This paper shows the results of research on the optical control of a GaAs chip monolithic amplifier, and is an extension of previous work by our group in the field of optical-microwave interaction [1-3]. The amplifier was originally designed for the transmitter stage of an indoor mobile communications system in the 2.4 GHz band. The possibilities of optical control of this amplifier are evidenc...

We completely describe the higher secant dimensions of all connected homogeneous projective varieties of dimension at most 3, in all possible equivariant embeddings. In particular, we calculate these dimensions for all Segre-Veronese embeddings of P1 × P1, P1 × P1 × P1, and P2 × P1, as well as for the variety F of incident point-line pairs in P2. For P2 × P1 and F the results are new, while the...

Let P1, P2 be graph properties. A vertex (P1,P2)-partition of a graph G is a partition {V1, V2} of V (G) such that for i = 1, 2 the induced subgraph G[Vi] has the property Pi. A property R = P1◦P2 is defined to be the set of all graphs having a vertex (P1,P2)-partition. A graph G ∈ P1◦P2 is said to be uniquely (P1,P2)-partitionable if G has exactly one vertex (P1,P2)-partition. In this note, we...

(2) ‖Hα(f1, f2)‖p ≤ Cα,p1,p2‖f1‖p1‖f2‖p2 with constants Cα,p1,p2 depending only on α, p1, p2 and p := p1p2 p1+p2 hold. The first result of this type is proved in [4], and the purpose of the current paper is to extend the range of exponents p1 and p2 for which (2) is known. In particular, the case p1 = 2, p2 = ∞ is solved to the affirmative. This was originally considered to be the most natural ...

(2) ‖Hα(f1, f2)‖p ≤ Cα,p1,p2‖f1‖p1‖f2‖p2 with constants Cα,p1,p2 depending only on α, p1, p2 and p := p1p2 p1+p2 hold. The first result of this type is proved in [4], and the purpose of the current paper is to extend the range of exponents p1 and p2 for which (2) is known. In particular, the case p1 = 2, p2 = ∞ is solved to the affirmative. This was originally considered to be the most natural ...

The tobacco etch potyvirus (TEV) polyprotein is proteolytically processed by three viral proteinases (NIa, HC-Pro, and P1). While the NIa and HC-Pro proteinases each provide multiple functions essential for viral infectivity, the role of the P1 proteinase beyond its autoproteolytic activity is understood poorly. To determine if P1 is necessary for genome amplification and/or virus movement from...

The proposal was tested that (P1 X P2) F1 leads to P1 irradiation bone marrow chimeras expressed predominantly P1-restricted T cells because donor derived stem cells were exposed to recipient derived antigen-presenting cells in the thymus. Because P1 recipient-derived antigen-presenting cells are replaced only slowly after 6-8 wk by (P1 X P2) donor-derived antigen-presenting cells in the thymus...

We have characterized Unstable factor for orange1 (Ufo1), a dominant, allele-specific modifier of expression of the maize pericarp color1 (p1) gene. The p1 gene encodes an Myb-homologous transcriptional activator of genes required for biosynthesis of red phlobaphene pigments. The P1-wr allele specifies colorless kernel pericarp and red cobs, whereas Ufo1 modifies P1-wr expression to confer pigm...

The sorption of nuclease P1 onto chitosan nano-particles is studied in this paper. The effect of some adsorption kinetics factors such as nuclease P1 concentration, chitosan nano-particles solution concentration, adsorption temperature, chitosan nano-particles size, solution pH, etc. is investigated. Adsorption of nuclease P1 onto chitosan nano-particles is fitted into Lagergren first-order equ...

BACKGROUND The pericarp color1 (p1) gene encodes for a myb-homologous protein that regulates the biosynthesis of brick-red flavonoid pigments called phlobahpenes. The pattern of pigmentation on the pericarp and cob glumes depends upon the allelic constitution at the p1 locus. p1 alleles have unique gene structure and copy number which have been proposed to influence the epigenetic regulation of...