Literature DB >> 12137226

The Human Genome Project and the future of diagnostics, treatment and prevention.

G J B van Ommen1.   

Abstract

The Human Genome Project, the mapping of our 30,000-50,000 genes and the sequencing of all of our DNA, will have major impact on biomedical research and the whole of therapeutic and preventive health care. The tracing of genetic diseases to their molecular causes is rapidly expanding diagnostic and preventive options. The increased insights into molecular pathways, gained from high-throughput 'functional genomics', using DNA-chip and protein-chip approaches and specially designed animal model systems, will open great prospects for pharmacological and genetic therapies. Powerful bioinformatics and biostatistics will further improve our pattern recognition and accelerate progress. A rapidly expanding area of high expectations is that of 'pharmacogenomics': the design of more effective drugs with lower toxicity through tailoring of drug treatment to individual, genetically determined differences in drug metabolism. Not only will this decrease the cost of health care through reduction of adverse drug reactions, but a better stratification of populations will also provide more statistical power farther upstream in drug trials. However, the optimal benefits from the current explosion of 'data mining' will only be realized when the basic data are made and kept publicly accessible, while at the same time safeguarding the protection of intellectual property arising from downstream inventions. This is one of the goals of HUGO, the international Human Genome Organization, established 13 years ago to assist coordination of data acquisition and exchange and societal implementation of the genome project. Additional points of attention in this historic endeavour are the prevention of stigmatization and discrimination and the safeguarding of a worldwide balance in the contribution by--and benefits to--different populations, while respecting the diversity in cultures and traditions.

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Year:  2002        PMID: 12137226     DOI: 10.1023/a:1015673727498

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  6 in total

1.  Only connect: personal genomics and the future of American medicine.

Authors:  Misha Angrist
Journal:  Mol Diagn Ther       Date:  2010-04-01       Impact factor: 4.074

2.  Identifying novel helix-loop-helix genes in Caenorhabditis elegans through a classroom demonstration of functional genomics.

Authors:  Vernetta Griffin; Tracee McMiller; Erika Jones; Casonya M Johnson
Journal:  Cell Biol Educ       Date:  2003

3.  Genotype and allele frequency of human multidrug resistance (MDR1) gene C3435T polymorphism in Denizli province of Turkey.

Authors:  Sebahat Turgut; Günfer Turgut; Erol Omer Atalay
Journal:  Mol Biol Rep       Date:  2006-11-02       Impact factor: 2.742

Review 4.  The Use of Omic Technologies Applied to Traditional Chinese Medicine Research.

Authors:  Dalinda Isabel Sánchez-Vidaña; Rahim Rajwani; Man-Sau Wong
Journal:  Evid Based Complement Alternat Med       Date:  2017-01-31       Impact factor: 2.629

5.  Identification of candidate biomarkers associated with apoptosis in melanosis coli: GNG5, LPAR3, MAPK8, and PSMC6.

Authors:  Xiaohang Hua; Jiangang Chen; Lingli Wu
Journal:  Biosci Rep       Date:  2019-01-18       Impact factor: 3.840

6.  Genetic analysis of the role of Alx4 in the coordination of lower body and external genitalia formation.

Authors:  Daisuke Matsumaru; Ryuma Haraguchi; Anne M Moon; Yoshihiko Satoh; Naomi Nakagata; Ken-ichi Yamamura; Naoki Takahashi; Sohei Kitazawa; Gen Yamada
Journal:  Eur J Hum Genet       Date:  2013-08-14       Impact factor: 4.246

  6 in total

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