Regenerative Medicine and Stem Cells Technologies

The one-day symposium on “Personalized Medicine” was held with the cooperation of council for the stem cells sciences and technologies in the center of international conferences of Alzahra University.

Patient-derived organoids, hollow spheres of cells cultured from tumors, can quickly and accurately predict how patients with pancreatic cancer respond to a variety of treatments, facilitating a precision-medicine approach to the deadly disease.

Dental cavities are the leading source of disability and pain: They affect 35 percent of the worlds population, with an economic impact in the hundreds of billions of dollars. Still, the methods for treating cavities and tooth enamel loss generally involve pain, cost—and drills.

Wake Forest Institute for Regenerative Medicine (WFIRM) scientists have developed a 3-D brain organoid that could have potential applications in drug discovery and disease modeling.

Glioma, a type of brain cancer, is normally treated by removing as much of the tumor as possible, followed by radiation or chemotherapy. With this treatment, patients survive an average of about 10 years, but the tumors inevitably grow back.

A clinical trial has begun which will use stem cell transplants to grow a new immune system for people with untreatable Crohns disease - a painful and chronic intestinal disease which affects at least 115,000 people in the UK.

A team of researchers at the University of California San Diego School of Medicine was recently granted $865,282 from the California Institute for Regenerative Medicine (CIRM) to investigate a stem cell therapy for pulmonary fibrosis.

Researchers from the Stowers Institute for Medical Research and collaborators have identified a way to expand blood-forming, adult stem cells from human umbilical cord blood (hUCB).

If dogs with arthritis can gain benefit from stem cell injections, maybe people can, too.

Among the most significant scientific advances in recent years are the discovery and development of new ways to genetically modify living things using a fast and affordable technology called CRISPR.