scholarly journals Fragile X mental retardation 1 and Filamin A interact genetically in Drosophila long-term memory

Author(s):  
Francois Bolduc
2010 ◽  
Vol 30 (19) ◽  
pp. 6782-6792 ◽  
Author(s):  
P. Banerjee ◽  
B. P. Schoenfeld ◽  
A. J. Bell ◽  
C. H. Choi ◽  
M. P. Bradley ◽  
...  

2008 ◽  
Vol 11 (10) ◽  
pp. 1143-1145 ◽  
Author(s):  
François V Bolduc ◽  
Kimberly Bell ◽  
Hilary Cox ◽  
Kendal S Broadie ◽  
Tim Tully

2019 ◽  
Vol 5 (2) ◽  
pp. 67-68
Author(s):  
Sultana MH Faradz ◽  
Tri Indah Winarni

Fragile X syndrome (FXS) is the most common cause of inherited intellectual disability (ID) and a leading cause of autism spectrum disorder (ASD). FXS is caused by an expansion of CGG repeats >200 in the 5′ untranslated region of the promotor region fragile X mental retardation 1 gene (FMR1), which is located on Xq27.3.  The abnormal CGG expansion leads to methylation and transcriptional silencing of the FMR1 gene, resulting in a reduction or loss of fragile X mental retardation 1 protein (FMRP) and causes long, thin, and immature dendritic spines, which lead to deficits in cognitive function, behavioral problems, and learning ability


Neuron ◽  
2006 ◽  
Vol 51 (4) ◽  
pp. 441-454 ◽  
Author(s):  
Lingfei Hou ◽  
Marcia D. Antion ◽  
Daoying Hu ◽  
Corinne M. Spencer ◽  
Richard Paylor ◽  
...  

Author(s):  
Catherine H. Choi ◽  
Brian P. Schoenfeld ◽  
Aaron J. Bell ◽  
Joseph Hinchey ◽  
Cory Rosenfelt ◽  
...  

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