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Genomic Disorders -

Genomic Disorders

The Genomic Basis of Disease
Buch | Softcover
426 Seiten
2010 | Softcover reprint of hardcover 1st ed. 2006
Humana Press Inc. (Verlag)
978-1-61737-642-9 (ISBN)
CHF 249,95 inkl. MwSt
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A grand summary and synthesis of the tremendous amount of data now available in the post genomic era on the structural features, architecture, and evolution of the human genome. Two appendices detail the genomic disorders, providing genomic features at the locus undergoing rearrangement, their clinical features, and frequency of detection.
A grand summary and synthesis of the tremendous amount of data now available in the post genomic era on the structural features, architecture, and evolution of the human genome. The authors demonstrate how such architectural features may be important to both evolution and to explaining the susceptibility to those DNA rearrangements associated with disease. Technologies to assay for such structural variation of the human genome and to model genomic disorders in mice are also presented. Two appendices detail the genomic disorders, providing genomic features at the locus undergoing rearrangement, their clinical features, and frequency of detection.

The CMT1A Duplication.- Genomic Structure.- Alu Elements.- The Impact of LINE-1 Retro transposition on the Human Genome.- Ancient Transposable Elements, Processed Pseudogenes, and Endogenous Retroviruses.- Segmental Duplications.- Non-B DNA and Chromosomal Rearrangements.- Genetic Basis of Olfactory Deficits.- Genomic Organization and Function of Human Centromeres.- Genome Evolution.- Primate Chromosome Evolution.- Genome Plasticity in Evolution.- Genomic Rearrangements and Disease Traits.- The CMT1A Duplication and HNPP Deletion.- Smith-Magenis Syndrome Deletion, Reciprocal Duplication dup(17)(p11.2p11.2), and Other Proximal 17p Rearrangements.- Chromosome 22q11.2 Rearrangement Disorders.- Neurofibromatosis 1.- Williams-Beuren Syndrome.- Sotos Syndrome.- X Chromosome Rearrangements.- Pelizaeus–Merzbacher Disease and Spastic Paraplegia Type 2.- Y-Chromosomal Rearrangements and Azoospermia.- Inversion Chromosomes.- Monosomy 1p36 As a Model for the Molecular Basis of Terminal Deletions.- inv dup(15) and inv dup(22).- Mechanisms Underlying Neoplasia-Associated Genomic Rearrangements.- Functional Aspects of Genome Structure.- Recombination Hotspots in Nonallelic Homologous Recombination.- Position Effects.- Genomic Disorders: Modeling And Assays.- Chromosome-Engineered Mouse Models.- Array-CGH for the Analysis of Constitutional Genomic Rearrangements.

Erscheint lt. Verlag 9.12.2010
Zusatzinfo 1 Illustrations, color; 111 Illustrations, black and white; XVIII, 426 p. 112 illus., 1 illus. in color.
Verlagsort Totowa, NJ
Sprache englisch
Maße 178 x 254 mm
Themenwelt Medizin / Pharmazie Medizinische Fachgebiete
Studium 2. Studienabschnitt (Klinik) Pathologie
ISBN-10 1-61737-642-6 / 1617376426
ISBN-13 978-1-61737-642-9 / 9781617376429
Zustand Neuware
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