191 research outputs found
Additivity properties of a Gaussian Channel
The Amosov-Holevo-Werner conjecture implies the additivity of the minimum
Re'nyi entropies at the output of a channel. The conjecture is proven true for
all Re'nyi entropies of integer order greater than two in a class of Gaussian
bosonic channel where the input signal is randomly displaced or where it is
coupled linearly to an external environment.Comment: 9 pages, 1 figure (minor error present in the published version
corrected
Minimum output entropy of bosonic channels: a conjecture
The von Neumann entropy at the output of a bosonic channel with thermal noise
is analyzed. Coherent-state inputs are conjectured to minimize this output
entropy. Physical and mathematical evidence in support of the conjecture is
provided. A stronger conjecture--that output states resulting from
coherent-state inputs majorize the output states from other inputs--is also
discussed.Comment: 15 pages, 12 figure
Classical capacity of the lossy bosonic channel: the exact solution
The classical capacity of the lossy bosonic channel is calculated exactly. It
is shown that its Holevo information is not superadditive, and that a
coherent-state encoding achieves capacity. The capacity of far-field,
free-space optical communications is given as an example.Comment: 4 pages, 2 figures (revised version
Proposed Experiment in Two-Qubit Linear Optical Photonic Gates for Maximal Success Rates
Here we propose an experiment in Linear Optical Quantum Computing (LOQC)
using the framework first developed by Knill, Laflamme, and Milburn. This
experiment will test the ideas of the authors' previous work on imperfect LOQC
gates using number-resolving photon detectors. We suggest a relatively simple
physical apparatus capable of producing CZ gates with controllable fidelity
less than 1 and success rates higher than the current theoretical maximum
(S=2/27) for perfect fidelity. These experimental setups are within the reach
of many experimental groups and would provide an interesting experiment in
photonic quantum computing.Comment: 9 pages, 3 figure
One-mode Bosonic Gaussian channels: a full weak-degradability classification
A complete degradability analysis of one-mode Gaussian Bosonic channels is
presented. We show that apart from the class of channels which are unitarily
equivalent to the channels with additive classical noise, these maps can be
characterized in terms of weak- and/or anti-degradability. Furthermore a new
set of channels which have null quantum capacity is identified. This is done by
exploiting the composition rules of one-mode Gaussian maps and the fact that
anti-degradable channels can not be used to transfer quantum information.Comment: 23 pages, 3 figure
A prospective open-label treatment trial of olanzapine monotherapy in children and adolescents with bipolar disorder
OBJECTIVE: The goal of this study was to assess the effectiveness and tolerability of olanzapine in the treatment of acute mania in children and adolescents.
METHODS: This was an 8-week, open-label, prospective study of olanzapine monotherapy (dose range 2.5-20 mg/day) involving 23 bipolar youths (manic, mixed, or hypomanic; 5-14 years old). Weekly assessments were made using the Young Mania Rating Scale (YMRS), Clinical Global Impressions Severity Scale (CGI-S), Brief Psychiatric Rating Scale, and Children\u27s Depression Rating Scale. Adverse events were assessed through self-reports, vital sign and weight monitoring, laboratory analytes, and extrapyramidal symptom rating scales (Barnes Akathisia Scale, Simpson-Angus Scale, and Abnormal Involuntary Movement Scale).
RESULTS: Twenty-two of the 23 youths (96%) completed the study. Olanzapine treatment was associated with significant improvement in mean YMRS score (-19.0 +/- 9.2, p \u3c 0.001). Using predefined criteria for improvement of \u3e or = 30% decline in the YMRS and a CGI-S Mania score of \u3c or = 3 at endpoint, the overall response rate was 61%. Overall, olanzapine was well tolerated, and extrapyramidal symptom measures were not significantly different from baseline. Body weight increased significantly over the study (5.0 +/- 2.3 kg, p \u3c 0.001).
CONCLUSIONS: Open-label olanzapine treatment was efficacious and well tolerated in the treatment of acute mania in youths with bipolar disorder. Future placebo-controlled, double-blind studies are warranted
Self-adjuvanting polymer-peptide conjugates as therapeutic vaccine candidates against cervical cancer
Dendrimers are structurally well-defined, synthetic polymers with sizes and physicochemical properties often resembling those of biomacromolecules (e.g. proteins). As a result they are promising candidates for peptide-based vaccine delivery platforms. Herein, we established a synthetic pathway to conjugate a human papillomavirus (HPV) E7 protein-derived peptide antigen to a star-polymer to create a macromolecular vaccine candidate to treat HPV-related cancers. These conjugates were able to reduce tumor growth and eradicate E7-expressing TC-1 tumors in mice after a single immunization, without the help of any external adjuvant
Diquat Derivatives: Highly Active, Two-Dimensional Nonlinear Optical Chromophores with Potential Redox Switchability
In this article, we present a detailed study of structureâactivity relationships in diquaternized 2,2â˛-bipyridyl (diquat) derivatives. Sixteen new chromophores have been synthesized, with variations in the amino electron donor substituents, Ď-conjugated bridge, and alkyl diquaternizing unit. Our aim is to combine very large, two-dimensional (2D) quadratic nonlinear optical (NLO) responses with reversible redox chemistry. The chromophores have been characterized as their PF_6^â salts by using various techniques including electronic absorption spectroscopy and cyclic voltammetry. Their visible absorption spectra are dominated by intense Ď â Ď^* intramolecular charge-transfer (ICT) bands, and all show two reversible diquat-based reductions. First hyperpolarizabilities β have been measured by using hyper-Rayleigh scattering with an 800 nm laser, and Stark spectroscopy of the ICT bands affords estimated static first hyperpolarizabilities β_0. The directly and indirectly derived β values are large and increase with the extent of Ď-conjugation and electron donor strength. Extending the quaternizing alkyl linkage always increases the ICT energy and decreases the E_(1/2) values for diquat reduction, but a compensating increase in the ICT intensity prevents significant decreases in Stark-based β_0 responses. Nine single-crystal X-ray structures have also been obtained. Time-dependent density functional theory clarifies the molecular electronic/optical properties, and finite field calculations agree with polarized HRS data in that the NLO responses of the disubstituted species are dominated by âoff-diagonalâ β_(zyy) components. The most significant findings of these studies are: (i) β_0 values as much as 6 times that of the chromophore in the technologically important material (E)-4â˛-(dimethylamino)-N-methyl-4-stilbazolium tosylate; (ii) reversible electrochemistry that offers potential for redox-switching of optical properties over multiple states; (iii) strongly 2D NLO responses that may be exploited for novel practical applications; (iv) a new polar material, suitable for bulk NLO behavior
Matrix gla protein in xenopus laevis: molecular cloning, tissue distribution, and evolutionary considerations
Matrix Gla protein (MGP) belongs to the family of vitamin K-dependent, Gla-containing proteins and in higher vertebrates, is found in the extracellular matrix of mineralized tissues and soft tissues. MGP synthesis is highly regulated at the transcription and posttranscription levels and is now known to be involved in the regulation of extracellular matrix calcification and maintenance of cartilage and soft tissue integrity during growth and development. However, its mode of action at the molecular level remains unknown. Because there is a large degree of conservation between amino,acid sequences of shark and human MGP, the function of MGP probably has been conserved throughout evolution. Given the complexity of the mammalian system, the study of MGP in a lower vertebrate might be advantageous to relate the onset of MGP expression with specific events during development. Toward this goal, MGP was purified from Xenopus long bones and its N-terminal amino acid sequence was determined and used to clone the Xenopus MGP complementary DNA (cDNA) by a mixture of reverse-transcription (RT)- and 5'- rapid amplification of cDNA ends (RACE)-polymerase chain reaction (PCR). MGP messenger RNA (mRNA) was present in all tissues analyzed although predominantly expressed in Xenopus bone and heart and its presence was detected early in development at the onset of chondrocranium development and long before the appearance of the first calcified structures and metamorphosis. These results show that in this system, as in mammals, MGP may be required to delay or prevent mineralization of cartilage and soft tissues during the early stages of development and indicate that Xenopus is an adequate model organism to further study MGP function during growth and development.NATO/CRG940751/SA5.2.05,
Praxis XXI/BIA 469/94,
(NIH; grant AR 25921)
(Praxis XXI/BPD/18816)
(Praxis XXI/BICJ-2985
Transcriptional Changes Common to Human Cocaine, Cannabis and Phencyclidine Abuse
A major goal of drug abuse research is to identify and understand drug-induced changes in brain function that are common to many or all drugs of abuse. As these may underlie drug dependence and addiction, the purpose of the present study was to examine if different drugs of abuse effect changes in gene expression that converge in common molecular pathways. Microarray analysis was employed to assay brain gene expression in postmortem anterior prefrontal cortex (aPFC) from 42 human cocaine, cannabis and/or phencyclidine abuse cases and 30 control cases, which were characterized by toxicology and drug abuse history. Common transcriptional changes were demonstrated for a majority of drug abuse cases (Nâ=â34), representing a number of consistently changed functional classes: Calmodulin-related transcripts (CALM1, CALM2, CAMK2B) were decreased, while transcripts related to cholesterol biosynthesis and trafficking (FDFT1, APOL2, SCARB1), and Golgi/endoplasmic reticulum (ER) functions (SEMA3B, GCC1) were all increased. Quantitative PCR validated decreases in calmodulin 2 (CALM2) mRNA and increases in apolipoprotein L, 2 (APOL2) and semaphorin 3B (SEMA3B) mRNA for individual cases. A comparison between control cases with and without cardiovascular disease and elevated body mass index indicated that these changes were not due to general cellular and metabolic stress, but appeared specific to the use of drugs. Therefore, humans who abused cocaine, cannabis and/or phencyclidine share a decrease in transcription of calmodulin-related genes and increased transcription related to lipid/cholesterol and Golgi/ER function. These changes represent common molecular features of drug abuse, which may underlie changes in synaptic function and plasticity that could have important ramifications for decision-making capabilities in drug abusers
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