Human genome mapping: a Jewish perspective.
نویسنده
چکیده
The Human Genome Project Science in the twentieth century has launched three great projects: (1) the Manhattan Project for the development of nuclear weapons, which took place in the United States between 1942 and 1945 under the technical supervision of Robert Oppenheimer; (2) the American Space Project, which started in the late 1950’s and led to the landing on the moon in 1968; and (3) the Human Genome Project, which is being conducted now in thousands of laboratories throughout the world. The Human Genome Project is one of the most ambitious projects ever undertaken in the life sciences. Billions of dollars have been allocated to numerous research groups all over the world in order to produce a map of the thousands of genes which constitute the human genome. A complete genome map should fully reveal to us which nucleotide “words” control which clinical conditions in man; in other words, which genetic components imply biologic anomaly or greater sensitivity to malignant disease, and which components determine psychological or intellectual characteristics. When the mapping is complete, it will be possible to check the hundreds of thousands of genes in any individual and to decipher the genetic information contained in them. The vast pool of raw data inherent in any genetic mapping can serve to achieve either positive or negative goals. The knowledge contained in the genes has great predictive capacity regarding the individual’s future, namely his chances of spontaneously contracting specific diseases, such as heart disease or cancer, at various ages and his chances of achieving success in sports or in intellectual endeavors. It follows that the project has far-reaching ramifications in many areas of society, e.g., work relations, insurance, the army, medicine, and family relations. Such knowledge is so powerful that it can destroy
منابع مشابه
I-49: Human Y Chromosome ProteomeProject
The success of the Human Genome Project (HGP) has provided a blueprint for the approximately 20,000 gene-encoded proteins potentially active in all of the hundreds of cell types that make up the human body. Yet we still have limited knowledge about a majority of the gene-encoded proteins which are the “building blocks of life” and “cellular machinery”. It is estimated that for nearly half of th...
متن کاملGenome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
The recent series of large genome-wide association studies in European and Japanese cohorts established that Parkinson disease (PD) has a substantial genetic component. To further investigate the genetic landscape of PD, we performed a genome-wide scan in the largest to date Ashkenazi Jewish cohort of 1130 Parkinson patients and 2611 pooled controls. Motivated by the reduced disease allele hete...
متن کاملWhat is it to do good medical ethics? An orthodox Jewish physician and ethicist's perspective.
This article, dedicated to the 40th anniversary of the Journal of Medical Ethics, approaches the question 'what does it mean to do good medical ethics?' first from a general perspective and then from the personal perspective of a Jewish Orthodox physician and ethicist who tries, both at a personal clinical level and in national and sometimes international discussions and debates, to reconcile h...
متن کاملIraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene.
Iraqi-Jewish optic atrophy plus is an autosomal recessive condition characterized by infantile optic atrophy, an early onset movement disorder, and 3-methylglutaconic aciduria. Other features include spastic paraplegia, mild ataxia, mild cognitive deficiency and dysarthria. This disorder was identified in inbred Iraqi-Jewish kindreds in which relationships between most of the affected individua...
متن کاملI-38: Chromosome Instability in The Cleavage Stage Embryo
Recently, we demonstrated chromosome instability (CIN) in human cleavage stage embryogenesis following in vitro fertilization (IVF). CIN not necessarily undermines normal human development (i.e. when remaining normal diploid blastomeres develop the embryo proper), however it can spark a spectrum of conditions, including loss of conception, genetic disease and genetic variation development. To s...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Assia--Jewish medical ethics
دوره 3 2 شماره
صفحات -
تاریخ انتشار 1998