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“The methyltransferase SETDB1 regulates a large neuron-specific topological chromatin domain.”, Nat Genet, vol. 49, no. 8, pp. 1239-1250, 2017.
, “Characterization of the honeybee AmNaV1 channel and tools to assess the toxicity of insecticides.”, Sci Rep, vol. 5, p. 12475, 2015.
, “Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics.”, Mol Pharmacol, vol. 86, no. 4, pp. 378-89, 2014.
, “Roundabout 1 exists predominantly as a basal dimeric complex and this is unaffected by binding of the ligand Slit2.”, Biochem J, vol. 461, no. 1, pp. 61-73, 2014.
, “Activity-dependent subcellular cotrafficking of the small GTPase Rem2 and Ca2+/CaM-dependent protein kinase IIα.”, PLoS One, vol. 7, no. 7, p. e41185, 2012.
, “Fragile X mental retardation protein interacts with the RNA-binding protein Caprin1 in neuronal RiboNucleoProtein complexes [corrected].”, PLoS One, vol. 7, no. 6, p. e39338, 2012.
, “VAMP4 directs synaptic vesicles to a pool that selectively maintains asynchronous neurotransmission.”, Nat Neurosci, vol. 15, no. 5, pp. 738-45, 2012.
, “The myosin Va head domain binds to the neurofilament-L rod and modulates endoplasmic reticulum (ER) content and distribution within axons.”, PLoS One, vol. 6, no. 2, p. e17087, 2011.
, “The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.”, Hum Mol Genet, vol. 16, no. 24, pp. 3047-58, 2007.
, “Wild-type superoxide dismutase acquires binding and toxic properties of ALS-linked mutant forms through oxidation.”, J Neurochem, vol. 102, no. 1, pp. 170-8, 2007.
, “Transition from reversible to persistent binding of CaMKII to postsynaptic sites and NR2B.”, J Neurosci, vol. 26, no. 4, pp. 1164-74, 2006.
, “The high and middle molecular weight neurofilament subunits regulate the association of neurofilaments with kinesin: inhibition by phosphorylation of the high molecular weight subunit.”, Brain Res Mol Brain Res, vol. 141, no. 2, pp. 151-5, 2005.
, “82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization.”, Hum Mol Genet, vol. 12, no. 14, pp. 1689-98, 2003.
, “Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs.”, Hum Mol Genet, vol. 12, no. 23, pp. 3087-96, 2003.
, “Modulations of anti-D affinity following promiscuous binding of the heavy chain with naïve light chains.”, Transfusion, vol. 43, no. 2, pp. 246-53, 2003.
, “Interaction with the NMDA receptor locks CaMKII in an active conformation.”, Nature, vol. 411, no. 6839, pp. 801-5, 2001.
, “Structural and functional characterization of the human FMR1 promoter reveals similarities with the hnRNP-A2 promoter region.”, Hum Mol Genet, vol. 6, no. 12, pp. 2051-60, 1997.
, “The fragile X mental retardation protein is associated with ribosomes.”, Nat Genet, vol. 12, no. 1, pp. 91-3, 1996.
, “Metal substitutions incarbonic anhydrase: a halide ion probe study.”, Biochem Biophys Res Commun, vol. 66, no. 4, pp. 1281-6, 1975.
, “Studies of oxygen binding energy to hemoglobin molecule.”, Biochem Biophys Res Commun, vol. 66, no. 4, pp. 1424-31, 1975.
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