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"Modulating Gene Expression: Abridging the RNAi and CRISPR-Cas9 Technologies" ed. by Aditi Singh, Mohammad W. Khan

Posted By: exLib
"Modulating Gene Expression: Abridging the RNAi and CRISPR-Cas9 Technologies" ed. by Aditi Singh, Mohammad W. Khan

"Modulating Gene Expression: Abridging the RNAi and CRISPR-Cas9 Technologies" ed. by Aditi Singh, Mohammad W. Khan
ITExLi | 2019 | ISBN: 838806989 9781838806989 1838806970 9781838806972 1838806962 9781838806965 | 119 pages | PDF | 8 MB

In this book, we will focus on the mechanisms, applications, regulations (their pros and cons), and various ways in which RNAi-based methods and CRIPSR-Cas9 technology have stimulated the modulation of gene expression, thereby making them a promising therapeutic tool to treat and prevent complex diseases and disorders.

RNA interference (RNAi) is a widely used technology for gene silencing and has become a key tool in a myriad of research and lead discoveries. In recent years, the mechanism of RNAi agents has been well investigated, and the technique has been optimized for better effectiveness and safety. On the other hand, the clustered regularly interspaced short palindromic repeats (CRISPR)-associated Cas9/gRNA system is a recent, novel, targeted genome-editing technique derived from the bacterial immune system. Recent advances in gene-editing research and technologies have enabled the CRISPR Cas9 system to become a popular tool for sequence-specific gene editing to correct and modify eukaryotic systems.

Contents
1.Introductory Chapter: Modulating Gene Expression - Abridging the RNAi and CRISPR-Cas9 Technologies
2.CRISPR-ERA for Switching Off (Onco) Genes
3.Gene Silencing Agents in Breast Cancer
4.Nontransformative Strategies for RNAi in Crop Protection
5.Strand Displacement Amplification for Multiplex Detection of Nucleic Acids
6.MultiSite Gateway Technology Is Useful for Donor DNA Plasmid Construction in CRISPR/Cas9-Mediated Knock-In System
7.Machine Learning and Rule Mining Techniques in the Study of Gene Inactivation and RNA Interference

1st true PDF with TOC BookMarkLinks