The relative cohomology Hdiff1(K(1|3), osp(2, 3);Dγ,µ(S1|3)) of the contact Lie superalgebra K(1|3) with coefficients in the space of differential operators Dγ,µ(S1|3) acting on tensor densities on S1|3, is calculated in N.Ben Fraj, I. Laraied, S. Omri (2013) and the generating 1-cocycles are expressed in terms of the infinitesimal super-Schwarzian derivative 1-cocycle s(Xf) = D1D2D3(f)α31/2, Xf \in K(1|3) which is invariant with respect to the conformal subsuperalgebra osp(2, 3) of K(1|3). In this work we study the supergroup case. We give an explicit construction of 1-cocycles of the group of contactomorphisms K(1|3) on the supercircle S1|3 generating the relative cohomology Hdiff1(K(1|3), PC(2, 3); Dγ,µ(S1|3) with coefficients in Dγ,µ(S1|3). We show that they possess properties similar to those of the super-Schwarzian derivative 1-cocycle S3(Φ) = EΦ-1 (D1(D2),D3)α31/2, Φ ∈ K(1|3) introduced by Radul which is invariant with respect to the conformal group PC(2, 3) of K(1|3). These cocycles are expressed in terms of S3(Φ) and possess its properties., Boujemaa Agrebaoui, Raja Hattab., and Obsahuje seznam literatury
The 14-3-3 proteins are a family of acidicr egulatory molecules found in all eukaryotes. 14-3-3 proteins function as molecular scaffolds by modulating the conformation of their binding partners. Through the functional modulation of a wide range of binding partners, 14-3-3 proteins are involved in many processes including cell cycle regulation, metabolism control, apoptosis, and control of gene transcription. This minireview includes a short overview of 14-3-3 proteins and then focuses on their role in the regulation of two important binding partners: FOXO forkhead transcription factors and an enzyme tyrosine hydroxylase., V. Obšilová, J. Šilhan, E. Bouřa, J. Teisinger, T. Obšil., and Obsahuje bibliografii a bibliografické odkazy
Speleothems in 6 sandstone caves in the Bohemian Paradise (Český ráj) were dated by means of 14C and U-series methods. Stable isotopes of C and O, FAAS, IR, XRD, XRF and SEM were used to characterize the carbonate material and its source. Stable isotopes (C and O) composition of speleothems in two caves corresponds to values characteristic for cave speleothems in Central Europe. In other caves they indicate evaporation and fast carbon dioxide escape during carbonate precipitation. The speleothems from the Krtola Cave were deposited between 8 and 13 kyr BP. Speleothems were deposited 5-8 kyr BP in the Sintrová, Mrtvé Údolí and U Studánky caves. Calcite coatings on smooth sandstone surfaces in studied caves demonstrate that cave walls did not retreat even a few mm in the last 5-8 kyr since speleothem deposition and are thus not evolving under recent climatic conditions. Most of the cave ceilings and walls are at present time indurated by hardened surfaces, which protect the sandstone from erosion. Sandstone caves probably intensively evolved either during or at the end of the Last Glacial period. There are two different erosion mechanisms which might have formed/reshaped the caves at that time: A) In the case of permafrost conditions: Repeated freeze/melt cycles affecting sandstone pore space followed by the transport of fallen sand grains by minor temporary trickles. We expect that heat was transmitted by air circulating between the cave and the surface; B) Seepage erosion of sandstone during the melting of permafrost, prior forming of case hardening., Jiří Bruthans, Jana Schweigstillová, Petr Jenč, Zdeňka Churáčková and Petr Bezdička., and Obsahuje bibliografii
Our own study as well as others have previously reported that hypoxia activates 15-lipoxygenase (15-LO) in the brain, causing a series of chain reactions, which exacerbates ischemic stroke. 15-hydroxyeicosatetraenoic acid (15-HETE) and 15-oxoeicosatetraenoic acid (15-oxo-ETE/15-KETE) are 15-LO-specific metabolites of arachidonic acid (AA). 15-HETE was found to be rapidly converted into 15-oxo-ETE by 15-hydroxyprostaglandin dehydrogenase (15-PGDH) in some circumstances. We have demonstrated that 15-HETE promotes cerebral vasoconstriction during hypoxia. However, the effect of 15-oxo-ETE upon the contraction of cerebral vasculature remains unclear. To investigate this effect and to clarify the underlying mechanism, we performed immunohistochemistry and Western blot to test the expression of 15-PGDH in rat cerebral tissue, examined internal carotid artery (ICA) tension in isolated rat ICA rings. Western blot and reverse transcription polymerase chain reaction (RT-PCR) were used to analyze the expression of voltage-gated potassium (Kv) channels (Kv2.1, Kv1.5, and Kv1.1) in cultured cerebral arterial smooth muscle cells (CASMCs). The results showed that the levels of 15-PGDH expression were drastically elevated in the cerebral of rats with hypoxia, and 15-oxo-ETE enhanced ICA contraction in a dose-dependent manner. This effect was more significant in the hypoxic rats than in the normoxic rats. We also found that 15-oxo-ETE significantly attenuated the expression of Kv2.1 and Kv1.5, but not Kv1.1. In conclusion, these results suggest that 15-oxo-ETE leads to the contraction of the ICA, especially under hypoxic conditions and that specific Kv channels may play an important role in 15-oxo- ETE-induced ICA constriction., Di Wang, Yu Liu, Ping Lu, Daling Zhu, Yulan Zhu., and Obsahuje bibliografii
An edge of $G$ is singular if it does not lie on any triangle of $G$; otherwise, it is non-singular. A vertex $u$ of a graph $G$ is called locally connected if the induced subgraph $G[N(u)]$ by its neighborhood is connected; otherwise, it is called locally disconnected. In this paper, we prove that if a connected claw-free graph $G$ of order at least three satisfies the following two conditions: (i) for each locally disconnected vertex $v$ of degree at least $3$ in $G,$ there is a nonnegative integer $s$ such that $v$ lies on an induced cycle of length at least $4$ with at most $s$ non-singular edges and with at least $s-5$ locally connected vertices; (ii) for each locally disconnected vertex $v$ of degree $2$ in $G,$ there is a nonnegative integer $s$ such that $v$ lies on an induced cycle $C$ with at most $s$ non-singular edges and with at least $s-3$ locally connected vertices and such that $G[V (C)\cap V_{2} (G)]$ is a path or a cycle, then $G$ has a 2-factor, and it is the best possible in some sense. This result generalizes two known results in Faudree, Faudree and Ryjáček (2008) and in Ryjáček, Xiong and Yoshimoto (2010).
Let $\tau $ be a type of algebras. A valuation of terms of type $\tau $ is a function $v$ assigning to each term $t$ of type $\tau $ a value $v(t) \geq 0$. For $k \geq 1$, an identity $s \approx t$ of type $\tau $ is said to be $k$-normal (with respect to valuation $v$) if either $s = t$ or both $s$ and $t$ have value $\geq k$. Taking $k = 1$ with respect to the usual depth valuation of terms gives the well-known property of normality of identities. A variety is called $k$-normal (with respect to the valuation $v$) if all its identities are $k$-normal. For any variety $V$, there is a least $k$-normal variety $N_k(V)$ containing $V$, namely the variety determined by the set of all $k$-normal identities of $V$. The concept of $k$-normalization was introduced by K. Denecke and S. L. Wismath in their paper (Algebra Univers., 50, 2003, pp.107-128) and an algebraic characterization of the elements of $N_k(V)$ in terms of the algebras in $V$ was given in (Algebra Univers., 51, 2004, pp. 395--409). In this paper we study the algebras of the variety $N_2(V)$ where $V$ is the type $(2,2)$ variety $L$ of lattices and our valuation is the usual depth valuation of terms. We introduce a construction called the {\it $3$-level inflation} of a lattice, and use the order-theoretic properties of lattices to show that the variety $N_2(L)$ is precisely the class of all $3$-level inflations of lattices. We also produce a finite equational basis for the variety $N_2(L)$.