Human Genome
Nova Science Publishers Inc (Verlag)
978-1-60741-695-1 (ISBN)
The sequencing of the human genome reveals our complete complement of genetic material. The sequenced human genome is one of the most international biomedical research projects ever, which is important in our current often all-too-fractured world. This book defines the function of all "unknown" human genes, delineates the functional and phenotypic significance of human genetic variants in humans, and explores the functions of the vast non-genic regions of the human genome. Human genome sequencing has revealed a great opportunity to deeply investigate the biology and evolution of the sex chromosome pair at a more global level, allowing new frontiers in the genetics research, such as a detailed knowledge of the sequence and the gene content of these chromosomes. This book provides the most current research done in this area.
Preface; CpG Islands in the Human Genome: Identification, Features, Mutations and Diseases; The Sex Chromosomes: Sequence, Evolution and Human Diseases; Role of Extrachromosomal Elements in HL-60 Human Leukemia Cells; Molecular Basis of Human Coagulopathies: From Southern Blots to Personalized Medicine; Wobble Splicing: Subtle Alternative Splicing at Tandem Splice Sites in Human Genome; Alternative Splicing Transcripts Affected by Junction Tandem Repeats in the Human Genome; Genetic Susceptibility to Complex Traits: Moving Towards Informed Analysis of Whole-Genome Screens; The Personal Genome: Science and Beyond; Unstable Repeat Expansion and Human Disease; SNPs and CNVs in Human Disorders; An Outlook on Uterine Neoplasms: From Hormonal and DNA Damaging to Cervical and Endometrial Cancer Development and Minimally Invasive Management; Lessons Learned in Human Tissue Banking for Acquiring High Quality Biospecimens for Translational Genomic Research: A Perspective of the IU; The Future of the Human Genomics Research: Three Unanswered Questions; Index.
| Erscheint lt. Verlag | 24.3.2010 |
|---|---|
| Zusatzinfo | Illustrations |
| Verlagsort | New York |
| Sprache | englisch |
| Maße | 260 x 180 mm |
| Gewicht | 824 g |
| Themenwelt | Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik |
| Naturwissenschaften ► Biologie ► Genetik / Molekularbiologie | |
| ISBN-10 | 1-60741-695-6 / 1607416956 |
| ISBN-13 | 978-1-60741-695-1 / 9781607416951 |
| Zustand | Neuware |
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