✦ LIBER ✦

The dual modulation of GIRK1/GIRK2 channels by opioid receptor ligands

✍ Scribed by Chris Ulens; Paul Daenens; Jan Tytgat

Book ID: 114017660
Publisher: Elsevier Science
Year: 1999
Tongue: English
Weight: 483 KB
Volume: 385
Category: Article
ISSN: 0014-2999
DOI: 10.1016/s0014-2999(99)00736-0

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Regulatory mechanisms underlying the mod

Regulatory mechanisms underlying the modulation of GIRK1/GIRK4 heteromeric channels by P2Y receptors

✍ Jie Wu; Wei-Guang Ding; Hiroshi Matsuura; Minoru Horie 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 377 KB

Effects of clozapine on the opioid recep

Effects of clozapine on the opioid receptors and the girk channel

✍ Toru Kobayashi; Kazutaka Ikeda; Toshiro Kumanishi 📂 Article 📅 1998 🏛 Elsevier Science 🌐 English ⚖ 118 KB

Single Channel Analysis of the Regulatio

Single Channel Analysis of the Regulation of GIRK1/GIRK4 Channels by Protein Phosphorylation

✍ Müllner, Carmen; Yakubovich, Daniel; Dessauer, Carmen W.; Platzer, Dieter; Schre 📂 Article 📅 2003 🏛 Biophysical Society 🌐 English ⚖ 237 KB

Girk channels are involved in the hypote

Girk channels are involved in the hypotensive effect of I1 imidazoline receptor selective ligands

✍ Pascal Bousquet; Guata Yoro Sy; Dragan Urosevic; Lyne Fellmann; Hugues Greney 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 62 KB

The modulation of GIRK channels by halot

The modulation of GIRK channels by halothane is essentially determined by its C terminus

✍ Lukas G. Weigl; Sergej Milovic; Bibiane Steinecker-Frohnwieser; Wolfgang Schreib 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 62 KB

Mutation analysis of the inwardly rectif

Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy

✍ Hallmann, Kerstin; Durner, Martina; Sander, Thomas; Steinlein, Ortrud K. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 2 views

Genetic factors play a major role in the etiology of idiopathic generalized epilepsy. However, in most syndromes, especially the common ones, multiple genetic factors seem to be involved. Mutations in K + channel genes have previously found to be associated with epilepsy both in humans and in mice.