Isbrandt D - Search Results

1

Lower force and impaired performance during high-intensity electrical stimulation in skeletal muscle of GAMT-deficient knockout mice.

Kan HE, Buse-Pot TE, Peco R, Isbrandt D, Heerschap A, de Haan A. Kan HE, et al. Among authors: isbrandt d. Am J Physiol Cell Physiol. 2005 Jul;289(1):C113-9. doi: 10.1152/ajpcell.00040.2005. Epub 2005 Mar 2. Am J Physiol Cell Physiol. 2005. PMID: 15743892 Free article.

2

Phosphorylated guanidinoacetate partly compensates for the lack of phosphocreatine in skeletal muscle of mice lacking guanidinoacetate methyltransferase.

Kan HE, Renema WK, Isbrandt D, Heerschap A. Kan HE, et al. Among authors: isbrandt d. J Physiol. 2004 Oct 1;560(Pt 1):219-29. doi: 10.1113/jphysiol.2004.067926. Epub 2004 Jul 29. J Physiol. 2004. PMID: 15284341 Free PMC article.

3

Creatine uptake in brain and skeletal muscle of mice lacking guanidinoacetate methyltransferase assessed by magnetic resonance spectroscopy.

Kan HE, Meeuwissen E, van Asten JJ, Veltien A, Isbrandt D, Heerschap A. Kan HE, et al. Among authors: isbrandt d. J Appl Physiol (1985). 2007 Jun;102(6):2121-7. doi: 10.1152/japplphysiol.01327.2006. Epub 2007 Mar 8. J Appl Physiol (1985). 2007. PMID: 17347380 Free article.

4

Disturbed energy metabolism and muscular dystrophy caused by pure creatine deficiency are reversible by creatine intake.

Nabuurs CI, Choe CU, Veltien A, Kan HE, van Loon LJ, Rodenburg RJ, Matschke J, Wieringa B, Kemp GJ, Isbrandt D, Heerschap A. Nabuurs CI, et al. Among authors: isbrandt d. J Physiol. 2013 Jan 15;591(2):571-92. doi: 10.1113/jphysiol.2012.241760. Epub 2012 Nov 5. J Physiol. 2013. PMID: 23129796 Free PMC article.

5

MR spectroscopy of muscle and brain in guanidinoacetate methyltransferase (GAMT)-deficient mice: validation of an animal model to study creatine deficiency.

Renema WK, Schmidt A, van Asten JJ, Oerlemans F, Ullrich K, Wieringa B, Isbrandt D, Heerschap A. Renema WK, et al. Among authors: isbrandt d. Magn Reson Med. 2003 Nov;50(5):936-43. doi: 10.1002/mrm.10627. Magn Reson Med. 2003. PMID: 14587004 Free article.

6

In vivo magnetic resonance spectroscopy of transgenic mice with altered expression of guanidinoacetate methyltransferase and creatine kinase isoenzymes.

Heerschap A, Kan HE, Nabuurs CI, Renema WK, Isbrandt D, Wieringa B. Heerschap A, et al. Among authors: isbrandt d. Subcell Biochem. 2007;46:119-48. doi: 10.1007/978-1-4020-6486-9_7. Subcell Biochem. 2007. PMID: 18652075 Review.

7

Severely altered guanidino compound levels, disturbed body weight homeostasis and impaired fertility in a mouse model of guanidinoacetate N-methyltransferase (GAMT) deficiency.

Schmidt A, Marescau B, Boehm EA, Renema WK, Peco R, Das A, Steinfeld R, Chan S, Wallis J, Davidoff M, Ullrich K, Waldschütz R, Heerschap A, De Deyn PP, Neubauer S, Isbrandt D. Schmidt A, et al. Among authors: isbrandt d. Hum Mol Genet. 2004 May 1;13(9):905-21. doi: 10.1093/hmg/ddh112. Epub 2004 Mar 17. Hum Mol Genet. 2004. PMID: 15028668

8

A Mouse Model of Creatine Transporter Deficiency Reveals Impaired Motor Function and Muscle Energy Metabolism.

Stockebrand M, Sasani A, Das D, Hornig S, Hermans-Borgmeyer I, Lake HA, Isbrandt D, Lygate CA, Heerschap A, Neu A, Choe CU. Stockebrand M, et al. Among authors: isbrandt d. Front Physiol. 2018 Jun 22;9:773. doi: 10.3389/fphys.2018.00773. eCollection 2018. Front Physiol. 2018. PMID: 30013483 Free PMC article.

9

Homoarginine levels are regulated by L-arginine:glycine amidinotransferase and affect stroke outcome: results from human and murine studies.

Choe CU, Atzler D, Wild PS, Carter AM, Böger RH, Ojeda F, Simova O, Stockebrand M, Lackner K, Nabuurs C, Marescau B, Streichert T, Müller C, Lüneburg N, De Deyn PP, Benndorf RA, Baldus S, Gerloff C, Blankenberg S, Heerschap A, Grant PJ, Magnus T, Zeller T, Isbrandt D, Schwedhelm E. Choe CU, et al. Among authors: isbrandt d. Circulation. 2013 Sep 24;128(13):1451-61. doi: 10.1161/CIRCULATIONAHA.112.000580. Epub 2013 Sep 4. Circulation. 2013. PMID: 24004504

10

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: isbrandt d. 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

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