119 research outputs found
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High energy beam transport beamline for LEDA
Here the authors describe the High Energy Beam Transport (HEBT) for the Low Energy Demonstration Accelerator (LEDA), which is part of the Accelerator Production of Tritium (APT) project. The authors used the TRACE 3-D linear design code for the first-order design and performed r-z and 3-D particle-in-cell (PIC) simulations to study the beam distribution and halo. TRACE 3-D predicts rms beam properties well. The PIC simulations are important for determining the presence of beam halo, which is present for some tunes. They propose halo experiments to help validate the simulation codes for modeling nonlinear space charge
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Design and Development of the LEDA Slow Wire Scanner Profile Measurement
The Low Energy Demonstration Accelerator (LEDA) [1, 2] is being developed at Los Alamos National Laboratory as part of the Accelerator Production of Tritium (APT) project. One of the diagnostics being developed to commission LEDA [3] is a slow wire scanner beam profile measurement. Initial profile measurements will be made at 6.7 MeV beam energy and 100 mA beam current. The wire scanner is an interceptive device that will move two silicon carbide coated graphite mono-filament fibers (wires) through the beam, in order to obtain the profile. Some of the design considerations discussed are; Mechanical design, wire temperature analysis, secondary electron detection, signal processing, and system control
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Noninterceptive beam energy measurements in line D of the Los Alamos Meson Physics Facility
Several members of the Accelerator and Operations Technology (AOT) division beam-diagnostics team performed time-of-flight (TOF) beam-energy measurements in line D of the Los Alamos Meson Physics Facility (LAMPF) using developmental beam time. These measurements provided information for a final design of an on-line beam energy measurement. The following paper discusses these measurements and how they apply to the final beam energy measurement design
BET Bromodomain Inhibition as a Therapeutic Strategy to Target c-Myc
SummaryMYC contributes to the pathogenesis of a majority of human cancers, yet strategies to modulate the function of the c-Myc oncoprotein do not exist. Toward this objective, we have targeted MYC transcription by interfering with chromatin-dependent signal transduction to RNA polymerase, specifically by inhibiting the acetyl-lysine recognition domains (bromodomains) of putative coactivator proteins implicated in transcriptional initiation and elongation. Using a selective small-molecule bromodomain inhibitor, JQ1, we identify BET bromodomain proteins as regulatory factors for c-Myc. BET inhibition by JQ1 downregulates MYC transcription, followed by genome-wide downregulation of Myc-dependent target genes. In experimental models of multiple myeloma, a Myc-dependent hematologic malignancy, JQ1 produces a potent antiproliferative effect associated with cell-cycle arrest and cellular senescence. Efficacy of JQ1 in three murine models of multiple myeloma establishes the therapeutic rationale for BET bromodomain inhibition in this disease and other malignancies characterized by pathologic activation of c-Myc.PaperFlic
Nanopore native RNA sequencing of a human poly(A) transcriptome
High-throughput complementary DNA sequencing technologies have advanced our understanding of transcriptome complexity and regulation. However, these methods lose information contained in biological RNA because the copied reads are often short and modifications are not retained. We address these limitations using a native poly(A) RNA sequencing strategy developed by Oxford Nanopore Technologies. Our study generated 9.9 million aligned sequence reads for the human cell line GM12878, using thirty MinION flow cells at six institutions. These native RNA reads had a median length of 771 bases, and a maximum aligned length of over 21,000 bases. Mitochondrial poly(A) reads provided an internal measure of read-length quality. We combined these long nanopore reads with higher accuracy short-reads and annotated GM12878 promoter regions to identify 33,984 plausible RNA isoforms. We describe strategies for assessing 3′ poly(A) tail length, base modifications and transcript haplotypes
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Position measurements for the isotope production facility and the switchyard kicker upgrade projects
The Los Alamos Neutron Science Center (LANSCE) is installing two beam lines to both improve operational tuning and provide new capabilities within the facility. The Isotope Production Facility (IPF) will provide isotopes for medical purposes by using the H' beam spur at 100 MeV and the Switchyard Kicker Upgrade (SYK) will allow the LANSCE 800-MeV H beam to be rapidly switched between various beam lines within the facility. The beam position measurements for both of these beam lines uses a standard micro-stripline beam position monitor (BPM) with both a 50-mm and 75-mm radius. The cable plant is unique in that it unambiguously provides a method of verifying the operation of the complete position measurement. The processing electronics module uses a log ratio technique with error corrections such that it has a dynamic range of -12 dBm to -85 dBm with errors less than 0.15 dB within this range. This paper will describe the primary components of these measurement systems and provide initial data of their operation
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