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Thomas Braulke

Showing results (31-40 of 106) with videos related to

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The Journal of Biological Chemistry|March 11, 2004
Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase AClaudia Heine, Bettina Koch, Stephan Storch, et al.
Journal of Cellular Biochemistry|March 21, 2007
Alteration of the insulin-like growth factor axis during in vitro differentiation of the human osteosarcoma cell line HOS 58Volker Viereck, Heide Siggelkow, Rajeswararao Pannem, et al.
Biochemical and Biophysical Research Communications|May 3, 2003
In vivo processed fragments of IGF binding protein-2 copurified with bioactive IGF-IILudger Ständker, Bernd Kübler, Maik Obendorf, et al.
Investigative Ophthalmology & Visual Science|October 3, 2013
Apoptotic photoreceptor loss and altered expression of lysosomal proteins in the nclf mouse model of neuronal ceroid lipofuscinosisUdo Bartsch, Giovanna Galliciotti, Guillermo F Jofre, et al.
The Biochemical Journal|September 28, 2002
A replacement of the active-site aspartic acid residue 293 in mouse cathepsin D affects its intracellular stability, processing and transport in HEK-293 cellsSanna Partanen, Stephan Storch, Hans-Gerhard Löffler, et al.
The Journal of Biological Chemistry|April 2, 2011
Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cellsJessica Lamp, Britta Keyser, David M Koeller, et al.
Biochimica Et Biophysica Acta|February 14, 2013
Cell biology and function of neuronal ceroid lipofuscinosis-related proteinsKatrin Kollmann, Kristiina Uusi-Rauva, Enzo Scifo, et al.
Human Mutation|December 19, 2009
Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6Anna-Katherina Kurze, Giovanna Galliciotti, Claudia Heine, et al.
The Journal of Biological Chemistry|August 20, 2014
Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activityBjörn Kowalewski, Torben Lübke, Katrin Kollmann, et al.
Human Molecular Genetics|September 9, 2008
Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH)Britta Keyser, Chris Mühlhausen, Achim Dickmanns, et al.
Pageof 11

Showing results (31-40 of 106) with videos related to

Sort By:
Pageof 11
The Journal of Biological Chemistry|March 11, 2004
Defective endoplasmic reticulum-resident membrane protein CLN6 affects lysosomal degradation of endocytosed arylsulfatase AClaudia Heine, Bettina Koch, Stephan Storch, et al.
Journal of Cellular Biochemistry|March 21, 2007
Alteration of the insulin-like growth factor axis during in vitro differentiation of the human osteosarcoma cell line HOS 58Volker Viereck, Heide Siggelkow, Rajeswararao Pannem, et al.
Biochemical and Biophysical Research Communications|May 3, 2003
In vivo processed fragments of IGF binding protein-2 copurified with bioactive IGF-IILudger Ständker, Bernd Kübler, Maik Obendorf, et al.
Investigative Ophthalmology & Visual Science|October 3, 2013
Apoptotic photoreceptor loss and altered expression of lysosomal proteins in the nclf mouse model of neuronal ceroid lipofuscinosisUdo Bartsch, Giovanna Galliciotti, Guillermo F Jofre, et al.
The Biochemical Journal|September 28, 2002
A replacement of the active-site aspartic acid residue 293 in mouse cathepsin D affects its intracellular stability, processing and transport in HEK-293 cellsSanna Partanen, Stephan Storch, Hans-Gerhard Löffler, et al.
The Journal of Biological Chemistry|April 2, 2011
Glutaric aciduria type 1 metabolites impair the succinate transport from astrocytic to neuronal cellsJessica Lamp, Britta Keyser, David M Koeller, et al.
Biochimica Et Biophysica Acta|February 14, 2013
Cell biology and function of neuronal ceroid lipofuscinosis-related proteinsKatrin Kollmann, Kristiina Uusi-Rauva, Enzo Scifo, et al.
Human Mutation|December 19, 2009
Pathogenic mutations cause rapid degradation of lysosomal storage disease-related membrane protein CLN6Anna-Katherina Kurze, Giovanna Galliciotti, Claudia Heine, et al.
The Journal of Biological Chemistry|August 20, 2014
Molecular characterization of arylsulfatase G: expression, processing, glycosylation, transport, and activityBjörn Kowalewski, Torben Lübke, Katrin Kollmann, et al.
Human Molecular Genetics|September 9, 2008
Disease-causing missense mutations affect enzymatic activity, stability and oligomerization of glutaryl-CoA dehydrogenase (GCDH)Britta Keyser, Chris Mühlhausen, Achim Dickmanns, et al.
Pageof 11