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ab17722 has been referenced in 39 publications.

  • Vershkov D  et al. FMR1 Reactivating Treatments in Fragile X iPSC-Derived Neural Progenitors In Vitro and In Vivo. Cell Rep 26:2531-2539.e4 (2019). PubMed: 30840878
  • Guimarães-Souza EM  et al. Retinal alterations in a pre-clinical model of an autism spectrum disorder. Mol Autism 10:19 (2019). PubMed: 31011411
  • Bao J  et al. Fmr1 protects cardiomyocytes against lipopolysaccharide-induced myocardial injury. Exp Ther Med 16:1825-1833 (2018). PubMed: 30186407
  • Hartmann H  et al. Proteomics and C9orf72 neuropathology identify ribosomes as poly-GR/PR interactors driving toxicity. Life Sci Alliance 1:e201800070 (2018). PubMed: 30456350
  • Antoniou A  et al. The dynamic recruitment of TRBP to neuronal membranes mediates dendritogenesis during development. EMBO Rep 19:N/A (2018). WB ; Rat . PubMed: 29263199
  • Khayachi A  et al. Sumoylation regulates FMRP-mediated dendritic spine elimination and maturation. Nat Commun 9:757 (2018). PubMed: 29472612
  • Soto-Acosta R  et al. Fragile X mental retardation protein is a Zika virus restriction factor that is antagonized by subgenomic flaviviral RNA. Elife 7:N/A (2018). PubMed: 30511641
  • Wilkinson B  et al. Synaptic GAP and GEF Complexes Cluster Proteins Essential for GTP Signaling. Sci Rep 7:5272 (2017). PubMed: 28706196
  • Marti AR  et al. No Escaping the Rat Race: Simulated Night Shift Work Alters the Time-of-Day Variation in BMAL1 Translational Activity in the Prefrontal Cortex. Front Neural Circuits 11:70 (2017). PubMed: 29085284
  • Filippini A  et al. Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse. RNA Biol 14:1580-1591 (2017). PubMed: 28640668
  • Zorio DA  et al. Cellular distribution of the fragile X mental retardation protein in the mouse brain. J Comp Neurol 525:818-849 (2017). PubMed: 27539535
  • Geng Q  et al. The Atypical Dual Specificity Phosphatase hYVH1 Associates with Multiple Ribonucleoprotein Particles. J Biol Chem 292:539-550 (2017). PubMed: 27856639
  • Akins MR  et al. Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains. Hum Mol Genet 26:192-209 (2017). PubMed: 28082376
  • Boland MJ  et al. Molecular analyses of neurogenic defects in a human pluripotent stem cell model of fragile X syndrome. Brain 140:582-598 (2017). PubMed: 28137726
  • Kang JY  et al. Deficits in the activity of presynaptic ?-aminobutyric acid type B receptors contribute to altered neuronal excitability in fragile X syndrome. J Biol Chem 292:6621-6632 (2017). PubMed: 28213518
  • Eliscovich C  et al. Imaging mRNA and protein interactions within neurons. Proc Natl Acad Sci U S A 114:E1875-E1884 (2017). WB, ICC/IF . PubMed: 28223507
  • Lechpammer M  et al. Dysregulation of FMRP/mTOR Signaling Cascade in Hypoxic-Ischemic Injury of Premature Human Brain. J Child Neurol 31:426-32 (2016). PubMed: 26239490
  • Wolfe SA  et al. FMRP regulates an ethanol-dependent shift in GABABR function and expression with rapid antidepressant properties. Nat Commun 7:12867 (2016). PubMed: 27666021
  • Guimarães-Souza EM  et al. Fragile X Mental Retardation Protein expression in the retina is regulated by light. Exp Eye Res 146:72-82 (2016). PubMed: 26719241
  • Kashima R  et al. Augmented noncanonical BMP type II receptor signaling mediates the synaptic abnormality of fragile X syndrome. Sci Signal 9:ra58 (2016). PubMed: 27273096
  • Telias M  et al. Functional Deficiencies in Fragile X Neurons Derived from Human Embryonic Stem Cells. J Neurosci 35:15295-306 (2015). PubMed: 26586818
  • Taha MS  et al. Subcellular fractionation and localization studies reveal a direct interaction of the fragile X mental retardation protein (FMRP) with nucleolin. PLoS One 9:e91465 (2014). IP, IF ; Human . PubMed: 24658146
  • Bartley CM  et al. FMRP S499 is phosphorylated independent of mTORC1-S6K1 activity. PLoS One 9:e96956 (2014). WB ; Mouse . PubMed: 24806451
  • Qin M  et al. Cerebral protein synthesis in a knockin mouse model of the fragile X premutation. ASN Neuro 6:N/A (2014). WB ; Mouse . PubMed: 25290064
  • Hamilton A  et al. Metabotropic glutamate receptor 5 knockout reduces cognitive impairment and pathogenesis in a mouse model of Alzheimer's disease. Mol Brain 7:40 (2014). WB ; Mouse . PubMed: 24886239
  • Avitzour M  et al. FMR1 epigenetic silencing commonly occurs in undifferentiated fragile X-affected embryonic stem cells. Stem Cell Reports 3:699-706 (2014). WB . PubMed: 25418717
  • Paul K  et al. Dampened dopamine-mediated neuromodulation in prefrontal cortex of fragile X mice. J Physiol 591:1133-43 (2013). Mouse . PubMed: 23148316
  • Giampetruzzi A  et al. FMRP and myelin protein expression in oligodendrocytes. Mol Cell Neurosci 56:333-41 (2013). PubMed: 23891804
  • Hoffman GE  et al. Ovarian abnormalities in a mouse model of fragile X primary ovarian insufficiency. J Histochem Cytochem 60:439-56 (2012). IHC-P ; Mouse . PubMed: 22470123
  • Jeon SJ  et al. Positive feedback regulation of Akt-FMRP pathway protects neurons from cell death. J Neurochem 123:226-38 (2012). PubMed: 22817682
  • Darnell JC  et al. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism. Cell 146:247-61 (2011). WB . PubMed: 21784246
  • Fatemi SH  et al. Metabotropic glutamate receptor 5 upregulation in children with autism is associated with underexpression of both Fragile X mental retardation protein and GABAA receptor beta 3 in adults with autism. Anat Rec (Hoboken) 294:1635-45 (2011). PubMed: 21901840
  • Qin M  et al. A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. Neurobiol Dis 42:85-98 (2011). PubMed: 21220020
  • Edbauer D  et al. Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132. Neuron 65:373-84 (2010). WB ; Mouse . PubMed: 20159450
  • Cheever A  et al. Fragile X protein family member FXR1P is regulated by microRNAs. RNA 16:1530-9 (2010). PubMed: 20519410
  • Dahlhaus R & El-Husseini A Altered neuroligin expression is involved in social deficits in a mouse model of the fragile X syndrome. Behav Brain Res 208:96-105 (2010). PubMed: 19932134
  • Pan J  et al. Inactivation of Nxf2 causes defects in male meiosis and age-dependent depletion of spermatogonia. Dev Biol 330:167-74 (2009). WB . PubMed: 19345203
  • Darnell JC  et al. Discrimination of common and unique RNA-binding activities among Fragile-X mental retardation protein paralogs. Hum Mol Genet : (2009). PubMed: 19487368
  • Zang JB  et al. A mouse model of the human Fragile X syndrome I304N mutation. PLoS Genet 5:e1000758 (2009). WB ; Mouse . PubMed: 20011099

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