Prof Whitelaw elaborated on advancements allowing scientists to rewrite the genome using the CRISPR technique, which enables correction of genetic flaws responsible for hereditary diseases.

The complexity of the central nervous system (CNS) and its pathologies necessitates an intricate understanding of the cellular and molecular mechanisms at play. Single-cell biology has emerged as a ...

Researchers in Lithuania present the molecular structure of a new, more-versatile CRISPR system for gene editing.

Agriculture can find solutions to counter the negative impacts of climate change on crops, but only if the sector is allowed to innovate, the International Seed Federation's chief told AFP.

The researchers identified the mechanism for this gigantic genome growth ... "In our research, we also used experiments with CRISPR-Cas transgenic mice to show that this simplification of the fins is ...

J INTS BIO announced research findings on its innovative brain tumor treatment, 'JIN-001,' developed in collaboration with MD Anderson Cancer Center, at the 2024 Society of Neuro-Oncology (SNO) Annual ...

CRISPR-based gene-editing tools are being developed to correct specific defective sections of the genome to cure inherited genetic diseases, with some applications already in clinical trials. However, ...

Cyclosporin H boosts a new lentivirus-delivered gene therapy with enhanced anti-sickling properties in blood stem cells from ...

Gliocidin selectively kills glioblastoma cells by inhibiting nucleotide synthesis, showing potential as a therapeutic option ...

This study presents important findings on cold tolerance shared between hibernating and non-hibernating mammals, identifying a key molecule, GPX4, through multi-species genome-wide CRISPR screens. The ...

A breakthrough tool called Helicase-Assisted Continuous Editing (HACE) allows scientists to create precise genetic mutations ...

With a bunch of gene therapy and gene editing programs in clinical trials, CRISPR Therapeutics (NASDAQ: CRSP) has an ...