Search Results - "McBride, Christie M."

  • Showing 1 - 6 results of 6
Refine Results
  1. 1

    Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER by Smith, Jennifer L, McBride, Christie M, Nataraj, Parvathi S, Bartos, Daniel C, January, Craig T, Delisle, Brian P

    “…The human ether-a-go-go related gene (hERG) encodes the voltage-gated K(+) channel that underlies the rapidly activating delayed-rectifier current in cardiac…”
    Get more information
    Journal Article
  2. 2

    Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor by McBride, Christie M., Smith, Ashley M., Smith, Jennifer L., Reloj, Allison R., Velasco, Ellyn J., Powell, Jonathan, Elayi, Claude S., Bartos, Daniel C., Burgess, Don E., Delisle, Brian P.

    Published in The Journal of membrane biology (01-05-2013)
    “…KCNH2 encodes the Kv11.1 channel, which conducts the rapidly activating delayed rectifier K + current ( I Kr ) in the heart. KCNH2 mutations cause type 2 long…”
    Get full text
    Journal Article
  3. 3
  4. 4
  5. 5
  6. 6

    Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residue in the Voltage Sensor by McBride, Christie M., Smith, Ashley M., Smith, Jennifer L., Reloj, Allison R., Velasco, Ellyn J., Powell, Jonathan, Elayi, Claude S., Bartos, Daniel C., Burgess, Don E., Delisle, Brian P.

    Published in The Journal of membrane biology (02-04-2013)
    “…KCNH2 encodes the Kv11.1 channel, which conducts the rapidly activating delayed rectifier K + current ( I Kr ) in the heart. KCNH2 mutations cause type 2 long…”
    Get full text
    Journal Article