Seneca S - Search Results

1

Defining the pathogenesis of the human Atp12p W94R mutation using a Saccharomyces cerevisiae yeast model.

Meulemans A, Seneca S, Pribyl T, Smet J, Alderweirldt V, Waeytens A, Lissens W, Van Coster R, De Meirleir L, di Rago JP, Gatti DL, Ackerman SH. Meulemans A, et al. Among authors: seneca s. J Biol Chem. 2010 Feb 5;285(6):4099-4109. doi: 10.1074/jbc.M109.046920. Epub 2009 Nov 20. J Biol Chem. 2010. PMID: 19933271 Free PMC article.

Studies in yeast have shown that a deficiency in Atp12p prevents assembly of the extrinsic domain (F(1)) of complex V and renders cells unable to make ATP through oxidative phosphorylation. De Meirleir et al. (De Meirleir, L., Seneca, S., Lissens, W., De Clercq, I., …

Studies in yeast have shown that a deficiency in Atp12p prevents assembly of the extrinsic domain (F(1)) of complex V and renders cells unab …

2

A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy.

Seneca S, Goemans N, Van Coster R, Givron P, Reybrouck T, Sciot R, Meulemans A, Smet J, Van Hove JL. Seneca S, et al. Am J Med Genet A. 2005 Aug 30;137(2):170-5. doi: 10.1002/ajmg.a.30854. Am J Med Genet A. 2005. PMID: 16059939

3

Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects.

de Paepe B, Smet J, Leroy JG, Seneca S, George E, Matthys D, van Maldergem L, Scalais E, Lissens W, de Meirleir L, Meulemans A, van Coster R. de Paepe B, et al. Among authors: seneca s. Pediatr Res. 2006 Jan;59(1):2-6. doi: 10.1203/01.pdr.0000191294.34122.ab. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16327006

4

A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.

Meulemans A, Seneca S, Smet J, De Paepe B, Lissens W, Van Coster R, Debeer A, De Meirleir L, Jaeken J. Meulemans A, et al. Among authors: seneca s. Eur J Paediatr Neurol. 2007 Jan;11(1):17-20. doi: 10.1016/j.ejpn.2006.10.004. Epub 2006 Dec 11. Eur J Paediatr Neurol. 2007. PMID: 17161635

5

Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.

Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S. Meulemans A, et al. Among authors: seneca s. Arch Neurol. 2007 Sep;64(9):1339-43. doi: 10.1001/archneur.64.9.1339. Arch Neurol. 2007. PMID: 17846276

6

The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders.

Meulemans A, Gerlo E, Seneca S, Lissens W, Smet J, Van Coster R, De Meirleir L. Meulemans A, et al. Among authors: seneca s. Acta Neurol Belg. 2007 Sep;107(3):78-83. Acta Neurol Belg. 2007. PMID: 18072335

7

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA.

Smet J, Seneca S, De Paepe B, Meulemans A, Verhelst H, Leroy J, De Meirleir L, Lissens W, Van Coster R. Smet J, et al. Among authors: seneca s. Electrophoresis. 2009 Oct;30(20):3565-72. doi: 10.1002/elps.200900213. Electrophoresis. 2009. PMID: 19862739

8

Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects.

De Paepe B, Smet J, Vanlander A, Seneca S, Lissens W, De Meirleir L, Vandewoestyne M, Deforce D, Rodenburg RJ, Van Coster R. De Paepe B, et al. Among authors: seneca s. Pediatr Res. 2012 Sep;72(3):232-40. doi: 10.1038/pr.2012.84. Epub 2012 Jun 22. Pediatr Res. 2012. PMID: 22728747

9

Effect of resveratrol on cultured skin fibroblasts from patients with oxidative phosphorylation defects.

De Paepe B, Vandemeulebroecke K, Smet J, Vanlander A, Seneca S, Lissens W, Van Hove JL, Deschepper E, Briones P, Van Coster R. De Paepe B, et al. Among authors: seneca s. Phytother Res. 2014 Feb;28(2):312-6. doi: 10.1002/ptr.4988. Epub 2013 Apr 26. Phytother Res. 2014. PMID: 23620374

10

Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II.

Van Coster R, Seneca S, Smet J, Van Hecke R, Gerlo E, Devreese B, Van Beeumen J, Leroy JG, De Meirleir L, Lissens W. Van Coster R, et al. Among authors: seneca s. Am J Med Genet A. 2003 Jul 1;120A(1):13-8. doi: 10.1002/ajmg.a.10202. Am J Med Genet A. 2003. PMID: 12794685

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