Maassen JA - Search Results

1

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.

2

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 Review.

3

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.

4

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

5

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.

6

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

7

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.

8

Variations in insulin secretion in carriers of gene variants in IRS-1 and -2.

't Hart LM, Nijpels G, Dekker JM, Maassen JA, Heine RJ, van Haeften TW. 't Hart LM, et al. Among authors: maassen ja. Diabetes. 2002 Mar;51(3):884-7. doi: 10.2337/diabetes.51.3.884. Diabetes. 2002. PMID: 11872698

9

Variations in insulin secretion in carriers of the E23K variant in the KIR6.2 subunit of the ATP-sensitive K(+) channel in the beta-cell.

't Hart LM, van Haeften TW, Dekker JM, Bot M, Heine RJ, Maassen JA. 't Hart LM, et al. Among authors: maassen ja. Diabetes. 2002 Oct;51(10):3135-8. doi: 10.2337/diabetes.51.10.3135. Diabetes. 2002. PMID: 12351459

10

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.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

172 results

Search Page