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Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.
Kahle KT, Merner ND, Friedel P, Silayeva L, Liang B, Khanna A, Shang Y, Lachance-Touchette P, Bourassa C, Levert A, Dion PA, Walcott B, Spiegelman D, Dionne-Laporte A, Hodgkinson A, Awadalla P, Nikbakht H, Majewski J, Cossette P, Deeb TZ, Moss SJ, Medina I, Rouleau GA. Kahle KT, et al. Among authors: medina i. EMBO Rep. 2014 Jul;15(7):766-74. doi: 10.15252/embr.201438840. Epub 2014 Jun 13. EMBO Rep. 2014. PMID: 24928908 Free PMC article.
Enhanced Synaptic Activity and Epileptiform Events in the Embryonic KCC2 Deficient Hippocampus.
Khalilov I, Chazal G, Chudotvorova I, Pellegrino C, Corby S, Ferrand N, Gubkina O, Nardou R, Tyzio R, Yamamoto S, Jentsch TJ, Hübner CA, Gaiarsa JL, Ben-Ari Y, Medina I. Khalilov I, et al. Among authors: medina i. Front Cell Neurosci. 2011 Nov 1;5:23. doi: 10.3389/fncel.2011.00023. eCollection 2011. Front Cell Neurosci. 2011. PMID: 22065950 Free PMC article.
A novel in vitro preparation: the intact hippocampal formation.
Khalilov I, Esclapez M, Medina I, Aggoun D, Lamsa K, Leinekugel X, Khazipov R, Ben-Ari Y. Khalilov I, et al. Among authors: medina i. Neuron. 1997 Oct;19(4):743-9. doi: 10.1016/s0896-6273(00)80956-3. Neuron. 1997. PMID: 9354321 Free article.
311 results