1,625 research outputs found
Emergence of a measurement basis in atom-photon scattering
The process of quantum measurement has been a long standing source of debate.
A measurement is postulated to collapse a wavefunction onto one of the states
of a predetermined set - the measurement basis. This basis origin is not
specified within quantum mechanics. According to the theory of decohernce, a
measurement basis is singled out by the nature of coupling of a quantum system
to its environment. Here we show how a measurement basis emerges in the
evolution of the electronic spin of a single trapped atomic ion due to
spontaneous photon scattering. Using quantum process tomography we visualize
the projection of all spin directions, onto this basis, as a photon is
scattered. These basis spin states are found to be aligned with the scattered
photon propagation direction. In accordance with decohernce theory, they are
subjected to a minimal increase in entropy due to the photon scattering, while,
orthogonal states become fully mixed and their entropy is maximally increased.
Moreover, we show that detection of the scattered photon polarization measures
the spin state of the ion, in the emerging basis, with high fidelity. Lastly,
we show that while photon scattering entangles all superpositions of pointer
states with the scattered photon polarization, the measurement-basis states
themselves remain classically correlated with it. Our findings show that photon
scattering by atomic spin superpositions fulfils all the requirements from a
quantum measurement process
High-fidelity state detection and tomography of a single ion Zeeman qubit
We demonstrate high-fidelity Zeeman qubit state detection in a single trapped
88 Sr+ ion. Qubit readout is performed by shelving one of the qubit states to a
metastable level using a narrow linewidth diode laser at 674 nm followed by
state-selective fluorescence detection. The average fidelity reached for the
readout of the qubit state is 0.9989(1). We then measure the fidelity of state
tomography, averaged over all possible single-qubit states, which is 0.9979(2).
We also fully characterize the detection process using quantum process
tomography. This readout fidelity is compatible with recent estimates of the
detection error-threshold required for fault-tolerant computation, whereas
high-fidelity state tomography opens the way for high-precision quantum process
tomography
Comparative Analysis of Carrier-Based Obturation and Lateral Compaction: A Retrospective Clinical Outcomes Study
The purpose of this retrospective study was to compare the outcome of primary endodontic treatment using a standardized cleaning and shaping technique and obturation with either lateral compaction or carrier-based obturation. Patients received primary endodontic treatment in the predoctoral dental clinic using a standardized cleaning and shaping protocol. All root canals were obturated using AH PlusTM sealer with lateral compaction of gutta-percha (LC) or carrier-based obturation (CBO). A total of 205 cases met the inclusion criteria. 71 teeth in 60 patients were recalled after 2 years and evaluated both clinically and radiographically by two independent examiners. Success was defined as a lack of clinical symptoms and a normal periodontal ligament space or reduction in size of a previously existing periapical radiolucency. Chi-square and logistic regression were used for statistical analysis with a significance level of P < 0.05. There was no difference in success rates between cases obturated with LC or CBO (P = 0.802); overall success rate was 83%. Molars had a significantly lower success rate (53%) than premolar and anterior teeth (89%) (P = 0.005), irrespective of the obturation technique used. When a standardized cleaning and shaping protocol was used by predoctoral dental students in a controlled university setting, there was no difference in success rates between cases obturated with LC or CBO
Proteasome Lid Bridges Mitochondrial Stress with Cdc53/Cullin1 NEDDylation Status
Cycles of Cdc53/Cullin1 rubylation (a.k.a NEDDylation) protect ubiquitin-E3 SCF (Skp1-Cullin1-F-box protein) complexes from self-destruction and play an important role in mediating the ubiquitination of key protein substrates involved in cell cycle progression, development, and survival. Cul1 rubylation is balanced by the COP9 signalosome (CSN), a multi-subunit derubylase that shows 1:1 paralogy to the 26 S proteasome lid. The turnover of SCF substrates and their relevance to various diseases is well studied, yet, the extent by which environmental perturbations influence Cul1 rubylation/derubylation cycles per se is still unclear. In this study, we show that the level of cellular oxidation serves as a molecular switch, determining Cullin1 rubylation/derubylation ratio. We describe a mutant of the proteasome lid subunit, Rpn11 that exhibits accumulated levels of Cullin1-Rub1 conjugates, a characteristic phenotype of csn mutants. By dissecting between distinct phenotypes of rpn11 mutants, proteasome and mitochondria dysfunction, we were able to recognize the high reactive oxygen species (ROS) production during the transition of cells into mitochondrial respiration, as a checkpoint of Cullin1 rubylation in a reversible manner. Thus, the study adds the rubylation cascade to the list of cellular pathways regulated by redox homeostasis
Development and Clinical Evaluation of a Root Coverage Procedure Using a Collagen Barrier Membrane
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/141360/1/jper0770.pd
How to Choose a Champion
League competition is investigated using random processes and scaling
techniques. In our model, a weak team can upset a strong team with a fixed
probability. Teams play an equal number of head-to-head matches and the team
with the largest number of wins is declared to be the champion. The total
number of games needed for the best team to win the championship with high
certainty, T, grows as the cube of the number of teams, N, i.e., T ~ N^3. This
number can be substantially reduced using preliminary rounds where teams play a
small number of games and subsequently, only the top teams advance to the next
round. When there are k rounds, the total number of games needed for the best
team to emerge as champion, T_k, scales as follows, T_k ~N^(\gamma_k) with
gamma_k=1/[1-(2/3)^(k+1)]. For example, gamma_k=9/5,27/19,81/65 for k=1,2,3.
These results suggest an algorithm for how to infer the best team using a
schedule that is linear in N. We conclude that league format is an ineffective
method of determining the best team, and that sequential elimination from the
bottom up is fair and efficient.Comment: 6 pages, 3 figure
Evaluation of a Collagen Membrane With and Without Bone Grafts in Treating Periodontal Intrabony Defects
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/141006/1/jper0838.pd
A framework for branched storytelling and matchmaking in multiplayer games
Video games often either have good single player campaign modes or good multi-player campaign-less modes. This paper presents a framework aimed at the full game development pipeline, from designers to programmers, to aid in creating multiplayer campaigns by providing components that help singleplayer story modes to be used in multiplayer interaction settings. We also propose a custom matchmaking system capable of matching players so as to intertwine their individual stories. The proposed framework has been validated in a case study. A set of experimental results show that the framework is capable of producing valuable story crossings and proper matchmaking.info:eu-repo/semantics/acceptedVersio
Dissection of the Carboxyl-Terminal Domain of the Proteasomal Subunit Rpn11 in Maintenance of Mitochondrial Structure and Function
We have previously demonstrated that the C-terminal part of Rpn11, a deubiquitinating enzyme in the lid of the proteasome, is essential for maintaining a correct cell cycle and normal mitochondrial morphology and function. The two roles are apparently unlinked as the mitochondrial role is mapped to the Carboxy-terminus, whereas the catalytic deubiquitinating activity is found within the N-terminal region. The mitochondrial defects are observed in rpn11-m1 (originally termed mpr1-1), a mutation that generates Rpn11 lacking the last 31 amino acids. No mitochondrial phenotypes are recorded for mutations in the MPN/JAMM motif. In the present study, we investigated the participation of the last 31 amino acids of the Rpn11 protein by analysis of intragenic revertants and site-specific mutants. We identified a putative -helix necessary for the maintenance of a correct cell cycle and determined that a very short region at the C-terminus of Rpn11 is essential for the maintenance of tubular mitochondrial morphology. Furthermore, we show that expression of the C-terminal part of Rpn11 is able to complement in trans all of the rpn11-m1 mitochondrial phenotypes. Finally, we investigate the mechanisms by which Rpn11 controls the mitochondrial shape and show that Rpn11 may regulate the mitochondrial fission and tubulation processes
Converting genetic network oscillations into somite spatial pattern
In most vertebrate species, the body axis is generated by the formation of
repeated transient structures called somites. This spatial periodicity in
somitogenesis has been related to the temporally sustained oscillations in
certain mRNAs and their associated gene products in the cells forming the
presomatic mesoderm. The mechanism underlying these oscillations have been
identified as due to the delays involved in the synthesis of mRNA and
translation into protein molecules [J. Lewis, Current Biol. {\bf 13}, 1398
(2003)]. In addition, in the zebrafish embryo intercellular Notch signalling
couples these oscillators and a longitudinal positional information signal in
the form of an Fgf8 gradient exists that could be used to transform these
coupled temporal oscillations into the observed spatial periodicity of somites.
Here we consider a simple model based on this known biology and study its
consequences for somitogenesis. Comparison is made with the known properties of
somite formation in the zebrafish embryo . We also study the effects of
localized Fgf8 perturbations on somite patterning.Comment: 7 pages, 7 figure
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