58 research outputs found
Magnetic Field Induced Charge Instabilities in Weakly Coupled Superlattices
Using a time dependent selfconsistent model for vertical sequential
tunneling,we study the appearance of charge instabilities that lead to the
formation of electric field domains in a weakly coupled doped superlattice in
the presence of high magnetic fields parallel to the transport direction. The
interplay between the high non linearity of the system --coming from the
Coulomb interaction-- and the inter-Landau-level scattering at the domain walls
(regions of charge accumulation inside the superlattice) gives rise to new
unstable negative differential conductance regions and extra stable branches in
the sawtooth-like I-V curves.Comment: 5 pages, 4 postscript figure
The nucleotide sequence of the 60kDa cysteine rich outer membrane protein ofChlamydia psittacistrain EAE/A22/M
An IL-27-Driven Transcriptional Network Identifies Regulators of IL-10 Expression across T Helper Cell Subsets.
Interleukin-27 (IL-27) is an immunoregulatory cytokine that suppresses inflammation through multiple mechanisms, including induction of IL-10, but the transcriptional network mediating its diverse functions remains unclear. Combining temporal RNA profiling with computational algorithms, we predict 79 transcription factors induced by IL-27 in T cells. We validate 11 known and discover 5 positive (Cebpb, Fosl2, Tbx21, Hlx, and Atf3) and 2 negative (Irf9 and Irf8) Il10 regulators, generating an experimentally refined regulatory network for Il10. We report two central regulators, Prdm1 and Maf, that cooperatively drive the expression of signature genes induced by IL-27 in type 1 regulatory T cells, mediate IL-10 expression in all T helper cells, and determine the regulatory phenotype of colonic Foxp3 <sup>+</sup> regulatory T cells. Prdm1/Maf double-knockout mice develop spontaneous colitis, phenocopying ll10-deficient mice. Our work provides insights into IL-27-driven transcriptional networks and identifies two shared Il10 regulators that orchestrate immunoregulatory programs across T helper cell subsets
Associations between serotype and susceptibility to antibiotics of Neisseria gonorrhoeae.
Viral gastroenteritis: small round structured viruses, caliciviruses and astroviruses. Part II. The epidemiological perspective.
Genome organization in the caliciviridae
Caliciviruses cause a wide spectrum of important diseases. These viruses have a positive-sense single-stranded RNA genome; recently, the complete genome sequences of several caliciviruses have been determined. This review outlines the genome organization and phylogenetic relationships of the animal and candidate human caliciviruses
Stable cloning of the amino terminus of the 60k outer membrane protein of Chlamydia trachomatis serovar L1
A mixed twenty-five base oligonucleotide probe was synthesized to the amino terminus of the 60 kDa cysteine-rich outer membrane protein of Chlamydia trachomatis serovar F. This probe hybridized to a single band in Southern blots of C. trachomatis serovar L1 DNA. However, repeated attempts at screening plasmid-based genomic libraries failed to yield positive signals. As an alternative approach, bacteriophage M13 was used as the primary cloning vector. With this vector two identical stable recombinants were isolated carrying a 2.2 kb Pst1 insert that hybridized to the oligonucleotide probe. Attempts to re-clone this fragment in plasmid-based vectors yielded very small unstable colonies. DNA encoding the amino terminus of the 60 kDa outer membrane protein was further localised to a 274 bp Sau3A fragment which was sub-cloned in both orientations in m13. DNA sequence analysis of this fragment from C. trachomatis serovar L1 demonstrated a perfect 15/15 amino acid match to the amino terminus of the 60 kDa outer membrane protein from C. trachomatis serovar F. On the basis of these results we suggest bacteriophage M13 as a general cloning vector to avoid the toxic effects of the amino termini of foreign outer membrane proteins in Escherichia coli
Viral gastroenteritis: the human caliciviruses
The caliciviruses are a major cause of viral gastroenteritis but the lack of diagnostic procedures has resulted in their role being under-rated. Norwalk-like viruses are detected by negative stain electron microscopy and their appearance results in their being called small round structured viruses. Spread is by food and contamination of the environment by vomitus. There are many genetic variants and only small numbers of virus particles are shed during infection. Sapporo-like viruses have a 3-fold axis of symmetry and are usually associated with paediatric gastroenteritis. Cell culture systems are lacking. There is no long-lived immunity following infection. Hand washing and protective clothing are essential during outbreaks
Molecular cloning and sequence analysis of a developmentally regulated cysteine-rich outer membrane protein from Chlamydia trachomatis.
Two overlapping genomic fragments have been cloned from Chlamydia trachomatis serovar L1 DNA. Sequence determination of 2530 bp has revealed two open reading frames coding for 'cysteine-rich' (Cr) proteins. One of these proteins was confirmed, by analysis of the inferred amino acid sequence, as the 60-kDa Cr outer membrane protein associated with differentiation of reticulate bodies (RBs) into elementary bodies (EBs). The other smaller 15-kDa protein contained a high percentage of methionine and cysteine and may correspond to a reported smaller and co-ordinately synthesised Cr outer-membrane protein also associated with RB to EB differentiation. Sequencing showed three potential stem-loop structures within the 5', 3' and intergenic regions of the cloned fragment. Southern-blot analysis revealed that the cloned fragment is conserved in ten serovars of C. trachomatis and that a strongly cross-hybridising fragment is also present in Chlamydia psittaci
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