ISBN: 9789048177264
Cancer genetics is a field of daunting breadth and depth. The literature describes hundreds of genes and genetic alterations that are variably associated with again as many disease states… Más…
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ISBN: 9789048177264
Cancer genetics is a field of daunting breadth and depth. The literature describes hundreds of genes and genetic alterations that are variably associated with again as many disease states… Más…
2010, ISBN: 9789048177264
Pasta blanda
[ED: Kartoniert / Broschiert], [PU: Springer Netherlands], Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. A concise guide to understandin… Más…
2010
ISBN: 904817726X
[EAN: 9789048177264], Nieuw boek, [SC: 7.07], [PU: Springer 2010-10], Books
2010, ISBN: 9789048177264
Buch, Softcover, Softcover reprint of hardcover 1st ed. 2008, [PU: Springer], Springer, 2010
2010, ISBN: 904817726X
[EAN: 9789048177264], Nieuw boek, [SC: 7.07], [PU: Springer -], Books
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Detalles del libro - Principles of Cancer Genetics
EAN (ISBN-13): 9789048177264
ISBN (ISBN-10): 904817726X
Tapa dura
Tapa blanda
Año de publicación: 2010
Editorial: Springer
340 Páginas
Peso: 0,515 kg
Idioma: eng/Englisch
Libro en la base de datos desde 2010-04-22T01:14:07+02:00 (Madrid)
Página de detalles modificada por última vez el 2023-10-23T16:07:00+02:00 (Madrid)
ISBN/EAN: 9789048177264
ISBN - escritura alterna:
90-481-7726-X, 978-90-481-7726-4
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Autor del libro: bunz, bünz
Título del libro: principles genetics, cancer and genetics, cancer principles practice oncology
Datos del la editorial
Autor: Fred Bunz
Título: Principles of Cancer Genetics
Editorial: Springer; Springer Netherland
326 Páginas
Año de publicación: 2010-10-19
Dordrecht; NL
Impreso en
Peso: 0,522 kg
Idioma: Inglés
84,98 € (DE)
87,36 € (AT)
94,00 CHF (CH)
POD
XII, 326 p.
BC; Cancer Research; Hardcover, Softcover / Medizin/Nichtklinische Fächer; Onkologie; Verstehen; BRCA; Bunz; Chromosom; Retinoblastom; cancer; genes; genetics; mutations; transcription; Oncology; Human Genetics; Biomedicine, general; Cancer Biology; Oncology; Medical Genetics; Biomedical Research; Genetik, Medizin; Medizinische Forschung; BB
Chapter 1: The Genetic Basis of Cancer The cancer gene theory Cancers are invasive tumors Cancer is a unique type of genetic disease What are cancer genes and how are they acquired? Mutations alter the human genome Genes and mutations Genetic variation and cancer genes Which mutations are important in cancer? Single nucleotide substitutions Gene silencing by cytosine methylation: epigenetics Environmental mutagens, mutations and cancer Inflammation promotes the propagation of cancer genes Darwinian selection and the clonal evolution of cancers Selective pressure and adaptation: hypoxia and altered metabolism Multiple somatic mutations punctuate clonal evolution How many mutations contribute to a cancer? Colorectal cancer: a model for understanding the process of tumorigenesis Do cancer cells divide more rapidly than normal cells? Germline cancer genes allow neoplasia to bypass steps in clonal evolution Cancer syndromes reveal rate-limiting steps in tumorigenesis Understanding cancer genetics Chapter 2: Oncogenes What is an oncogene? The discovery of transmissible cancer genes Viral oncogenes are derived from the host genome The search for activated oncogenes: the RAS gene family Complex genomic rearrangements: the MYC gene family Proto-oncogene activation by gene amplification Proto-oncogene activation by chromosomal translocation Chromosomal translocations in liquid and solid tumors Chronic myeloid leukemia and the Philadelphia chromosome Ewing’s sarcoma and the oncogenic activation of a transcription factor Oncogene discovery in the genomic era: mutations in PIK3CA Selection of tumor-associated mutations Multiple modes of proto-oncogene activation Oncogenes are dominant cancer genes Germline mutations of RET and MET confer cancer predisposition Proto-oncogene activation and tumorigenesis Chapter 3: Tumor SuppressorGenes What is a tumor suppressor gene? The discovery of recessive cancer phenotypes Retinoblastoma and Knudson’s two-hit hypothesis Chromosomal localization of the retinoblastoma gene The mapping and cloning of the retinoblastoma gene Tumor suppressor gene inactivation: the second ‘hit’ and loss of heterozygosity Recessive genes, dominant traits APC inactivation in inherited and sporadic colorectal cancers P53 inactivation: a frequent event in tumorigenesis Functional inactivation of p53: tumor suppressor genes and oncogenes interact Germline inheritance of mutant P53: Li Fraumeni syndrome Cancer predisposition: allelic penetrance, relative risk and odds ratios Breast cancer susceptibility: BRCA1 and BRCA2 Genetic losses on chromosome 9: CDKN2A Complexity at CDKN2A: neighboring and overlapping genes Genetic losses on chromosome 10: PTEN SMAD4 and the maintenance of stromal architecture Two distinct genes underlie neurofibromatosis Multiple endocrine neoplasia type 1 Most tumor suppressor genes are tissue-specific Modeling cancer syndromes in mice Tumor suppressor gene inactivation during colorectal tumorigenesis Inherited tumor suppressor gene mutations: gatekeepers and landscapers Maintaining the genome: caretakers Chapter 4: Genetic Instability and Cancer What is genetic instability? The majority of cancer cells are aneuploid Aneuploid cancer cells exhibit chromosome instability Chromosome instability arises early in colorectal tumorigenesis Chromosomal instability accelerates clonal evolution What causes aneuploidy? Transition from tetraploidy to aneuploidy during tumorigenesis Multiple forms of genetic instability in cancer Defects in mismatch repair cause hereditary nonpolyposis colorectal cancer Mismatch repair-deficient cancers have a distinct spectrum of mutations Defects in nucleotide excision repair cause xerodermaMás, otros libros, que pueden ser muy parecidos a este:
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