Genomic Disorders The Genomic Basis of Disease /

• Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
• Άλλοι συγγραφείς: Lupski, James R. (Επιμελητής έκδοσης), Stankiewicz, Pawel (Επιμελητής έκδοσης)
• Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
• Γλώσσα: English
• Έκδοση: Totowa, NJ : Humana Press, 2006.
• Θέματα: Medicine.; Pathology.; Medicine & Public Health.

 It is now abundantly clear that architectural features of the human genome can lead to DNA rearrangements that cause both disease and behavioral traits. In Genomic Disorders: The Genomic Basis of Disease, distinguished experts and pioneers in the field of genomics and genome rearrangements summarize and synthesize the tremendous amount of data now available in the postgenomic era on the structural features, architecture, and evolution of the human genome. The authors demonstrate how such architectural features may be important to evolution and explaining the susceptibility to those DNA rearrangements associated with disease. Technologies to assay for such structural variation of the human genome and 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. Comprehensive and clinically relevant, Genomic Disorders: The Genomic Basis of Disease offers genome and clinical genetics researchers not only an up-to-date survey of genome architecture, but also details those rearrangements that can be the underlying cause or basis of many human traits and disorders. 

 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.