Publishing research using ab30868? Please let us know so that we can cite the reference in this datasheet.

ab30868 has been referenced in 16 publications.

  • Muona M  et al. Dysfunctional ADAM22 implicated in progressive encephalopathy with cortical atrophy and epilepsy. Neurol Genet 2:e46 (2016). PubMed: 27066583
  • Dazzo E  et al. Secretion-Positive LGI1 Mutations Linked to Lateral Temporal Epilepsy Impair Binding to ADAM22 and ADAM23 Receptors. PLoS Genet 12:e1006376 (2016). PubMed: 27760137
  • Kole MJ  et al. Selective Loss of Presynaptic Potassium Channel Clusters at the Cerebellar Basket Cell Terminal Pinceau in Adam11 Mutants Reveals Their Role in Ephaptic Control of Purkinje Cell Firing. J Neurosci 35:11433-44 (2015). PubMed: 26269648
  • Dazzo E  et al. Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy. Am J Hum Genet 96:992-1000 (2015). PubMed: 26046367
  • Simabukuro MM  et al. GABAA receptor and LGI1 antibody encephalitis in a patient with thymoma. Neurol Neuroimmunol Neuroinflamm 2:e73 (2015). PubMed: 25738169
  • Lovero KL  et al. The LGI1-ADAM22 protein complex directs synapse maturation through regulation of PSD-95 function. Proc Natl Acad Sci U S A 112:E4129-37 (2015). PubMed: 26178195
  • Yokoi N  et al. Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsy. Nat Med 21:19-26 (2015). PubMed: 25485908
  • Boillot M  et al. Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures. Brain 137:2984-96 (2014). Mouse . PubMed: 25234641
  • Ohkawa T  et al. Autoantibodies to epilepsy-related LGI1 in limbic encephalitis neutralize LGI1-ADAM22 interaction and reduce synaptic AMPA receptors. J Neurosci 33:18161-74 (2013). Human . PubMed: 24227725
  • Zhou YD  et al. Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses. J Neurosci 32:903-10 (2012). WB ; Mouse . PubMed: 22262888
  • Fukata Y  et al. Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy. Proc Natl Acad Sci U S A 107:3799-804 (2010). PubMed: 20133599
  • Ogawa Y  et al. ADAM22, a Kv1 channel-interacting protein, recruits membrane-associated guanylate kinases to juxtaparanodes of myelinated axons. J Neurosci 30:1038-48 (2010). WB . PubMed: 20089912
  • Chabrol E  et al. Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. Brain 133:2749-62 (2010). WB ; Mouse . PubMed: 20659958
  • Lai M  et al. Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series. Lancet Neurol 9:776-85 (2010). PubMed: 20580615
  • de Bellescize J  et al. A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes. Epilepsy Res 85:118-22 (2009). WB . PubMed: 19268539
  • Striano P  et al. A novel loss-of-function LGI1 mutation linked to autosomal dominant lateral temporal epilepsy. Arch Neurol 65:939-42 (2008). WB ; Human . PubMed: 18625862

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