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

T Hennet

Showing results (21-30 of 31) with videos related to

Pageof 4
Sort By:
Proceedings of the National Academy of Sciences of the United States of America|January 20, 1999
A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferasesD Zhou, A Dinter, R Gutiérrez Gallego, et al.
Free Radical Research|August 1, 1996
TNF alpha alters mitochondrial membrane potential in L929 but not in TNF alpha-resistant L929.12 cells: relationship with the expression of stress proteins, annexin 1 and superoxide dismutase activityB S Polla, M R Jacquier-Sarlin, S Kantengwa, et al.
Journal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literatureM Di Rocco, T Hennet, C E Grubenmann, et al.
Human Genetics|July 29, 2000
Multi-allelic origin of congenital disorder of glycosylation (CDG)-IcT Imbach, S Grünewald, B Schenk, et al.
Journal of Medical Genetics|July 6, 2004
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)E Schollen, C G Frank, L Keldermans, et al.
The Journal of Clinical Investigation|January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type IeT Imbach, B Schenk, E Schollen, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patientM T García-Silva, G Matthijs, E Schollen, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Proceedings of the National Academy of Sciences of the United States of America|January 20, 1999
A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferasesD Zhou, A Dinter, R Gutiérrez Gallego, et al.
Free Radical Research|August 1, 1996
TNF alpha alters mitochondrial membrane potential in L929 but not in TNF alpha-resistant L929.12 cells: relationship with the expression of stress proteins, annexin 1 and superoxide dismutase activityB S Polla, M R Jacquier-Sarlin, S Kantengwa, et al.
Journal of Inherited Metabolic Disease|October 27, 2009
RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylationJ Jaeken, W Vleugels, L Régal, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
Congenital disorder of glycosylation (CDG) Ig: report on a patient and review of the literatureM Di Rocco, T Hennet, C E Grubenmann, et al.
Human Genetics|July 29, 2000
Multi-allelic origin of congenital disorder of glycosylation (CDG)-IcT Imbach, S Grünewald, B Schenk, et al.
Journal of Medical Genetics|July 6, 2004
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)E Schollen, C G Frank, L Keldermans, et al.
The Journal of Clinical Investigation|January 22, 2000
Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type IeT Imbach, B Schenk, E Schollen, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Congenital disorder of glycosylation (CDG) type Ie. A new patientM T García-Silva, G Matthijs, E Schollen, et al.
The Journal of Clinical Investigation|December 26, 2001
MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfB Schenk, T Imbach, C G Frank, et al.
Annals of Neurology|June 14, 2000
Clinical and biochemical characteristics of congenital disorder of glycosylation type Ic, the first recognized endoplasmic reticulum defect in N-glycan synthesisS Grünewald, T Imbach, K Huijben, et al.
Pageof 4