1. Ando M, Takeuchi S. (1999) Immunological identification of an inward rectifier K+ channel (Kir4.1) in the intermediate cell (melanocyte) of the cochlear stria vascularis of gerbils and rats.
Cell Tissue Res, 298 (1): 179-83.
[PMID:10555552]
2. Bockenhauer D, Feather S, Stanescu HC, Bandulik S, Zdebik AA, Reichold M, Tobin J, Lieberer E, Sterner C, Landoure G et al.. (2009) Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
N Engl J Med, 360 (19): 1960-70.
[PMID:19420365]
3. Bond CT, Pessia M, Xia XM, Lagrutta A, Kavanaugh MP, Adelman JP. (1994) Cloning and expression of a family of inward rectifier potassium channels.
Recept Channels, 2 (3): 183-91.
[PMID:7874445]
4. Connors NC, Adams ME, Froehner SC, Kofuji P. (2004) The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia.
J Biol Chem, 279 (27): 28387-92.
[PMID:15102837]
5. Ferraro TN, Golden GT, Smith GG, Martin JF, Lohoff FW, Gieringer TA, Zamboni D, Schwebel CL, Press DM, Kratzer SO, Zhao H, Berrettini WH, Buono RJ. (2004) Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
Mamm Genome, 15 (4): 239-51.
[PMID:15112102]
6. Fujita A, Horio Y, Higashi K, Mouri T, Hata F, Takeguchi N, Kurachi Y. (2002) Specific localization of an inwardly rectifying K(+) channel, Kir4.1, at the apical membrane of rat gastric parietal cells; its possible involvement in K(+) recycling for the H(+)-K(+)-pump.
J Physiol (Lond.), 540 (Pt 1): 85-92.
[PMID:11927671]
7. Furutani K, Ohno Y, Inanobe A, Hibino H, Kurachi Y. (2009) Mutational and in silico analyses for antidepressant block of astroglial inward-rectifier Kir4.1 channel.
Mol Pharmacol, 75 (6): 1287-95.
[PMID:19264848]
8. Gilliam D, O'Brien DP, Coates JR, Johnson GS, Johnson GC, Mhlanga-Mutangadura T, Hansen L, Taylor JF, Schnabel RD. (2014) A homozygous KCNJ10 mutation in Jack Russell Terriers and related breeds with spinocerebellar ataxia with myokymia, seizures, or both.
J Vet Intern Med, 28 (3): 871-7.
[PMID:24708069]
9. Hibino H, Horio Y, Inanobe A, Doi K, Ito M, Yamada M, Gotow T, Uchiyama Y, Kawamura M, Kubo T et al.. (1997) An ATP-dependent inwardly rectifying potassium channel, KAB-2 (Kir4. 1), in cochlear stria vascularis of inner ear: its specific subcellular localization and correlation with the formation of endocochlear potential.
J Neurosci, 17 (12): 4711-21.
[PMID:9169531]
10. Higashi K, Fujita A, Inanobe A, Tanemoto M, Doi K, Kubo T, Kurachi Y. (2001) An inwardly rectifying K(+) channel, Kir4.1, expressed in astrocytes surrounds synapses and blood vessels in brain.
Am J Physiol, Cell Physiol, 281 (3): C922-31.
[PMID:11502569]
11. Horio Y, Hibino H, Inanobe A, Yamada M, Ishii M, Tada Y, Satoh E, Hata Y, Takai Y, Kurachi Y. (1997) Clustering and enhanced activity of an inwardly rectifying potassium channel, Kir4.1, by an anchoring protein, PSD-95/SAP90.
J Biol Chem, 272 (20): 12885-8.
[PMID:9148889]
12. Huang C, Sindic A, Hill CE, Hujer KM, Chan KW, Sassen M, Wu Z, Kurachi Y, Nielsen S, Romero MF et al.. (2007) Interaction of the Ca2+-sensing receptor with the inwardly rectifying potassium channels Kir4.1 and Kir4.2 results in inhibition of channel function.
Am J Physiol Renal Physiol, 292 (3): F1073-81.
[PMID:17122384]
13. Ishii M, Fujita A, Iwai K, Kusaka S, Higashi K, Inanobe A, Hibino H, Kurachi Y. (2003) Differential expression and distribution of Kir5.1 and Kir4.1 inwardly rectifying K+ channels in retina.
Am J Physiol, Cell Physiol, 285 (2): C260-7.
[PMID:12686518]
14. Ishii M, Horio Y, Tada Y, Hibino H, Inanobe A, Ito M, Yamada M, Gotow T, Uchiyama Y, Kurachi Y. (1997) Expression and clustered distribution of an inwardly rectifying potassium channel, KAB-2/Kir4.1, on mammalian retinal Müller cell membrane: their regulation by insulin and laminin signals.
J Neurosci, 17 (20): 7725-35.
[PMID:9315894]
15. Ito M, Inanobe A, Horio Y, Hibino H, Isomoto S, Ito H, Mori K, Tonosaki A, Tomoike H, Kurachi Y. (1996) Immunolocalization of an inwardly rectifying K+ channel, K(AB)-2 (Kir4.1), in the basolateral membrane of renal distal tubular epithelia.
FEBS Lett, 388 (1): 11-5.
[PMID:8654579]
16. Kaiser M, Maletzki I, Hülsmann S, Holtmann B, Schulz-Schaeffer W, Kirchhoff F, Bähr M, Neusch C. (2006) Progressive loss of a glial potassium channel (KCNJ10) in the spinal cord of the SOD1 (G93A) transgenic mouse model of amyotrophic lateral sclerosis.
J Neurochem, 99 (3): 900-12.
[PMID:16925593]
17. Kharade SV, Kurata H, Bender AM, Blobaum AL, Figueroa EE, Duran A, Kramer M, Days E, Vinson P, Flores D et al.. (2018) Discovery, Characterization, and Effects on Renal Fluid and Electrolyte Excretion of the Kir4.1 Potassium Channel Pore Blocker, VU0134992.
Mol Pharmacol, 94 (2): 926-937.
[PMID:29895592]
18. Kofuji P, Ceelen P, Zahs KR, Surbeck LW, Lester HA, Newman EA. (2000) Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina.
J Neurosci, 20 (15): 5733-40.
[PMID:10908613]
19. Konstas AA, Korbmacher C, Tucker SJ. (2003) Identification of domains that control the heteromeric assembly of Kir5.1/Kir4.0 potassium channels.
Am J Physiol, Cell Physiol, 284 (4): C910-7.
[PMID:12456399]
20. Kurschner C, Mermelstein PG, Holden WT, Surmeier DJ. (1998) CIPP, a novel multivalent PDZ domain protein, selectively interacts with Kir4.0 family members, NMDA receptor subunits, neurexins, and neuroligins.
Mol Cell Neurosci, 11 (3): 161-72.
[PMID:9647694]
21. Lachheb S, Cluzeaud F, Bens M, Genete M, Hibino H, Lourdel S, Kurachi Y, Vandewalle A, Teulon J, Paulais M. (2008) Kir4.1/Kir5.1 channel forms the major K+ channel in the basolateral membrane of mouse renal collecting duct principal cells.
Am J Physiol Renal Physiol, 294 (6): F1398-407.
[PMID:18367659]
22. Li L, Head V, Timpe LC. (2001) Identification of an inward rectifier potassium channel gene expressed in mouse cortical astrocytes.
Glia, 33 (1): 57-71.
[PMID:11169792]
23. Lourdel S, Paulais M, Cluzeaud F, Bens M, Tanemoto M, Kurachi Y, Vandewalle A, Teulon J. (2002) An inward rectifier K(+) channel at the basolateral membrane of the mouse distal convoluted tubule: similarities with Kir4-Kir5.1 heteromeric channels.
J Physiol (Lond.), 538 (Pt 2): 391-404.
[PMID:11790808]
24. Marcus DC, Wu T, Wangemann P, Kofuji P. (2002) KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.
Am J Physiol, Cell Physiol, 282 (2): C403-7.
[PMID:11788352]
25. Nagelhus EA, Horio Y, Inanobe A, Fujita A, Haug FM, Nielsen S, Kurachi Y, Ottersen OP. (1999) Immunogold evidence suggests that coupling of K+ siphoning and water transport in rat retinal Müller cells is mediated by a coenrichment of Kir4.1 and AQP4 in specific membrane domains.
Glia, 26 (1): 47-54.
[PMID:10088671]
26. Neusch C, Rozengurt N, Jacobs RE, Lester HA, Kofuji P. (2001) Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.
J Neurosci, 21 (15): 5429-38.
[PMID:11466414]
27. Pessia M, Imbrici P, D'Adamo MC, Salvatore L, Tucker SJ. (2001) Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1.
J Physiol (Lond.), 532 (Pt 2): 359-67.
[PMID:11306656]
28. Pessia M, Tucker SJ, Lee K, Bond CT, Adelman JP. (1996) Subunit positional effects revealed by novel heteromeric inwardly rectifying K+ channels.
EMBO J, 15 (12): 2980-7.
[PMID:8670799]
29. Poopalasundaram S, Knott C, Shamotienko OG, Foran PG, Dolly JO, Ghiani CA, Gallo V, Wilkin GP. (2000) Glial heterogeneity in expression of the inwardly rectifying K(+) channel, Kir4.1, in adult rat CNS.
Glia, 30 (4): 362-72.
[PMID:10797616]
30. Scholl UI, Choi M, Liu T, Ramaekers VT, Häusler MG, Grimmer J, Tobe SW, Farhi A, Nelson-Williams C, Lifton RP. (2009) Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.
Proc Natl Acad Sci USA, 106 (14): 5842-7.
[PMID:19289823]
31. Schoots O, Wilson JM, Ethier N, Bigras E, Hebert TE, Van Tol HH. (1999) Co-expression of human Kir3 subunits can yield channels with different functional properties.
Cell Signal, 11 (12): 871-83.
[PMID:10659995]
32. Shuck ME, Piser TM, Bock JH, Slightom JL, Lee KS, Bienkowski MJ. (1997) Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3).
J Biol Chem, 272 (1): 586-93.
[PMID:8995301]
33. Sicca F, Imbrici P, D'Adamo MC, Moro F, Bonatti F, Brovedani P, Grottesi A, Guerrini R, Masi G, Santorelli FM et al.. (2011) Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
Neurobiol Dis, 43 (1): 239-47.
[PMID:21458570]
34. Su S, Ohno Y, Lossin C, Hibino H, Inanobe A, Kurachi Y. (2007) Inhibition of astroglial inwardly rectifying Kir4.1 channels by a tricyclic antidepressant, nortriptyline.
J Pharmacol Exp Ther, 320 (2): 573-80.
[PMID:17071817]
35. Takumi T, Ishii T, Horio Y, Morishige K, Takahashi N, Yamada M, Yamashita T, Kiyama H, Sohmiya K, Nakanishi S et al.. (1995) A novel ATP-dependent inward rectifier potassium channel expressed predominantly in glial cells.
J Biol Chem, 270 (27): 16339-46.
[PMID:7608203]
36. Tanemoto M, Kittaka N, Inanobe A, Kurachi Y. (2000) In vivo formation of a proton-sensitive K+ channel by heteromeric subunit assembly of Kir5.1 with Kir4.1.
J Physiol (Lond.), 525 Pt 3: 587-92.
[PMID:10856114]
37. Tong X, Ao Y, Faas GC, Nwaobi SE, Xu J, Haustein MD, Anderson MA, Mody I, Olsen ML, Sofroniew MV et al.. (2014) Astrocyte Kir4.1 ion channel deficits contribute to neuronal dysfunction in Huntington's disease model mice.
Nat Neurosci, 17 (5): 694-703.
[PMID:24686787]
38. Tucker SJ, Imbrici P, Salvatore L, D'Adamo MC, Pessia M. (2000) pH dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia.
J Biol Chem, 275 (22): 16404-7.
[PMID:10764726]
39. Yang T, Gurrola 2nd JG, Wu H, Chiu SM, Wangemann P, Snyder PM, Smith RJ. (2009) Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.
Am J Hum Genet, 84 (5): 651-7.
[PMID:19426954]