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

G A Jansen

Showing results (1-10 of 32) with videos related to

Pageof 4
Sort By:
Anesthesiology|February 1, 1975
A new six-way stopcockG A Jansen
Southern Medical Journal|September 1, 1971
Rapid method for simultaneous qualitative assay of narcotics, cocaine, quinine and propoxyphene in the urineG A Jansen, I Bickers
Journal of Inherited Metabolic Disease|March 1, 1997
Plasmalogens and oxidative stress: evidence against a major role of plasmalogens in protection against the superoxide anion radicalG A Jansen, R J Wanders
Biochimica Et Biophysica Acta|November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemiaG A Jansen, R J Wanders
Anesthesiology|March 1, 1970
Morphine metabolism and morphine tolerance in goldfishG A Jansen, N M Greene
Journal of Neuropathology and Experimental Neurology|November 15, 2001
Refsum disease, peroxisomes and phytanic acid oxidation: a reviewR J Wanders, G A Jansen, O H Skjeldal
Biochemical Society Transactions|May 18, 2000
Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid alpha- and beta-oxidation systems in humansR J Wanders, E G van Grunsven, G A Jansen
Archives of Disease in Childhood|November 26, 1997
Increased plasma malondialdehyde associated with cerebellar structural defectsV T Ramaekers, B Bosman, G A Jansen, et al.
The New England Journal of Medicine|July 10, 1997
Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's diseaseG A Jansen, R J Wanders, P A Watkins, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Phytanic acid alpha-oxidation in man: identification of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal enzyme with normal activity in Zellweger syndromeG A Jansen, S Denis, N M Verhoeven, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Anesthesiology|February 1, 1975
A new six-way stopcockG A Jansen
Southern Medical Journal|September 1, 1971
Rapid method for simultaneous qualitative assay of narcotics, cocaine, quinine and propoxyphene in the urineG A Jansen, I Bickers
Journal of Inherited Metabolic Disease|March 1, 1997
Plasmalogens and oxidative stress: evidence against a major role of plasmalogens in protection against the superoxide anion radicalG A Jansen, R J Wanders
Biochimica Et Biophysica Acta|November 25, 1993
L-2-hydroxyglutarate dehydrogenase: identification of a novel enzyme activity in rat and human liver. Implications for L-2-hydroxyglutaric acidemiaG A Jansen, R J Wanders
Anesthesiology|March 1, 1970
Morphine metabolism and morphine tolerance in goldfishG A Jansen, N M Greene
Journal of Neuropathology and Experimental Neurology|November 15, 2001
Refsum disease, peroxisomes and phytanic acid oxidation: a reviewR J Wanders, G A Jansen, O H Skjeldal
Biochemical Society Transactions|May 18, 2000
Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid alpha- and beta-oxidation systems in humansR J Wanders, E G van Grunsven, G A Jansen
Archives of Disease in Childhood|November 26, 1997
Increased plasma malondialdehyde associated with cerebellar structural defectsV T Ramaekers, B Bosman, G A Jansen, et al.
The New England Journal of Medicine|July 10, 1997
Phytanoyl-coenzyme A hydroxylase deficiency -- the enzyme defect in Refsum's diseaseG A Jansen, R J Wanders, P A Watkins, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Phytanic acid alpha-oxidation in man: identification of 2-hydroxyphytanoyl-CoA lyase, a peroxisomal enzyme with normal activity in Zellweger syndromeG A Jansen, S Denis, N M Verhoeven, et al.
Pageof 4