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Kirstine Calloe
Kirstine Calloe
Dirección de correo verificada de sund.ku.dk
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Managing the complexity of communication: regulation of gap junctions by post-translational modification
LN Axelsen, K Calloe, NH Holstein-Rathlou, MS Nielsen
Frontiers in pharmacology 4, 53537, 2013
1442013
The small molecule NS11021 is a potent and specific activator of Ca2+-activated big-conductance K+ channels
BH Bentzen, A Nardi, K Calloe, LS Madsen, SP Olesen, M Grunnet
Molecular pharmacology 72 (4), 1033-1044, 2007
1402007
Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
JM Cordeiro, M Marieb, R Pfeiffer, K Calloe, E Burashnikov, ...
Journal of molecular and cellular cardiology 46 (5), 695-703, 2009
1312009
A transient outward potassium current activator recapitulates the electrocardiographic manifestations of Brugada syndrome
K Calloe, JM Cordeiro, JM Di Diego, RS Hansen, M Grunnet, SP Olesen, ...
Cardiovascular research 81 (4), 686-694, 2009
1252009
A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation
MS Olesen, L Refsgaard, AG Holst, AP Larsen, S Grubb, S Haunsø, ...
Cardiovascular research 98 (3), 488-495, 2013
1242013
The acrylamide (S)-1 differentially affects Kv7 (KCNQ) potassium channels
BH Bentzen, N Schmitt, K Calloe, WD Brown, M Grunnet, SP Olesen
Neuropharmacology 51 (6), 1068-1077, 2006
1082006
The KCNQ5 potassium channel from mouse: a broadly expressed M-current like potassium channel modulated by zinc, pH, and volume changes
HS Jensen, K Callø, T Jespersen, BS Jensen, SP Olesen
Molecular brain research 139 (1), 52-62, 2005
792005
Patient iPSC-derived neurons for disease modeling of frontotemporal dementia with mutation in CHMP2B
Y Zhang, B Schmid, NK Nikolaisen, MA Rasmussen, BI Aldana, M Agger, ...
Stem cell reports 8 (3), 648-658, 2017
772017
Structure of the human ClC-1 chloride channel
K Wang, SS Preisler, L Zhang, Y Cui, JW Missel, C Grønberg, K Gotfryd, ...
PLoS biology 17 (4), e3000218, 2019
752019
A common single nucleotide polymorphism can exacerbate long-QT type 2 syndrome leading to sudden infant death
E Nof, JM Cordeiro, GJ Pérez, FS Scornik, K Calloe, B Love, ...
Circulation: Cardiovascular Genetics 3 (2), 199-206, 2010
662010
Diet-induced pre-diabetes slows cardiac conductance and promotes arrhythmogenesis
LN Axelsen, K Calloe, TH Braunstein, M Riemann, JP Hofgaard, B Liang, ...
Cardiovascular diabetology 14, 1-14, 2015
612015
Differential effects of the transient outward K+ current activator NS5806 in the canine left ventricle
K Calloe, T Jespersen, A Lundby, C Antzelevitch, SP Olesen, JM Cordeiro
Biophysical Journal 96 (3), 659a, 2009
592009
A novel nonsense variant in Nav1. 5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias
MS Olesen, NF Jensen, AG Holst, JB Nielsen, J Tfelt-Hansen, ...
Canadian Journal of Cardiology 27 (4), 523. e17-523. e23, 2011
562011
Activation, Permeability, and Inhibition of Astrocytic and Neuronal Large Pore (Hemi) channels*♦
DB Hansen, ZC Ye, K Calloe, TH Braunstein, JP Hofgaard, BR Ransom, ...
Journal of Biological Chemistry 289 (38), 26058-26073, 2014
542014
Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders
M Gilling, HB Rasmussen, K Calloe, AF Sequeira, M Baretto, G Oliveira, ...
Frontiers in genetics 4, 54, 2013
542013
Characterization and Mechanisms of Action of Novel NaV1.5 Channel Mutations Associated With Brugada Syndrome
K Calloe, MM Refaat, S Grubb, J Wojciak, J Campagna, NM Thomsen, ...
Circulation: Arrhythmia and Electrophysiology 6 (1), 177-184, 2013
542013
Characterizations of a loss-of-function mutation in the Kir3. 4 channel subunit
K Calloe, LS Ravn, N Schmitt, JL Sui, M Duno, S Haunso, M Grunnet, ...
Biochemical and Biophysical Research Communications 364 (4), 889-895, 2007
532007
Effect of the Ito activator NS5806 on cloned Kv4 channels depends on the accessory protein KChIP2
A Lundby, T Jespersen, N Schmitt, M Grunnet, SP Olesen, JM Cordeiro, ...
British journal of pharmacology 160 (8), 2028-2044, 2010
512010
The novel C-terminal KCNQ1 mutation M520R alters protein trafficking
N Schmitt, K Calloe, NH Nielsen, M Buschmann, EJ Speckmann, ...
Biochemical and biophysical research communications 358 (1), 304-310, 2007
422007
Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome
M Grunnet, ER Behr, K Calloe, J Hofman-Bang, J Till, M Christiansen, ...
Heart Rhythm 2 (11), 1238-1249, 2005
412005
El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.
Artículos 1–20