|
|
|||
|
||||
OverviewThis text describes the clinical pathological and molecular genetic features that characterize Wilms tumour, the most common renal tumour of infancy. The book notes that the heterogeneity observed at the clinical pathological level is also seen at the molecular genetic level. This suggests that the molecular events leading to Wilms tumour are complex, but at the same time provide a paradigm for other embryonal and adult malignancies. Full Product DetailsAuthor: Max J. Coppes , C. E. Campbell , Bryan Williams , B. WilliamsPublisher: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG Imprint: Springer-Verlag Berlin and Heidelberg GmbH & Co. K Edition: illustrated edition Weight: 0.655kg ISBN: 9783540593966ISBN 10: 3540593969 Pages: 170 Publication Date: 03 August 1995 Audience: College/higher education , Professional and scholarly , Postgraduate, Research & Scholarly , Professional & Vocational Format: Hardback Publisher's Status: Active Availability: Out of stock The supplier is temporarily out of stock of this item. It will be ordered for you on backorder and shipped when it becomes available. Table of Contents1. Clinical Presentation and Treatment.- 2. Histopathology.- 3. Genetics of Wilms Tumor.- 4. Cloning and Characterization of the WT1 Locus.- 5. Developmental and Tissue-Specific Expression Patterns of the Wilms Tumor Suppressor Gene WT1.- 6. Cellular Functions of WT1.- 7. Naturally Occurring Mutations in the WT1 Gene.- 8. Other Loci Implicated in Wilms Tumor.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
||||