Localization of KCNQ5 in the normal and epileptic human temporal neocortex and hippocampal formation

The KCNQ family of voltage-dependent non-inactivating K + channels is composed of five members, four of which (KCNQ2–5) are expressed in the CNS and are responsible for the M-current. Mutations in either KCNQ2 or KCNQ3 lead to a hereditary form of dominant generalized epilepsy. Using specific antise...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Neuroscience 2003-01, Vol.120 (2), p.353-364
Hauptverfasser:	Yus-nájera, E, Muñoz, A, Salvador, N, Jensen, B.S, Rasmussen, H.B, Defelipe, J, Villarroel, A
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Biological and medical sciences Blotting, Western Cell Line epilepsy Epilepsy - metabolism Epilepsy - pathology Female Fetus Fluorescent Antibody Technique - methods Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy hippocampus Hippocampus - cytology Hippocampus - metabolism human brain Humans Immunohistochemistry - methods KCNQ channels KCNQ Potassium Channels KCNQ2 Potassium Channel KCNQ3 Potassium Channel Kidney M-current Male Medical sciences Middle Aged neocortex Nervous system (semeiology, syndromes) Neurology Potassium Channels - genetics Potassium Channels - immunology Potassium Channels - metabolism Potassium Channels, Voltage-Gated Precipitin Tests - methods Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - immunology Recombinant Fusion Proteins - metabolism Temporal Lobe - cytology Temporal Lobe - metabolism Transfection - methods
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!