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Produktbild: Genetics and Genomics for the Cardiologist
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Genetics and Genomics for the Cardiologist

Aus der Reihe Basic Science for the Cardiologist

97,99 €

inkl. gesetzl. MwSt., Versandkostenfrei

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

23.10.2012

Abbildungen

XIII, 227 p.

Verlag

Springer Us

Seitenzahl

227

Maße (L/B/H)

23,5/15,5/1,4 cm

Gewicht

376 g

Auflage

Softcover reprint of the original 1st edition 2002

Sprache

Englisch

ISBN

978-1-4613-5357-7

Beschreibung

Produktdetails

Einband

Taschenbuch

Erscheinungsdatum

23.10.2012

Abbildungen

XIII, 227 p.

Verlag

Springer Us

Seitenzahl

227

Maße (L/B/H)

23,5/15,5/1,4 cm

Gewicht

376 g

Auflage

Softcover reprint of the original 1st edition 2002

Sprache

Englisch

ISBN

978-1-4613-5357-7

Herstelleradresse

Springer-Verlag GmbH
Tiergartenstr. 17
69121 Heidelberg
DE

Email: GPSR Kontakt

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  • Produktbild: Genetics and Genomics for the Cardiologist
  • 1: The Human Genome.- 1.1 Size and characteristics of nuclear and mitochondrial genome in humans.- 1.2 Structural and functional organization of human chromosomes.- 1.3 Structural and functional organization of human genes.- 1.4 Artificial banding of human chromosomes.- 1.5 Replication of human DNA and the origin of new mutations.- 1.6 Effects of mutations in DNA sequences.- 1.7 DNA markers.- 1.8 Chromosomal basis of inheritance.- 1.9 The main reference database for human disease genes.- 1.10 The Human Mutation Database and the nomenclature for human mutations.- 2: From Genome to Clinical Phenotype.- 2.1 Analyzing the human transcriptome.- 2.2 The differential expression of human genes.- 2.3 From transcriptome to proteome and metabolome.- 2.4 The transcriptome of the human heart.- 2.5 Genotype and phenotype.- 2.6 Molecular explanation of dominance of some mutations.- 2.7 Gene dosage.- 2.8 Peculiarity of phenotypes due to mutations in mitochondrial DNA.- 2.9 Multi-factorial diseases.- 3: Identifying Disease Genes in Humans.- 3.1 Starting with the family.- 3.2 The positional candidate gene approach.- 3.3 Linkage analysis in Mendelian diseases.- 3.4 Linkage analysis in multifactorial diseases.- 3.5 Detecting pathogenic mutations.- 3.6 Establishing the pathogenic role of specific mutations.- 3.7 Establishing genotype-phenotype correlations.- 4: Inherited Structural and Functional Defects of Myocardium.- 4.1 Cardiomyopathies.- 4.2 Genetic heterogeneity of cardiomyopathies and the “final common pathway” hypothesis.- 4.3 Arrhythmic disorders.- 4.4 Genetic basis of congenital heart defects in humans.- 4.5 Transgenic animals and the genetic dissection of developmental phenotypes.- 4.6 Understanding cardiovascular development.- 5: Inherited Cardiovascular Disorders.- 5.1Structural defects of vessels.- 5.2 Coronary atherosclerosis and myocardial infarction.- 5.3 Genetics of hypertension.- 5.4 Understanding hypertension through animal models.- 6: Genetics and Genomics Applied to Diagnosis and Therapy.- 6.1 Growing interest for genetic tests.- 6.2 Purposes and methods of genetic testing.- 6.3 Novel genetic tests.- 6.4 Genetic risk assessment.- 6.5 Genetic tests: some ethical and legal aspects.- 6.6 Genetics and genomics applied to drug therapy: pharmacogenetics and pharmacogenomics.- 6.7 Pharmacogenetics in Cardiology.- 6.8 Pharmacogenomics and beyond.- 6.9 Gene-based therapeutics.- Conclusion.- References.- Appendix I: Updated information from the Web.- Appendix II: OMIM IDs for monogenic disorders relevant to Cardiology.- Appendix III: Genes encoding ionic channels and expressed in human heart.- Credits.