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hemimegalencephaly/gama aminobuterna kiselina

Veza se sprema u međuspremnik
ČlanciKliničkim ispitivanjimaPatenti
4 rezultati

Altered expression of neurotransmitter-receptor subunit and uptake site mRNAs in hemimegalencephaly.

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OBJECTIVE Hemimegalencephaly (HMEG) is characterized by unilateral hemispheric enlargement and severe cytoarchitectural abnormalities that are highly associated with intractable epilepsy. No studies have defined alterations in neurotransmitter-receptor subunit gene expression in HMEG. We hypothesize

Human cortical neuronal cell line: establishment from a patient with unilateral megalencephaly.

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A cell line has been established in continuous culture of human cerebral cortical neurons obtained from a patient with unilateral megalencephaly, a disorder associated with continued proliferation of immature neuronal cells. When differentiated in the presence of nerve growth factor,

Rapid neurite formation in a human cortical neuronal cell line.

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The subclone HCN-1 was derived from parental cell lines from cortical tissue of a patient with unilateral megalencephaly growth and immunochemistry staining characteristics [G. V. Ronnett et al. (1990) Human cortical neuronal cell line: establishment from a patient with unilateral megalencephaly.

Pacemaker GABA synaptic activity may contribute to network synchronization in pediatric cortical dysplasia.

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Spontaneous pacemaker γ-aminobutyric acid (GABA) receptor-mediated synaptic activity (PGA) occurs in a subset of tissue samples from pediatric epilepsy surgery patients. In the present study, based on single-cell electrophysiological recordings from 120 cases, we describe the etiologies, cell types,
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