Defensive K channel

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Defensive k-alliances in graphs

Let Γ = (V,E) be a simple graph of order n and degree sequence δ1 ≥ δ2 ≥ · · · ≥ δn. For a nonempty set X ⊆ V , and a vertex v ∈ V , δX(v) denotes the number of neighbors v has in X. A nonempty set S ⊆ V is a defensive k-alliance in Γ = (V,E) if δS(v) ≥ δS̄(v) + k, ∀v ∈ S. The defensive k-alliance number of Γ, denoted by ak(Γ), is defined as the minimum cardinality of a defensive k-alliance in Γ...

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Global defensive k-alliances in graphs

Let Γ = (V,E) be a simple graph. For a nonempty set X ⊆ V , and a vertex v ∈ V , δX(v) denotes the number of neighbors v has in X. A nonempty set S ⊆ V is a defensive k-alliance in Γ = (V,E) if δS(v) ≥ δS̄(v)+k, ∀v ∈ S. A defensive k-alliance S is called global if it forms a dominating set. The global defensive k-alliance number of Γ, denoted by γ k(Γ), is the minimum cardinality of a defensive ...

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Boundary defensive k-alliances in graphs

We define a boundary defensive k-alliance in a graph as a set S of vertices with the property that every vertex in S has exactly k more neighbors in S than it has outside of S. In this paper we study mathematical properties of boundary defensive k-alliances. In particular, we obtain several bounds on the cardinality of every boundary defensive k-alliance. Moreover, we consider the case in which...

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A tripartite SNARE-K+ channel complex mediates in channel-dependent K+ nutrition in Arabidopsis.

A few membrane vesicle trafficking (SNARE) proteins in plants are associated with signaling and transmembrane ion transport, including control of plasma membrane ion channels. Vesicle traffic contributes to the population of ion channels at the plasma membrane. Nonetheless, it is unclear whether these SNAREs also interact directly to affect channel gating and, if so, what functional impact this...

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Determining K+ Channel Activation Curves from K+ Channel Currents Often Requires the Goldman–Hodgkin–Katz Equation

Potassium ion current in nerve membrane, I(K), has traditionally been described by I(K) = g(K)(V - E(K)), where g(K) is the K ion conductance, V is membrane potential and E(K) is the K(+) Nernst potential. This description has been unchallenged by most investigators in neuroscience since its introduction almost 60 years ago. The problem with the I(K) approximately (V - E(K)) proportionality is ...

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ژورنال

عنوان ژورنال: Acta Physiologica

سال: 2015

ISSN: 1748-1708

DOI: 10.1111/apha.12557