LM t Hart, T Hansen, I Rietveld, JM Dekker, … - Diabetes, 2005 - Am Diabetes Assoc Previously, we have shown that a mutation in the mitochondrial DNA–encoded
tRNA Leu(UUR) gene is associated with type 2 diabetes. One of the consequences
of this mutation is a reduced aminoacylation of tRNA Leu(UUR) . In this ... Cited by 13 - Related articles - All 8 versions
JA Maassen, LM t Hart, GM Janssen, E … - Biochemical Society transactions, 2006 - ncbi.nlm.nih.gov Multiple pathogenic pathways are able to deregulate glucose homoeostasis leading
to diabetes. The 3243A>G mutation in the mtDNA (mitochondrial DNA)-encoded
tRNALeu,UUR gene was found by us to be associated with a particular ... Cited by 9 - Related articles - BL Direct - All 4 versions
JA Maassen, RS Jahangir Tafrechi, GMC … - Endocrinology and metabolism clinics of North America, 2006 - Elsevier Mitochondria are distinct organelles within eukaryotic cells. From an
evolutionary point of view, it is assumed that mitochondria originated from
bacteria by endosymbiotic mechanisms with proeukaryotic cells [2]. ... Cited by 10 - Related articles - All 4 versions
EC van Hove, T Hansen, JM Dekker, E Reiling … - DIABETES, 2006 - Am Diabetes Assoc Page 1. Brief Genetics Report The HADHSC Gene Encoding Short-Chain L -3-Hydroxyacyl-
CoA Dehydrogenase (SCHAD) and Type 2 Diabetes Susceptibility ... Related articles
GC Scheper, T van der Klok, RJ van Andel, … - Nature genetics, 2007 - nature.com Leukoencephalopathy with brain stem and spinal cord involvement and lactate
elevation (LBSL) has recently been defined based on a highly characteristic
constellation of abnormalities observed by magnetic resonance imaging and ... Cited by 34 - Related articles - BL Direct - All 5 versions
N Abahuni, S Gispert, P Bauer, O Riess, R … - Neuroscience Letters, 2007 - Elsevier Mitochondrial dysfunction occurs early in late-onset sporadic Parkinson's
disease (PD), but the mitochondrial protein network mediating PD pathogenesis is
largely unknown. Mutations in the mitochondrial serine-threonine kinase ... Cited by 6 - Related articles - All 2 versions
EC van Hove, T Hansen, JM Dekker, E Reiling … - Diabetes, 2006 - Am Diabetes Assoc The short-chain l-3-hydroxyacyl-CoA dehydrogenase (SCHAD) protein is involved in
the penultimate step of mitochondrial fatty acid oxidation. Previously, it has
been shown that mutations in the corresponding gene (HADHSC) are associated ... Cited by 1 - Related articles - BL Direct - All 7 versions
S Seneca, N Goemans, R Van Coster, P … - American Journal of Medical Genetics Part A, 2005 - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Cited by 9 - Related articles - BL Direct - All 7 versions
- ►nih.gov GC Petzold, G Bohner, R Klingebiel, N … - British Medical Journal, 2006 - jnnp.bmj.com Comment We describe a patient with repeated ICA vasospasm of unknown origin.
Because of the consanguinity of his parents and the Friedreich's foot seen in
various genetic neurological disorders, 1 genetic screening was undertaken, ... Cited by 8 - Related articles - BL Direct - All 4 versions
