MeSH tree: C16.320.322
Patients with X-linked severe combined immunodeficiency disorder (SCID-X1), sometimes called "bubble boy disease," are born with a defective gene that prevents them from producing immune cells. Gene therapy from St. Jude ...
Oct 6, 2023
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88
Researchers from Umeå University have unveiled how the most common white blood cells, neutrophils, counter Candida albicanstoxin and stop it in its tracks. Their results have been published in EMBO Reports.
Oct 5, 2023
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29
Developing brains become shaped by the sights, sounds, and experiences of early life. The brain's circuits grow more stable as we age. However, some experiences later in life open up opportunities for these circuits to be ...
Oct 4, 2023
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42
Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy diagnosed in childhood, with approximately 20,000 new cases reported each year. It is a progressive muscle disorder that results in the loss of muscle ...
Sep 29, 2023
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84
UC Davis MIND Institute Director Leonard Abbeduto is calling for a major shift in the way research into autism and other neurodevelopmental disabilities is conducted. He has co-authored a paper titled "Toward Equity in Research ...
Aug 29, 2023
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43
Autism spectrum disorder is a much more prevalent co-occurring condition in individuals with fragile X than previously realized, according to new research. It is also underdiagnosed in community settings.
Aug 29, 2023
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94
Duchenne muscular dystrophy (DMD) is a muscle degeneration disorder caused by mutations affecting the dystrophin gene. On August 24 in the journal Stem Cell Reports, researchers show how a dual CRISPR RNA method restored ...
Aug 24, 2023
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164
Duchenne muscular dystrophy (DMD) is a common progressive muscular disorder. It is an X-chromosome-linked disorder that gradually weakens various muscle groups including those supporting the heart, thus resulting into early ...
Aug 17, 2023
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60
A new method allows large quantities of muscle stem cells to be safely obtained in cell culture. This provides a potential for treating patients with muscle diseases—and for those who would like to eat meat, but don't want ...
Aug 16, 2023
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85
Fragile X syndrome is a genetic disorder caused by a mutation in a gene that lies at the tip of the X chromosome. It is linked to autism spectrum disorders. People with fragile X experience a range of symptoms that include ...
Jul 27, 2023
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