Sauter K - Search Results

1

L-arginine:glycine amidinotransferase deficiency protects from metabolic syndrome.

Choe CU, Nabuurs C, Stockebrand MC, Neu A, Nunes P, Morellini F, Sauter K, Schillemeit S, Hermans-Borgmeyer I, Marescau B, Heerschap A, Isbrandt D. Choe CU, et al. Among authors: sauter k. Hum Mol Genet. 2013 Jan 1;22(1):110-23. doi: 10.1093/hmg/dds407. Epub 2012 Oct 1. Hum Mol Genet. 2013. PMID: 23026748

2

Differential regulation of AMPK activation in leptin- and creatine-deficient mice.

Stockebrand M, Sauter K, Neu A, Isbrandt D, Choe CU. Stockebrand M, et al. Among authors: sauter k. FASEB J. 2013 Oct;27(10):4147-56. doi: 10.1096/fj.12-225136. Epub 2013 Jun 28. FASEB J. 2013. PMID: 23825223

3

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

Stockebrand M, Nejad AS, Neu A, Kharbanda KK, Sauter K, Schillemeit S, Isbrandt D, Choe CU. Stockebrand M, et al. Among authors: sauter k. Amino Acids. 2016 Aug;48(8):2025-39. doi: 10.1007/s00726-016-2202-7. Epub 2016 Mar 3. Amino Acids. 2016. PMID: 26940723

4

C-terminal HERG (LQT2) mutations disrupt IKr channel regulation through 14-3-3epsilon.

Choe CU, Schulze-Bahr E, Neu A, Xu J, Zhu ZI, Sauter K, Bähring R, Priori S, Guicheney P, Mönnig G, Neapolitano C, Heidemann J, Clancy CE, Pongs O, Isbrandt D. Choe CU, et al. Among authors: sauter k. Hum Mol Genet. 2006 Oct 1;15(19):2888-902. doi: 10.1093/hmg/ddl230. Epub 2006 Aug 21. Hum Mol Genet. 2006. PMID: 16923798

5

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

Neu A, Eiselt M, Paul M, Sauter K, Stallmeyer B, Isbrandt D, Schulze-Bahr E. Neu A, et al. Among authors: sauter k. Hum Mutat. 2010 Aug;31(8):E1609-21. doi: 10.1002/humu.21302. Hum Mutat. 2010. PMID: 20564468

6

Identification and functional characterization of a novel KCNE2 (MiRP1) mutation that alters HERG channel kinetics.

Isbrandt D, Friederich P, Solth A, Haverkamp W, Ebneth A, Borggrefe M, Funke H, Sauter K, Breithardt G, Pongs O, Schulze-Bahr E. Isbrandt D, et al. Among authors: sauter k. J Mol Med (Berl). 2002 Aug;80(8):524-32. doi: 10.1007/s00109-002-0364-0. Epub 2002 Jun 28. J Mol Med (Berl). 2002. PMID: 12185453

7

Contribution of N- and C-terminal Kv4.2 channel domains to KChIP interaction [corrected].

Callsen B, Isbrandt D, Sauter K, Hartmann LS, Pongs O, Bähring R. Callsen B, et al. Among authors: sauter k. J Physiol. 2005 Oct 15;568(Pt 2):397-412. doi: 10.1113/jphysiol.2005.094359. Epub 2005 Aug 11. J Physiol. 2005. PMID: 16096338 Free PMC article.

8

Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA).

Isbrandt D, Leicher T, Waldschütz R, Zhu X, Luhmann U, Michel U, Sauter K, Pongs O. Isbrandt D, et al. Among authors: sauter k. Genomics. 2000 Mar 1;64(2):144-54. doi: 10.1006/geno.2000.6117. Genomics. 2000. PMID: 10729221

9

N-type inactivation features of Kv4.2 channel gating.

Gebauer M, Isbrandt D, Sauter K, Callsen B, Nolting A, Pongs O, Bähring R. Gebauer M, et al. Among authors: sauter k. Biophys J. 2004 Jan;86(1 Pt 1):210-23. doi: 10.1016/S0006-3495(04)74097-7. Biophys J. 2004. PMID: 14695263 Free PMC article.

10

Biophysical properties of Kv3.1 channels in SH-SY5Y human neuroblastoma cells.

Friederich P, Dilger JP, Isbrandt D, Sauter K, Pongs O, Urban BW. Friederich P, et al. Among authors: sauter k. Recept Channels. 2003;9(6):387-96. doi: 10.3109/714041019. Recept Channels. 2003. PMID: 14698966

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