand factor A2 domain by nattokinase
FEBS Letters, EarlyView.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
Stability of vector bundles from F-theory [PDF]
, 1999 We use a recently proposed formulation of stable holomorphic vector bundles $V$ on elliptically fibered Calabi--Yau n-fold $Z_n$ in terms of toric geometry to describe stability conditions on $V$.
Mayr, P., Berglund, Per
core +1 more source
Modelling stem cell differentiation related processes—A practical overview for biologists
FEBS Letters, EarlyView.Stem cell differentiation is complex and difficult to control experimentally. This review introduces suitable computational modelling approaches that can support stem cell research, from mechanistic ODE and abstract models to multiscale and deep learning methods.
Ricco Zeegelaar +4 more
wiley +1 more source
Computing Brane and Flux Superpotentials in F-theory Compactifications [PDF]
, 2010 In four-dimensional F-theory compactifications with N=1 supersymmetry the fields describing the dynamics of space-time filling 7-branes are part of the complex structure moduli space of the internal Calabi-Yau fourfold.
Ha, Tae-Won +5 more
core +1 more source
Orientifold limits of singular F-theory vacua
Nuclear Physics B, 2020 We construct global orientifold limits of singular F-theory vacua whose associated gauge groups are SO(3), SO(5), SO(6), F4, SU(4), and Spin(7). For each limit we show a universal tadpole relation is satisfied, which is a homological identity whose ...
James Fullwood, Dongxu Wang
doaj +1 more source
Design and analysis strategies for robust microbiome ageing research
FEBS Letters, EarlyView.The gut microbiome changes with age and associates with age‐related morbidity and mortality, establishing it as a potential biomarker and intervention target for ageing. Realising this potential requires methodological rigour, yet distinguishing biological signals from methodological artefacts remains challenging across cohorts. This review provides an
Mark Olenik +5 more
wiley +1 more source
Discrete family symmetry from F-theory GUTs [PDF]
, 2014 We consider realistic F-theory GUT models based on discrete family symmetries $A_4$ and $S_3$, combined with $SU(5)$ GUT, comparing our results to existing field theory models based on these groups.
Stephen F. King +7 more
core +1 more source
F-theory with hyperelliptic fibrations
Journal of High Energy PhysicsWe discuss the role of hyperelliptic fibrations in F-theory. For each even integer n we give a noncompact Calabi-Yau threefold X containing a hyperelliptically fibered surface Y, such that X and Y are homotopy equivalent and c 2(X) = n.
E. Ballico +3 more
doaj +1 more source
Vortex spin-torque oscillator stabilized by phase locked loop using integrated circuits
AIP Advances, 2017 Spin-torque nano-oscillators (STO) are candidates for the next technological implementation of spintronic devices in commercial electronic systems.
Martin Kreissig +11 more
doaj +1 more source