4 Einträge gefunden

1. Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6.

   1. Kurze, Anna-Katharina
   2. Galliciotti, Giovanna
   3. Heine, Claudia
   4. Mole, Sara E
   5. Quitsch, Arne
   6. Braulke, Thomas

   2010 - Forschungsinformationssystem des UKE
2. Accumulation of bis(monoacylglycero)phosphate and gangliosides in mouse models of neuronal ceroid lipofuscinosis.

   1. Jabs, Sabrina
   2. Quitsch, Arne
   3. Käkelä, Reijo
   4. Koch, Bettina
   5. Tyynelä, Jaana
   6. Helmut, Brade
   7. Glatzel, Markus

   2008 - Forschungsinformationssystem des UKE
3. Topology and endoplasmic reticulum retention signals of the lysosomal storage disease-related membrane protein CLN6.

   1. Heine, Claudia
   2. Quitsch, Arne
   3. Storch, Stephan
   4. Martin, Yella
   5. Lonka, Liina
   6. Lehesjoki, Anna-Elina
   7. Mole, Sara E

   2007 - Forschungsinformationssystem des UKE
4. C-terminal prenylation of the CLN3 membrane glycoprotein is required for efficient endosomal sorting to lysosomes.

   1. Storch, Stephan
   2. Pohl, Sandra
   3. Quitsch, Arne
   4. Falley, Katrin
   5. Braulke, Thomas

   2007 - Forschungsinformationssystem des UKE