Results 41 to 50 of about 389,954 (327)
We find and propose an explanation for a large variety of modularity-related symmetries in problems of 3-manifold topology and physics of 3d N $$ \mathcal{N} $$ = 2 theories where such structures a priori are not manifest.
Miranda C.N. Cheng +4 more
doaj +1 more source
Bounds for twisted symmetric square L-functions via half-integral weight periods
We establish the first moment bound $$\begin{align*}\sum_{\varphi} L(\varphi \otimes \varphi \otimes \Psi, \tfrac{1}{2}) \ll_\varepsilon p^{5/4+\varepsilon} \end{align*}$$ for triple product L-functions, where $\Psi $ is a fixed Hecke ...
Paul D. Nelson
doaj +1 more source
Mapping the evolution of mitochondrial complex I through structural variation
Respiratory complex I (CI) is crucial for bioenergetic metabolism in many prokaryotes and eukaryotes. It is composed of a conserved set of core subunits and additional accessory subunits that vary depending on the organism. Here, we categorize CI subunits from available structures to map the evolution of CI across eukaryotes. Respiratory complex I (CI)
Dong‐Woo Shin +2 more
wiley +1 more source
Poincaré series for modular graph forms at depth two. Part II. Iterated integrals of cusp forms
We continue the analysis of modular invariant functions, subject to inhomogeneous Laplace eigenvalue equations, that were determined in terms of Poincaré series in a companion paper. The source term of the Laplace equation is a product of (derivatives of)
Daniele Dorigoni +2 more
doaj +1 more source
Ordinary pseudorepresentations and modular forms
In this short note, we observe that the techniques of our recent work "Pseudo-modularity and Iwasawa theory" can be used to provide a new proof of some of the residually reducible modularity lifting results of Skinner and Wiles.
Wake, Preston, Wang-Erickson, Carl
core +1 more source
Fluorescent probes allow dynamic visualization of phosphoinositides in living cells (left), whereas mass spectrometry provides high‐sensitivity, isomer‐resolved quantitation (right). Their synergistic use captures complementary aspects of lipid signaling. This review illustrates how these approaches reveal the spatiotemporal regulation and quantitative
Hiroaki Kajiho +3 more
wiley +1 more source
Heterotic-string amplitudes at one loop: modular graph forms and relations to open strings
We investigate one-loop four-point scattering of non-abelian gauge bosons in heterotic string theory and identify new connections with the corresponding open-string amplitude.
Jan E. Gerken +2 more
doaj +1 more source
sl(2)ˆ Decomposition of denominator formulae of some BKM Lie superalgebras - II
The square-root of Siegel modular forms of CHL ZN orbifolds of type II compactifications are denominator formulae for some Borcherds-Kac-Moody Lie superalgebras for N=1,2,3,4.
Suresh Govindarajan, Mohammad Shabbir
doaj +1 more source
Hecke operators on Hilbert-Siegel modular forms
We define Hilbert-Siegel modular forms and Hecke "operators" acting on them. As with Hilbert modular forms, these linear transformations are not linear operators until we consider a direct product of spaces of modular forms (with varying groups), modulo ...
Caulk, Suzanne, Walling, Lynne H.
core +1 more source
Bifidobacterium bifidum establishes symbiosis with infants by metabolizing lacto‐N‐biose I (LNB) from human milk oligosaccharides (HMOs). The extracellular multidomain enzyme LnbB drives this process, releasing LNB via its catalytic glycoside hydrolase family 20 (GH20) lacto‐N‐biosidase domain.
Xinzhe Zhang +5 more
wiley +1 more source

