New York, April 4 (IANS) US scientists are using new advances in CRISPR gene-editing technology to uncover new biology that could lead to long-lasting treatments and new therapeutic strategies for ...

Scientists are testing CRISPR gene editing as a potential HIV cure after successfully removing the virus from infected cells in lab studies. Here’s what the research means and what comes next.

PHILADELPHIA (WPVI) -- Researchers at Temple University's School of Medicine and a team at the University of Nebraska Medical Center say they have, for the first time, eliminated the DNA of HIV-1, the ...

Clustered regularly interspaced short palindromic repeats (CRISPR)-based therapeutics are rapidly gaining traction for the management of infectious diseases. Programs targeting pathogens such as the ...

Clustered Regularly Interspaced Short Palindromic Repeats, or CRISPR for short forms part of a new ground-breaking gene-editing technology, known as CRISPR-Cas9. Many developments to CRISPR technology ...

Programs targeting pathogens such as HIV, herpes simplex virus (HSV), and drug-resistant Escherichia coli are advancing in clinical trials, signaling a transformative shift in the infectious disease ...

Scientific breakthroughs are transforming HIV care, with long-acting drugs like lenacapavir and CRISPR-based gene editing offering the possibility of yearly treatment and even complete removal of HIV ...