An improved gradient bound for 2D MBE

2020 ◽  
Vol 269 (12) ◽  
pp. 11165-11171
Author(s):  
Dong Li ◽  
Fan Wang ◽  
Kai Yang
Keyword(s):  
2020 ◽  
Vol 20 (2) ◽  
pp. 245-251
Author(s):  
Roberta Filippucci ◽  
Patrizia Pucci ◽  
Philippe Souplet

AbstractWe consider the elliptic equation {-\Delta u=u^{q}|\nabla u|^{p}} in {\mathbb{R}^{n}} for any {p>2} and {q>0}. We prove a Liouville-type theorem, which asserts that any positive bounded solution is constant. The proof technique is based on monotonicity properties for the spherical averages of sub- and super-harmonic functions, combined with a gradient bound obtained by a local Bernstein argument. This solves, in the case of bounded solutions, a problem left open in [2], where the case {0<p<2} is considered. Some extensions to elliptic systems are also given.


2016 ◽  
Vol 19 (04) ◽  
pp. 1650041 ◽  
Author(s):  
Feida Jiang ◽  
Ni Xiang ◽  
Jinju Xu

This paper concerns the gradient estimates for Neumann problem of a certain Monge–Ampère type equation with a lower order symmetric matrix function in the determinant. Under a one-sided quadratic structure condition on the matrix function, we present two alternative full discussions of the global gradient bound for the elliptic solutions.


1976 ◽  
Vol 54 (5) ◽  
pp. 698-707 ◽  
Author(s):  
Gilles Forget ◽  
Seymour Heisler

A bovine adrenocortical particulate fraction prepared by zonal ultracentrifugation and banding between ρ20 1.08 and 1.101 in a linear sucrose gradient bound 7.3 times more [3H]angiotensin II (ATII) per milligram protein than the original homogenate. Enzyme marker and electron microscope studies indicated that this fraction was largely devoid of mitochondria while being enriched in smooth membranes of predominantly plasmalemmal origin. The binding of labeled ATII was maximal after 10 min incubation (22 °C) and remained at equilibrium for at least 20 min thereafter. [3H]ATII binding was completely inhibited by saturating concentrations of nonradioactive ATII. The high-affinity binding site in the preparation had a specific binding capacity of 2.38 pmol∙mg−1, with an equilibrium constant of 2.36 × 108 M−1. Inhibition–displacement studies with unlabeled ATI, ATII, ATII fragments, analogs, and antagonists show that the receptor fraction has the highest affinity for the intact native octapeptide. ACTH and bradykinin had no specific effects on [3H]ATII binding. The current study suggests that the receptor fraction may be of use in a highly sensitive ATII radioligand assay.


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