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ab17722 has been referenced in 16 publications.

  • 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
  • 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
  • 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
  • Darnell JC  et al. FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism. Cell 146:247-61 (2011). WB . PubMed: 21784246
  • 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