Search research articles
Contact Us
Filters
Showing results (221-230 of 497) with videos related to
Page
of 50
Sort By:
Biochimie
|
January 1, 1993
Postnatal diagnosis of peroxisomal disorders: a biochemical approach
R J Wanders, R B Schutgens, P G Barth, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase
H J ten Brink, B T Poll-The, J M Saudubray, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 6, 2000
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle
W Röschinger, A C Muntau, M Duran, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2001
Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes
G A Jansen, D M van den Brink, R Ofman, et al.
European Journal of Cell Biology
|
June 29, 1999
Immunological analyses of alkyl-dihydroxyacetone-phosphate synthase in human peroxisomal disorders
J Biermann, J Gootjes, B M Humbel, et al.
The EMBO Journal
|
November 2, 1999
Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carnitine transporter, Agp2p
C W van Roermund, E H Hettema, M van den Berg, et al.
The Journal of Cell Biology
|
August 10, 2000
Pex11p plays a primary role in medium-chain fatty acid oxidation, a process that affects peroxisome number and size in Saccharomyces cerevisiae
C W van Roermund, H F Tabak, M van Den Berg, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: high frequency of 3 mutations in the mevalonate kinase gene
S M Houten, J Frenkel, W Kuis, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
A far advanced case of gyrate atrophy in a 12-year-old girl
H D Bakker, N G Abeling, M J van Schooneveld, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Di- and trihydroxycholestanoic acidaemia with hepatic failure
H Przyrembel, R J Wanders, C W van Roermund, et al.
Page
of 50
Search research articles
Search
Showing results (221-230 of 497) with videos related to
Sort By:
Page
of 50
Biochimie
|
January 1, 1993
Postnatal diagnosis of peroxisomal disorders: a biochemical approach
R J Wanders, R B Schutgens, P G Barth, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Pristanic acid does not accumulate in peroxisomal acyl-CoA oxidase deficiency: evidence for a distinct peroxisomal pristanyl-CoA oxidase
H J ten Brink, B T Poll-The, J M Saudubray, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 6, 2000
Carnitine-acylcarnitine translocase deficiency: metabolic consequences of an impaired mitochondrial carnitine cycle
W Röschinger, A C Muntau, M Duran, et al.
Biochemical and Biophysical Research Communications
|
May 9, 2001
Identification of pristanal dehydrogenase activity in peroxisomes: conclusive evidence that the complete phytanic acid alpha-oxidation pathway is localized in peroxisomes
G A Jansen, D M van den Brink, R Ofman, et al.
European Journal of Cell Biology
|
June 29, 1999
Immunological analyses of alkyl-dihydroxyacetone-phosphate synthase in human peroxisomal disorders
J Biermann, J Gootjes, B M Humbel, et al.
The EMBO Journal
|
November 2, 1999
Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carnitine transporter, Agp2p
C W van Roermund, E H Hettema, M van den Berg, et al.
The Journal of Cell Biology
|
August 10, 2000
Pex11p plays a primary role in medium-chain fatty acid oxidation, a process that affects peroxisome number and size in Saccharomyces cerevisiae
C W van Roermund, H F Tabak, M van Den Berg, et al.
Journal of Inherited Metabolic Disease
|
July 15, 2000
Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: high frequency of 3 mutations in the mevalonate kinase gene
S M Houten, J Frenkel, W Kuis, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
A far advanced case of gyrate atrophy in a 12-year-old girl
H D Bakker, N G Abeling, M J van Schooneveld, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Di- and trihydroxycholestanoic acidaemia with hepatic failure
H Przyrembel, R J Wanders, C W van Roermund, et al.
Page
of 50