Essays on Egg Cell

- If Adam Smith were faced with the problem of procuring donor organs, he might suggest that we would be better off relying on donors’ self-interest rather than their benevolence, and advocate a market solution to distributing this scarce resource. Karl Polanyi, however, might argue that society would be harmed by allowing the market to displace the gift relationships created by voluntary donation. Although both died before successful organ transplantation was possible, use what you have learned of their theories to state the position you think each would take on whether and why organ donations should be organized on a market ...

The advancement of technology has precipitated a revolution in scientific understanding over the last several decades. Advancements in research tools has led to new insights into every facet of scientific discovery within the realms of chemistry, physics, and biology and all the sub-disciplines forming their constitution. Increased discovery has brought with it opportunities for cross discipline cooperation which has resulted in the formation of new disciplines and has galvanized scientists to press the boundaries of research and application as has never been seen in human history. One such field testing those limits is genetics. Today’s geneticists have expanded beyond ...

Introduction

Science, technology when applied to the natural way how a human’s body and all of its corresponding organ systems operate can be referred to as biotechnology. Biotechnology has emerged as one of the most lucrative and fast developing field of medicine combined with technology. It can be defined as the utilization of organisms (e.g. humans, animals, plants, etc.) or any living system to create, develop, or improve products that can be used to make a particular task easier, or more efficient . In an era characterized by rapid and even unpredictable improvements in technology, one can assume that the same rate ...

Abstract

Tay-Sachs disease (TSD) is a group of autosomal recessive lipid lysosomal storage disorders caused by mutations of the HEXA gene, which codes for the alpha subunit of the enzyme Hexosaminidase A, one of three enzymes responsible for the normal degradation of GM2 ganglioside, a substance found in high concentration in the plasma membrane of neuronal cells. The classic acute infantile form, discussed here, is a neurodegenerative disorder with onset at four to eight months of age in which acquired capabilities are lost and general neurologic deterioration occurs, with death by age two to four years. It occurs with highest frequency in the ...