By Andrew Joseph - Stat News When the genome-editing tool CRISPR is thought of as a potential medicine, the targets that first come to mind are diseases like sickle cell or other conditions caused by particular mutations. Use CRISPR to fix that mutation, the idea...

By The Harvard Gazette For more than 20 years, scientists have been able to unravel the sequence of the human genome, the precise recipe of everyone’s DNA. That has led to incredible advances in discovering genes responsible for countless diseases. But within the last...

Growing and selection are crucial. by Josh Conway - Lifespan.io CRISPR is still imperfect While the accuracy of genetic modification through the well-known CRISPR/Cas9 system continues to improve, the technology remains imperfect. Small mistakes were initially...

— Difficult infection took weeks to identify; doctors warn about unproven treatments by Sophie Putka - MedPage Today A woman with multiple sclerosis (MS) who had intrathecal injections of umbilical cord stem cells in Mexico ended up with a severe Mycobacterium...

by William A. Haseltine - Forbes Induced pluripotent stem cells (iPSC), a continuing muse in cell therapy research, could potentially be used to improve flaws associated with conventional CAR T therapy. What if an effective cancer treatment became cheaper and easier...

By Izzy Wood -  Drug Target Review US researchers combine revascularisation techniques to allow new blood vessels to rapidly form in an architecturally organised manner. The ability to regenerate and pattern blood vessels remains an elusive milestone in regenerative...

By Genetic and Engineering News Alzheimer’s disease (AD) is the sixth leading cause of death in the United States. However, the exact cause of AD remains unknown. Existing approved treatments for AD are designed to target the already existing AD neuropathology,...

By McMaster University McMaster researchers have uncovered a fast and effective way to detect cancer stem cells before the disease recurs in adults who previously underwent treatment. Mick Bhatia, a professor in the department of Biochemistry and Biomedical Sciences,...

By Michael Irving - New Atlas Yale scientists have discovered a new potential treatment avenue to fight cancer. Using CRISPR gene-editing, the team eliminated extra chromosomes from cancer cells and found that they could no longer grow out of control. Healthy human...

By Anna Lazarus Caplan - People It was just after his eighth birthday when Hanif Mouehla found himself fighting for his life after being diagnosed with sickle cell disease. Inspired by the care he received, the 17-year-old is now eyeing the pre-med track at Harvard...

by Mrigakshi Dixit - Interesting Engineering Named Lantidra, it's a cellular therapy developed using deceased donor pancreatic cells for the treatment of type 1 diabetes in adults. Therapy suitable for patients with hypoglycemia Type 1 diabetes makes the pancreas...