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Journal of Inherited Metabolic Disease
|
June 29, 1999
Molecular basis of Sjögren-Larsson syndrome: frequency of the 1297-1298 del GA and 943C-->T mutation in 29 patients
L Ijlst, W Oostheim, M van Werkhoven, et al.
Annual Review of Biochemistry
|
January 1, 1992
Biochemistry of peroxisomes
H van den Bosch, R B Schutgens, R J Wanders, et al.
Clinical Genetics
|
February 1, 1986
Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome
E M Bleeker-Wagemakers, J W Oorthuys, R J Wanders, et al.
Biochemical and Biophysical Research Communications
|
December 5, 1998
The structure and organization of the human carnitine/acylcarnitine translocase (CACT1) gene2
V Iacobazzi, M A Naglieri, C A Stanley, 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 syndrome
G A Jansen, S Denis, N M Verhoeven, et al.
European Journal of Biochemistry
|
July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondria
R J Wanders, A K Groen, C W Van Roermund, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
H Przyrembel, C Jakobs, L IJlst, et al.
Biochemistry International
|
September 1, 1989
Studies on the formation of lactate and pyruvate from glucose in cultured skin fibroblasts: implications for detection of respiratory chain defects
F A Wijburg, N Feller, H R Scholte, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Signals on proteins, intracellular targeting and inborn errors of organellar metabolism
J M Tager, J M Aerts, C van den Bogert, et al.
The Journal of Biological Chemistry
|
March 4, 2000
Molecular and biochemical characterization of rat gamma-trimethylaminobutyraldehyde dehydrogenase and evidence for the involvement of human aldehyde dehydrogenase 9 in carnitine biosynthesis
F M Vaz, S W Fouchier, R Ofman, et al.
Page
of 50
Search research articles
Search
Showing results (121-130 of 497) with videos related to
Sort By:
Page
of 50
Journal of Inherited Metabolic Disease
|
June 29, 1999
Molecular basis of Sjögren-Larsson syndrome: frequency of the 1297-1298 del GA and 943C-->T mutation in 29 patients
L Ijlst, W Oostheim, M van Werkhoven, et al.
Annual Review of Biochemistry
|
January 1, 1992
Biochemistry of peroxisomes
H van den Bosch, R B Schutgens, R J Wanders, et al.
Clinical Genetics
|
February 1, 1986
Long term survival of a patient with the cerebro-hepato-renal (Zellweger) syndrome
E M Bleeker-Wagemakers, J W Oorthuys, R J Wanders, et al.
Biochemical and Biophysical Research Communications
|
December 5, 1998
The structure and organization of the human carnitine/acylcarnitine translocase (CACT1) gene2
V Iacobazzi, M A Naglieri, C A Stanley, 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 syndrome
G A Jansen, S Denis, N M Verhoeven, et al.
European Journal of Biochemistry
|
July 16, 1984
Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondria
R J Wanders, A K Groen, C W Van Roermund, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
H Przyrembel, C Jakobs, L IJlst, et al.
Biochemistry International
|
September 1, 1989
Studies on the formation of lactate and pyruvate from glucose in cultured skin fibroblasts: implications for detection of respiratory chain defects
F A Wijburg, N Feller, H R Scholte, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Signals on proteins, intracellular targeting and inborn errors of organellar metabolism
J M Tager, J M Aerts, C van den Bogert, et al.
The Journal of Biological Chemistry
|
March 4, 2000
Molecular and biochemical characterization of rat gamma-trimethylaminobutyraldehyde dehydrogenase and evidence for the involvement of human aldehyde dehydrogenase 9 in carnitine biosynthesis
F M Vaz, S W Fouchier, R Ofman, et al.
Page
of 50