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- Braulke, Thomas
- Mühlhausen, Chris
- Ullrich, Kurt 8
- Keyser, Britta 3
- Muschol, Nicole 3
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10 Einträge gefunden
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Disease-causing mutations affecting surface residues of mitochondrial glutaryl-CoA dehydrogenase impair stability, heteromeric complex formation, and mitochondria architecture
- Schmiesing, Jessica
- Lohmöller, Benjamin
- Schweizer, Michaela
- Tidow, Henning
- Gersting, Søren W
- Muntau, Ania C
- Braulke, Thomas
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Interaction of glutaric aciduria type 1-related glutaryl-CoA dehydrogenase with mitochondrial matrix proteins
2014 - Forschungsinformationssystem des UKE - frei zugänglich -
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Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cells.
2011 - Forschungsinformationssystem des UKE -
The mutation p.Ser298Pro in the sulphamidase gene (SGSH) is associated with a slowly progressive clinical phenotype in mucopolysaccharidosis type IIIA (Sanfilippo A syndrome)
- Meyer, Ann
- Kossow, Kai
- Gal, Andreas
- Steglich, Cordula
- Mühlhausen, Chris
- Ullrich, Kurt
- Braulke, Thomas
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Membrane translocation of glutaric acid and its derivatives.
2008 - Forschungsinformationssystem des UKE -
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Organic anion transporters OAT1 and OAT4 mediate the high affinity transport of glutarate derivatives accumulating in patients with glutaric acidurias.
- Hagos, Yohannes
- Krick, Wolfgang
- Braulke, Thomas
- Mühlhausen, Chris
- Burckhardt, Gerhard
- Burckhardt, Birgitta C
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Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A).
2007 - Forschungsinformationssystem des UKE -
Endothelial effects of 3-hydroxyglutaric acid: implications for glutaric aciduria type I.
- Mühlhausen, Chris
- Ott, Nicola
- Chalajour, Fariba
- Tilki, Derya
- Freudenberg, Folke
- Shahhossini, Mona
- Thiem, Joachim