Results 61 to 70 of about 142,767 (307)
FEBS Letters, EarlyView.Septin 9 polybasic domains couple phosphoinositide‐rich membrane binding to centrosome positioning, Golgi organization, and microtubule acetylation to control epithelial polarity. Their loss disrupts this axis, causing centrosome mispositioning, Golgi fragmentation, reduced microtubule acetylation, and polarity inversion via upregulation of the ...
Ting ting Cai +4 more
wiley +1 more source
AN INTRODUCTION TO THE THEORY OF DIFFERENTIABLE STRUCTURES ON INFINITE INTEGRAL DOMAINS [PDF]
Journal of Sciences, Islamic Republic of Iran, 1990 A special class of differentiable functions on an infinite integral domain which is not a field is introduced.
doaj
On singular integral equations with variable limits of integration
Қарағанды университетінің хабаршысы. Математика сериясы, 2019 The wide range of problems of mathematical physics is reduced to a special Volterra integral equation of the second kind or to integral equations with variable limits of integration.
D.M. Akhmanova +2 more
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FEBS Letters, EarlyView.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
Accurate Nonstandard Path Integral Models for Arbitrary Dielectric Boundaries in 2-D NS-FDTD Domains
SensorsAn efficient path integral (PI) model for the accurate analysis of curved dielectric structures on coarse grids via the two-dimensional nonstandard finite-difference time-domain (NS-FDTD) technique is introduced in this paper.
Tadao Ohtani +2 more
doaj +1 more source
Conducive integral domains as pullbacks
Manuscripta Mathematica, 1986 A ''conducive domain'' is a (commutative unitary integral) domain R, with quotient field F, such that for every overring T of R, \(R\subseteq T\subsetneqq F\), the conductor \((R:T)=\{x\in F;\quad xT\subseteq R\}\) is nonzero [cf. \textit{E. Bastida} and \textit{R. Gilmer}, Mich. Math. J. 20, 79- 95 (1973; Zbl 0239.13001) and \textit{D. E.
BARUCCI, Valentina, D. Dobbs, M. Fontana
openaire +4 more sources
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
Modulation of Homer1 EVH1 domain internal dynamics by putative autism‐associated mutations
FEBS Letters, EarlyView.The putative autism‐associated M65I and S97L variants of the EVH1 domain of the postsynaptic scaffold protein Homer1 do not exhibit substantial changes in their overall structure or partner binding. Both of them, but especially the M65I variant, show altered internal dynamics relative to the wild‐type domain on the μs‐ms timescale, indicated by the ...
Fanni Farkas +6 more
wiley +1 more source
Electron transfer between complexes III and IV in S. cerevisiae mitochondrial membranes
FEBS Letters, EarlyView.Mitochondrial oxidative phosphorylation in S. cerevisiae mitoplasts is limited by complex IV catalytic capacity, rather than two‐dimensional cytochrome c diffusion. At physiological cytochrome c : supercomplex ratios at salinity equivalent to that of 20 mm monovalent salt, activity is maximized, indicating that this low ionic strength accurately mimics
Ana Paula Lobez +2 more
wiley +1 more source