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Luis María Vaschetto - CRISPR-/Cas9 Based Genome Editing for Treating Genetic Disorders and Diseases, Häftad

Häftad, Engelska, 2024

CRISPR-/Cas9 Based Genome Editing for Treating Genetic Disorders and Diseases

Av Luis María Vaschetto

969 kr

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Beskrivning
The CRISPR-Cas9 genome-editing system is creating a revolution in the science world. In the laboratory, CRISPR-Cas9 can efficiently be used to target specific genes, correct mutations and regulate gene expression of a wide array of cells and organisms, including human cells. CRISPR-/Cas9 Based Genome Editing for Treating Genetic Disorders and Diseases is a unique reading material for college students, academicians, and other health professionals interested in learning about the broad range of applications of CRISPR/Cas9 genetic scissors. Some topics included in this book are: the role of the CRISPR/Cas9 system in neuroscience, gene therapy, epigenome editing, genome mapping, cancer, virus infection control strategies, regulatory challenges and bioethical considerations.
Produktinformation
  • Utgivningsdatum: 2024-05-27
  • Mått: 156 x 234 x 15 mm
  • Vikt: 500 g
  • Format: Häftad
  • Språk: Engelska
  • Antal sidor: 262
  • Förlag: Taylor & Francis Ltd
  • ISBN: 9780367542870
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Mer information

Luis María Vaschetto received his Doctorate in Biological Sciences from Universidad Nacional de Córdoba (Argentina). He was a postdoctoral researcher at the Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) and a research associate at South Dakota State University (SDSU). His research focuses on understanding the epigenetic mechanisms involved in plant and animal development, as well as their effects on human health and diseases.

Recensioner i media

'Overall, this is an excellent book and a valuable contribution to the burgeoning field of human genome editing. Each chapter is well sourced and has an extensive list of references. Indeed, more than 25 percent of the 259 numberedpages in the book are devoted to references. This book offers an excellent starting point for exploration of genome editing in humans and is highly recommended.'- Mark F. Sanders, PhD, UC Davis College of Biological Sciences

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