5 Einträge gefunden

1. Transcriptomic and metabolic analyses reveal salvage pathways in creatine-deficient AGAT(-/-) mice

   1. Stockebrand, Malte
   2. Nejad, Ali Sasani
   3. Neu, Axel
   4. Kharbanda, Kusum K
   5. Sauter, Kathrin
   6. Schillemeit, Stefan
   7. Isbrandt, Dirk

   2016 - Forschungsinformationssystem des UKE
2. Differential regulation of AMPK activation in leptin- and creatine-deficient mice

   1. Stockebrand, Malte
   2. Sauter, Kathrin
   3. Neu, Axel
   4. Isbrandt, Dirk
   5. Choe, Chi-un

   2013 - Forschungsinformationssystem des UKE
3. L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.

   1. Choe, Chi-Un
   2. Nabuurs, Christine
   3. Stockebrand, Malte
   4. Neu, Axel
   5. Nunes, Patricia
   6. Morellini, Fabio
   7. Sauter, Kathrin

   2013 - Forschungsinformationssystem des UKE
4. 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
5. 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