Sex-specific behavioral deficits induced at early life by prenatal exposure to the cannabinoid receptor agonist WIN 55,212-2 depend on mGlu5 receptor signaling.
Manduca A, Servadio M, Melancia F, Schiavi S, Manzoni O, Trezza V - British journal of pharmacology - Oct 2019
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Cannabinoid Exposure via Lactation in Rats Disrupts Perinatal Programming of the Gamma-Aminobutyric Acid Trajectory and Select Early-Life Behaviors.
Scheyer AF, Borsoi M, Wager-Miller J, Pelissier-Alicot AL, Murphy MN, Mackie K, Manzoni OJJ - Biological psychiatry - Sep 2019
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Somatic double-hit in MTOR and RPS6 in hemimegalencephaly with intractable epilepsy.
Pelorosso C, Watrin F, Conti V, Buhler E, Gelot A, Yang X, Mei D, McEvoy-Venneri J, Manent JB, Cetica V, Ball LL, Buccoliero AM, Vinck A, Barba C, Gleeson JG, Guerrini R, Represa A - Human molecular genetics - Aou 2019
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Impaired vocal communication, sleep-related discharges, and transient alteration of slow-wave sleep in developing mice lacking the GluN2A subunit of N-methyl-d-aspartate receptors.
Salmi M, Del Gallo F, Minlebaev M, Zakharov A, Pauly V, Perron P, Pons-Bennaceur A, Corby-Pellegrino S, Aniksztejn L, Lenck-Santini PP, Epsztein J, Khazipov R, Burnashev N, Bertini G, Szepetowski P - Epilepsia - Jul 2019
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Report on three additional patients and genotype-phenotype correlation in SLC25A22-related disorders group.
Lemattre C, Imbert-Bouteille M, Gatinois V, Benit P, Sanchez E, Guignard T, Tran Mau-Them F, Haquet E, Rivier F, Carme E, Roubertie A, Boland A, Lechner D, Meyer V, Thevenon J, Duffourd Y, Rivière JB, Deleuze JF, Wells C, Molinari F, Rustin P, Blanchet P, Geneviève D - European journal of human genetics : EJHG - Jul 2019
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Early alterations in a mouse model of Rett syndrome: the GABA developmental shift is abolished at birth.
Lozovaya N, Nardou R, Tyzio R, Chiesa M, Pons-Bennaceur A, Eftekhari S, Bui TT, Billon-Grand M, Rasero J, Bonifazi P, Guimond D, Gaiarsa JL, Ferrari DC, Ben-Ari Y - Scientific reports - Jun 2019
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Extracellular mild acidosis decreases the Ca permeability of the human NMDA receptors.
Plutino S, Sciaccaluga M, Fucile S - Cell calcium - Jun 2019
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Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations.
Lesca G, Møller RS, Rudolf G, Hirsch E, Hjalgrim H, Szepetowski P - Epileptic disorders : international epilepsy journal with videotape - Mai 2019
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