Genetic Polymorphism and Disease

Genetic Polymorphism and Disease

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Genetic Polymorphism and Disease

By Syed Sameer Aga, Mujeeb Zafar Banday, Saniya Nissar

By Syed Sameer Aga, Mujeeb Zafar Banday, Saniya Nissar

Genetic polymorphisms are an essential element in understanding the variations in phenotypes and their role in determining the risk or even causing various diseases, including genetic disorders and multifactorial diseases. They also serve as crucial genetic markers that aid in studying genetic and evolutionary aspects of individuals, populations, and organisms, allowing us to trace evolutionary and parental lineages. Polymorphisms in critical metabolic, signal transduction, cell cycle, or DNA repair genes significantly impact gene expression, leading to susceptibility to diseases such as cancers, cardiovascular diseases, immune disorders, and neurological pathologies. In their book, “Genetic Polymorphisms: Techniques and Their Role in Human Diseases,” Syed Sameer Aga, Mujeeb Zafar Banday, and Saniya Nissar collate comprehensive reviews on the roles played by polymorphisms in disease mechanisms and explore various techniques for identifying Single Nucleotide Polymorphisms (SNPs) and their impact on enzyme and protein functionality.

The book starts by introducing the concept of genetic polymorphism and its various types. It then delves into the fascinating world of genetic polymorphisms and their role in modulating the risk of various human diseases. The authors discuss in detail the impact of these polymorphisms on critical metabolic pathways, signal transduction mechanisms, cell cycle regulation, and DNA repair processes. They highlight the importance of these genetic variants as potential markers for disease susceptibility and their impact on individual variations in response to therapeutics.

One of the strengths of this book lies in its exploration of various molecular techniques used for detecting genetic polymorphisms. The authors provide a detailed understanding of advanced laboratory techniques such as Polymerase Chain Reaction (PCR), real-time PCR, DNA sequencing, and microarray analysis. By highlighting the advantages and limitations of each technique, readers gain valuable insights into the best practices for studying genetic polymorphisms. The book also emphasizes the need for robust data analysis and interpretation to draw accurate conclusions from genetic polymorphism studies.

The authors also focus on Single Nucleotide Polymorphisms (SNPs) and their role in modulating the susceptibility to human diseases. They explain how SNPs can impact protein structure and function, leading to altered enzymatic activity and signaling pathways. The book provides extensive examples of polymorphisms in key genes associated with specific diseases, showcasing the clinical relevance of these genetic variants. This knowledge can aid in developing personalized medicine approaches by identifying individuals who are more likely to respond to certain treatments based on their genetic makeup.

Throughout the book, Aga, Banday, and Nissar provide a comprehensive analysis of genetic polymorphisms and present their role in disease mechanisms in a concise and accessible manner. Their writing style is engaging, making complex scientific concepts understandable to a wide range of readers, including researchers, healthcare professionals, and students studying genetics or related fields.

“Genetic Polymorphisms: Techniques and Their Role in Human Diseases” is an essential reference book for anyone interested in understanding the impact of genetic variations on disease susceptibility and treatment outcomes. The authors’ thorough exploration of molecular techniques for detecting genetic polymorphisms, coupled with their in-depth analysis of the role of polymorphisms in disease mechanisms, makes this book a valuable resource for researchers and clinicians alike.

Order your copy of “Genetic Polymorphisms: Techniques and Their Role in Human Diseases” today and delve into the fascinating world of genetics and its impact on human health. With its comprehensive coverage and insightful analysis, this book is a must-have for anyone interested in the field of genetics and personalized medicine.

Product Details

  • Describes the genetic polymorphism and its various types
  • Discusses the role of genetic polymorphisms in modulating the risk of various human diseases
  • Explores various molecular techniques used for detecting GPs
  • Characterizes the role of SNPs in modulating the susceptibility of human diseases
  • Provides a genetic basis for individual variations in response to therapeutics
  • Publisher ‏ : ‎ CRC Press; 1st edition (December 6, 2022)
  • Language ‏ : ‎ English
  • Hardcover ‏ : ‎ 540 pages
  • ISBN-10 ‏ : ‎ 1032153164
  • ISBN-13 ‏ : ‎ 978-1032153162

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