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CRISPR and Gene Editing in Drug Development: A Revolution in Precision Medicine


Article Information

Title: CRISPR and Gene Editing in Drug Development: A Revolution in Precision Medicine

Authors: Khushboo Gupta, Ashley Christeena Thomas, Vandana Santwani, Binit Kumar Sarangi, Ankush Chandrakar, Sandip Prasad Tiwari

Journal: Journal of Neonatal Surgery

HEC Recognition History
Category From To
Y 2023-07-01 2024-09-30
Y 2022-07-01 2023-06-30

Publisher: EL-MED-Pub Publishers

Country: Pakistan

Year: 2025

Volume: 14

Issue: 27S

Language: en

Keywords: AI in genomics

Categories

Abstract

The discovery and implementation of CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology have transformed the landscape of biotechnology and precision medicine. As a revolutionary gene-editing tool, CRISPR enables targeted, efficient, and cost-effective modification of DNA, offering promising therapeutic interventions for a wide range of genetic and acquired diseases. This article provides an in-depth overview of CRISPR’s origins, mechanisms, and applications in drug development, from treating genetic disorders and enhancing cancer immunotherapies to accelerating drug discovery and developing tools against infectious diseases. It also addresses ethical considerations, regulatory frameworks, and future innovations such as base and prime editing. By exploring current trends and interdisciplinary applications, this article underscores the pivotal role CRISPR plays in shaping the future of medicine, agriculture, and synthetic biology


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