(1) For all subsets A, B of E2 T such that A meets B holds proj1 ◦A meets proj1◦B. (2) Let A, B be subsets of E2 T and s be a real number. If A misses B and A⊆HorizontalLine(s) and B⊆ HorizontalLine(s), then proj1◦A misses proj1◦B. (3) For every closed subset S of E2 T such that S is Bounded holds proj1 ◦ S is closed. (4) For every compact subset S of E2 T holds proj1 ◦ S is compact. (5) Let p,...

Mono- and polyclonal antibodies directed against different domains of the potato leafroll luteovirus (PLRV) P1 (ORF1) protein were applied to the analysis of P1 expression during PLRV replication in planta. Western analyses detected P1 and a protein of approximately 25 kDa (P1-C25) that accumulated to readily detectable amounts in PLRV-infected plants, but was not detected by in vitro cell-free...

A Mycoplasma pneumoniae cytadhesin P1 gene with novel nucleotide sequence variation has been identified. Four clinical strains of M. pneumoniae were found to carry this type of P1 gene. This new P1 gene is similar to the known group II P1 genes but possesses novel sequence variation of approximately 300 bp in the RepMP2/3 region. The position of the new variable region is distant from the previ...

ly seen, the main problem of the theory of Eisenstein series is to analyze thespace L(ξ) or the spaces L({P}, ξ) in terms of the cusp forms on the various M . Thisanalysis is carried out—in principle—in the text. However, one can be satisfied with amore perspicuous statement if one is content to analyze L(ξ) in terms of the representationsoccurring discretely in the spaces of au...

approved: Richard 0. Hampton Pea seed-borne mosaic potyvirus pathotype 1 (PSbMV-P1) has the ability to infect most genotypes of Pisum sativum. The exception are those genotypes that are homozygous recessive for the sbm-1 gene. The life cycle of PSbMV pathotype 4 (PSbMV-P4) is unaffected by the sbm-1/sbm-1 genotype. Infectious clones of Pl-P4 recombinants were used to define the genomic segment ...

Allelic variation at the Zea mays (maize) pericarp color1 (p1) gene has been attributed to epigenetic gene regulation. A p1 distal enhancer, 5.2 kb upstream of the transcriptional start site, has demonstrated variation in DNA methylation in different p1 alleles/epialleles. In addition, DNA methylation of sequences within the 3' end of intron 2 also plays a role in tissue-specific expression of ...

A transgene carrying a distal enhancer element of the maize P1-rr promoter caused silencing of an endogenous P1-rr allele in the progeny of transgenic maize plants. Expression of both the transgene and the endogenous P1-rr allele was reduced in the affected plants. The silenced phenotype was observed in the progeny of seven of eight crosses involving three independent transgenic events tested (...

The bifurcations of generic heteroclinic loop with one nonhyperbolic equilibrium p1 and one hyperbolic saddle p2 are investigated, where p1 is assumed to undergo transcritical bifurcation. Firstly, we discuss bifurcations of heteroclinic loop when transcritical bifurcation does not happen, the persistence of heteroclinic loop, the existence of homoclinic loop connecting p1 (resp. p2) and the co...

The expression of a molecular cDNA clone (P1 KIN) of the human RNA-dependent P1/eIF-2 alpha protein kinase (PKR) was examined in transfected monkey cells and in cell-free protein-synthesizing systems. Expression of the wild-type (wt) P1 KIN cDNA, which encodes an active protein kinase, was compared with that of the phosphotransfer catalytic domain II Lys-296-->Arg (K296R) mutant cDNA, which doe...

Mycoplasma pneumoniae strains traditionally are divided into two types, based on sequence variation in the P1 gene. Recently, however, we have identified 8 P1 subtypes by restriction fragment length polymorphism analysis. In the present study the P1 gene sequences of three P1 type 1 and two P1 type 2 M. pneumoniae strains were analyzed. A new P1 gene sequence in a type 1 strain with partial sim...