Search For "muscle diseases"
Researchers discover muscle disorder caused by key protein mutations
Updated : 1 year, 9 months ago IST
A new study discovered that the SMCHD1 protein controls how genes are digested, which influences the course of Facioscapulohumeral Muscular Dystrophy (FSHD). This finding about SMCHD1's role in gene regulation is significant because it opens new avenues for creating tailored therapeutic tech
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Study suggests new approach for evaluating muscle coordination, fatigue
Updated : 5 months, 1 week ago IST
Surface electromyography (sEMG) is a conventional technique for measuring muscle electrical activity during exercise. This strategy has been used for over 70 years and consists of two conventional procedures. The first uses a pair of electrodes (metals that transmit electricity through non-m
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Study gives more insight into how warming-up enhances muscle performance
Updated : 2 years, 4 months ago IST
Everyone understands the benefits of warming up your muscles before a workout. But what happens when we warm up our muscles, and are all muscles the same? You might be shocked to learn that the science behind this commonplace activity hasn't always been obvious.
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Study reveals cause of heart muscle disease in children is key to effectiv
Updated : 2 years, 9 months ago IST
Cardiomyopathy treatment for children should be personalised based on the root cause, symptoms, and course of the ailment in each child.
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Researchers discover ceramides role in aging muscle health
Updated : 2 years, 4 months ago IST
Mice experience inactivity, muscle loss, and strength loss as they age, just like humans do. The ceramide content of mice's muscles increases as they age, according to a group of researchers at EPFL lead by Johan Auwerx.
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Study: New technologies can be key to producing effective therapies for fa
Updated : 3 years, 5 months ago IST
Portsmouth [England], September 27 (ANI): A genetic mutation causes Duchenne muscular dystrophy (DMD), which affects one in every 5,000 boys born. Because the affected gene is located on the X chromosome, girls are carriers of the mutant gene but only very rarely develop the disease (one
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