Analysis of the Fragile X mental retardation protein isoforms 1, 2 and 3 interactions with the G-quadruplex forming semaphorin 3F mRNA

2012 ◽  
Vol 8 (2) ◽  
pp. 642-649 ◽  
Author(s):  
Timothy L. Evans ◽  
Anna C. Blice-Baum ◽  
Mihaela-Rita Mihailescu
2015 ◽  
Vol 11 (12) ◽  
pp. 3222-3230 ◽  
Author(s):  
Snezana Stefanovic ◽  
Brett A. DeMarco ◽  
Ayana Underwood ◽  
Kathryn R. Williams ◽  
Gary J. Bassell ◽  
...  

Fragile X syndrome, the most common cause of inherited intellectual disability, is caused by a trinucleotide CGG expansion in the 5′-untranslated region of the FMR1 gene, which leads to the loss of expression of the fragile X mental retardation protein (FMRP).


2017 ◽  
Vol 13 (8) ◽  
pp. 1448-1457 ◽  
Author(s):  
Damian S. McAninch ◽  
Ashley M. Heinaman ◽  
Cara N. Lang ◽  
Kathryn R. Moss ◽  
Gary J. Bassell ◽  
...  

SMNDC1 mRNA adopts a 5′-UTR G quadruplex structure recognized specifically by FMRP, potentially affecting spliceosome assembly in FXS.


2019 ◽  
Vol 10 ◽  
pp. 117864181882526
Author(s):  
Jiang Zhang ◽  
Guangli Wang ◽  
Wei-Wu He ◽  
Molly Losh ◽  
Elizabeth Berry-Kravis ◽  
...  

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