Results 51 to 60 of about 9,021,127 (291)
Meromorphic solutions of a third order nonlinear differential equation [PDF]
We prove that all the meromorphic solutions of the nonlinear differential equation c0 u"' + 6 u^4 + c1 u" + c2 u u' + c3 u^3 + c4 u'+ c5 u^2 + c6 u +c7=0 are elliptic or degenerate elliptic, and we build them explicitly.Comment: 12 pages, to appear ...
Conte, Robert, Tuen-Wai, Ng
core +2 more sources
Sequence determinants of RNA G‐quadruplex unfolding by Arg‐rich regions
We show that Arg‐rich peptides selectively unfold RNA G‐quadruplexes, but not RNA stem‐loops or DNA/RNA duplexes. This length‐dependent activity is inhibited by acidic residues and is conserved among SR and SR‐related proteins (SRSF1, SRSF3, SRSF9, U1‐70K, and U2AF1).
Naiduwadura Ivon Upekala De Silva +10 more
wiley +1 more source
Third-order chromatic dispersion stabilizes Kerr frequency combs
Using numerical simulations of an extended Lugiato-Lefever equation, we analyze the stability and nonlinear dynamics of Kerr frequency combs generated in microresonators and fiber resonators taking into account third-order dispersion effects.
Coen, Stephane +4 more
core +1 more source
Cell wall target fragment discovery using a low‐cost, minimal fragment library
LoCoFrag100 is a fragment library made up of 100 different compounds. Similarity between the fragments is minimized and 10 different fragments are mixed into a single cocktail, which is soaked to protein crystals. These crystals are analysed by X‐ray crystallography, revealing the binding modes of the bound fragment ligands.
Kaizhou Yan +5 more
wiley +1 more source
Filter for third order phase locked loops [PDF]
Filters for third-order phase-locked loops are used in receivers to acquire and track carrier signals, particularly signals subject to high doppler-rate changes in frequency.
Crow, R. B., Tausworthe, R. C.
core +1 more source
Structural biology of ferritin nanocages
Ferritin is a conserved iron‐storage protein that sequesters iron as a ferric mineral core within a nanocage, protecting cells from oxidative damage and maintaining iron homeostasis. This review discusses ferritin biology, structure, and function, and highlights recent cryo‐EM studies revealing mechanisms of ferritinophagy, cellular iron uptake, and ...
Eloise Mastrangelo, Flavio Di Pisa
wiley +1 more source
CMB temperature anisotropies from third order gravitational perturbations
In this paper we present a complete computation of the Cosmic Microwave Background (CMB) anisotropies up to third order from gravitational perturbations accounting for scalar, vector and tensor perturbations.
Bartolo, N. +3 more
core +2 more sources
The third-order law for magnetohydrodynamic turbulence with constant shear [PDF]
The scaling laws of mixed third‐order structure functions for isotropic, homogeneous, and incompressible magnetohydrodynamic (MHD) turbulence have been recently applied in solar wind studies, even though there is recognition that isotropy is not well ...
Matthaeus, William H. +3 more
core +2 more sources
Structural and biochemical characterisations show that the planar cell polarity (PCP) protein Inturned harbours a unique PDZ‐like domain that does not bind canonical PDZ‐binding motifs (PBMs) like that of another PCP protein Vangl2. In contrast, the apical‐basal polarity protein Scribble contains four PDZ domains that bind Vangl2, but one PDZ domain ...
Stephan Wilmes +4 more
wiley +1 more source
On Third-Order Bronze Fibonacci Numbers
In this study, we firstly obtain De Moivre-type identities for the second-order Bronze Fibonacci sequences. Next, we construct and define the third-order Bronze Fibonacci, third-order Bronze Lucas and modified third-order Bronze Fibonacci sequences. Then,
Mücahit Akbiyik, Jeta Alo
doaj +1 more source

