4 Einträge gefunden

1. The W101C KCNJ5 Mutation Induces Slower Pacing by Constitutively Active GIRK Channels in hiPSC-Derived Cardiomyocytes

   1. Kayser, Anne
   2. Dittmann, Sven
   3. Šarić, Tomo
   4. Mearini, Giulia
   5. Verkerk, Arie O
   6. Schulze-Bahr, Eric

   2023 - Forschungsinformationssystem des UKE - frei zugänglich
2. A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

   1. Neu, Axel
   2. Eiselt, Michele
   3. Paul, Matthias
   4. Sauter, Kathrin
   5. Stallmeyer, Birgit
   6. Isbrandt, Dirk
   7. Schulze-Bahr, Eric

   2010 - Forschungsinformationssystem des UKE
3. Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.

   1. Kruse, Martin
   2. Schulze-Bahr, Eric
   3. Corfield, Valerie
   4. Beckmann, Alf
   5. Stallmeyer, Birgit
   6. Kurtbay, Güven
   7. Ohmert, Iris

   2009 - Forschungsinformationssystem des UKE
4. C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.

   1. Choe, Chi-Un
   2. Schulze-Bahr, Eric
   3. Neu, Axel
   4. Xu, Jun
   5. Zhu, Zheng I
   6. Sauter, Kathrin
   7. Bähring, Robert

   2006 - Forschungsinformationssystem des UKE