An experimental gene therapy seems to slow the progression of Huntington’s disease by about 75 per cent, and researchers are ...
Major is one of the first pediatric patients in Florida to receive gene therapy for sickle cell disease since the FDA ...
A cutting-edge therapy using base-edited immune cells is offering a major breakthrough for patients with one of the toughest forms of blood cancer, T-cell acute lymphoblastic leukaemia. By precisely ...
TOMI Environmental Solutions, Inc.® ('TOMI”) (NASDAQ: TOMZ), a global leader in disinfection and decontamination solutions, ...
In the big picture, matched sibling donor transplants remain the standard of care, Boelens said. But gene therapy is ...
The treatment uses a modified, harmless virus to deliver healthy genes to a patient’s cells to treat genetic diseases. Read ...
Caden Major was born with sickle cell disease – an inherited blood disorder affecting red blood cells. Now at 19 years old, ...
Xmoor Pharma has established a strategic collaboration with the Translational Research Office (TRO) and University College ...
Scientists have successfully transplanted gene-edited insulin-producing cells into a man with type 1 diabetes—allowing him to ...
JABSOM Cell and Molecular Biology researcher Dr. Jesse Owens has spent the better part of two decades chasing a vision that ...
News Medical on MSN
‘Ready-made’ T-cell gene therapy tackles ‘incurable’ T-cell leukemia
A groundbreaking new treatment using genome-edited immune cells, developed by scientists at UCL (University College London) and Great Ormond Street Hospital (GOSH), has shown promising results in ...
A patient with synovial sarcoma, a soft-tissue cancer that usually occurs in the large joints of the arms and legs, is the ...
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