Results 31 to 40 of about 2,049,523 (298)
Zeros of Dedekind zeta functions under GRH
, 2015 Assuming GRH, we prove an explicit upper bound for the number of zeros of a Dedekind zeta function having imaginary part in $[T-a,T+a]$. We also prove a bound for the multiplicity of the zeros.Comment: Some misprints corrected, simplified proof for a ...
Grenié, Loïc, Molteni, Giuseppe
core +1 more source
Multiplicity and concentration results for a fractional Schrödinger-Poisson type equation with magnetic field [PDF]
Proceedings of the Royal Society of Edinburgh: Section A Mathematics, 2018 This paper is devoted to the study of fractional Schrödinger-Poisson type equations with magnetic field of the type $$\varepsilon^{2s}(-\Delta)_{A/\varepsilon}^{s}u + V(x)u + {\rm e}^{-2t}(\vert x \vert^{2t-3} \ast \vert u\vert ^{2})u = f(\vert u \vert ...
V. Ambrosio
semanticscholar +1 more source
Generalized multiresolution analyses with given multiplicity functions [PDF]
, 2007 Generalized multiresolution analyses are increasing sequences of subspaces of a Hilbert space $\H$ that fail to be multiresolution analyses in the sense of wavelet theory because the core subspace does not have an orthonormal basis generated by a fixed ...
Baggett, Lawrence W. +5 more
core +4 more sources
Infection Models for Pine Wilt Disease on the Basis of Vector Behaviors
Population Ecology, EarlyView.Infection models for pine wilt disease without vector density were built to estimate the transmission coefficient of the pathogenic nematode. The models successfully simulated the annual change in the density of infected trees for four pine stands. ABSTRACT Pine wilt disease is caused by the pinewood nematode (Bursaphelenchus xylophilus Steiner et ...
Katsumi Togashi
wiley +1 more source
Phage therapy dosing: The problem(s) with multiplicity of infection (MOI)
Bacteriophage, 2016 The concept of bacteriophage multiplicity of infection (MOI) – ratios of phages to bacteria – historically has been less easily applied than many phage workers would prefer or, perhaps, may be aware.
S. Abedon
semanticscholar +1 more source
Population Ecology, EarlyView.Population size and dynamics fundamentally shape speciation by influencing genetic drift, founder events, and adaptive potential. Small populations may speciate rapidly due to stronger drift, whereas large populations harbor more genetic diversity, which can alter divergence trajectories. We highlight theoretical models that incorporate population size
Ryo Yamaguchi +3 more
wiley +1 more source
Social Education Research, 2021 History of mathematics (HOM) was incorporated into peer teaching during lesson study as a strategy to augment the mathematics self-efficacy of female pre-service teachers in Ghana.
Samuel Baah-Duodu +4 more
semanticscholar +1 more source
Fermionic one-loop amplitudes of the RNS superstring
, 2018 We investigate massless n-point one-loop amplitudes of the open RNS superstring with two external fermions and determine their worldsheet integrands.
Lee, Seungjin, Schlotterer, Oliver
core +1 more source
Structural dynamics of the plant hormone receptor ETR1 in a native‐like membrane environment
FEBS Letters, EarlyView.The present study unveils the structural and signaling dynamics of ETR1, a key plant ethylene receptor. Using an optimized nanodisc system and solution NMR, we captured full‐length ETR1 in a native‐like membrane environment. Our findings reveal dynamic domain uncoupling and Cu(I)‐induced rigidification, providing the first evidence of metal‐triggered ...
Moritz Lemke +2 more
wiley +1 more source
, 2014 For any given bounded symmetric domain, we prove the existence of commutative $C^*$-algebras generated by Toeplitz operators acting on any weighted Bergman space.
Dawson, Matthew +2 more
core +1 more source