These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 8986828)

  • 1. A regenerative link in the ionic fluxes through the weaver potassium channel underlies the pathophysiology of the mutation.
    Silverman SK; Kofuji P; Dougherty DA; Davidson N; Lester HA
    Proc Natl Acad Sci U S A; 1996 Dec; 93(26):15429-34. PubMed ID: 8986828
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The weaver mutation changes the ion selectivity of the affected inwardly rectifying potassium channel GIRK2.
    Tong Y; Wei J; Zhang S; Strong JA; Dlouhy SR; Hodes ME; Ghetti B; Yu L
    FEBS Lett; 1996 Jul; 390(1):63-8. PubMed ID: 8706831
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Nonselective and G betagamma-insensitive weaver K+ channels.
    Navarro B; Kennedy ME; Velimirovíc B; Bhat D; Peterson AS; Clapham DE
    Science; 1996 Jun; 272(5270):1950-3. PubMed ID: 8658170
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional analysis of the weaver mutant GIRK2 K+ channel and rescue of weaver granule cells.
    Kofuji P; Hofer M; Millen KJ; Millonig JH; Davidson N; Lester HA; Hatten ME
    Neuron; 1996 May; 16(5):941-52. PubMed ID: 8630252
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The inwardly rectifying K(+) channel subunit GIRK1 rescues the GIRK2 weaver phenotype.
    Hou P; Yan S; Tang W; Nelson DJ
    J Neurosci; 1999 Oct; 19(19):8327-36. PubMed ID: 10493734
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Voltage-gated calcium channels mediate intracellular calcium increase in weaver dopaminergic neurons during stimulation of D2 and GABAB receptors.
    Guatteo E; Bengtson CP; Bernardi G; Mercuri NB
    J Neurophysiol; 2004 Dec; 92(6):3368-74. PubMed ID: 15240766
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The weaver mouse gain-of-function phenotype of dopaminergic midbrain neurons is determined by coactivation of wvGirk2 and K-ATP channels.
    Liss B; Neu A; Roeper J
    J Neurosci; 1999 Oct; 19(20):8839-48. PubMed ID: 10516303
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Asymmetrical contributions of subunit pore regions to ion selectivity in an inward rectifier K+ channel.
    Silverman SK; Lester HA; Dougherty DA
    Biophys J; 1998 Sep; 75(3):1330-9. PubMed ID: 9726934
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence that neuronal G-protein-gated inwardly rectifying K+ channels are activated by G beta gamma subunits and function as heteromultimers.
    Kofuji P; Davidson N; Lester HA
    Proc Natl Acad Sci U S A; 1995 Jul; 92(14):6542-6. PubMed ID: 7604029
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Involvement of GIRK2 in postnatal development of the weaver cerebellum.
    Liesi P; Stewart RR; Wright JM
    J Neurosci Res; 2000 Apr; 60(2):164-73. PubMed ID: 10740221
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Pore mutation in a G-protein-gated inwardly rectifying K+ channel subunit causes loss of K+-dependent inhibition in weaver hippocampus.
    Jarolimek W; Bäurle J; Misgeld U
    J Neurosci; 1998 Jun; 18(11):4001-7. PubMed ID: 9592081
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The weaver mutation causes a loss of inward rectifier current regulation in premigratory granule cells of the mouse cerebellum.
    Rossi P; De Filippi G; Armano S; Taglietti V; D'Angelo E
    J Neurosci; 1998 May; 18(10):3537-47. PubMed ID: 9570785
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional effects of the mouse weaver mutation on G protein-gated inwardly rectifying K+ channels.
    Slesinger PA; Patil N; Liao YJ; Jan YN; Jan LY; Cox DR
    Neuron; 1996 Feb; 16(2):321-31. PubMed ID: 8789947
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparative expression of the inward rectifier K+ channel GIRK2 in the cerebellum of normal and weaver mutant mice.
    Lauritzen I; De Weille J; Adelbrecht C; Lesage F; Murer G; Raisman-Vozari R; Lazdunski M
    Brain Res; 1997 Apr; 753(1):8-17. PubMed ID: 9125426
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation.
    Patil N; Cox DR; Bhat D; Faham M; Myers RM; Peterson AS
    Nat Genet; 1995 Oct; 11(2):126-9. PubMed ID: 7550338
    [TBL] [Abstract][Full Text] [Related]  

  • 16. betaL-betaM loop in the C-terminal domain of G protein-activated inwardly rectifying K(+) channels is important for G(betagamma) subunit activation.
    Finley M; Arrabit C; Fowler C; Suen KF; Slesinger PA
    J Physiol; 2004 Mar; 555(Pt 3):643-57. PubMed ID: 14724209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Control of channel activity through a unique amino acid residue of a G protein-gated inwardly rectifying K+ channel subunit.
    Chan KW; Sui JL; Vivaudou M; Logothetis DE
    Proc Natl Acad Sci U S A; 1996 Nov; 93(24):14193-8. PubMed ID: 8943083
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The weaver mutation of GIRK2 results in a loss of inwardly rectifying K+ current in cerebellar granule cells.
    Surmeier DJ; Mermelstein PG; Goldowitz D
    Proc Natl Acad Sci U S A; 1996 Oct; 93(20):11191-5. PubMed ID: 8855331
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heteromeric channel formation and Ca(2+)-free media reduce the toxic effect of the weaver Kir 3.2 allele.
    Tucker SJ; Pessia M; Moorhouse AJ; Gribble F; Ashcroft FM; Maylie J; Adelman JP
    FEBS Lett; 1996 Jul; 390(3):253-7. PubMed ID: 8706871
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Normal cerebellar development but susceptibility to seizures in mice lacking G protein-coupled, inwardly rectifying K+ channel GIRK2.
    Signorini S; Liao YJ; Duncan SA; Jan LY; Stoffel M
    Proc Natl Acad Sci U S A; 1997 Feb; 94(3):923-7. PubMed ID: 9023358
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.