Results 61 to 70 of about 575,106 (294)
Biomolecular condensates formed by fused in sarcoma (FUS) are dissolved by high ATP concentrations yet persist in cells. Using a reconstituted system, we demonstrate that valosin‐containing protein (VCP), an AAA+ ATPase, counteracts ATP‐driven dissolution of FUS condensates through its D2 ATPase activity.
Hitomi Kimura +2 more
wiley +1 more source
On higher spin partition functions
We observe that the partition function of the set of all free massless higher spins s=0,1,2,3,... in flat space is equal to one: the ghost determinants cancel against the "physical" ones or, equivalently, the (regularized) total number of degrees of ...
Beccaria, M., Tseytlin, A. A.
core +1 more source
Approximating the Bethe partition function
When belief propagation (BP) converges, it does so to a stationary point of the Bethe free energy $F$, and is often strikingly accurate. However, it may converge only to a local optimum or may not converge at all. An algorithm was recently introduced for attractive binary pairwise MRFs which is guaranteed to return an $ε$-approximation to the global ...
Weller, Adrian, Jebara, Tony
openaire +4 more sources
Diversity and complexity in neural organoids
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
Kostant partition functions for affine Kac-Moody algebras
Employing the method of generating functions in conjunction with various number-thoretic identities, we obtain recursion relations for the Kostant partition functions for the affine Kac-Moody algebras The partition functions for the higher rank algebras ...
T. S. Santhanam, R. Chakrabarti
doaj +1 more source
Surprises for QCD at Nonzero Chemical Potential [PDF]
In this lecture we compare different QCD-like partition functions with bosonic quarks and fermionic quarks at nonzero chemical potential. Although it is not a surprise that the ground state properties of a fermionic quantum system and a bosonic quantum ...
Splittorff, K., Verbaarschot, J. J. M.
core +3 more sources
Congruences of the Partition Function
Let $p(n)$ denote the partition function. In this article, we will show that congruences of the form $$ p(m^j\ell^kn+B)\equiv 0\mod m \text{for all} n\ge 0 $$ exist for all primes $m$ and $\ell$ satisfying $m\ge 13$ and $\ell\neq 2,3,m$. Here the integer $k$ depends on the Hecke eigenvalues of a certain invariant subspace of $S_{m/2-1}(Γ_0(576),χ_{12})$
openaire +2 more sources
Parking Functions and Noncrossing Partitions [PDF]
A parking function is a sequence $(a_1,\dots,a_n)$ of positive integers such that, if $b_1\leq b_2\leq \cdots\leq b_n$ is the increasing rearrangement of the sequence $(a_1,\dots, a_n),$ then $b_i\leq i$. A noncrossing partition of the set $[n]=\{1,2,\dots,n\}$ is a partition $\pi$ of the set $[n]$ with the property that if $a < b < c < d ...
openaire +2 more sources
Mitochondrial remodeling shapes neural and glial lineage progression by matching metabolic supply with demand. Elevated OXPHOS supports differentiation and myelin formation, while myelin compaction lowers mitochondrial dependence, revealing mitochondria as key drivers of developmental energy adaptation.
Sahitya Ranjan Biswas +3 more
wiley +1 more source
5d partition functions with a twist
We derive the partition function of 5d N = 1 $$ \mathcal{N}=1 $$ gauge theories on the manifold S b 3 × Σ g $$ {S}_b^3 \times {\varSigma}_{\mathfrak{g}} $$ with a partial topological twist along the Riemann surface, Σ g $$ {\varSigma}_{\mathfrak{g}} $$ .
P. Marcos Crichigno +2 more
doaj +1 more source

