In a comprehensive Genomic Press Interview, researchers from the University of Texas Health Science Center at San Antonio and Hirosaki University have uncovered critical new insights into the ...
According to the Cleveland Clinic, Fragile X syndrome is the most common inherited cause of intellectual disability ...
The cover artistically integrates multiple elements central to investigating the developmental origins of Fragile X syndrome. A vibrant DNA double helix structure rendered in rainbow iridescent colors ...
Fragile X syndrome (FXS) is an inherited genetic developmental condition that strongly impacts brain development. Despite the ...
Salk neuroscientists found how specialized brain cells called astrocytes contribute to fragile X syndrome symptoms: through a protein pathway that, when suppressed, can alleviate some symptoms in a ...
Researchers discovered that suppressing BMP signaling in astrocytes reduces seizures and restores brain balance in Fragile X syndrome models.
A new study shows that enhancing activity of a specific component of 'NMDA' receptors normalizes protein synthesis, neural activity and seizure susceptibility in the hippocampus of fragile X lab mice.
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