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Thomas Braulke

Showing results (41-50 of 106) with videos related to

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Carbohydrate Research|March 7, 2006
In vitro sulfation of N-acetyllactosaminide by soluble recombinant human beta-Gal-3'-sulfotransferaseP Greimel, Sabrina Jabs, Stefan Storch, et al.
Pediatrics|October 17, 2007
Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A)Ann Meyer, Kai Kossow, Andreas Gal, et al.
Journal of Neurochemistry|September 18, 2007
Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissueSandra Pohl, Hannah M Mitchison, Alfried Kohlschütter, et al.
Traffic (Copenhagen, Denmark)|July 30, 2015
Mannose 6-phosphate-independent Lysosomal Sorting of LIMP-2Judith Blanz, Friederike Zunke, Sandra Markmann, et al.
Human Molecular Genetics|September 20, 2015
Subunit interactions of the disease-related hexameric GlcNAc-1-phosphotransferase complexRaffaella De Pace, Renata Voltolini Velho, Marisa Encarnação, et al.
Plos One|September 21, 2011
N-glycans and glycosylphosphatidylinositol-anchor act on polarized sorting of mouse PrP(C) in Madin-Darby canine kidney cellsBerta Puig, Hermann C Altmeppen, Dana Thurm, et al.
Nature Medicine|October 4, 2005
Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferaseStephan Tiede, Stephan Storch, Torben Lübke, et al.
Endocrinology|April 9, 2004
Insulin-like growth factor (IGF)-binding protein-1 is highly induced during acute carbon tetrachloride liver injury and potentiates the IGF-I-stimulated activation of rat hepatic stellate cellsJens-Gerd Scharf, Frank Dombrowski, Ruslan Novosyadlyy, et al.
FEBS Letters|January 22, 2002
Decreased intracellular degradation of insulin-like growth factor binding protein-3 in cathepsin L-deficient fibroblastsOlaf Zwad, Bernd Kübler, Wera Roth, et al.
Human Mutation|November 9, 2004
A novel mutation in UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) in two siblings with mucolipidosis type III alters a used glycosylation siteStephan Tiede, Michael Cantz, Annick Raas-Rothschild, et al.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Carbohydrate Research|March 7, 2006
In vitro sulfation of N-acetyllactosaminide by soluble recombinant human beta-Gal-3'-sulfotransferaseP Greimel, Sabrina Jabs, Stefan Storch, et al.
Pediatrics|October 17, 2007
Scoring evaluation of the natural course of mucopolysaccharidosis type IIIA (Sanfilippo syndrome type A)Ann Meyer, Kai Kossow, Andreas Gal, et al.
Journal of Neurochemistry|September 18, 2007
Increased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissueSandra Pohl, Hannah M Mitchison, Alfried Kohlschütter, et al.
Traffic (Copenhagen, Denmark)|July 30, 2015
Mannose 6-phosphate-independent Lysosomal Sorting of LIMP-2Judith Blanz, Friederike Zunke, Sandra Markmann, et al.
Human Molecular Genetics|September 20, 2015
Subunit interactions of the disease-related hexameric GlcNAc-1-phosphotransferase complexRaffaella De Pace, Renata Voltolini Velho, Marisa Encarnação, et al.
Plos One|September 21, 2011
N-glycans and glycosylphosphatidylinositol-anchor act on polarized sorting of mouse PrP(C) in Madin-Darby canine kidney cellsBerta Puig, Hermann C Altmeppen, Dana Thurm, et al.
Nature Medicine|October 4, 2005
Mucolipidosis II is caused by mutations in GNPTA encoding the alpha/beta GlcNAc-1-phosphotransferaseStephan Tiede, Stephan Storch, Torben Lübke, et al.
Endocrinology|April 9, 2004
Insulin-like growth factor (IGF)-binding protein-1 is highly induced during acute carbon tetrachloride liver injury and potentiates the IGF-I-stimulated activation of rat hepatic stellate cellsJens-Gerd Scharf, Frank Dombrowski, Ruslan Novosyadlyy, et al.
FEBS Letters|January 22, 2002
Decreased intracellular degradation of insulin-like growth factor binding protein-3 in cathepsin L-deficient fibroblastsOlaf Zwad, Bernd Kübler, Wera Roth, et al.
Human Mutation|November 9, 2004
A novel mutation in UDP-N-acetylglucosamine-1-phosphotransferase gamma subunit (GNPTAG) in two siblings with mucolipidosis type III alters a used glycosylation siteStephan Tiede, Michael Cantz, Annick Raas-Rothschild, et al.
Pageof 11