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 *

238 related articles for article (PubMed ID: 24939841)

  • 1. Altered inhibition of Cx26 hemichannels by pH and Zn2+ in the A40V mutation associated with keratitis-ichthyosis-deafness syndrome.
    Sanchez HA; Bienkowski R; Slavi N; Srinivas M; Verselis VK
    J Biol Chem; 2014 Aug; 289(31):21519-32. PubMed ID: 24939841
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Differentially altered Ca2+ regulation and Ca2+ permeability in Cx26 hemichannels formed by the A40V and G45E mutations that cause keratitis ichthyosis deafness syndrome.
    Sánchez HA; Mese G; Srinivas M; White TW; Verselis VK
    J Gen Physiol; 2010 Jul; 136(1):47-62. PubMed ID: 20584891
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The D50N mutation and syndromic deafness: altered Cx26 hemichannel properties caused by effects on the pore and intersubunit interactions.
    Sanchez HA; Villone K; Srinivas M; Verselis VK
    J Gen Physiol; 2013 Jul; 142(1):3-22. PubMed ID: 23797419
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Keratitis-ichthyosis-deafness syndrome-associated Cx26 mutants produce nonfunctional gap junctions but hyperactive hemichannels when co-expressed with wild type Cx43.
    García IE; Maripillán J; Jara O; Ceriani R; Palacios-Muñoz A; Ramachandran J; Olivero P; Perez-Acle T; González C; Sáez JC; Contreras JE; Martínez AD
    J Invest Dermatol; 2015 May; 135(5):1338-1347. PubMed ID: 25625422
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Aberrant hemichannel properties of Cx26 mutations causing skin disease and deafness.
    Gerido DA; DeRosa AM; Richard G; White TW
    Am J Physiol Cell Physiol; 2007 Jul; 293(1):C337-45. PubMed ID: 17428836
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.
    Zhang Y; Hao H
    Biochem Biophys Res Commun; 2013 Jul; 436(3):424-9. PubMed ID: 23756814
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The human Cx26-D50A and Cx26-A88V mutations causing keratitis-ichthyosis-deafness syndrome display increased hemichannel activity.
    Mhaske PV; Levit NA; Li L; Wang HZ; Lee JR; Shuja Z; Brink PR; White TW
    Am J Physiol Cell Physiol; 2013 Jun; 304(12):C1150-8. PubMed ID: 23447037
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathological hemichannels associated with human Cx26 mutations causing Keratitis-Ichthyosis-Deafness syndrome.
    Levit NA; Mese G; Basaly MG; White TW
    Biochim Biophys Acta; 2012 Aug; 1818(8):2014-9. PubMed ID: 21933663
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro.
    de Wolf E; van de Wiel J; Cook J; Dale N
    Physiol Rep; 2016 Nov; 4(22):. PubMed ID: 27884957
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The Cx26-G45E mutation displays increased hemichannel activity in a mouse model of the lethal form of keratitis-ichthyosis-deafness syndrome.
    Mese G; Sellitto C; Li L; Wang HZ; Valiunas V; Richard G; Brink PR; White TW
    Mol Biol Cell; 2011 Dec; 22(24):4776-86. PubMed ID: 22031297
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The syndromic deafness mutation G12R impairs fast and slow gating in Cx26 hemichannels.
    García IE; Villanelo F; Contreras GF; Pupo A; Pinto BI; Contreras JE; Pérez-Acle T; Alvarez O; Latorre R; Martínez AD; González C
    J Gen Physiol; 2018 May; 150(5):697-711. PubMed ID: 29643172
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Aberrant connexin26 hemichannels underlying keratitis-ichthyosis-deafness syndrome are potently inhibited by mefloquine.
    Levit NA; Sellitto C; Wang HZ; Li L; Srinivas M; Brink PR; White TW
    J Invest Dermatol; 2015 Apr; 135(4):1033-1042. PubMed ID: 25229253
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Syndromic deafness mutations at Asn 14 differentially alter the open stability of Cx26 hemichannels.
    Sanchez HA; Slavi N; Srinivas M; Verselis VK
    J Gen Physiol; 2016 Jul; 148(1):25-42. PubMed ID: 27353444
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Connexin mutations causing skin disease and deafness increase hemichannel activity and cell death when expressed in Xenopus oocytes.
    Lee JR; Derosa AM; White TW
    J Invest Dermatol; 2009 Apr; 129(4):870-8. PubMed ID: 18987669
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Connexin26 hemichannels with a mutation that causes KID syndrome in humans lack sensitivity to CO2.
    Meigh L; Hussain N; Mulkey DK; Dale N
    Elife; 2014 Nov; 3():e04249. PubMed ID: 25422938
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Altered cellular localization and hemichannel activities of KID syndrome associated connexin26 I30N and D50Y mutations.
    Aypek H; Bay V; Meşe G
    BMC Cell Biol; 2016 Feb; 17():5. PubMed ID: 26831144
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Emerging issues of connexin channels: biophysics fills the gap.
    Harris AL
    Q Rev Biophys; 2001 Aug; 34(3):325-472. PubMed ID: 11838236
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome.
    Taki T; Takeichi T; Sugiura K; Akiyama M
    Sci Rep; 2018 Aug; 8(1):12824. PubMed ID: 30150638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Opposing modulation of Cx26 gap junctions and hemichannels by CO
    Nijjar S; Maddison D; Meigh L; de Wolf E; Rodgers T; Cann MJ; Dale N
    J Physiol; 2021 Jan; 599(1):103-118. PubMed ID: 33022747
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome.
    Neoh CY; Chen H; Ng SK; Lane EB; Common JE
    Int J Dermatol; 2009 Oct; 48(10):1078-81. PubMed ID: 19785089
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.