Results 151 to 160 of about 14,329 (173)

Genetic Reduction of the Translational Repressors FMRP and 4E-BP2 Preserves Memory in Mouse Models of Alzheimer's Disease. [PDF]

open access: yesAging Cell
Ribeiro FC   +11 more
europepmc   +1 more source

FMR1 reduction alters cellular and circuit properties in human cortex

open access: yes
Singh A   +17 more
europepmc   +1 more source

Ablation of Fmrp in Adult Neural Stem Cells Disrupts Hippocampus-Dependent Learning

open access: yesNature Medicine, 2011
Deficiency in fragile X mental retardation protein (FMRP) results in fragile X syndrome (FXS), an inherited form of intellectual disability. Despite extensive research, it is unclear how FMRP deficiency contributes to the cognitive deficits in FXS.
Peng Jin, Amelia J Eisch, Weixiang Guo
exaly   +2 more sources

FMRP Drives mRNP Targets Into Translationally Silenced Complexes

open access: yesMolecular Cell
Fragile X Syndrome (FXS) is due to a deficiency in the ubiquitously expressed RNA-binding protein FMRP. While the mechanism of FMRP-mediated translational repression has been attributed primarily to ribosome stalling, we show using immunoprecipitations ...
Eric A J Simko   +2 more
exaly   +3 more sources

Fragile X Mental Retardation Protein (FMRP) Controls Diacylglycerol Kinase Activity in Neurons [PDF]

open access: yesProceedings of the National Academy of Sciences of the United States of America, 2016
Fragile X syndrome (FXS) is caused by the absence of the Fragile X Mental Retardation Protein (FMRP) in neurons. In the mouse, the lack of FMRP is associated with an excessive translation of hundreds of neuronal proteins, notably including postsynaptic ...
Barbara Bardoni   +2 more
exaly   +2 more sources
Some of the next articles are maybe not open access.

Related searches:

Home - About - Disclaimer - Privacy