Results 111 to 120 of about 3,204,490 (302)
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
Certain Subclasses of Multivalent Analytic Functions
Two new subclasses and of multivalent analytic functions are introduced. Distortion inequalities and inclusion relation for and are obtained. Some results of the partial sums of functions in these classes are also given.
Yi-Ling Cang, Jin-Lin Liu
doaj +1 more source
Zeros of Gaussian Analytic Functions [PDF]
We prove and discuss three results on zero distribution of gaussian analytic functions: (i) the Edeleman-Kostlan formula for the expectation of the counting measure; (ii) a variation on the theme of Calabi's rigidity theorem; (iii) Offord's estimate of exponential decay of the tail probabilities of an anlytic function having an access or deficiency of ...
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
On some classes of analytic functions
Let m1, m2 be any numbers and let Vm1,m2 be the class of functions of analytic in the unit disc E={z:|z|
Khalida I. Noor, Haila Madifer
doaj +1 more source
DIATOMIC ANALYTIC MOLECULAR PARTITION FUNCTIONS FOR STELLAR ATMOSPHERES [PDF]
Approximate partition functions and their derivatives for diatomic molecules are formulated taking into account the finite number of levels. A procedure is developed to derive compact analytic expressions, without free parameters, necessary for the ...
OCTAVIO CARDONA NUÑEZ +1 more
core
Hyperosmotic stress induces PARP1‐mediated HPF1‐dependent mono(ADP‐ribosyl)ation
Sorbitol‐induced hyperosmotic stress rapidly induces reversible mono(ADP‐ribosyl)ation (MARylation) on PARP1 without the signs of genotoxic signaling. We show that PARP1 autoMARylation is HPF1 dependent and forms hydroxylamine‐resistant O‐glycosidic linkages.
Anna Georgina Kopasz +11 more
wiley +1 more source
Coefficient inequalities for certain analytic functions
For real α(α>1), we introduce subclasses M(α) and N(α) of analytic functions f(z) with f(0)=0 and f′(0)=1 in U. The object of the present paper is to consider the coefficient inequalities for functions f(z) to be in the classes M(α) and N(α).
Junichi Nishiwaki, Shigeyoshi Owa
doaj +1 more source
An isoform of 14‐3‐3 protein regulates transbilayer lipid movement at the plasma membrane
Loss of 14‐3‐3ζ in CHO cells confers resistance to exogenous phosphatidylserine (PS) and impairs endocytosis‐independent inward flip‐flop of fluorescent PS at the plasma membrane. RNAi‐mediated knockdown reproduces this defect, while no additive effect is seen in ATP11C‐deficient cells.
Akiko Yamaji‐Hasegawa +3 more
wiley +1 more source
q-Blossoming for analytic functions
We construct aᅠq-analog of the blossom for analytic functions, the analyticᅠq-blossom. Thisᅠq-analog also extends the notion ofᅠq-blossoming from polynomials to analytic functions.
Goldman, Ron, Simeonov, Plamen
core +1 more source

