scholarly journals Biophysical characterization of G-quadruplex forming FMR1 mRNA and of its interactions with different fragile X mental retardation protein isoforms

RNA ◽  
2013 ◽  
Vol 20 (1) ◽  
pp. 103-114 ◽  
Author(s):  
A. C. Blice-Baum ◽  
M.-R. Mihailescu
Keyword(s):  
Mental Retardation ◽  
Fragile X ◽  
Protein Isoforms ◽  
Biophysical Characterization ◽  
Fragile X Mental Retardation ◽  
G Quadruplex ◽  
Mental Retardation Protein ◽  
Fmr1 Mrna

scholarly journals Expression and Characterization of Human Fragile X Mental Retardation Protein Isoforms and Interacting Proteins in Human Cells

2019 ◽  
Vol 10 ◽  
pp. 117864181882526
Author(s):  
Jiang Zhang ◽  
Guangli Wang ◽  
Wei-Wu He ◽  
Molly Losh ◽  
Elizabeth Berry-Kravis ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Fragile X ◽  
Human Cells ◽  
Protein Isoforms ◽  
Interacting Proteins ◽  
Fragile X Mental Retardation ◽  
Mental Retardation Protein

scholarly journals Characterization of Fragile X Mental Retardation Protein Recruitment and Dynamics in Drosophila Stress Granules

PLoS ONE ◽  
2013 ◽  
Vol 8 (2) ◽  
pp. e55342 ◽  
Author(s):  
Cristina Gareau ◽  
Elise Houssin ◽  
David Martel ◽  
Laetitia Coudert ◽  
Samia Mellaoui ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Fragile X ◽  
Stress Granules ◽  
Fragile X Mental Retardation ◽  
Mental Retardation Protein ◽  
Protein Recruitment

scholarly journals Fragile X mental retardation protein interactions with a G quadruplex structure in the 3′-untranslated region of NR2B mRNA

2015 ◽  
Vol 11 (12) ◽  
pp. 3222-3230 ◽  
Author(s):  
Snezana Stefanovic ◽  
Brett A. DeMarco ◽  
Ayana Underwood ◽  
Kathryn R. Williams ◽  
Gary J. Bassell ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Intellectual Disability ◽  
Protein Interactions ◽  
Untranslated Region ◽  
Fragile X ◽  
Common Cause ◽  
Fragile X Mental Retardation ◽  
Quadruplex Structure ◽  
G Quadruplex ◽  
Mental Retardation Protein

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).

scholarly journals Identification and characterization of the methyl arginines in the fragile X mental retardation protein Fmrp

2005 ◽  
Vol 15 (1) ◽  
pp. 87-96 ◽  
Author(s):  
April Stetler ◽  
Claudia Winograd ◽  
Joyce Sayegh ◽  
Anne Cheever ◽  
Erin Patton ◽  
...  
Keyword(s):  
Mental Retardation ◽  
Fragile X ◽  
Fragile X Mental Retardation ◽  
Mental Retardation Protein ◽  
Identification And Characterization

scholarly journals Characterization of Fragile X Mental Retardation Protein granules formation and dynamics in Drosophila

Biology Open ◽  
2012 ◽  
Vol 2 (1) ◽  
pp. 68-81 ◽  
Author(s):  
C. Gareau ◽  
D. Martel ◽  
L. Coudert ◽  
S. Mellaoui ◽  
R. Mazroui
Keyword(s):  
Mental Retardation ◽  
Fragile X ◽  
Fragile X Mental Retardation ◽  
Mental Retardation Protein ◽  
Protein Granules
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