Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Anke Penno

Showing results (11-20 of 16) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 16 results.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Neuromolecular Medicine|January 9, 2015
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificityDaniela Ernst, Sinéad M Murphy, Karthik Sathiyanadan, et al.
The Journal of Biological Chemistry|March 5, 2017
Identification of a feedback loop involving β-glucosidase 2 and its product sphingosine sheds light on the molecular mechanisms in Gaucher diseaseSophie Schonauer, Heinz G Körschen, Anke Penno, et al.
Journal of Lipid Research|November 25, 2016
Localization of 1-deoxysphingolipids to mitochondria induces mitochondrial dysfunctionIrina Alecu, Andrea Tedeschi, Natascha Behler, et al.
American Journal of Human Genetics|October 6, 2010
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type IAnnelies Rotthier, Michaela Auer-Grumbach, Katrien Janssens, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 20, 2009
Overexpression of the wild-type SPT1 subunit lowers desoxysphingolipid levels and rescues the phenotype of HSAN1Florian S Eichler, Thorsten Hornemann, Alex McCampbell, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
The Journal of Biological Chemistry|January 26, 2010
Hereditary sensory neuropathy type 1 is caused by the accumulation of two neurotoxic sphingolipidsAnke Penno, Mary M Reilly, Henry Houlden, et al.
Neuromolecular Medicine|January 9, 2015
Novel HSAN1 mutation in serine palmitoyltransferase resides at a putative phosphorylation site that is involved in regulating substrate specificityDaniela Ernst, Sinéad M Murphy, Karthik Sathiyanadan, et al.
The Journal of Biological Chemistry|March 5, 2017
Identification of a feedback loop involving β-glucosidase 2 and its product sphingosine sheds light on the molecular mechanisms in Gaucher diseaseSophie Schonauer, Heinz G Körschen, Anke Penno, et al.
Journal of Lipid Research|November 25, 2016
Localization of 1-deoxysphingolipids to mitochondria induces mitochondrial dysfunctionIrina Alecu, Andrea Tedeschi, Natascha Behler, et al.
American Journal of Human Genetics|October 6, 2010
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type IAnnelies Rotthier, Michaela Auer-Grumbach, Katrien Janssens, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 20, 2009
Overexpression of the wild-type SPT1 subunit lowers desoxysphingolipid levels and rescues the phenotype of HSAN1Florian S Eichler, Thorsten Hornemann, Alex McCampbell, et al.
Pageof 2