Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kristian L. Poulsen"'
Autor:
Maria de los Angeles Tejada, Mostafa Hotait, Georges Nemer, Kirstine Calloe, Marwan M. Refaat, Abdallah Rebeiz, Dan A. Klaerke, Kristian L. Poulsen
Publikováno v:
Pacing and Clinical Electrophysiology. 38:1304-1309
Background Loss-of-function mutations in the voltage gated potassium channel Kv11.1 have been associated with the Long QT Syndrome (LQTS) type 2. We identified the p.T613A mutation in Kv11.1 in a family with LQTS. T613A is located in the outer part o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a91139593ed0e030229f7722831a76f2
https://doi.org/10.1111/pace.12693
https://doi.org/10.1111/pace.12693
Autor:
Kristian L, Poulsen, Mostafa, Hotait, Kirstine, Calloe, Dan A, Klaerke, Abdallah, Rebeiz, Georges, Nemer, Maria A, Tejada, Marwan M, Refaat
Publikováno v:
Pacing and clinical electrophysiology : PACE. 38(11)
Loss-of-function mutations in the voltage gated potassium channel Kv 11.1 have been associated with the Long QT Syndrome (LQTS) type 2. We identified the p.T613A mutation in Kv 11.1 in a family with LQTS. T613A is located in the outer part of the por
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::074bf65c04a2e277ced4a479d329054d
https://pubmed.ncbi.nlm.nih.gov/26173150
https://pubmed.ncbi.nlm.nih.gov/26173150
Autor:
Philip J. Pedersen, Dan A. Klaerke, Kristian L. Poulsen, Maria de los Angeles Tejada, Emma Rie Olander, Kirstine Calloe, Frank Hauser, Kirsten B. Thomsen, Søren Grubb, Rikke Buhl
Publikováno v:
Pedersen, P J, Thomsen, K B, Olander, E R, Hauser, F, Tejada, M D L A, Poulsen, K L, Grubb, S J, Buhl, R, Callø, K & Klærke, D A 2015, ' Molecular cloning and functional expression of the Equine K+ channel KV11.1 (Ether à Go-Go-related/KCNH2 gene) and the regulatory subunit KCNE2 from equine myocardium ', PloS one, vol. 10, no. 9, e0138320 . https://doi.org/10.1371/journal.pone.0138320
PLoS ONE
PLoS ONE, Vol 10, Iss 9, p e0138320 (2015)
PLoS ONE
PLoS ONE, Vol 10, Iss 9, p e0138320 (2015)
The KCNH2 and KCNE2 genes encode the cardiac voltage-gated K+ channel KV11.1 and its auxiliary β subunit KCNE2. KV11.1 is critical for repolarization of the cardiac action potential. In humans, mutations or drug therapy affecting the KV11.1 channel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::269d699d6f9f710336b95f896c804f06
https://curis.ku.dk/portal/da/publications/molecular-cloning-and-functional-expression-of-the-equine-k-channel-kv111-ether-a-gogorelatedkcnh2-gene-and-the-regulatory-subunit-kcne2-from-equine-myocardium(7cd56f01-5880-4d74-b3ea-733438a73f49).html
https://curis.ku.dk/portal/da/publications/molecular-cloning-and-functional-expression-of-the-equine-k-channel-kv111-ether-a-gogorelatedkcnh2-gene-and-the-regulatory-subunit-kcne2-from-equine-myocardium(7cd56f01-5880-4d74-b3ea-733438a73f49).html
Autor:
Philip J. Pedersen, Kirstine Calloe, Søren Grubb, Rikke Buhl, Maria de los Angeles Tejada, Kristian L. Poulsen, Dan A. Klaerke
Publikováno v:
Biophysical Journal. (2):113a
The heart rate in horses can vary between 30 and 250 beats per minute. This suggests an important role for a dynamic regulation of the repolarizing potassium currents.Methods and Results: Kv7.1 and KCNE1 that underlie the slow delayed rectifying curr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68001094c7e9544e5d1db969ba921996