Lidt om Jordnødkager.

Lidt om Jordnødkager

Mindre Meddelelser

Mindre Meddelelse

Agrikulturkemisk Konsulentvirksomhed i 1908.

Agrikulturkemisk Konsulentvirksomhed i 1908

Planters Evne til direkte at binde Luftens Kvælstof i Følge de af Th. Jamieson i 1905 udførte Undersøgelser med nogle supplerende Bemærkninger.

Planters Evne til direkte at binde Luftens Kvælstof i Følge de af Th. Jamieson i 1905 udførte Undersøgelser med nogle supplerende Bemærkninger

Vore Kunstgødninger. 1. Kvælstofgødninger i 1905.

Vore Kunstgødninger. 1. Kvælstofgødninger i 1905

Relative commutants of strongly self-absorbing C*-algebras

The relative commutant $A'\cap A^{\mathcal{U}}$ of a strongly self-absorbing algebra $A$ is indistinguishable from its ultrapower $A^{\mathcal{U}}$. This applies both to the case when $A$ is the hyperfinite II$_1$ factor and to the case when it is a strongly self-absorbing C*-algebra. In the latter case we prove analogous results for $\ell_\infty(A)/c_0(A)$ and reduced powers corresponding to other filters on $\bf N$. Examples of algebras with approximately inner flip and approximately inner half-flip are provided, showing the optimality of our results. We also prove that strongly self-absorbing algebras are smoothly classifiable, unlike the algebras with approximately inner half-flip.Comment: Some minor correction

The topological dimension of type I C*-algebras

While there is only one natural dimension concept for separable, metric spaces, the theory of dimension in noncommutative topology ramifies into different important concepts. To accommodate this, we introduce the abstract notion of a noncommutative dimension theory by proposing a natural set of axioms. These axioms are inspired by properties of commutative dimension theory, and they are for instance satisfied by the real and stable rank, the decomposition rank and the nuclear dimension. We add another theory to this list by showing that the topological dimension, as introduced by Brown and Pedersen, is a noncommutative dimension theory of type I C*-algebras. We also give estimates of the real and stable rank of a type I C*-algebra in terms of its topological dimension.Comment: 20 pages; minor correction

A Simple Separable Exact C*-Algebra not Anti-isomorphic to Itself

We give an example of an exact, stably finite, simple. separable C*-algebra D which is not isomorphic to its opposite algebra. Moreover, D has the following additional properties. It is stably finite, approximately divisible, has real rank zero and stable rank one, has a unique tracial state, and the order on projections over D is determined by traces. It also absorbs the Jiang-Su algebra Z, and in fact absorbs the 3^{\infty} UHF algebra. We can also explicitly compute the K-theory of D, namely K_0 (D) = Z[1/3] with the standard order, and K_1 (D) = 0, as well as the Cuntz semigroup of D.Comment: 16 pages; AMSLaTeX. The material on other possible K-groups for such an algebra has been moved to a separate paper (1309.4142 [math.OA]

Monoids of intervals of simple refinement monoids and non-stable K-Theory of multiplier algebras

We show that the representation of the monoid of intervals of a simple refinement monoid in terms of affine semicontinuous functions, given by Perera in 2001, fails to be faithful in the case of strictly perforated monoids. We give some potential applications of this result in the context of monoids of intervals and K-Theory of multiplier rings

Centralized Modularity of N-Linked Glycosylation Pathways in Mammalian Cells

Glycosylation is a highly complex process to produce a diverse repertoire of cellular glycans that are attached to proteins and lipids. Glycans are involved in fundamental biological processes, including protein folding and clearance, cell proliferation and apoptosis, development, immune responses, and pathogenesis. One of the major types of glycans, N-linked glycans, is formed by sequential attachments of monosaccharides to proteins by a limited number of enzymes. Many of these enzymes can accept multiple N-linked glycans as substrates, thereby generating a large number of glycan intermediates and their intermingled pathways. Motivated by the quantitative methods developed in complex network research, we investigated the large-scale organization of such N-linked glycosylation pathways in mammalian cells. The N-linked glycosylation pathways are extremely modular, and are composed of cohesive topological modules that directly branch from a common upstream pathway of glycan synthesis. This unique structural property allows the glycan production between modules to be controlled by the upstream region. Although the enzymes act on multiple glycan substrates, indicating cross-talk between modules, the impact of the cross-talk on the module-specific enhancement of glycan synthesis may be confined within a moderate range by transcription-level control. The findings of the present study provide experimentally-testable predictions for glycosylation processes, and may be applicable to therapeutic glycoprotein engineering