<i>Fmr1</i> Deletion and Early-Life Stress Interact to Increase Cell Proliferation and Glial Populations at the Expense of Immature Neurons in the Adult Dentate Gyrus. [PDF]
Latchney SE +4 more
europepmc +1 more source
Mapping RNA-Binding Proteins on the Ribosome by Tethered Micrococcal Nuclease. [PDF]
Yao CY, Joseph S.
europepmc +1 more source
Contribution of astrocytic calcium signaling to auditory hypersensitivity in a mouse model of fragile X syndrome. [PDF]
Bergdolt L +12 more
europepmc +1 more source
Lampbrush Chromosomes and Fragile X Mental Retardation Protein, FMRP
Fragile X Syndrome is the most common form of inherited mental retardation, occurring in 1/4000 males and 1/8000 females. This syndrome is caused by the lack of expression of the Fragile X mental retardation protein, or FMRP.
Miri Kim (2113432)
core
Integrated genetic analysis reveals synaptic m<sup>6</sup>A enrichment in high-risk autism genes. [PDF]
Doijad S, Sakthivel D, Gowda NKC.
europepmc +1 more source
Large-scale analysis of FMR1 CGG repeat length and risk of premature ovarian insufficiency in over 92 000 women. [PDF]
Morbey EJ +7 more
europepmc +1 more source
Circular RNA <i>circHomer1</i> mediates hippocampal functions via ribonucleoprotein granule transport and dendritic targeting of synaptic RNAs. [PDF]
Cai Y +15 more
europepmc +1 more source
A rapid and dynamic role for FMRP in the plasticity of adult neurons. [PDF]
Gundermann DG +3 more
europepmc +1 more source
Reelin signaling as a translational rheostat: linking synaptic homeostasis to neurodevelopment and neurodegeneration. [PDF]
Durakoglugil MS.
europepmc +1 more source

