BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 33840812)

  • 1. Biallelic loss-of-function variants in KCNJ16 presenting with hypokalemic metabolic acidosis.
    Webb BD; Hotchkiss H; Prasun P; Gelb BD; Satlin L
    Eur J Hum Genet; 2021 Oct; 29(10):1566-1569. PubMed ID: 33840812
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.
    Paulais M; Bloch-Faure M; Picard N; Jacques T; Ramakrishnan SK; Keck M; Sohet F; Eladari D; Houillier P; Lourdel S; Teulon J; Tucker SJ
    Proc Natl Acad Sci U S A; 2011 Jun; 108(25):10361-6. PubMed ID: 21633011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.
    Schlingmann KP; Renigunta A; Hoorn EJ; Forst AL; Renigunta V; Atanasov V; Mahendran S; Barakat TS; Gillion V; Godefroid N; Brooks AS; Lugtenberg D; Lake J; Debaix H; Rudin C; Knebelmann B; Tellier S; Rousset-Rouvière C; Viering D; de Baaij JHF; Weber S; Palygin O; Staruschenko A; Kleta R; Houillier P; Bockenhauer D; Devuyst O; Vargas-Poussou R; Warth R; Zdebik AA; Konrad M
    J Am Soc Nephrol; 2021 Jun; 32(6):1498-1512. PubMed ID: 33811157
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic mutation of Kcnj16 identifies Kir5.1-containing channels as key regulators of acute and chronic pH homeostasis.
    Puissant MM; Muere C; Levchenko V; Manis AD; Martino P; Forster HV; Palygin O; Staruschenko A; Hodges MR
    FASEB J; 2019 Apr; 33(4):5067-5075. PubMed ID: 30605394
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Inwardly rectifying K
    Wang WH; Lin DH
    Am J Physiol Cell Physiol; 2022 Aug; 323(2):C277-C288. PubMed ID: 35759440
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of inwardly rectifying K+ channel 5.1 (Kir5.1) in the regulation of renal membrane transport.
    Lin DH; Duan XP; Zheng JY; Wang WH
    Curr Opin Nephrol Hypertens; 2022 Sep; 31(5):479-485. PubMed ID: 35894283
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Deletion of Kir5.1 Impairs Renal Ability to Excrete Potassium during Increased Dietary Potassium Intake.
    Wu P; Gao ZX; Zhang DD; Su XT; Wang WH; Lin DH
    J Am Soc Nephrol; 2019 Aug; 30(8):1425-1438. PubMed ID: 31239388
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Loss of transcriptional activation of the potassium channel Kir5.1 by HNF1β drives autosomal dominant tubulointerstitial kidney disease.
    Kompatscher A; de Baaij JHF; Aboudehen K; Hoefnagels APWM; Igarashi P; Bindels RJM; Veenstra GJC; Hoenderop JGJ
    Kidney Int; 2017 Nov; 92(5):1145-1156. PubMed ID: 28577853
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Relationship between the renin-angiotensin-aldosterone system and renal Kir5.1 channels.
    Manis AD; Palygin O; Khedr S; Levchenko V; Hodges MR; Staruschenko A
    Clin Sci (Lond); 2019 Dec; 133(24):2449-2461. PubMed ID: 31799617
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Essential role of Kir5.1 channels in renal salt handling and blood pressure control.
    Palygin O; Levchenko V; Ilatovskaya DV; Pavlov TS; Pochynyuk OM; Jacob HJ; Geurts AM; Hodges MR; Staruschenko A
    JCI Insight; 2017 Sep; 2(18):. PubMed ID: 28931751
    [TBL] [Abstract][Full Text] [Related]  

  • 11.
    Poli G; Hasan S; Belia S; Cenciarini M; Tucker SJ; Imbrici P; Shehab S; Pessia M; Brancorsini S; D'Adamo MC
    Int J Mol Sci; 2021 Jun; 22(11):. PubMed ID: 34205849
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Kir4.1/Kir5.1 Activity Is Essential for Dietary Sodium Intake-Induced Modulation of Na-Cl Cotransporter.
    Wu P; Gao ZX; Su XT; Wang MX; Wang WH; Lin DH
    J Am Soc Nephrol; 2019 Feb; 30(2):216-227. PubMed ID: 30559144
    [TBL] [Abstract][Full Text] [Related]  

  • 13. KCNJ10 determines the expression of the apical Na-Cl cotransporter (NCC) in the early distal convoluted tubule (DCT1).
    Zhang C; Wang L; Zhang J; Su XT; Lin DH; Scholl UI; Giebisch G; Lifton RP; Wang WH
    Proc Natl Acad Sci U S A; 2014 Aug; 111(32):11864-9. PubMed ID: 25071208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lethal digenic mutations in the K
    Hasan S; Balobaid A; Grottesi A; Dabbagh O; Cenciarini M; Rawashdeh R; Al-Sagheir A; Bove C; Macchioni L; Pessia M; Al-Owain M; D'Adamo MC
    J Neurophysiol; 2017 Oct; 118(4):2402-2411. PubMed ID: 28747464
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Deletion of renal Nedd4-2 abolishes the effect of high sodium intake (HS) on Kir4.1, ENaC, and NCC and causes hypokalemia during high HS.
    Zhang DD; Duan XP; Xiao Y; Wu P; Gao ZX; Wang WH; Lin DH
    Am J Physiol Renal Physiol; 2021 May; 320(5):F883-F896. PubMed ID: 33818128
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Src family protein tyrosine kinase regulates the basolateral K channel in the distal convoluted tubule (DCT) by phosphorylation of KCNJ10 protein.
    Zhang C; Wang L; Thomas S; Wang K; Lin DH; Rinehart J; Wang WH
    J Biol Chem; 2013 Sep; 288(36):26135-26146. PubMed ID: 23873931
    [TBL] [Abstract][Full Text] [Related]  

  • 17. EAST/SeSAME Syndrome and Beyond: The Spectrum of Kir4.1- and Kir5.1-Associated Channelopathies.
    Lo J; Forst AL; Warth R; Zdebik AA
    Front Physiol; 2022; 13():852674. PubMed ID: 35370765
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel mutations in the KCNJ10 gene associated to a distinctive ataxia, sensorineural hearing loss and spasticity clinical phenotype.
    Morin M; Forst AL; Pérez-Torre P; Jiménez-Escrig A; Barca-Tierno V; García-Galloway E; Warth R; Lopez-Sendón Moreno JL; Moreno-Pelayo MA
    Neurogenetics; 2020 Apr; 21(2):135-143. PubMed ID: 32062759
    [TBL] [Abstract][Full Text] [Related]  

  • 19. KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function.
    Reichold M; Zdebik AA; Lieberer E; Rapedius M; Schmidt K; Bandulik S; Sterner C; Tegtmeier I; Penton D; Baukrowitz T; Hulton SA; Witzgall R; Ben-Zeev B; Howie AJ; Kleta R; Bockenhauer D; Warth R
    Proc Natl Acad Sci U S A; 2010 Aug; 107(32):14490-5. PubMed ID: 20651251
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.
    D'Adamo MC; Shang L; Imbrici P; Brown SD; Pessia M; Tucker SJ
    J Biol Chem; 2011 Jan; 286(1):192-8. PubMed ID: 21047793
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.