Ion Channels in the Heart

Yazar: Bartos, Daniel C., Grandi, Eleonora, Ripplinger, Crystal M.
Yayımlandı Compr Physiol (2015)

Depolarization of Cardiac Membrane Potential Synchronizes Calcium Sparks and Waves in Tissue

Yazar: Sato, Daisuke, Bartos, Daniel C., Ginsburg, Kenneth S., Bers, Donald M.
Baskı/Yayın Bilgisi 2014

Quantitative analysis of the Ca(2+)‐dependent regulation of delayed rectifier K(+) current I (Ks) in rabbit ventricular myocytes

Yazar: Bartos, Daniel C., Morotti, Stefano, Ginsburg, Kenneth S., Grandi, Eleonora, Bers, Donald M.
Yayımlandı J Physiol (2017)

Trafficking-deficient hERG K(+) channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER

Yazar: Smith, Jennifer L., McBride, Christie M., Nataraj, Parvathi S., Bartos, Daniel C., January, Craig T., Delisle, Brian P.
Baskı/Yayın Bilgisi 2011

The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most

Yazar: Ackerman, Jaeger P., Bartos, Daniel C., Kapplinger, Jamie D., Tester, David J., Delisle, Brian P., Ackerman, Michael J.
Yayımlandı Mayo Clin Proc (2016)

A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation

Yazar: Bartos, Daniel C., Giudicessi, John R., Tester, David J., Ackerman, Michael J., Ohno, Seiko, Horie, Minoru, Gollob, Michael H., Burgess, Don E., Delisle, Brian P.
Yayımlandı Heart Rhythm (2013)

The Cardiomyocyte Molecular Clock Regulates the Circadian Expression of Kcnh2 and Contributes to Ventricular Repolarization

Yazar: Schroder, Elizabeth A., Burgess, Don E., Zhang, Xiping, Lefta, Mellani, Smith, Jennifer L., Patwardhan, Abhijit, Bartos, Daniel C., Elayi, Claude S., Esser, Karyn A., Delisle, Brian P.
Yayımlandı Heart Rhythm (2015)

Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residue in the Voltage Sensor

Yazar: 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.
Baskı/Yayın Bilgisi 2013

Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum

Yazar: Smith, Jennifer L., Reloj, Allison R., Nataraj, Parvathi S., Bartos, Daniel C., Schroder, Elizabeth A., Moss, Arthur J., Ohno, Seiko, Horie, Minoru, Anderson, Corey L., January, Craig T., Delisle, Brian P.
Baskı/Yayın Bilgisi 2013

R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation

Yazar: Bartos, Daniel C., Duchatelet, Sabine, Burgess, Don E., Klug, Didier, Denjoy, Isabelle, Peat, Rachel, Lupoglazoff, Jean-Marc, Fressart, Véronique, Berthet, Myriam, Ackerman, Michael J., January, Craig T., Guicheney, Pascale, Delisle, Brian P.
Baskı/Yayın Bilgisi 2010

A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation

Yazar: Bartos, Daniel C., Anderson, Jeffrey B., Bastiaenen, Rachel, Johnson, Jonathan N., Gollob, Michael H, Tester, David J., Burgess, Don E., Homfray, Tessa, Behr, Elijah R., Ackerman, Michael J., Guicheney, Pascale, Delisle, Brian P.
Baskı/Yayın Bilgisi 2013

High-risk Long QT Syndrome Mutations in the Kv7.1 (KCNQ1) Pore Disrupt the Molecular Basis for Rapid K(+) Permeation

Yazar: Burgess, Don E., Bartos, Daniel C., Reloj, Allison R., Campbell, Kenneth S., Johnson, Jonathan N., Tester, David J., Ackerman, Michael J., Fressart, Véronique, Denjoy, Isabelle, Guicheney, Pascale, Moss, Arthur J., Ohno, Seiko, Horie, Minoru, Delisle, Brian P.
Baskı/Yayın Bilgisi 2012

Potassium channels in the heart: structure, function and regulation

Yazar: Grandi, Eleonora, Sanguinetti, Michael C., Bartos, Daniel C., Bers, Donald M., Chen‐Izu, Ye, Chiamvimonvat, Nipavan, Colecraft, Henry M., Delisle, Brian P., Heijman, Jordi, Navedo, Manuel F., Noskov, Sergei, Proenza, Catherine, Vandenberg, Jamie I., Yarov‐Yarovoy, Vladimir
Yayımlandı J Physiol (2016)

Long QT Syndrome–Associated Mutations in Intrauterine Fetal Death

Yazar: Crotti, Lia, Tester, David J., White, Wendy M., Bartos, Daniel C., Insolia, Roberto, Besana, Alessandra, Kunic, Jennifer D., Will, Melissa L., Velasco, Ellyn J., Bair, Jennifer J., Ghidoni, Alice, Cetin, Irene, Van Dyke, Daniel L., Wick, Myra J., Brost, Brian, Delisle, Brian P., Facchinetti, Fabio, George, Alfred L., Schwartz, Peter J., Ackerman, Michael J.
Baskı/Yayın Bilgisi 2013