The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2

[1]  D. Cox,et al.  Functional Effects of the Mouse weaver Mutation on G Protein–Gated Inwardly Rectifying K+ Channels , 1996, Neuron.

[2]  David R. Cox,et al.  A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation , 1995, Nature Genetics.

[3]  M. Lazdunski,et al.  Heterologous multimeric assembly is essential for K+ channel activity of neuronal and cardiac G-protein-activated inward rectifiers. , 1995, Biochemical and biophysical research communications.

[4]  H. Lester,et al.  Evidence that neuronal G-protein-gated inwardly rectifying K+ channels are activated by G beta gamma subunits and function as heteromultimers. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[5]  O. Saksela,et al.  Increased proteolytic activity of the granule neurons may contribute to neuronal death in the weaver mouse cerebellum. , 1995, Developmental biology.

[6]  D. Clapham,et al.  The G-protein-gated atrial K+ channel IKAch is a heteromultimer of two inwardly rectifying K+-channel proteins , 1995, Nature.

[7]  H. Schulman,et al.  The human mu opioid receptor: modulation of functional desensitization by calcium/calmodulin-dependent protein kinase and protein kinase C , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[8]  C. Chavkin,et al.  Agonist-induced Desensitization of the Mu Opioid Receptor-coupled Potassium Channel (GIRK1) (*) , 1995, The Journal of Biological Chemistry.

[9]  Y. Chen,et al.  Differential regulation by cAMP-dependent protein kinase and protein kinase C of the mu opioid receptor coupling to a G protein-activated K+ channel. , 1994, The Journal of biological chemistry.

[10]  H. Lester,et al.  Atrial G protein-activated K+ channel: expression cloning and molecular properties. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[11]  Yoshihiro Kubo,et al.  Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel , 1993, Nature.

[12]  N. Davidson,et al.  Expression of an atrial G-protein-activated potassium channel in Xenopus oocytes. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[13]  Lei Yu,et al.  Molecular cloning and functional expression of a mu opioid receptor from rat brain , 1994, Regulatory Peptides.

[14]  R. Kramer,et al.  Molecular cloning and single-channel properties of the cyclic nucleotide-gated channel from catfish olfactory neurons , 1992, Neuron.

[15]  A. Brown,et al.  The nature and origin of spontaneous noise in G protein-gated ion channels , 1991, The Journal of general physiology.

[16]  T. Schwarz,et al.  Alteration of ionic selectivity of a K+ channel by mutation of the H5 region , 1991, Nature.

[17]  W. Giles,et al.  Regulation of spontaneous opening of muscarinic K+ channels in rabbit atrium. , 1991, The Journal of physiology.

[18]  T. Snutch.  The use of Xenopus oocytes to probe synaptic communication , 1988, Trends in Neurosciences.

[19]  R. Nicoll,et al.  Pharmacologically distinct actions of serotonin on single pyramidal neurones of the rat hippocampus recorded in vitro. , 1987, The Journal of physiology.

[20]  N. Davidson,et al.  Equilibrium properties of mouse-Torpedo acetylcholine receptor hybrids expressed in Xenopus oocytes , 1987, The Journal of general physiology.

[21]  R. Nicoll,et al.  A G protein couples serotonin and GABAB receptors to the same channels in hippocampus. , 1986, Science.

[22]  W. Trautwein,et al.  Acetylcholine activation of single muscarinic K+ channels in isolated pacemaker cells of the mammalian heart , 1983, Nature.

[23]  B. Ghetti,et al.  Dopamine deficiency in the weaver mutant mouse , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[24]  P. Rakić,et al.  Sequence of developmental abnormalities leading to granule cell deficit in cerebellar cortex of weaver mutant mice , 1973, The Journal of comparative neurology.

[25]  N. Dascal,et al.  The use of Xenopus oocytes for the study of ion channels. , 1987, CRC critical reviews in biochemistry.