Results 61 to 70 of about 15,646,549 (216)

Functional Role of Phospholipase D in Bone Metabolism. [PDF]

open access: yesJ Bone Metab, 2023
Kim HJ, Lee DK, Choi JY.
europepmc   +1 more source

Expression of Phospholipase D Family Member 6 in Bovine Testes and Its Molecular Characteristics. [PDF]

open access: yesInt J Mol Sci, 2023
Yang R   +10 more
europepmc   +1 more source

On the relation between cluster and classical tilting [PDF]

open access: yesarXiv, 2008
Let D be a triangulated category with a cluster tilting subcategory U. The quotient category D/U is abelian; suppose that it has finite global dimension. We show that projection from D to D/U sends cluster tilting subcategories of D to support tilting subcategories of D/U, and that, in turn, support tilting subcategories of D/U can be lifted uniquely
arxiv  

Chromatic number and complete graph substructures for degree sequences [PDF]

open access: yesarXiv, 2009
Given a graphic degree sequence $D$, let $\chi(D)$ (respectively $\omega(D)$, $h(D)$, and $H(D)$) denote the maximum value of the chromatic number (respectively, the size of the largest clique, largest clique subdivision, and largest clique minor) taken over all simple graphs whose degree sequence is $D$. It is proved that $\chi(D)\le h(D)$.
arxiv  

Brown Spider Venom Phospholipase-D Activity upon Different Lipid Substrates. [PDF]

open access: yesToxins (Basel), 2023
Chaves-Moreira D   +9 more
europepmc   +1 more source

Reducts of the Generic Digraph [PDF]

open access: yesarXiv, 2014
The generic digraph $(D,E)$ is the unique countable homogeneous digraph that embeds all finite digraphs. In this paper, we determine the lattice of reducts of $(D,E)$, where a structure $\mathcal{M}$ is a reduct of $(D,E)$ if it has domain $D$ and all its $\emptyset$-definable relations are $\emptyset$-definable relations of $(D,E)$.
arxiv  

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