2018-12-11 02:09:42 Source: Science and Technology every day
Lateral atleotrophic sclerosis (ALS), also known as a motor neuron disease, is marked by the presence of unusual forms of protons such as superoxide dismutase 1 (SOD1), gather in neurons and then die to die. Researchers at the University of Zurich Renewable Medicine Institute, Tobias Welt, have referred to human antibodies from a healthy group of elderly people who recognize superoxide removal in a sklerosis patient backbone device at the thistle. Engine 1 is unusual. When they are added to an animal model of lateralopic amyotrophic sclerosis, the antibody can delay a sporting entertainment event, prolonging the duration of the animal's duration, reduce the neurons and a collection of superoxide dismutase 1 collections . These results show that this human antibody may have the potential to treat an amyotrophic side-side sclerosis side; including unfolding on superoxide dismutase 1.
(Source article: Science and Technology in the day)