Physiological Aspects of Genetics

A considerable amount of evidence indicates that desoxyribonucleic acid is capable of duplicating itself, a property also possessed by genes. (By a self-duplicating material, we mean one which plays some essential role in its own production.) Watson & Crick (1) have proposed a new structure for desoxyribonucleic acid which not only takes into account the existing analytical and x-ray diffraction data but also seems capable of explaining the mechanism of duplication. Their model consists of two helical chains coiled around the same axis, the purine and pyrimidine bases on the inside, the phosphate groups on the outside. The chains are held together by hydrogen bonds between the bases, the adenine residues of either chain being bonded specifically to thymine in the other, and similarly guanine to cytosine. The sequence of bases along one chain is not restricted, but once fixed the sequence along the other chain is determined. This complementarity, which is the most novel feature of the structure, suggests that duplication takes place by separation of the two chains, followed by the synthesis of its complement alongside each chain. The model is supported by recent x-ray diffraction studies (2, 3)

Kinetic study of crystallisation of sol-gel derived calcia-alumina binary compounds

In-situ High Temperature X-ray Diffraction (HTXRD) and Differential Scanning Calorimetric (DSC) studies were performed on a sol-gel derived binary compound of a calcia-alumina (C12A7) system consisting of calcium oxide (CaO) and aluminium oxide (Al2O3) in a ratio of 12:7 for in situ investigation into the phase transformations under progressively increasing thermal activation from roomerature to 1200 °C. The crystallisation of amorphous samples formulated at roomerature on magnesium oxide (MgO) single crystal (100) substrates was found to be complete on heat treatment at 1100 °C for 3 h. This observation was further supported by independent Fourier Transform Infrared (FTIR) and Raman Spectroscopies. Values of 348 kJ/mol and 375 kJ/mol were estimated from Kissinger plots for activation energies of crystallisation of CaO and Al2O3 constituents, respectively

City-Size and Health Outcomes: Lessons from the USA

In this paper, we compare health outcomes in cities of different sizes. Using 2001 National Health Interview Survey data for adult urban-US population, it is shown that individual health is better in bigger cities compared to small or medium sized ones. This result holds after controlling for potentially confounding variables including age, gender, education, marital status, smoking, income, asset-ownership, and race. Possible sources of selection bias are controlled using many model specifications and population sub-groupings. Although, stiff challenges for healthcare delivery exist for large cities, an aggressive urban health policy should also put strong emphasis on improving health in small and medium sized cities to reduce urban health disparities in the USA. Policy implications for other developed and developing countries are also hypothesized.