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Biomedical Sciences - Human Genetics | Neurofibromatosis Type 1 - Molecular and Cellular Biology

Neurofibromatosis Type 1

Molecular and Cellular Biology

Upadhyaya, Meena, Cooper, David N (Eds.)

2012, XVI, 717 p. 75 illus., 60 illus. in color.

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  • Represents the most comprehensive and up to date account of this common neuroectodermal disorder
  • An outstanding panel of scientists and clinicians covering all aspects of NF1 biology
  • Lessons learned  from the molecular biology of NF1 tumorigenesis can be extrapolated to many other cancers

Neurofibromatosis type 1 (NF1), caused by mutational inactivation of the NF1 tumour suppressor gene, is one of the most common dominantly inherited human disorders, affecting 1 in 3000 individuals worldwide. This book presents in concise fashion, but as comprehensively as possible, our current state of knowledge on the molecular genetics, molecular biology and cellular biology of this tumour predisposition syndrome.

Written by internationally recognized experts in the field, the 44 chapters that constitute this edited volume provide the reader with a broad overview of the clinical features of the disease, the structure and expression of the NF1 gene, its germ line and somatic mutational spectra and genotype-phenotype relationships, the structure and function of its protein product (neurofibromin), NF1 modifying loci, the molecular pathology of NF1-associated tumours, animal models of the disease, psycho-social aspects and future prospects for therapeutic treatment.

Neurofibromatosis Type 1: Molecular and Cellular Biology will be of great value to medical geneticists, molecular and cellular biologists, oncologists, dermatologists, neurologists, genetic counsellors and general practitioners alike.

 

Content Level » Research

Keywords » NF1 gene - genotype-phenotype correlations - mutation - neurofibromatosis type 1

Related subjects » Cancer Research - Human Genetics - Molecular Medicine - Neuroscience - Oncology & Hematology

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