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Author: Felix Mitelman Publisher: Wiley-Liss ISBN: 9780471111832 Category : Medical Languages : en Pages : 4252
Book Description
A systematic, concise and uniform presentation of the chromosome changes reported in human neoplastic disorders. Due to the dramatic increase of data, especially on solid tumors which typically have very complex karyotypes, the number of entries has almost doubled in the present edition. This version contains several improvements: all karyotypes have been adjusted according to the ISCN (1991) nomenclature recommendations, extremely complex karyotypes are now displayed unabridged, clonal aberrations are classified by conventional criteria as nonneoplastic disorders/lesions and morphological diagnoses (particularly those of solid tumors) have been reorganized and extended to make retrieval of data on specific tumor types more accessible.
Author: Felix Mitelman Publisher: Wiley-Liss ISBN: 9780471111832 Category : Medical Languages : en Pages : 4252
Book Description
A systematic, concise and uniform presentation of the chromosome changes reported in human neoplastic disorders. Due to the dramatic increase of data, especially on solid tumors which typically have very complex karyotypes, the number of entries has almost doubled in the present edition. This version contains several improvements: all karyotypes have been adjusted according to the ISCN (1991) nomenclature recommendations, extremely complex karyotypes are now displayed unabridged, clonal aberrations are classified by conventional criteria as nonneoplastic disorders/lesions and morphological diagnoses (particularly those of solid tumors) have been reorganized and extended to make retrieval of data on specific tumor types more accessible.
Author: Sverre Heim Publisher: John Wiley & Sons ISBN: 1118795512 Category : Medical Languages : en Pages : 645
Book Description
The first three editions of this acclaimed book presented a much-needed conceptual synthesis of this rapidly moving field. Now, Cancer Cytogenetics, Fourth Edition, offers a comprehensive, expanded, and up-to-date review of recent dramatic advances in this area, incorporating a vast amount of new data from the latest basic and clinical investigations. New contributors reflecting broader international authorship and even greater expertise Greater emphasis throughout on the clinical importance and application of information about cytogenetic and molecular aberrations Includes a complete coverage of chromosome aberrations in cancer based on an assessment of the 60,000 neoplasms cytogenetically investigated to date Now produced in full color for enhanced clarity Covers how molecular genetic data (PCR-based and sequencing information) are collated with the cytogenetic data where pertinent Discusses how molecular cytogenetic data (based on studies using FISH, CGH, SNP, etc) are fused with karyotyping data to enable an as comprehensive understanding of cancer cytogenetics as is currently possible
Author: Felix Mitelman Publisher: ISBN: Category : Medical Languages : en Pages : 742
Book Description
The new electronic edition of Mitelman's Catalog of Chromosome Aberrations in Cancer continues its legacy as the most complete, up-to-date sourcebook available on the chromosomal changes that have been reported in cases of human neoplastic disorder. Replacing the print version, this CD-ROM is an interactive database which combines all of the information found in the print edition, along with new databases which are currently not included in print. In addition, this electronic version offers all the advantages of searchability and hyperlinked cross references which are unique to this format.
Author: Henry H Q Heng Publisher: World Scientific ISBN: 9814520861 Category : Medical Languages : en Pages : 463
Book Description
Cancer research is at a crossroads. Traditionally, cancer has been thought of as a disease of gene mutation, where the stepwise accumulation of cancer gene mutations is the key, and the identification of common gene mutations has been considered to be essential for diagnosis and treatment. Despite extensive research efforts and accumulated knowledge on cancer genes and pathways, the clinical benefits of this traditional approach have been limited. Recently, cancer genome sequencing has revealed an extensive amount of genetic heterogeneity where the long-expected common mutation drivers have been difficult, if not impossible, to identify. These realities ultimately challenge the conceptual framework of current cancer biology.This book introduces a new concept of genome theory of cancer evolution, in an attempt to unify the field. Many important and representative, but often confusing, questions and paradoxes are critically analyzed. By comparing gene- and genome-based theories, the hidden flaws of many popular viewpoints are addressed. This discussion is intended to initiate a much-needed critical re-evaluation of current cancer research.
Author: Henry H. Heng Publisher: Academic Press ISBN: 0128136367 Category : Medical Languages : en Pages : 564
Book Description
Genome Chaos: Rethinking Genetics, Evolution, and Molecular Medicine transports readers from Mendelian Genetics to 4D-genomics, building a case for genes and genomes as distinct biological entities, and positing that the genome, rather than individual genes, defines system inheritance and represents a clear unit of selection for macro-evolution. In authoring this thought-provoking text, Dr. Heng invigorates fresh discussions in genome theory and helps readers reevaluate their current understanding of human genetics, evolution, and new pathways for advancing molecular and precision medicine. - Bridges basic research and clinical application and provides a foundation for re-examining the results of large-scale omics studies and advancing molecular medicine - Gathers the most pressing questions in genomic and cytogenomic research - Offers alternative explanations to timely puzzles in the field - Contains eight evidence-based chapters that discuss 4d-genomics, genes and genomes as distinct biological entities, genome chaos and macro-cellular evolution, evolutionary cytogenetics and cancer, chromosomal coding and fuzzy inheritance, and more
Author: Thomas Liehr Publisher: Academic Press ISBN: 0128235802 Category : Science Languages : en Pages : 430
Book Description
Cytogenomics demonstrates that chromosomes are crucial in understanding the human genome and that new high-throughput approaches are central to advancing cytogenetics in the 21st century. After an introduction to (molecular) cytogenetics, being the basic of all cytogenomic research, this book highlights the strengths and newfound advantages of cytogenomic research methods and technologies, enabling researchers to jump-start their own projects and more effectively gather and interpret chromosomal data. Methods discussed include banding and molecular cytogenetics, molecular combing, molecular karyotyping, next-generation sequencing, epigenetic study approaches, optical mapping/karyomapping, and CRISPR-cas9 applications for cytogenomics. The book's second half demonstrates recent applications of cytogenomic techniques, such as characterizing 3D chromosome structure across different tissue types and insights into multilayer organization of chromosomes, role of repetitive elements and noncoding RNAs in human genome, studies in topologically associated domains, interchromosomal interactions, and chromoanagenesis. This book is an important reference source for researchers, students, basic and translational scientists, and clinicians in the areas of human genetics, genomics, reproductive medicine, gynecology, obstetrics, internal medicine, oncology, bioinformatics, medical genetics, and prenatal testing, as well as genetic counselors, clinical laboratory geneticists, bioethicists, and fertility specialists. - Offers applied approaches empowering a new generation of cytogenomic research using a balanced combination of classical and advanced technologies - Provides a framework for interpreting chromosome structure and how this affects the functioning of the genome in health and disease - Features chapter contributions from international leaders in the field
Author: Ilan R. Kirsch Publisher: CRC Press ISBN: 9780849388934 Category : Science Languages : en Pages : 556
Book Description
The Causes and Consequences of Chromosomal Aberrations explores one of the most dramatic examples of genomic instability-chromosomal aberrations. It describes some of the more recent techniques used to map genes within the human genome, study chromosomal aberrations at the cellular level, and define the organization of the interphase nucleus. General overviews are provided to build a conceptual framework for understanding the generality and specificity of chromosomal aberrations. The Causes and Consequences of Chromosomal Aberrations also explores the role of recombinases and topoisomerases in the development of chromosomal aberrations. It contains studies of chromosomal aberrations, which offer separate instructive treatises on specific malignancies. The Causes and Consequences of Chromosomal Aberrations is useful to medical and graduate students, physicians, molecular biologists, and cytogeneticists. It will benefit anyone interested in the concepts, contributions, and development in the field of molecular cytogenetics.
Author: Felix Mitelman
Author: Felix Mitelman
Author: Sverre Heim
Author: Felix Mitelman
Author: Felix Mitelman
Author: Henry H Q Heng
Author: Henry H. Heng
Author: 
Author: 
Author: Thomas Liehr
Author: Ilan R. Kirsch