A Primer Of Human Genetics Ebook

This 4th edition is thoroughly updated version of the 3rd edition with its intact simple to-the-point presentation of knowledge, which makes the book examination friendly. This edition will be useful not only to the undergraduates, but also to the postgraduates, immunologists and geneticists. A chapter on "Stem Cell Therapy" Inclusion of Summary at the end of each chapter The concept of personalized medicine under Pharmacogenetics Information updation in nearly all chapters A chapter on "Stem Cell Therapy" Inclusion of Summary at the end of each chapter The concept of personalized medicine under Pharmacogenetics Information updation in nearly all chapters

Basic Genetics is a concise introductory textbook that focuses not only on understanding and explaining the main points of genetics, but also upon covering the required essential traditional subjects in the field. The main goal of this textbook is to help first year students who are taking their first course in human genetics to understand the different topics within genetics. It is of particular interest for those who are preparing themselves to study medicine or other medical sciences. This textbook presents only the essential required information. Some of the different subjects included in the eight chapters are: cell cycle and cellular division, Mendelian principles of heredity, the molecular basis of genetic material, gene expression and gene expression control, genetic variations and genetic engineering, as well as human genetics. In addition, Basic Genetics contains multiple choice questions covering each topic and their answers. These questions are absolutely essential for students' self- assessment. These different topics of basic genetics have also been illustrated by simple diagrams in full color.

Begins with molecular characterization of the human genome (rather than the conventional descriptions of Mendelian inheritance, pedigree analysis, and chromosome abnormalities), and maintains this emphasis on understanding human genetics in molecular terms throughout. Suitable as a text for biology

A chapter on "Stem Cell Therapy" Inclusion of Summary at the end of each chapter The concept of personalized medicine under Pharmacogenetics Information updation in nearly all chapters

The present edition of the book is a thoroughly revised and updated version of the previous edition. The presentation of the knowledge is simple and to the point, making the book examination friendly About the Author : - Professor SD Gangane is currently the Head of the Department of Anatomy and Genetic Division, Grant Medical College. Formerly he was serving as Head, Department of Anatomy, RCSM Government Medical College, Kohlapur, Maharashtra.

A Primer of Human Genetics is an introductory textbook designed to give students the foundation they need to understand and appreciate the extraordinary shifts in human genetics that have accompanied the arrival of genomics. The book lays out the key concepts of human evolution, quantitative genetics, and personalized medicine before describing the tools that are missing from most contemporary textbooks: genome-wide association studies, whole-genome resequencing, gene expression and epigenome profiling, and integrative genomics. The final section provides an up-to-date survey of specific findings in six major domains of human disease: immunological, metabolic, cardiovascular, cancer, neuropsychological, and aging disorders. After reading this textbook, not only will students be better equipped to read current literature, they will gain a sense of the impact that the revolution in genomics has had for our understanding of the human condition, as well as of the major trends in human genetics research. Students are assumed to have a core understanding of genetics such as would be obtained in a general genetics class. Each chapter is approximately 20 pages long, and organized under up to ten sub-headings, most of which incorporate an illustrative figure. Chapter summary points recap the key messages, and references point students to key reviews and contemporary highlights. Several of the chapters contain a single box, which provides extra material on topics such as 'Consent and Responsible Conduct of Research' and 'Methylation Analysis in Biology.'

"More than a million people have had their genomes sequenced, most of them since the last edition of this book was published in 2014. When I wrote the first edition, the idea to sequence "the" human genome was just becoming reality. The growing field of genomics, of considering all of our genes, is now revealing that we are much more alike than different, yet those differences among 3 million of our 3.2 billion DNA building blocks hold clues to our variation and diversity. It has been a privilege to chronicle the evolution of human genetics, from an academic subfield of life science and a minor medical specialty to a growing body of knowledge that will affect us all. The twelfth edition opens with the hypothetical "Eve's Genome" and ends with "Do You Want Your Genome Sequenced?" In between, the text touches on what exome and genome sequencing have revealed about single-gene diseases so rare that they affect only a single family to clues to such common and complex conditions as intellectual disability and autism. Exome and genome sequencing are also important in such varied areas as understanding our origins, solving crimes, and tracking epidemics. In short, DNA sequencing will affect most of us. As the cost of genome sequencing plummets, we all may be able to look to our genomes for echoes of our pasts and hints of our futures-if we so choose. We may also learn what we can do to counter our inherited tendencies and susceptibilities. Genetic knowledge is informative and empowering. This book shows you how and why this is true"--

Genetics has become an integral part of medical teaching at undergraduate and postgraduate levels. It is a science where conceptual and terminological changes occur every day. This book provides information about various aspects of human genetics in a brief, simple, comprehensive and yet interesting manner so as to sustain and drive the interest and enthusiasm of the reader. The two main parts of the book, Principles of Genetics and Applications of Genetics strive to provide current, relevant information in a clear and concise form. With updated text detailing new advances in DNA replication and gene expression, detailed illustrations and examples, chapter summaries and a comprehensive glossary, this book attempts to help the reader learn about and keep abreast with the changes in the fascinating field of genetics.

Significant advances in our knowledge of genetics were made during the twentieth century but in the most recent decades, genetic research has dramatically increased its impact throughout society. Genetic issues are now playing a large role in health and public policy, and new knowledge in this field will continue to have significant implications for individuals and society. Written for the non-majors human genetics course, Human Genetics, Third Edition will increase the genetics knowledge of students who are learning about human genetics for the first time. This thorough revision of the best-selling Human Genome, Second Edition includes entirely new chapters on forensics, stem cell biology, bioinformatics, and societal/ethical issues associated with the field. New special features boxes make connections between human genetics and human health and disease. Carefully crafted pedagogy includes chapter-opening case studies that set the stage for each chapter; concept statements interspersed throughout the chapter that keep first-time students focused on key concepts; and end-of-chapter questions and critical thinking activities. This new edition will contribute to creating a genetically literate student population that understands basic biological research, understands elements of the personal and health implications of genetics, and participates effectively in public policy issues involving genetic information. Includes topical material on forensics, disease studies, and the human genome project to engage non-specialist students Full, 4-color illustration program enhances and reinforces key concepts and themes Uniform organization of chapters includes interest boxes that focus on human health and disease, chapter-opening case studies, and concept statements to engage non-specialist readers