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Search results 1 to 100 out of 137 for Kcnj10

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Category: Publication
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Type Details Score
Publication
11788352 | J:75599
First Author: Marcus DC
Year: 2002
Journal: Am J Physiol Cell Physiol
Title: KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.
Volume: 282
Issue: 2
Pages: C403-7
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Publication
19420365 | J:226598
First Author: Bockenhauer D
Year: 2009
Journal: N Engl J Med
Title: Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
Volume: 360
Issue: 19
Pages: 1960-70
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Publication
20651251 | J:163627
First Author: Reichold M
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function.
Volume: 107
Issue: 32
Pages: 14490-5
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Publication
25834074 | J:280287
First Author: Zhang C
Year: 2015
Journal: Am J Physiol Renal Physiol
Title: KCNJ10 (Kir4.1) is expressed in the basolateral membrane of the cortical thick ascending limb.
Volume: 308
Issue: 11
Pages: F1288-96
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Publication
26887833 | J:280415
First Author: Su XT
Year: 2016
Journal: Am J Physiol Renal Physiol
Title: Disruption of KCNJ10 (Kir4.1) stimulates the expression of ENaC in the collecting duct.
Volume: 310
Issue: 10
Pages: F985-93
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Publication
15112102 | J:89732
First Author: Ferraro TN
Year: 2004
Journal: Mamm Genome
Title: Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene.
Volume: 15
Issue: 4
Pages: 239-51
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Publication
25071208 | J:213940
First Author: Zhang C
Year: 2014
Journal: Proc Natl Acad Sci U S A
Title: KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1).
Volume: 111
Issue: 32
Pages: 11864-9
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Publication
17959752 | J:130279
First Author: Singh R
Year: 2008
Journal: Am J Physiol Renal Physiol
Title: Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.
Volume: 294
Issue: 1
Pages: F139-48
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Publication
19426954 | J:150860
First Author: Yang T
Year: 2009
Journal: Am J Hum Genet
Title: Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.
Volume: 84
Issue: 5
Pages: 651-7
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Publication
25099735 | J:223117
First Author: Wang L
Year: 2014
Journal: Am J Physiol Cell Physiol
Title: Kcnj10 is a major type of K+ channel in mouse corneal epithelial cells and plays a role in initiating EGFR signaling.
Volume: 307
Issue: 8
Pages: C710-7
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Publication
21748805 | J:175546
First Author: Haj-Yasein NN
Year: 2011
Journal: Glia
Title: Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human Kir4.1 gene (KCNJ10).
Volume: 59
Issue: 11
Pages: 1635-42
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Publication
37126448 | J:337577
First Author: Oudart M
Year: 2023
Journal: Cell Rep
Title: The ribosome-associated protein RACK1 represses Kir4.1 translation in astrocytes and influences neuronal activity.
Volume: 42
Issue: 5
Pages: 112456
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Publication
26319417 | J:231402
First Author: Fan L
Year: 2015
Journal: Biochim Biophys Acta
Title: Vasopressin-induced stimulation of the Na(+)-activated K(+) channels is responsible for maintaining the basolateral K(+) conductance of the thick ascending limb (TAL) in EAST/SeSAME syndrome.
Volume: 1852
Issue: 11
Pages: 2554-62
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Publication
25848073 | J:322093
First Author: Wang L
Year: 2015
Journal: J Am Soc Nephrol
Title: Caveolin-1 Deficiency Inhibits the Basolateral K+ Channels in the Distal Convoluted Tubule and Impairs Renal K+ and Mg2+ Transport.
Volume: 26
Issue: 11
Pages: 2678-90
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Publication
26546361 | J:234526
First Author: Slaats GG
Year: 2015
Journal: J Cell Sci
Title: Screen-based identification and validation of four new ion channels as regulators of renal ciliogenesis.
Volume: 128
Issue: 24
Pages: 4550-9
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Publication
23457544 | J:197180
First Author: Buniello A
Year: 2013
Journal: PLoS One
Title: Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness.
Volume: 8
Issue: 2
Pages: e56274
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29483225 | J:284338
First Author: Wu P
Year: 2018
Journal: Hypertension
Title: AT2R (Angiotensin II Type 2 Receptor)-Mediated Regulation of NCC (Na-Cl Cotransporter) and Renal K Excretion Depends on the K Channel, Kir4.1.
Volume: 71
Issue: 4
Pages: 622-630
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Publication
28052988 | J:287780
First Author: Cuevas CA
Year: 2017
Journal: J Am Soc Nephrol
Title: Potassium Sensing by Renal Distal Tubules Requires Kir4.1.
Volume: 28
Issue: 6
Pages: 1814-1825
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Publication
30517856 | J:271539
First Author: Saritas T
Year: 2018
Journal: Cell Rep
Title: Optical Clearing in the Kidney Reveals Potassium-Mediated Tubule Remodeling.
Volume: 25
Issue: 10
Pages: 2668-2675.e3
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Publication
17942730 | J:126082
First Author: Djukic B
Year: 2007
Journal: J Neurosci
Title: Conditional knock-out of Kir4.1 leads to glial membrane depolarization, inhibition of potassium and glutamate uptake, and enhanced short-term synaptic potentiation.
Volume: 27
Issue: 42
Pages: 11354-65
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Publication
21106816 | J:166979
First Author: Chever O
Year: 2010
Journal: J Neurosci
Title: Implication of Kir4.1 channel in excess potassium clearance: an in vivo study on anesthetized glial-conditional Kir4.1 knock-out mice.
Volume: 30
Issue: 47
Pages: 15769-77
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Publication
30271961 | J:278523
 
First Author: Song F
Year: 2018
Journal: Commun Biol
Title: Kir4.1 channels in NG2-glia play a role in development, potassium signaling, and ischemia-related myelin loss.
Volume: 1
Pages: 80
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Publication
30110571 | J:280290
First Author: Malik S
Year: 2018
Journal: Am J Physiol Renal Physiol
Title: Potassium conservation is impaired in mice with reduced renal expression of Kir4.1.
Volume: 315
Issue: 5
Pages: F1271-F1282
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Publication
10908613 | J:63635
First Author: Kofuji P
Year: 2000
Journal: J Neurosci
Title: Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina.
Volume: 20
Issue: 15
Pages: 5733-40
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Publication
19515915 | J:155644
First Author: Seifert G
Year: 2009
Journal: J Neurosci
Title: Analysis of astroglial K+ channel expression in the developing hippocampus reveals a predominant role of the Kir4.1 subunit.
Volume: 29
Issue: 23
Pages: 7474-88
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Publication
12618319 | J:108878
First Author: Rozengurt N
Year: 2003
Journal: Hear Res
Title: Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit.
Volume: 177
Issue: 1-2
Pages: 71-80
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Publication
21367857 | J:171122
First Author: Song P
Year: 2011
Journal: J Biol Chem
Title: Kir4.1 channel expression is essential for parietal cell control of acid secretion.
Volume: 286
Issue: 16
Pages: 14120-8
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Publication
16306174 | J:135777
First Author: Neusch C
Year: 2006
Journal: J Neurophysiol
Title: Lack of the Kir4.1 channel subunit abolishes K+ buffering properties of astrocytes in the ventral respiratory group: impact on extracellular K+ regulation.
Volume: 95
Issue: 3
Pages: 1843-52
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11466414 | J:77663
First Author: Neusch C
Year: 2001
Journal: J Neurosci
Title: Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.
Volume: 21
Issue: 15
Pages: 5429-38
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Publication
22290828 | J:181361
First Author: Bay V
Year: 2012
Journal: Glia
Title: Relationship between glial potassium regulation and axon excitability: a role for glial Kir4.1 channels.
Volume: 60
Issue: 4
Pages: 651-60
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17344384 | J:120107
First Author: Metea MR
Year: 2007
Journal: J Neurosci
Title: Neurovascular coupling is not mediated by potassium siphoning from glial cells.
Volume: 27
Issue: 10
Pages: 2468-71
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Publication
20074622 | J:159727
First Author: Tang X
Year: 2010
Journal: Neuroscience
Title: Inwardly rectifying potassium channel Kir4.1 is responsible for the native inward potassium conductance of satellite glial cells in sensory ganglia.
Volume: 166
Issue: 2
Pages: 397-407
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Publication
22431254 | J:323157
First Author: Stephan J
Year: 2012
Journal: Glia
Title: Kir4.1 channels mediate a depolarization of hippocampal astrocytes under hyperammonemic conditions in situ.
Volume: 60
Issue: 6
Pages: 965-78
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19382212 | J:156198
First Author: Tang X
Year: 2009
Journal: Glia
Title: Heterogeneity of Kir4.1 channel expression in glia revealed by mouse transgenesis.
Volume: 57
Issue: 16
Pages: 1706-15
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22546335 | J:192434
 
First Author: Udagawa T
Year: 2012
Journal: Neuroscience
Title: Inwardly rectifying potassium channel Kir4.1 is localized at the calyx endings of vestibular afferents.
Volume: 215
Pages: 209-16
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Publication
- | J:65830
   
First Author: Inanobe A
Year: 2000
Journal: GenBank Submission
Title: Mus musculus mRNA for ATP-dependent inward rectifier potassium channel Kir4.1, complete cds
Pages: AB039879
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Publication
37116573 | J:341770
 
First Author: Liu JY
Year: 2023
Journal: Neurosci Lett
Title: Inward rectifying K(ir)4.1 channels regulate oligodendrocyte precursor cell differentiation and CNS myelination in vivo.
Volume: 807
Pages: 137278
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29596047 | J:263279
   
First Author: Larson VA
Year: 2018
Journal: Elife
Title: Oligodendrocytes control potassium accumulation in white matter and seizure susceptibility.
Volume: 7
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15359216 | J:93207
 
First Author: Wu J
Year: 2004
Journal: Mol Vis
Title: Contribution of Kir4.1 to the mouse electroretinogram.
Volume: 10
Pages: 650-4
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14722723 | J:86322
First Author: Hitzemann R
Year: 2003
Journal: Mamm Genome
Title: A strategy for the integration of QTL, gene expression, and sequence analyses.
Volume: 14
Issue: 11
Pages: 733-47
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23986512 | J:203001
First Author: Zaika OL
Year: 2013
Journal: Am J Physiol Renal Physiol
Title: Direct inhibition of basolateral Kir4.1/5.1 and Kir4.1 channels in the cortical collecting duct by dopamine.
Volume: 305
Issue: 9
Pages: F1277-87
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Publication
30559144 | J:290704
First Author: Wu P
Year: 2019
Journal: J Am Soc Nephrol
Title: Kir4.1/Kir5.1 Activity Is Essential for Dietary Sodium Intake-Induced Modulation of Na-Cl Cotransporter.
Volume: 30
Issue: 2
Pages: 216-227
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Publication
31239388 | J:294659
First Author: Wu P
Year: 2019
Journal: J Am Soc Nephrol
Title: Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake.
Volume: 30
Issue: 8
Pages: 1425-1438
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Publication
21256195 | J:170603
 
First Author: Hsu MS
Year: 2011
Journal: Neuroscience
Title: Laminar-specific and developmental expression of aquaporin-4 in the mouse hippocampus.
Volume: 178
Pages: 21-32
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Publication
36527899 | J:332767
 
First Author: Hong X
Year: 2023
Journal: EBioMedicine
Title: Kir4.1 channel activation in NG2 glia contributes to remyelination in ischemic stroke.
Volume: 87
Pages: 104406
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Publication
27161034 | J:239936
 
First Author: Battefeld A
Year: 2016
Journal: Nat Commun
Title: Myelinating satellite oligodendrocytes are integrated in a glial syncytium constraining neuronal high-frequency activity.
Volume: 7
Pages: 11298
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17869537 | J:132623
First Author: Zhang H
Year: 2008
Journal: Mol Cell Neurosci
Title: Aquaporin-4 independent Kir4.1 K+ channel function in brain glial cells.
Volume: 37
Issue: 1
Pages: 1-10
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21446052 | J:171206
First Author: Strohschein S
Year: 2011
Journal: Glia
Title: Impact of aquaporin-4 channels on K+ buffering and gap junction coupling in the hippocampus.
Volume: 59
Issue: 6
Pages: 973-80
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17525153 | J:124606
First Author: Ruiz-Ederra J
Year: 2007
Journal: J Biol Chem
Title: Evidence against functional interaction between aquaporin-4 water channels and Kir4.1 potassium channels in retinal Müller cells.
Volume: 282
Issue: 30
Pages: 21866-72
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31695761 | J:285979
First Author: Kim MA
Year: 2019
Journal: Theranostics
Title: Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing.
Volume: 9
Issue: 24
Pages: 7184-7199
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Publication
30803043 | J:274735
First Author: Rao SB
Year: 2019
Journal: Glia
Title: Targeted deletion of β1-syntrophin causes a loss of Kir 4.1 from Müller cell endfeet in mouse retina.
Volume: 67
Issue: 6
Pages: 1138-1149
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Publication
29464197 | J:262199
 
First Author: Kahanovitch U
Year: 2018
Journal: eNeuro
Title: MeCP2 Deficiency Leads to Loss of Glial Kir4.1.
Volume: 5
Issue: 1
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29897283 | J:281038
First Author: Wang MX
Year: 2018
Journal: Am J Physiol Renal Physiol
Title: Kir5.1 regulates Nedd4-2-mediated ubiquitination of Kir4.1 in distal nephron.
Volume: 315
Issue: 4
Pages: F986-F996
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Publication
35997251 | J:327955
   
First Author: Mapps AA
Year: 2022
Journal: Elife
Title: Satellite glia modulate sympathetic neuron survival, activity, and autonomic function.
Volume: 11
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30204081 | J:268839
   
First Author: Schirmer L
Year: 2018
Journal: Elife
Title: Oligodendrocyte-encoded Kir4.1 function is required for axonal integrity.
Volume: 7
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27122158 | J:235679
First Author: Zhang C
Year: 2016
Journal: Am J Physiol Cell Physiol
Title: Caveolin-1 regulates corneal wound healing by modulating Kir4.1 activity.
Volume: 310
Issue: 11
Pages: C993-C1000
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17065440 | J:114967
First Author: Menichella DM
Year: 2006
Journal: J Neurosci
Title: Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity.
Volume: 26
Issue: 43
Pages: 10984-91
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Publication
34205849 | J:307601
 
First Author: Poli G
Year: 2021
Journal: Int J Mol Sci
Title: Kcnj16 (Kir5.1) Gene Ablation Causes Subfertility and Increases the Prevalence of Morphologically Abnormal Spermatozoa.
Volume: 22
Issue: 11
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15310750 | J:93983
First Author: Hibino H
Year: 2004
Journal: J Biol Chem
Title: Differential assembly of inwardly rectifying K+ channel subunits, Kir4.1 and Kir5.1, in brain astrocytes.
Volume: 279
Issue: 42
Pages: 44065-73
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31736353 | J:294764
First Author: Thomson MN
Year: 2020
Journal: Am J Physiol Renal Physiol
Title: WNK bodies cluster WNK4 and SPAK/OSR1 to promote NCC activation in hypokalemia.
Volume: 318
Issue: 1
Pages: F216-F228
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24081156 | J:217962
First Author: Sibille J
Year: 2014
Journal: J Physiol
Title: Astroglial potassium clearance contributes to short-term plasticity of synaptically evoked currents at the tripartite synapse.
Volume: 592
Issue: 1
Pages: 87-102
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33086039 | J:300547
First Author: Yu X
Year: 2020
Journal: Neuron
Title: Context-Specific Striatal Astrocyte Molecular Responses Are Phenotypically Exploitable.
Volume: 108
Issue: 6
Pages: 1146-1162.e10
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Publication
21283711 | J:169570
First Author: Hirrlinger PG
Year: 2011
Journal: PLoS One
Title: Genetic deletion of laminin isoforms β2 and γ3 induces a reduction in Kir4.1 and aquaporin-4 expression and function in the retina.
Volume: 6
Issue: 1
Pages: e16106
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Publication
31042800 | J:276025
First Author: Luo Q
Year: 2019
Journal: Invest Ophthalmol Vis Sci
Title: The Diurnal Rhythm of Insulin Receptor Substrate-1 (IRS-1) and Kir4.1 in Diabetes: Implications for a Clock Gene Bmal1.
Volume: 60
Issue: 6
Pages: 1928-1936
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9367690 | J:44256
First Author: Tada Y
Year: 1997
Journal: Genomics
Title: Assignment of the glial inwardly rectifying potassium channel KAB-2/Kir4.1 (Kcnj10) gene to the distal region of mouse chromosome 1.
Volume: 45
Issue: 3
Pages: 629-30
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Publication
38032389 | J:343429
 
First Author: Altas B
Year: 2024
Journal: J Cell Biol
Title: Nedd4-2-dependent regulation of astrocytic Kir4.1 and Connexin43 controls neuronal network activity.
Volume: 223
Issue: 1
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Publication
25716834 | J:219851
First Author: Robel S
Year: 2015
Journal: J Neurosci
Title: Reactive astrogliosis causes the development of spontaneous seizures.
Volume: 35
Issue: 8
Pages: 3330-45
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29606582 | J:262438
First Author: Kelley KW
Year: 2018
Journal: Neuron
Title: Kir4.1-Dependent Astrocyte-Fast Motor Neuron Interactions Are Required for Peak Strength.
Volume: 98
Issue: 2
Pages: 306-319.e7
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Publication
32152201 | J:289982
First Author: Morell RJ
Year: 2020
Journal: J Neurosci
Title: Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39.
Volume: 40
Issue: 15
Pages: 2976-2992
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11919667 | J:91457
First Author: Buck KJ
Year: 2002
Journal: Psychopharmacology (Berl)
Title: Mapping murine loci for physical dependence on ethanol.
Volume: 160
Issue: 4
Pages: 398-407
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Publication
16910173 | J:114154
First Author: Jones LC
Year: 2006
Journal: Nutr Neurosci
Title: Quantitative genetic analysis of brain copper and zinc in BXD recombinant inbred mice.
Volume: 9
Issue: 1-2
Pages: 81-92
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Publication
38278860 | J:344965
First Author: Udagawa T
Year: 2024
Journal: Sci Rep
Title: Loss of Pax3 causes reduction of melanocytes in the developing mouse cochlea.
Volume: 14
Issue: 1
Pages: 2210
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10547923 | J:58134
First Author: Mayeda AR
Year: 1999
Journal: Behav Genet
Title: A QTL for the genetic variance in free-running period and level of locomotor activity between inbred strains of mice.
Volume: 29
Issue: 3
Pages: 171-6
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Publication
14532115 | J:86183
First Author: Boettger T
Year: 2003
Journal: EMBO J
Title: Loss of K-Cl co-transporter KCC3 causes deafness, neurodegeneration and reduced seizure threshold.
Volume: 22
Issue: 20
Pages: 5422-34
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9647694 | J:48437
First Author: Kurschner C
Year: 1998
Journal: Mol Cell Neurosci
Title: CIPP, a novel multivalent PDZ domain protein, selectively interacts with Kir4.0 family members, NMDA receptor subunits, neurexins, and neuroligins.
Volume: 11
Issue: 3
Pages: 161-72
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Publication
27488639 | J:234621
First Author: Shibata S
Year: 2016
Journal: J Neurosci
Title: Hepatocyte Growth Factor-c-MET Signaling Mediates the Development of Nonsensory Structures of the Mammalian Cochlea and Hearing.
Volume: 36
Issue: 31
Pages: 8200-9
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Publication
30753104 | J:287221
First Author: Partearroyo T
Year: 2019
Journal: FASEB J
Title: Betaine-homocysteine S-methyltransferase deficiency causes increased susceptibility to noise-induced hearing loss associated with plasma hyperhomocysteinemia.
Volume: 33
Issue: 5
Pages: 5942-5956
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Publication
11709546 | J:72911
First Author: Murdoch JN
Year: 2001
Journal: Hum Mol Genet
Title: Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification.
Volume: 10
Issue: 22
Pages: 2593-601
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Publication
11431695 | J:70272
First Author: Kibar Z
Year: 2001
Journal: Nat Genet
Title: Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail.
Volume: 28
Issue: 3
Pages: 251-5
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Publication
10479680 | J:57542
First Author: Kurschner C
Year: 1999
Journal: J Neurosci
Title: Neuronal interleukin-16 (NIL-16): a dual function PDZ domain protein.
Volume: 19
Issue: 18
Pages: 7770-80
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Publication
11401431 | J:68343
First Author: Doudney K
Year: 2001
Journal: Genomics
Title: Comparative physical and transcript maps of approximately 1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23.
Volume: 72
Issue: 2
Pages: 180-92
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Publication
22472609 | J:315134
First Author: Ezan P
Year: 2012
Journal: J Cereb Blood Flow Metab
Title: Deletion of astroglial connexins weakens the blood-brain barrier.
Volume: 32
Issue: 8
Pages: 1457-67
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

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