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Anke Penno

Showing results (1-10 of 16) with videos related to

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Biochimica Et Biophysica Acta|December 19, 2012
Phospholipids and lipid dropletsAnke Penno, Gregor Hackenbroich, Christoph Thiele
Journal of Lipid Research|August 28, 2016
A highly sensitive protocol for microscopy of alkyne lipids and fluorescently tagged or immunostained proteinsAnne Gaebler, Anke Penno, Lars Kuerschner, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|July 31, 2019
Brain endothelial specific gene therapy improves experimental Sandhoff diseaseGodwin Dogbevia, Hanna Grasshoff, Alaa Othman, et al.
Journal of Lipid Research|February 3, 2009
An improved method to determine serine palmitoyltransferase activityMarkus F Rütti, Stéphane Richard, Anke Penno, et al.
Journal of Lipid Research|November 23, 2016
Cytotoxic 1-deoxysphingolipids are metabolized by a cytochrome P450-dependent pathwayIrina Alecu, Alaa Othman, Anke Penno, et al.
The Journal of Biological Chemistry|August 4, 2009
The SPTLC3 subunit of serine palmitoyltransferase generates short chain sphingoid basesThorsten Hornemann, Anke Penno, Markus F Rütti, et al.
Autophagy|August 25, 2020
1-Deoxysphingolipids cause autophagosome and lysosome accumulation and trigger NLRP3 inflammasome activationMario A Lauterbach, Victor Saavedra, Matthew S J Mangan, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
The Journal of Clinical Investigation|November 3, 2011
Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1Kevin Garofalo, Anke Penno, Brian P Schmidt, et al.
Human Mutation|May 28, 2011
Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type IAnnelies Rotthier, Anke Penno, Bernd Rautenstrauss, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Biochimica Et Biophysica Acta|December 19, 2012
Phospholipids and lipid dropletsAnke Penno, Gregor Hackenbroich, Christoph Thiele
Journal of Lipid Research|August 28, 2016
A highly sensitive protocol for microscopy of alkyne lipids and fluorescently tagged or immunostained proteinsAnne Gaebler, Anke Penno, Lars Kuerschner, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|July 31, 2019
Brain endothelial specific gene therapy improves experimental Sandhoff diseaseGodwin Dogbevia, Hanna Grasshoff, Alaa Othman, et al.
Journal of Lipid Research|February 3, 2009
An improved method to determine serine palmitoyltransferase activityMarkus F Rütti, Stéphane Richard, Anke Penno, et al.
Journal of Lipid Research|November 23, 2016
Cytotoxic 1-deoxysphingolipids are metabolized by a cytochrome P450-dependent pathwayIrina Alecu, Alaa Othman, Anke Penno, et al.
The Journal of Biological Chemistry|August 4, 2009
The SPTLC3 subunit of serine palmitoyltransferase generates short chain sphingoid basesThorsten Hornemann, Anke Penno, Markus F Rütti, et al.
Autophagy|August 25, 2020
1-Deoxysphingolipids cause autophagosome and lysosome accumulation and trigger NLRP3 inflammasome activationMario A Lauterbach, Victor Saavedra, Matthew S J Mangan, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
The Journal of Clinical Investigation|November 3, 2011
Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1Kevin Garofalo, Anke Penno, Brian P Schmidt, et al.
Human Mutation|May 28, 2011
Characterization of two mutations in the SPTLC1 subunit of serine palmitoyltransferase associated with hereditary sensory and autonomic neuropathy type IAnnelies Rotthier, Anke Penno, Bernd Rautenstrauss, et al.
Pageof 2