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- Braulke, Thomas
- Storch, Stephan 11
- Pohl, Sandra 10
- Ullrich, Kurt 6
- Mühlhausen, Chris 5
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32 Einträge gefunden
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Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6.
- Kurze, Anna-Katharina
- Galliciotti, Giovanna
- Heine, Claudia
- Mole, Sara E
- Quitsch, Arne
- Braulke, Thomas
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Protein kinase a dependent phosphorylation of apical membrane antigen 1 plays an important role in erythrocyte invasion by the malaria parasite.
- Leykauf, Kerstin
- Treeck, Moritz
- Gilson, Paul R
- Nebl, Thomas
- Braulke, Thomas
- Cowman, Alan F
- Gilberger, Tim W
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Lysosomal targeting of the CLN7 membrane glycoprotein and transport via the plasma membrane require a dileucine motif.
2010 - Forschungsinformationssystem des UKE -
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Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases.
2009 - Forschungsinformationssystem des UKE -
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Mannose phosphorylation in health and disease.
- Kollmann, Katrin
- Pohl, Sandra
- Marschner, Katrin
- Encarnação, Marisa
- Sakwa, Imme
- Stephan, Tiede
- Poorthuis, Ben J
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Molecular order in mucolipidosis II and III nomenclature.
- Cathey, Sara S
- Kudo, Mariko
- Stephan, Tiede
- Raas-Rothschild, Annick
- Braulke, Thomas
- Beck, Michael
- Taylor, Harold A
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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 -
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