658 research outputs found
Building CMS Pixel Barrel Detectur Modules
For the barrel part of the CMS pixel tracker about 800 silicon pixel detector
modules are required. The modules are bump bonded, assembled and tested at the
Paul Scherrer Institute. This article describes the experience acquired during
the assembly of the first ~200 modules.Comment: 5 pages, 7 figures, Vertex200
CMS Barrel Pixel Detector Overview
The pixel detector is the innermost tracking device of the CMS experiment at
the LHC. It is built from two independent sub devices, the pixel barrel and the
end disks. The barrel consists of three concentric layers around the beam pipe
with mean radii of 4.4, 7.3 and 10.2 cm. There are two end disks on each side
of the interaction point at 34.5 cm and 46.5 cm. This article gives an overview
of the pixel barrel detector, its mechanical support structure, electronics
components, services and its expected performance.Comment: Proceedings of Vertex06, 15th International Workshop on Vertex
Detector
Compact frontend-electronics and bidirectional 3.3 Gbps optical datalink for the H1-experiment
Compact Frontend-Electronics and Bidirectional 3.3 Gbps Optical Datalink for Fast Proportional Chamber Readout
The 9600 channels of the multi-wire proportional chamber of the H1 experiment
at HERA have to be read out within 96 ns and made available to the trigger
system. The tight spatial conditions at the rear end flange require a compact
bidirectional readout electronics with minimal power consumption and dead
material.
A solution using 40 identical optical link modules, each transferring the
trigger information with a physical rate of 4 x 832 Mbps via optical fibers,
has been developed and commisioned. The analog pulses from the chamber can be
monitored and the synchronization to the global HERA clock signal is ensured.Comment: 13 pages, 10 figure
1,2-Bis{bis[4-(trifluoromethyl)phenyl]phosphino}ethane
Crystals of the title compound, C30H20F12P2 or R
2PCH2CH2PR
2 (R = 4-C6H4CF3), were inadvertently prepared while attempting to recrystallize a crude sample of trans-Re(Cl)(N2)(R
2PCH2CH2PR
2)2 from diethyl ether. The molecule lies on a center of inversion. One of the rings lies approximately in the P—C—C—P plane; the dihedral angle is 174.53°.The other ring is not quite perpendicular; the dihedral angle is 71.1°. The compound is isostructural with the R = Ph, 4-C6H4CH3 and 4-C6H4CH2CH3 analogues. It is well known that the basicity of phosphines and diphosphines can be altered by changing the electron-donating ability of R; however, the structural parameters for the title compound do not significantly differ from those of the aforementioned substituted-phenyl compounds
Cellular mechano-environment regulates the mammary circadian clock
Circadian clocks drive B24 h rhythms in tissue physiology. They rely on transcriptional/ translational feedback loops driven by interacting networks of clock complexes. However, little is known about how cell-intrinsic circadian clocks sense and respond to their microenvironment. Here, we reveal that the breast epithelial clock is regulated by the mechano-chemical stiffness of the cellular microenvironment in primary cell culture. Moreover, the mammary clock is controlled by the periductal extracellular matrix in vivo, which contributes to a dampened circadian rhythm during ageing. Mechanistically, the tension sensing cell-matrix adhesion molecule, vinculin, and the Rho/ROCK pathway, which transduces signals provided by extracellular stiffness into cells, regulate the activity of the core circadian clock complex. We also show that genetic perturbation, or age-associated disruption of self-sustained clocks, compromises the self-renewal capacity of mammary epithelia. Thus, circadian clocks are mechano-sensitive, providing a potential mechanism to explain how ageing influences their amplitude and function
Neurotransmitter release regulated by a MALS–liprin-α presynaptic complex
Synapses are highly specialized intercellular junctions organized by adhesive and scaffolding molecules that align presynaptic vesicular release with postsynaptic neurotransmitter receptors. The MALS/Veli–CASK–Mint-1 complex of PDZ proteins occurs on both sides of the synapse and has the potential to link transsynaptic adhesion molecules to the cytoskeleton. In this study, we purified the MALS protein complex from brain and found liprin-α as a major component. Liprin proteins organize the presynaptic active zone and regulate neurotransmitter release. Fittingly, mutant mice lacking all three MALS isoforms died perinatally with difficulty breathing and impaired excitatory synaptic transmission. Excitatory postsynaptic currents were dramatically reduced in autaptic cultures from MALS triple knockout mice due to a presynaptic deficit in vesicle cycling. These findings are consistent with a model whereby the MALS–CASK–liprin-α complex recruits components of the synaptic release machinery to adhesive proteins of the active zone
Differential usage of three exons generates at least five different mRNAs encoding human leukocyte common antigens.
Variants of BALB/c 3T3 cells lacking complex gangliosides retain a fibronectin matrix and spread normally on fibronectin-coated substrates.
Mechanical Design and Material Budget of the CMS Barrel Pixel Detector
The Compact Muon Solenoid experiment at the Large Hadron Collider at CERN
includes a silicon pixel detector as its innermost component. Its main task is
the precise reconstruction of charged particles close to the primary
interaction vertex. This paper gives an overview of the mechanical requirements
and design choices for the barrel pixel detector. The distribution of material
in the detector as well as its description in the Monte Carlo simulation are
discussed in detail
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