Divergent Views on Abortion and the Period of Ensoulment

A Muslim woman in her sixteenth week of pregnancy was informed that her ultrasound scan showed spina bifida, and laboratory results confirmed the diagnosis. The child would have various complications and, most probably, would need medical care for life. With the consent of her husband she decided to terminate the pregnancy. Her decision sparked controversy among Muslim clerics in her community, sparking debate between those who would allow abortion for medical reasons and those who oppose abortion for any reason. This paper will review the philosophical and theological arguments of the pro-life and pro-choice groups as well as the Islamic perspective concerning a woman’s autonomy over her reproductive system, the sanctity of the fetus and the embryo, therapeutic abortion, and ensoulment

Practical Secrecy at the Physical Layer: Key Extraction Methods with Applications in Cognitive Radio

The broadcast nature of wireless communication imposes the risk of information leakage to adversarial or unauthorized receivers. Therefore, information security between intended users remains a challenging issue. Currently, wireless security relies on cryptographic techniques and protocols that lie at the upper layers of the wireless network. One main drawback of these existing techniques is the necessity of a complex key management scheme in the case of symmetric ciphers and high computational complexity in the case of asymmetric ciphers. On the other hand, physical layer security has attracted significant interest from the research community due to its potential to generate information-theoretic secure keys. In addition, since the vast majority of physical layer security techniques exploit the inherent randomness of the communication channel, key exchange is no longer mandatory. However, additive white Gaussian noise, interference, channel estimation errors and the fact that communicating transceivers employ different radio frequency (RF) chains are among the reasons that limit utilization of secret key generation (SKG) algorithms to high signal to noise ratio levels. The scope of this dissertation is to design novel secret key generation algorithms to overcome this main drawback. In particular, we design a channel based SKG algorithm that increases the dynamic range of the key generation system. In addition, we design an algorithm that exploits angle of arrival (AoA) as a common source of randomness to generate the secret key. Existing AoA estimation systems either have high hardware and computation complexities or low performance, which hinder their incorporation within the context of SKG. To overcome this challenge, we design a novel high performance yet simple and efficient AoA estimation system that fits the objective of collecting sequences of AoAs for SKG. Cognitive radio networks (CRNs) are designed to increase spectrum usage efficiency by allowing secondary users (SUs) to exploit spectrum slots that are unused by the spectrum owners, i.e., primary users (PUs). Hence, spectrum sensing (SS) is essential in any CRN. CRNs can work both in opportunistic (interweaved) as well as overlay and/or underlay (limited interference) fashions. CRNs typically operate at low SNR levels, particularly, to support overlay/underlay operations. Similar to other wireless networks, CRNs are susceptible to various physical layer security attacks including spectrum sensing data falsification and eavesdropping. In addition to the generalized SKG methods provided in this thesis and due to the peculiarity of CRNs, we further provide a specific method of SKG for CRNs. After studying, developing and implementing several SS techniques, we design an SKG algorithm that exploits SS data. Our algorithm does not interrupt the SS operation and does not require additional time to generate the secret key. Therefore, it is suitable for CRNs

Quantifying uncertainty from aerosol and atmospheric parameters and their impact on climate sensitivity

Climate sensitivity in Earth system models (ESMs) is an emergent property that is affected by structural (missing or inaccurate model physics) and parametric (variations in model parameters) uncertainty. This work provides the first quantitative assessment of the role of compensation between uncertainties in aerosol forcing and atmospheric parameters, and their impact on the climate sensitivity of the Community Atmosphere Model, Version 4 (CAM4). Running the model with prescribed ocean and ice conditions, we perturb four parameters related to sulfate and black carbon aerosol radiative forcing and distribution, as well as five atmospheric parameters related to clouds, convection, and radiative flux. In this experimental setup where aerosols do not affect the properties of clouds, the atmospheric parameters explain the majority of variance in climate sensitivity, with two parameters being the most important: one controlling low cloud amount, and one controlling the timescale for deep convection. Although the aerosol parameters strongly affect aerosol optical depth, their impacts on climate sensitivity are substantially weaker than the impacts of the atmospheric parameters, but this result may depend on whether aerosol–cloud interactions are simulated. Based on comparisons to inter-model spread of other ESMs, we conclude that structural uncertainties in this configuration of CAM4 likely contribute 3 times more to uncertainty in climate sensitivity than parametric uncertainties. We provide several parameter sets that could provide plausible (measured by a skill score) configurations of CAM4, but with different sulfate aerosol radiative forcing, black carbon radiative forcing, and climate sensitivity.</p

Rapid Isocratic Liquid Chromatographic Separation and Quantification of Tryptophan and Six kynurenine Metabolites in Biological Samples with Ultraviolet and Fluorimetric Detection

A simple, rapid isocratic liquid chromatographic procedure with ultraviolet and fluorimetric detection is described for the separation and quantification of L-tryptophan (Trp) and six of its kynurenine metabolites (kynurenine, 3-hydroxykynurenine, and 3-hydroxyanthranilic, kynurenic, xanthurenic and anthranilic acids). Using the Perkin Elmer LC 200 system, a reverse phase Synergi 4 μ fusion-RP80 A column (250 × 4.6 mm) (Phenomenex), and a mobile phase of 10 mM sodium dihydrogen phosphate: methanol (73:27, by vol) at pH 2.8 and a flow rate of 1.0–1.2 ml/min at 37 °C, a run took ∼13 min. The run took <7 min at 40 °C and a 1.4 ml/min flow rate. Limits of detection of all 7 analytes were 5–72 nM and their recoveries from human plasma and rat serum and liver varied between 62% and 111%. This simple method is suitable for high throughput work and can be further developed to include quinolinic acid and other Trp metabolites

Application of the Phenomenex EZ:faast™ amino acid analysis kit for rapid gas-chromatographic determination of concentrations of plasma tryptophan and its brain uptake competitors

The Phenomenex EZ:faast™ amino acid analysis kit is available for gas (GC) or liquid (LC) chromatographic analysis of amino acids (AA) using mass spectrometry (MS) and other GC detectors. We used it for rapid GC determination of plasma tryptophan, its brain uptake competitors (Val, Leu, Ile, Phe and Tyr) and many other amino acids. Based on solid-phase extraction, this fast method enables one person to process two plasma samples in 8–10 min and six samples in ∼15 min up to GC injection and a 7-min GC run per plasma sample. Using a Perkin-Elmer Clarus 500 GC, a Total Chrome software, a flame-ionisation detector (FID) and norvaline as internal standard, we used this method to analyse ∼1,000 plasma samples from normal subjects undergoing acute tryptophan depletion and loading tests. The limit of detection for most amino acids is 1 nmol/ml (1 μM) and in many cases less. With manual injection, coefficients of variation for the above six amino acids were 1.5–6.2% (intra-assay) and 3.8–9.7% (inter-assay). This simple, rapid and elegant method will be valuable to the amino acid analyst and researcher, as it can save much manpower time and meet urgent emergency requests and the demands of a high-throughput laboratory

Specificity of the Acute Tryptophan and Tyrosine Plus Phenylalanine Depletion and Loading Tests Part II: Normalisation of the Tryptophan and the Tyrosine Plus Phenylalanine to Competing Amino Acid Ratios in a New Control Formulation

Current formulations for acute tryptophan (Trp) or tyrosine (Tyr) plus phenylalanine (Phe) depletion and loading cause undesirable decreases in ratios of Trp or Tyr + Phe to competing amino acids (CAA), thus undermining the specificities of these tests. Branched-chain amino acids (BCAA) cause these unintended decreases, and lowering their content in a new balanced control formulation in the present study led to normalization of all ratios. Four groups (n = 12 each) of adults each received one of four 50 g control formulations, with 0% (traditional), 20%, 30%, or 40% less of the BCAA. The free and total [Trp]/[CAA] and [Phe + Tyr]/[BCAA + Trp] ratios all decreased significantly during the first 5 h following the traditional formulation, but were fully normalized by the formulation containing 40% less of the BCAA. We recommend the latter as a balanced control formulation and propose adjustments in the depletion and loading formulations to enhance their specificities for 5-HT and the catecholamines

Specificity of the Acute Tryptophan and Tyrosine Plus Phenylalanine Depletion and Loading Tests I. Review of Biochemical Aspects and Poor Specificity of Current Amino Acid Formulations

The acute tryptophan or tyrosine plus phenylalanine depletion and loading tests are powerful tools for studying the roles of serotonin, dopamine and noradrenaline in normal subjects and those with behavioural disorders. The current amino acid formulations for these tests, however, are associated with undesirable decreases in ratios of tryptophan or tyrosine plus phenylalanine to competing amino acids resulting in loss of specificity. This could confound biochemical and behavioural findings. Compositions of current formulations are reviewed, the biochemical principles underpinning the tests are revisited and examples of unintended changes in the above ratios and their impact on monoamine function and behaviour will be demonstrated from data in the literature. The presence of excessive amounts of the 3 branched-chain amino acids Leu, Ile and Val is responsible for these unintended decreases and the consequent loss of specificity. Strategies for enhancing the specificity of the different formulations are proposed

Molecular markers as a prognostic system for hepatocellular carcinoma

AbstractThe gene expression profile p16, c-erbB-3 and bcl2 in hepatocellular carcinoma (HCC) patients with and without associated HCV infection, was assessed. Forty-eight subjects were included in the study and divided equally into two groups: HCC with and without HCV associated infection. Adjacent paracancerous tissues were assessed as control samples. Correlations with various clinico-pathological parameters of the tumour were assessed: stage, grade, and tumour size. The c-erbB-3 oncogene was expressed in 83.33% (40/48) of the total HCC sample and in 31.25% (15/48) of the noncancerous lesions. C-erbB-3 was expressed in 87.5% (21/24) of the HCC cases with associated HCV infection and in 79.16% (19/24) of the HCC cases without associated HCV infection. Gene expression of c-erbB-3 was significantly correlated with the clinico-pathological parameters of the tumour. P16 gene expression was found in 12.5% (6/48) of the total HCC sample and in 25% (12/48) of the para-cancerous lesions. P16 was expressed in 12.5% (3/24) of HCC cases with and without associated HCV infection. Gene expression of p16 exhibited significant negative correlation with clinico-pathological parameters of the tumour. Bcl2 gene expression was found in 20.8% (10/48) of the total HCC sample and in the para-cancerous lesions. Bcl2 was expressed in 20.8% (5/24) of the HCC cases with and without HCV associated infection. Gene expression of bcl2 did not show significant correlations with the clinico-pathological parameters of the tumour. In conclusion, gene expression profiles of p16 and c-erbB-3 could be used as prognostic molecular markers in HCC