| scholarly article | Q13442814 |
| P50 | author | Stéphanie Baulac | Q47402324 |
| P2093 | author name string | Xuan Wang | |
| Dawei Zhang | |||
| Ekim Ozkaynak | |||
| Ekkehard M Kasper | |||
| Yu-Dong Zhou | |||
| Eric Leguern | |||
| Matthew P Anderson | |||
| P2860 | cites work | LGI1 is a Nogo receptor 1 ligand that antagonizes myelin-based growth inhibition | Q24312114 |
| Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features | Q24643177 | ||
| Signaling mechanisms linking neuronal activity to gene expression and plasticity of the nervous system | Q24650727 | ||
| LGI1, a putative tumor metastasis suppressor gene, controls in vitro invasiveness and expression of matrix metalloproteinases in glioma cells through the ERK1/2 pathway | Q28253059 | ||
| The classical complement cascade mediates CNS synapse elimination | Q28261273 | ||
| Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission | Q28264840 | ||
| Experience-driven plasticity of visual cortex limited by myelin and Nogo receptor | Q28274782 | ||
| ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy | Q28506819 | ||
| Functional interaction between matrix metalloproteinase-3 and semaphorin-3C during cortical axonal growth and guidance | Q28506945 | ||
| Abnormal functional organization in the dorsal lateral geniculate nucleus of mice lacking the beta 2 subunit of the nicotinic acetylcholine receptor | Q28509430 | ||
| Visual response properties in the dorsal lateral geniculate nucleus of mice lacking the beta2 subunit of the nicotinic acetylcholine receptor | Q28511869 | ||
| The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1 | Q28567361 | ||
| In vivo time-lapse imaging and serial section electron microscopy reveal developmental synaptic rearrangements | Q30428647 | ||
| Activity patterns govern synapse-specific AMPA receptor trafficking between deliverable and synaptic pools | Q30439413 | ||
| Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. | Q30479847 | ||
| Enhanced synaptic connectivity and epilepsy in C1q knockout mice | Q30494456 | ||
| Reexpression of LGI1 in glioma cells results in dysregulation of genes implicated in the canonical axon guidance pathway. | Q33653166 | ||
| Synapse elimination and indelible memory | Q33864501 | ||
| Long-term depression in the CNS. | Q34121481 | ||
| Emergence of lamina-specific retinal ganglion cell connectivity by axon arbor retraction and synapse elimination | Q34777417 | ||
| Synaptic development of the mouse dorsal lateral geniculate nucleus | Q34783980 | ||
| Experience-dependent retinogeniculate synapse remodeling is abnormal in MeCP2-deficient mice | Q34856164 | ||
| Axon retraction and degeneration in development and disease | Q36196519 | ||
| Spontaneous patterned retinal activity and the refinement of retinal projections | Q36310213 | ||
| Organization and remodeling of the olivocerebellar climbing fiber projection | Q36417573 | ||
| Refinement of the retinogeniculate pathway | Q37192008 | ||
| Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy. | Q37381254 | ||
| LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. | Q37384880 | ||
| Synapse elimination in the central nervous system | Q37501163 | ||
| Wiring and rewiring of the retinogeniculate synapse | Q37874006 | ||
| Arrested glutamatergic synapse development in human partial epilepsy | Q41131473 | ||
| Vision triggers an experience-dependent sensitive period at the retinogeniculate synapse | Q42054778 | ||
| Developmental remodelling of the lemniscal synapse in the ventral basal thalamus of the mouse. | Q42492907 | ||
| Development of single retinofugal axon arbors in normal and β2 knock-out mice | Q42700713 | ||
| Structural and functional composition of the developing retinogeniculate pathway in the mouse | Q46839109 | ||
| Distinct roles for spontaneous and visual activity in remodeling of the retinogeniculate synapse | Q48394935 | ||
| Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity | Q48573266 | ||
| Developmental remodeling of the retinogeniculate synapse. | Q49063133 | ||
| Synaptic dynamism measured over minutes to months: age-dependent decline in an autonomic ganglion. | Q52006102 | ||
| In vivo time-lapse imaging of synaptic takeover associated with naturally occurring synapse elimination | Q78789949 | ||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 903-910 | |
| P577 | publication date | 2012-01-01 | |
| P1433 | published in | Journal of Neuroscience | Q1709864 |
| P1476 | title | Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses | |
| P478 | volume | 32 |
| Q38710287 | Autoimmune synaptopathies |
| Q35834299 | Axon targeting of the alpha 7 nicotinic receptor in developing hippocampal neurons by Gprin1 regulates growth |
| Q55456679 | Clinical characteristics and short-term prognosis of LGI1 antibody encephalitis: a retrospective case study. |
| Q34370543 | Epigenomic profiling of men exposed to early-life stress reveals DNA methylation differences in association with current mental state |
| Q47952463 | Errant gardeners: glial-cell-dependent synaptic pruning and neurodevelopmental disorders |
| Q38012351 | Genetics of epilepsy and relevance to current practice |
| Q27303973 | Glutamatergic neuron-targeted loss of LGI1 epilepsy gene results in seizures |
| Q26998200 | LGI proteins in the nervous system |
| Q36583967 | LGI1 acts presynaptically to regulate excitatory synaptic transmission during early postnatal development |
| Q38695397 | LGI1 tunes intrinsic excitability by regulating the density of axonal Kv1 channels. |
| Q90193710 | Relevance of Surface Neuronal Protein Autoantibodies as Biomarkers in Seizure-Associated Disorders |
| Q30475064 | The temporal and spatial expression pattern of the LGI1 epilepsy predisposition gene during mouse embryonic cranial development |
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