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1 to 25 of 113  Show
  1. 1
    "Molecular cloning and expression of a human heart inward rectifier potassium channel."
    Raab-Graham K.F., Radeke C.M., Vandenberg C.A.
    NeuroReport 5:2501-2505(1994) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA].
    Category: Sequences.
    Tissue: Heart.
    Source: UniProtKB/Swiss-Prot (reviewed).
  2. 2
    Tang W., Qin C.L., Yang X.C.
    Submitted (APR-1995) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE [MRNA].
    Category: Sequences.
    Tissue: Brain.
    Source: UniProtKB/Swiss-Prot (reviewed).
  3. 3
    "Cloning and functional expression of a human gene, hIRK1, encoding the heart inward rectifier K+-channel."
    Wood L.S., Tsai T.-D., Lee K.S., Vogeli G.
    Gene 163:313-317(1995) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA].
    Category: Sequences.
    Tissue: Heart.
    Source: UniProtKB/Swiss-Prot (reviewed).
  4. 4
    "Inwardly rectifying whole cell potassium current in human blood eosinophils."
    Tare M., Prestwich S.A., Gordienko D.V., Parveen S., Carver J.E., Robinson C., Bolton T.B.
    J. Physiol. (Lond.) 506:303-318(1998) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA].
    Category: Sequences.
    Tissue: Blood.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  6. 6
    "Inward rectifier K+ channel from human heart and brain: cloning and stable expression in a human cell line."
    Ashen M.D., O'Rourke B., Kluge K.A., Johns D.C., Tomaselli G.F.
    Am. J. Physiol. 268:H506-H511(1995) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 1-143.
    Category: Sequences.
    Tissue: Fetal brain and Heart.
    Source: UniProtKB/Swiss-Prot (reviewed).
  7. 7
    "Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome."
    Preisig-Muller R., Schlichthorl G., Goerge T., Heinen S., Bruggemann A., Rajan S., Derst C., Veh R.W., Daut J.
    Proc. Natl. Acad. Sci. U.S.A. 99:7774-7779(2002) [PubMed] [Europe PMC] [Abstract]
    Cited for: INTERACTION WITH KCNJ4.
    Category: Interaction.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 and mapped to 2 other entries.

  8. 8
    "Nitric oxide increases cardiac IK1 by nitrosylation of cysteine 76 of Kir2.1 channels."
    Gomez R., Caballero R., Barana A., Amoros I., Calvo E., Lopez J.A., Klein H., Vaquero M., Osuna L., Atienza F., Almendral J., Pinto A., Tamargo J., Delpon E.
    Circ. Res. 105:383-392(2009) [PubMed] [Europe PMC] [Abstract]
    Cited for: S-NITROSYLATION AT CYS-76.
    Category: PTM / Processing.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 4 other entries.

  9. 9
    "Cell-free identification of novel N-myristoylated proteins from complementary DNA resources using bioorthogonal myristic acid analogues."
    Takamitsu E., Fukunaga K., Iio Y., Moriya K., Utsumi T.
    Anal. Biochem. 464:83-93(2014) [PubMed] [Europe PMC] [Abstract]
    Cited for: MYRISTOYLATION AT GLY-2, SUBCELLULAR LOCATION.
    Category: Subcellular Location, PTM / Processing.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  10. 10
    Cited for: CHARACTERIZATION OF VARIANTS LQT7 VAL-71 AND TRP-218, VARIANTS LQT7 VAL-300; 95-SER--PHE-98 DEL AND SER-314-315-TYR DEL.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  11. 11
    "KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes."
    Andelfinger G., Tapper A.R., Welch R.C., Vanoye C.G., George A.L. Jr., Benson D.W.
    Am. J. Hum. Genet. 71:663-668(2002) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LQT7 TRP-67.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  12. 12
    "Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)."
    Tristani-Firouzi M., Jensen J.L., Donaldson M.R., Sansone V., Meola G., Hahn A., Bendahhou S., Kwiecinski H., Fidzianska A., Plaster N., Fu Y.-H., Ptacek L.J., Tawil R.
    J. Clin. Invest. 110:381-388(2002) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS LQT7 LEU-186; HIS-216 AND MET-302.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  13. 13
    Cited for: VARIANT ATFB9 ILE-93, CHARACTERIZATION OF VARIANT ATFB9 ILE-93.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  14. 14
    Cited for: VARIANT SQT3 ASN-172, CHARACTERIZATION OF VARIANT SQT3 ASN-172.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  15. 15
    "Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome."
    Lu C.W., Lin J.H., Rajawat Y.S., Jerng H., Rami T.G., Sanchez X., DeFreitas G., Carabello B., DeMayo F., Kearney D.L., Miller G., Li H., Pfaffinger P.J., Bowles N.E., Khoury D.S., Towbin J.A.
    J. Med. Genet. 43:653-659(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT LQT7 ARG-75, CHARACTERIZATION OF VARIANT LQT7 ARG-75.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 and mapped to 1 other entries.

  16. 16
    "Corticosteroid-exacerbated symptoms in an Andersen's syndrome kindred."
    Bendahhou S., Fournier E., Gallet S., Menard D., Larroque M.M., Barhanin J.
    Hum. Mol. Genet. 16:900-906(2007) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANTS LQT7 PHE-54 AND PRO-305, CHARACTERIZATION OF VARIANTS LQT7 PHE-54 AND PRO-305.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  17. 17
    "Targeting of an A kinase-anchoring protein, AKAP79, to an inwardly rectifying potassium channel, Kir2.1."
    Dart C., Leyland M.L.
    J. Biol. Chem. 276:20499-20505(2001) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:P63252.

    This publication is mapped to 3 other entries.

  18. 18
    "Characterization of inwardly rectifying K(+) conductance across the basolateral membrane of rat tracheal epithelia."
    Jeong J.S., Lee H.J., Jung J.S., Shin S.H., Son Y.J., Yoon J.H., Lee S.H., Lee H.S., Yun I., Hwang T.H.
    Biochem. Biophys. Res. Commun. 288:914-920(2001) [PubMed] [Europe PMC] [Abstract]
    Annotation: molecular cloning from and conductance in nasal mucosal epitheliumImported.
    Source: GeneRIF:3759.

    This publication is mapped to 1 other entry.

  19. 19
    "Modulation of the inward rectifier potassium channel IRK1 by the Ras signaling pathway."
    Giovannardi S., Forlani G., Balestrini M., Bossi E., Tonini R., Sturani E., Peres A., Zippel R.
    J. Biol. Chem. 277:12158-12163(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Modulation of the inward rectifier potassium channel IRK1 by the Ras signaling pathwayImported.
    Source: GeneRIF:3759.

    This publication is mapped to 3 other entries.

  20. 20
    "Novel KCNJ2 mutation in familial periodic paralysis with ventricular dysrhythmia."
    Ai T., Fujiwara Y., Tsuji K., Otani H., Nakano S., Kubo Y., Horie M.
    Circulation 105:2592-2594(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: Thr192Ala missense mutation found in familial periodic paralysis with ventricular dysrhythmia and marked QT prolongationImported.
    Source: GeneRIF:3759.

    This publication is mapped to 1 other entry.

  21. 21
    "Multiple forms of synaptic plasticity triggered by selective suppression of activity in individual neurons."
    Burrone J., O'Byrne M., Murthy V.N.
    Nature 420:414-418(2002) [PubMed] [Europe PMC] [Abstract]
    Annotation: effect of suppressing excitability in single neurons within a network of active hippocampal neurons by overexpressing an inward-rectifier potassium channelImported.
    Source: GeneRIF:3759.

    This publication is mapped to 1 other entry.

  22. 22
    "Plasticity of KIR channels in human smooth muscle cells from internal thoracic artery."
    Karkanis T., Li S., Pickering J.G., Sims S.M.
    Am. J. Physiol. Heart Circ. Physiol. 284:H2325-34(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: expression of Kir2.1 protein in proliferative smooth muscle cells consistent with the higher current densityImported.
    Source: GeneRIF:3759.

    This publication is mapped to 4 other entries.

  23. 23
    "Direct interaction between the actin-binding protein filamin-A and the inwardly rectifying potassium channel, Kir2.1."
    Sampson L.J., Leyland M.L., Dart C.
    J. Biol. Chem. 278:41988-41997(2003) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Annotation: filamin-A was found to have no effect on Kir2.1 channel behavior but rather increased the number of functional channels resident within the membraneImported.
    Source: IntAct:P63252, GeneRIF:3759.

    This publication is mapped to 16 other entries.

  24. 24
    "Role of the small GTPase Rho in modulation of the inwardly rectifying potassium channel Kir2.1."
    Jones S.V.
    Mol. Pharmacol. 64:987-993(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: the small GTPase Rho transduces the m1 muscarinic receptor-induced inhibition of Kir2.1 via an unidentified mechanism.Imported.
    Source: GeneRIF:3759.

    This publication is mapped to 1 other entry.

  25. 25
    "Defective potassium channel Kir2.1 trafficking underlies Andersen-Tawil syndrome."
    Bendahhou S., Donaldson M.R., Plaster N.M., Tristani-Firouzi M., Fu Y.H., Ptacek L.J.
    J. Biol. Chem. 278:51779-51785(2003) [PubMed] [Europe PMC] [Abstract]
    Annotation: data show that the Andersen-Tawil syndrome phenotype may occur through a dominant-negative effect as well as through haplo-insufficiency and reveal amino acids critical in trafficking and conductance of the inward rectifier K+ channels.Imported.
    Source: GeneRIF:3759.

    This publication is mapped to 1 other entry.

1 to 25 of 113  Show