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 *

157 related articles for article (PubMed ID: 31781151)

  • 21. Novel KCNJ10 Gene Variations Compromise Function of Inwardly Rectifying Potassium Channel 4.1.
    Méndez-González MP; Kucheryavykh YV; Zayas-Santiago A; Vélez-Carrasco W; Maldonado-Martínez G; Cubano LA; Nichols CG; Skatchkov SN; Eaton MJ
    J Biol Chem; 2016 Apr; 291(14):7716-26. PubMed ID: 26867573
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human Kir4.1 gene (KCNJ10).
    Haj-Yasein NN; Jensen V; Vindedal GF; Gundersen GA; Klungland A; Ottersen OP; Hvalby O; Nagelhus EA
    Glia; 2011 Nov; 59(11):1635-42. PubMed ID: 21748805
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1.
    Sicca F; Imbrici P; D'Adamo MC; Moro F; Bonatti F; Brovedani P; Grottesi A; Guerrini R; Masi G; Santorelli FM; Pessia M
    Neurobiol Dis; 2011 Jul; 43(1):239-47. PubMed ID: 21458570
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Discovery, Characterization, and Effects on Renal Fluid and Electrolyte Excretion of the Kir4.1 Potassium Channel Pore Blocker, VU0134992.
    Kharade SV; Kurata H; Bender AM; Blobaum AL; Figueroa EE; Duran A; Kramer M; Days E; Vinson P; Flores D; Satlin LM; Meiler J; Weaver CD; Lindsley CW; Hopkins CR; Denton JS
    Mol Pharmacol; 2018 Aug; 94(2):926-937. PubMed ID: 29895592
    [TBL] [Abstract][Full Text] [Related]  

  • 25. MeCP2 Deficiency Leads to Loss of Glial Kir4.1.
    Kahanovitch U; Cuddapah VA; Pacheco NL; Holt LM; Mulkey DK; Percy AK; Olsen ML
    eNeuro; 2018; 5(1):. PubMed ID: 29464197
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mislocalization of K+ channels causes the renal salt wasting in EAST/SeSAME syndrome.
    Tanemoto M; Abe T; Uchida S; Kawahara K
    FEBS Lett; 2014 Mar; 588(6):899-905. PubMed ID: 24561201
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The salt-wasting phenotype of EAST syndrome, a disease with multifaceted symptoms linked to the KCNJ10 K+ channel.
    Bandulik S; Schmidt K; Bockenhauer D; Zdebik AA; Humberg E; Kleta R; Warth R; Reichold M
    Pflugers Arch; 2011 Apr; 461(4):423-35. PubMed ID: 21221631
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [The function and regulation of basolateral Kir4.1 and Kir4.1/Kir5.1 in renal tubules].
    Xiao Y; Meng XX; Zhang H; Guo XW; Gu RM
    Sheng Li Xue Bao; 2018 Dec; 70(6):600-606. PubMed ID: 30560268
    [TBL] [Abstract][Full Text] [Related]  

  • 29. SeSAME/EAST syndrome--phenotypic variability and delayed activity of the distal convoluted tubule.
    Scholl UI; Dave HB; Lu M; Farhi A; Nelson-Williams C; Listman JA; Lifton RP
    Pediatr Nephrol; 2012 Nov; 27(11):2081-2090. PubMed ID: 22907601
    [TBL] [Abstract][Full Text] [Related]  

  • 30. EAST syndrome: Clinical, pathophysiological, and genetic aspects of mutations in KCNJ10.
    Abdelhadi O; Iancu D; Stanescu H; Kleta R; Bockenhauer D
    Rare Dis; 2016; 4(1):e1195043. PubMed ID: 27500072
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A case series of adult patients affected by EAST/SeSAME syndrome suggests more severe disease in subjects bearing
    Suzumoto Y; Columbano V; Gervasi L; Giunta R; Mattina T; Trimarchi G; Capolongo G; Simeoni M; Perna AF; Zacchia M; Toriello G; Pollastro RM; Rapisarda F; Capasso G; Trepiccione F
    Intractable Rare Dis Res; 2021 May; 10(2):95-101. PubMed ID: 33996354
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Lack of the Kir4.1 channel subunit abolishes K+ buffering properties of astrocytes in the ventral respiratory group: impact on extracellular K+ regulation.
    Neusch C; Papadopoulos N; Müller M; Maletzki I; Winter SM; Hirrlinger J; Handschuh M; Bähr M; Richter DW; Kirchhoff F; Hülsmann S
    J Neurophysiol; 2006 Mar; 95(3):1843-52. PubMed ID: 16306174
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Role of Astrocytic Inwardly Rectifying Potassium (Kir) 4.1 Channels in Epileptogenesis.
    Kinboshi M; Ikeda A; Ohno Y
    Front Neurol; 2020; 11():626658. PubMed ID: 33424762
    [TBL] [Abstract][Full Text] [Related]  

  • 34. DNA methylation: A mechanism for sustained alteration of KIR4.1 expression following central nervous system insult.
    Boni JL; Kahanovitch U; Nwaobi SE; Floyd CL; Olsen ML
    Glia; 2020 Jul; 68(7):1495-1512. PubMed ID: 32068308
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome.
    Thompson DA; Feather S; Stanescu HC; Freudenthal B; Zdebik AA; Warth R; Ognjanovic M; Hulton SA; Wassmer E; van't Hoff W; Russell-Eggitt I; Dobbie A; Sheridan E; Kleta R; Bockenhauer D
    J Physiol; 2011 Apr; 589(Pt 7):1681-9. PubMed ID: 21300747
    [TBL] [Abstract][Full Text] [Related]  

  • 36. KCNJ10 (Kir4.1) is expressed in the basolateral membrane of the cortical thick ascending limb.
    Zhang C; Wang L; Su XT; Lin DH; Wang WH
    Am J Physiol Renal Physiol; 2015 Jun; 308(11):F1288-96. PubMed ID: 25834074
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome in a European child with
    Papavasiliou A; Foska K; Ioannou J; Nagel M
    SAGE Open Med Case Rep; 2017; 5():2050313X17723549. PubMed ID: 28835827
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.
    Sicca F; Ambrosini E; Marchese M; Sforna L; Servettini I; Valvo G; Brignone MS; Lanciotti A; Moro F; Grottesi A; Catacuzzeno L; Baldini S; Hasan S; D'Adamo MC; Franciolini F; Molinari P; Santorelli FM; Pessia M
    Sci Rep; 2016 Sep; 6():34325. PubMed ID: 27677466
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations.
    Bockenhauer D; Feather S; Stanescu HC; Bandulik S; Zdebik AA; Reichold M; Tobin J; Lieberer E; Sterner C; Landoure G; Arora R; Sirimanna T; Thompson D; Cross JH; van't Hoff W; Al Masri O; Tullus K; Yeung S; Anikster Y; Klootwijk E; Hubank M; Dillon MJ; Heitzmann D; Arcos-Burgos M; Knepper MA; Dobbie A; Gahl WA; Warth R; Sheridan E; Kleta R
    N Engl J Med; 2009 May; 360(19):1960-70. PubMed ID: 19420365
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.