Results 111 to 120 of about 13,308 (213)
Subcellular targeting and local translation of mRNAs are critical for axon development. However, the precise local control of mRNA translation requires investigation.
Bin Wang +8 more
doaj +1 more source
BDNF Regulates the Expression of Fragile X Mental Retardation Protein mRNA in the Hippocampus
Both fragile X mental retardation protein (FMRP) and brain-derived neurotrophic factor (BDNF) are implicated in the maturation of neurons and in the higher cognitive functions.
Maija Castrén +7 more
doaj +1 more source
Fragile X syndrome, the most frequent form of familial mental retardation, is caused by mutation of the Fmr1 gene. Fmr1 encodes the Fragile X Mental Retardation Protein (FMRP), an mRNA binding protein regulating local, postsynaptic mRNA translation ...
Chanxia Li +3 more
doaj +1 more source
(A) Binding of PSD-95 Q11234 11-2AP by FMRP ISO1 (Kd = 128 ± 27 nM; shown by red circles), and FMRP S500D (Kd = 66 ± 10 nM; shown by black squares). (B) Binding of PSD-95 Q2 4-2AP by FMRP ISO1 (Kd = 195 ± 16 nM; shown by red circles) and by FMRP S500D ...
Kathryn R. Moss (6719051) +6 more
core +1 more source
FMRP Associates with Cytoplasmic Granules at the Onset of Meiosis in the Human Oocyte.
Germ cell development and primordial follicle formation during fetal life is critical in establishing the pool of oocytes that subsequently determines the reproductive lifespan of women.
Roseanne Rosario +6 more
doaj +1 more source
Function of FMRP by analyzing its interactors
Le Syndrome de l'X fragile (FXS) est la forme la plus fréquente de retard mental héréditaire. Il est causé par l’inactivation du gène FMR1 codant une RNA Binding Protein (FMRP) impliquée dans le contrôle de la traduction.
Abekhoukh-Achiou, Sabiha
core
FMRP 1C3 Western Blot (Millipore MAB2160) post-IP v1
Protocol for using Mouse-FMRP antibody follow immunoprecipitation of FMRP using a rabbit antibody such as Abcam #17722
core +1 more source
Engineering Recombinant Antibodies for the Detection of Axonal FMRP Spliceforms [PDF]
Epigenetic silencing of the fragile X mental retardation protein (FMRP) is understood to be the primary causative agent of fragile X syndrome (FXS), a well characterized cause of intellectual disability and autism.
Doll, Steven Gardner
core
Toward peptide-based protein replacement in fragile X syndrome: Evaluating the N-tat strategy
Fragile X syndrome (FXS), a leading inherited cause of intellectual disability and autism, arises from loss of the RNA-binding protein FMRP and consequent dysregulation of synaptic mRNA translation.
Oliver A. Kent
doaj +1 more source
The present invention provides compositions and methods for down-modulating the expression and/or the immuno-suppressive activity of i) the FMRP protein, ii) an mRNA encoding the FMRP protein, and/or iii) the FMR1 gene for the treatment and/or prevention
Hanahan, Douglas, Zeng, Qiqun
core

