The knowledge of fifth, sixth, seventh, eighth and ninth graders regarding the United Nations

Thesis (Ed.M.)--Boston Universit

Interferometry with Photon-Subtracted Thermal Light

We propose and implement a quantum procedure for enhancing the sensitivity with which one can determine the phase shift experienced by a weak light beam possessing thermal statistics in passing through an interferometer. Our procedure entails subtracting exactly one (which can be generalized to m) photons from the light field exiting an interferometer containing a phase-shifting element in one of its arms. As a consequence of the process of photon subtraction, and somewhat surprisingly, the mean photon number and signal-to-noise ratio of the resulting light field are thereby increased, leading to enhanced interferometry. This method can be used to increase measurement sensitivity in a variety of practical applications, including that of forming the image of an object illuminated only by weak thermal light

Enhanced Thermal Object Imaging by Photon Addition or Subtraction

Long-baseline interferometry (LBI) is used to reconstruct the image of faint thermal objects. The image quality, for a given exposure time, is in general limited by a low signal-to-noise ratio (SNR). We show theoretically that a significant increase of the SNR, in a LBI, is possible by adding or subtracting photons to the thermal beam. At low photon counts, photon addition-subtraction technology strongly enhances the image quality. We have experimentally realized a nondeterministic physical protocol for photon subtraction. Our theoretical predictions are supported by experimental results.Comment: 4 pages, 5 figure

Quantum-enhanced interferometry with weak thermal light

We propose and implement a procedure for enhancing the sensitivity with which one can determine the phase shift experienced by a thermal light beam possessing on average fewer than four photons in passing through an interferometer. Our procedure entails subtracting exactly one (which can be generalized to m) photon from the light field exiting an interferometer containing a phase-shifting element in one of its arms. As a consequence of the process of photon subtraction, the mean photon number and signal-to-noise ratio (SNR) of the resulting light field are increased, leading to an enhancement of the SNR of the interferometric signal for that fraction of the incoming data that leads to photon subtraction

A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer

ATP Binding Cassette B1 (ABCB1) is a transporter with a broad substrate specificity involved in the elimination of several carcinogens from the gut. Several polymorphic variants within the ABCB1 gene have been reported as modulators of ABCB1-mediated transport. We investigated the impact of ABCB1 genetic variants on colorectal cancer (CRC) risk. A hybrid tagging/functional approach was performed to select 28 single nucleotide polymorphisms (SNPs) that were genotyped in 1,321 Czech subjects, 699 CRC cases and 622 controls. In addition, six potentially functional SNPs were genotyped in 3,662 German subjects, 1,809 cases and 1,853 controls from the DACHS study. We found that three functional SNPs (rs1202168, rs1045642 and rs868755) were associated with CRC risk in the German population. Carriers of the rs1202168_T and rs868755_T alleles had an increased risk for CRC (Ptrend = 0.016 and 0.029, respectively), while individuals bearing the rs1045642_C allele showed a decreased risk of CRC (Ptrend = 0.022). We sought to replicate the most significant results in an independent case-control study of 3,803 subjects, 2,169 cases and 1,634 controls carried out in the North of Germany. None of the SNPs tested were significantly associated with CRC risk in the replication study. In conclusion, in this study of about 8,800 individuals we show that ABCB1 gene polymorphisms play at best a minor role in the susceptibility to CRC

TWO-PHOTON MULTIWAVE MIXING (DOPPLER-FREE SPECTROSCOPY).

This dissertation examines aspects of the interaction of multiple coherent light fields for the two-photon two-level model. In this model the interacting energy levels are not connected by an atomic dipole and a two-photon transition between them is necessary. We employ the density matrix formalism allowing easy comparison between the one- and two-photon two-level models. Significant differences are found due to dynamic Stark shifts and conjugate scattering off the pump-induced two-photon coherence. Averages over Doppler broadening are performed and the new upper-level relaxation mechanisms of decay to an intermediate nonresonant level and ionization from the upper state are included. The new relaxation mechanisms, introduced to the theory to better model experiments, are similar except that ionization is intensity dependent. They cause the resulting probe absorption spectra to become more complex and in general asymmetric. Doppler broadening is also important in experiments using gases. We analytically average over a Lorentzian velocity distribution for both co- and counterpropagating pump and probe beams. For copropagating fields the results are similar to those for the one-photon case averaged over inhomogeneous broadening, whereas counterpropagating pump and probe fields yield the so-called Doppler-free configuration that is normally only modelled to third order in the pump amplitude. We consider the pump field amplitude to all orders and find that as long as the width of the Doppler velocity distribution is significantly larger than the two-photon Rabi frequency the results are Doppler-free. The final part of the dissertation treats the question of two-photon squeezed states. This requires quantized sidemodes. Squeezed states are minimum uncertainty states with unequal variances in the two quadratures of the electromagnetic field amplitude. One way to generate these states is via multiwave mixing and we present here the first calculation for nondegenerate two-photon multiwave mixing as it applies to squeezed states. We find that in general two-photon squeezed states require lower intensities and detuning than those predicted by the one-photon model

Resveratrol increases F508del-CFTR dependent salivary secretion in cystic fibrosis mice

Cystic fibrosis (CF) is a fatal genetic disease associated with widespread exocrine gland dysfunction. Studies have suggested activating effects of resveratrol, a naturally-occurring polyphenol compound with antioxidant and anti-inflammatory properties, on CF transmembrane conductance regulator (CFTR) protein function. We assayed, in F508del-CFTR homozygous (CF) and in wild-type mice, the effect of resveratrol on salivary secretion in basal conditions, in response to inhibition by atropine (basal β-adrenergic-dependent component) and to stimulation by isoprenaline (CFTR-dependent component). Both components of the salivary secretion were smaller in CF mice than in controls. Two hours after intraperitoneal administration of resveratrol (50 mg/kg) dissolved in DMSO, the compound was detected in salivary glands. As in both CF and in wild-type mice, DMSO alone increased the response to isoprenaline in males but not in females, the effect of resveratrol was only measured in females. In wild-type mice, isoprenaline increased secretion by more than half. In CF mice, resveratrol rescued the response to isoprenaline, eliciting a 2.5-fold increase of β-adrenergic-stimulated secretion. We conclude that the salivary secretion assay is suitable to test DMSO-soluble CFTR modulators in female mice. We show that resveratrol applied in vivo to mice reaches salivary glands and increases β-adrenergic secretion. Immunolabelling of CFTR in human bronchial epithelial cells suggests that the effect is associated with increased CFTR protein expression. Our data support the view that resveratrol is beneficial for treating CF. The salivary secretion assay has a potential application to test efficacy of novel CF therapies

Resveratrol increases F508del-CFTR dependant salivary secretion in cystic fibrosis mice

Cystic fibrosis (CF) is a fatal genetic disease associated with widespread exocrine gland dysfunction. Studies have suggested activating effects of resveratrol, a naturally-occurring polyphenol compound with antioxidant and anti-inflammatory properties, on CF transmembrane conductance regulator (CFTR) protein function. We assayed, in F508del-CFTR homozygous (CF) and in wild-type mice, the effect of resveratrol on salivary secretion in basal conditions, in response to inhibition by atropine (basal β-adrenergic-dependent component) and to stimulation by isoprenaline (CFTR-dependent component). Both components of the salivary secretion were smaller in CF mice than in controls. Two hours after intraperitoneal administration of resveratrol (50 mg/kg) dissolved in DMSO, the compound was detected in salivary glands. As in both CF and in wild-type mice, DMSO alone increased the response to isoprenaline in males but not in females, the effect of resveratrol was only measured in females. In wild-type mice, isoprenaline increased secretion by more than half. In CF mice, resveratrol rescued the response to isoprenaline, eliciting a 2.5-fold increase of β-adrenergic-stimulated secretion. We conclude that the salivary secretion assay is suitable to test DMSO-soluble CFTR modulators in female mice. We show that resveratrol applied in vivo to mice reaches salivary glands and increases β-adrenergic secretion. Immunolabelling of CFTR in human bronchial epithelial cells suggests that the effect is associated with increased CFTR protein expression. Our data support the view that resveratrol is beneficial for treating CF. The salivary secretion assay has a potential application to test efficacy of novel CF therapies