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microRNAs and Fragile X Syndrome
2015Fragile X syndrome (FXS) is one of the major causes for autism and mental retardation in humans. The etiology of FXS is linked to the expansion of the CGG trinucleotide repeats, r(CGG), suppressing the fragile X mental retardation 1 (FMR1) gene on the X chromosome, resulting in a loss of fragile X mental retardation protein (FMRP) expression, which is ...
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Fragile X Syndrome: Introduction
2019Fragile X syndrome (FXS) is one of the most common reasons for intellectual disability (ID). First described in the 1940s, it took many years to understand the disease. The awe-inspiring breakthroughs in both science and technology facilitated the recognition of the unique inheritance pattern and the genetic mechanism of fragile X.
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ATP Synthase c-Subunit Leak Causes Aberrant Cellular Metabolism in Fragile X Syndrome
Cell, 2020Pawel Licznerski +2 more
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Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene
Cell, 2018X Shawn Liu, Hao Wu, Xuebing Wu
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Metformin for Treatment of Fragile X Syndrome and Other Neurological Disorders
Annual Review of Medicine, 2019Ilse Gantois +2 more
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Syntactic Complexity During Conversation of Boys With Fragile X Syndrome and Down Syndrome
Journal of Speech, Language, and Hearing Research, 2018Joanne E Roberts, John Sideris
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Fragile X syndrome and associated disorders: Clinical aspects and pathology
Neurobiology of Disease, 2020Maria Jimena Salcedo-Arellano +2 more
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A Comparison of Phonological Skills of Boys With Fragile X Syndrome and Down Syndrome
Journal of Speech, Language, and Hearing Research, 2018Joanne Roberts, Martie L Skinner
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