Maassen JA - Search Results

1

Phosphorus-31 magnetic resonance spectroscopy of skeletal muscle in maternally inherited diabetes and deafness A3243G mitochondrial mutation carriers.

van Elderen SG, Doornbos J, van Essen EH, Lemkes HH, Maassen JA, Smit JW, de Roos A. van Elderen SG, et al. Among authors: maassen ja. J Magn Reson Imaging. 2009 Jan;29(1):127-31. doi: 10.1002/jmri.21620. J Magn Reson Imaging. 2009. PMID: 19097109

2

New insights in the molecular pathogenesis of the maternally inherited diabetes and deafness syndrome.

Maassen JA, Jahangir Tafrechi RS, Janssen GM, Raap AK, Lemkes HH, 't Hart LM. Maassen JA, et al. Endocrinol Metab Clin North Am. 2006 Jun;35(2):385-96, x-xi. doi: 10.1016/j.ecl.2006.02.014. Endocrinol Metab Clin North Am. 2006. PMID: 16632100 Review.

3

Mitochondrial diabetes: molecular mechanisms and clinical presentation.

Maassen JA, 'T Hart LM, Van Essen E, Heine RJ, Nijpels G, Jahangir Tafrechi RS, Raap AK, Janssen GM, Lemkes HH. Maassen JA, et al. Diabetes. 2004 Feb;53 Suppl 1:S103-9. doi: 10.2337/diabetes.53.2007.s103. Diabetes. 2004. PMID: 14749274 Review.

4

Genetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE study.

Reiling E, van Vliet-Ostaptchouk JV, van 't Riet E, van Haeften TW, Arp PA, Hansen T, Kremer D, Groenewoud MJ, van Hove EC, Romijn JA, Smit JW, Nijpels G, Heine RJ, Uitterlinden AG, Pedersen O, Slagboom PE, Maassen JA, Hofker MH, 't Hart LM, Dekker JM. Reiling E, et al. Among authors: maassen ja. Eur J Hum Genet. 2009 Aug;17(8):1056-62. doi: 10.1038/ejhg.2009.4. Epub 2009 Feb 11. Eur J Hum Genet. 2009. PMID: 19209188 Free PMC article.

5

Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis.

Maassen JA. Maassen JA. Am J Med Genet. 2002 May 30;115(1):66-70. doi: 10.1002/ajmg.10346. Am J Med Genet. 2002. PMID: 12116179 Review.

6

Molecular mechanisms of mitochondrial diabetes (MIDD).

Maassen JA, Janssen GM, 't Hart LM. Maassen JA, et al. Ann Med. 2005;37(3):213-21. doi: 10.1080/07853890510007188. Ann Med. 2005. PMID: 16019720 Free article. Review.

7

Lessons that can be learned from patients with diabetogenic mutations in mitochondrial DNA: implications for common type 2 diabetes.

Maassen JA, 't Hart LM, Ouwens DM. Maassen JA, et al. Curr Opin Clin Nutr Metab Care. 2007 Nov;10(6):693-7. doi: 10.1097/MCO.0b013e3282f0b774. Curr Opin Clin Nutr Metab Care. 2007. PMID: 18089949 Review.

8

Evidence that the mitochondrial leucyl tRNA synthetase (LARS2) gene represents a novel type 2 diabetes susceptibility gene.

't Hart LM, Hansen T, Rietveld I, Dekker JM, Nijpels G, Janssen GM, Arp PA, Uitterlinden AG, Jørgensen T, Borch-Johnsen K, Pols HA, Pedersen O, van Duijn CM, Heine RJ, Maassen JA. 't Hart LM, et al. Among authors: maassen ja. Diabetes. 2005 Jun;54(6):1892-5. doi: 10.2337/diabetes.54.6.1892. Diabetes. 2005. PMID: 15919814 Free article.

9

The association of mitochondrial content with prevalent and incident type 2 diabetes.

Reiling E, Ling C, Uitterlinden AG, Van't Riet E, Welschen LM, Ladenvall C, Almgren P, Lyssenko V, Nijpels G, van Hove EC, Maassen JA, de Geus EJ, Boomsma DI, Dekker JM, Groop L, Willemsen G, 't Hart LM. Reiling E, et al. Among authors: maassen ja. J Clin Endocrinol Metab. 2010 Apr;95(4):1909-15. doi: 10.1210/jc.2009-1775. Epub 2010 Feb 11. J Clin Endocrinol Metab. 2010. PMID: 20150578

10

Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutation.

Jahangir Tafrechi RS, Svensson PJ, Janssen GM, Szuhai K, Maassen JA, Raap AK. Jahangir Tafrechi RS, et al. Among authors: maassen ja. Mutat Res. 2005 Oct 15;578(1-2):43-52. doi: 10.1016/j.mrfmmm.2005.02.002. Mutat Res. 2005. PMID: 16202796

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