Results 61 to 70 of about 13,110,779 (313)
Diversity and complexity in neural organoids
FEBS Letters, EarlyView.Neural organoid research aims to expand genetic diversity on one side and increase tissue complexity on the other. Chimeroids integrate multiple donor genomes within single organoids. Self‐organising multi‐identity organoids, exogenous cell seeding, or enforced assembly of region‐specific organoids contribute to tissue complexity.
Ilaria Chiaradia, Madeline A. Lancaster
wiley +1 more source
An isoform of 14‐3‐3 protein regulates transbilayer lipid movement at the plasma membrane
FEBS Letters, EarlyView.Loss of 14‐3‐3ζ in CHO cells confers resistance to exogenous phosphatidylserine (PS) and impairs endocytosis‐independent inward flip‐flop of fluorescent PS at the plasma membrane. RNAi‐mediated knockdown reproduces this defect, while no additive effect is seen in ATP11C‐deficient cells.
Akiko Yamaji‐Hasegawa +3 more
wiley +1 more source
Scale transition and enforcement of RVE boundary conditions in second-order computational homogenization [PDF]
, 2008 Formulation of the scale transition equations coupling the microscopic and macroscopic variables in the second-order computational homogenization of heterogeneous materials and the enforcement of generalized boundary conditions for the representative ...
Bicanic, Nenad +2 more
core +1 more source
Frontiers in Applied Mathematics and StatisticsThis study primarily seeks to expand upon these developments by encompassing neutral differential equations of mixed type, incorporating both delay and advanced terms, particularly in the case of the canonical operator.
Ahmed M. Hassan +4 more
doaj +1 more source
Oscillatory behavior of the second order noncanonical differential equations
Electronic Journal of Qualitative Theory of Differential Equations, 2019 Establishing monotonical properties of nonoscillatory solutions we introduce new oscillatory criteria for the second order noncanonical differential equation with delay/advanced argument \begin{equation*} (r(t)y'(t))'+p(t)y(\tau(t))=0. \end{equation*}
Blanka Baculíková
doaj +1 more source
FEBS Letters, EarlyView.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
Second order tangency conditions and differential inclusions: a counterexample and a remedy
Electronic Journal of Differential Equations, 2009 In this paper we show that second order tangency conditions are superfluous not to say useless while discussing the existence condition for certain second order differential inclusions. In this regard, a counterexample is provided even in the simpler
Corneliu Ursescu
doaj
FEBS Letters, EarlyView.Embryo‐like structures (stembryos) are an innovative tool, but they are hindered by experimental variability and limited developmental potential. DNA methylation is crucial for mammalian development, but its status in stembryo models is poorly characterized.
Sara Canil +4 more
wiley +1 more source
Multivalued second order differential problem
Annales Universitatis Paedagogicae Cracoviensis: Studia Mathematica, 2012 Let $K$ be a closed convex cone with nonempty interior in a real Banach space and let $F,G,Hcolon K o cc(K)$ be three given continuous additive set-valued functions.
Ewelina Mainka-Niemczyk
doaj
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