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Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1991
Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patients
R J Wanders, M Casteels, G P Mannaerts, et al.
European Journal of Clinical Investigation
|
July 28, 2001
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency
P P Van Veldhoven, E Meyhi, R H Squires, et al.
Cellular and Molecular Life Sciences : CMLS
|
June 21, 2006
Thiamine pyrophosphate: an essential cofactor for the alpha-oxidation in mammals--implications for thiamine deficiencies?
M Sniekers, V Foulon, G P Mannaerts, et al.
Lipids
|
June 1, 2001
Oxidative catabolism of alpha-tocopherol in rat liver microsomes
H Van Houte, E De Hoffmann, P P Van Veldhoven, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation
L Van Maldergem, M Espeel, R J Wanders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Di- and trihydroxycholestanaemia in twin sisters
R J Wanders, C W van Roermund, A Schelen, et al.
European Journal of Biochemistry
|
September 15, 1996
Further characterization of the peroxisomal 3-hydroxyacyl-CoA dehydrogenases from rat liver. Relationship between the different dehydrogenases and evidence that fatty acids and the C27 bile acids di- and tri-hydroxycoprostanic acids are metabolized by separate multifunctional proteins
M Dieuaide-Noubhani, D Novikov, E Baumgart, et al.
European Journal of Biochemistry
|
July 15, 1996
Rat pristanoyl-CoA oxidase. cDNA cloning and recognition of its C-terminal (SQL) by the peroxisomal-targeting signal 1 receptor
J C Vanhooren, M Fransen, B de Béthune, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 26, 1996
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome
E Baumgart, J C Vanhooren, M Fransen, et al.
Journal of Neuropathology and Experimental Neurology
|
April 10, 2002
The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation
M Baes, P Gressens, S Huyghe, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 143) with videos related to
Sort By:
Page
of 15
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 31, 1991
Accumulation and impaired in vivo metabolism of di- and trihydroxycholestanoic acid in two patients
R J Wanders, M Casteels, G P Mannaerts, et al.
European Journal of Clinical Investigation
|
July 28, 2001
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency
P P Van Veldhoven, E Meyhi, R H Squires, et al.
Cellular and Molecular Life Sciences : CMLS
|
June 21, 2006
Thiamine pyrophosphate: an essential cofactor for the alpha-oxidation in mammals--implications for thiamine deficiencies?
M Sniekers, V Foulon, G P Mannaerts, et al.
Lipids
|
June 1, 2001
Oxidative catabolism of alpha-tocopherol in rat liver microsomes
H Van Houte, E De Hoffmann, P P Van Veldhoven, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal beta-oxidation
L Van Maldergem, M Espeel, R J Wanders, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1991
Di- and trihydroxycholestanaemia in twin sisters
R J Wanders, C W van Roermund, A Schelen, et al.
European Journal of Biochemistry
|
September 15, 1996
Further characterization of the peroxisomal 3-hydroxyacyl-CoA dehydrogenases from rat liver. Relationship between the different dehydrogenases and evidence that fatty acids and the C27 bile acids di- and tri-hydroxycoprostanic acids are metabolized by separate multifunctional proteins
M Dieuaide-Noubhani, D Novikov, E Baumgart, et al.
European Journal of Biochemistry
|
July 15, 1996
Rat pristanoyl-CoA oxidase. cDNA cloning and recognition of its C-terminal (SQL) by the peroxisomal-targeting signal 1 receptor
J C Vanhooren, M Fransen, B de Béthune, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 26, 1996
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome
E Baumgart, J C Vanhooren, M Fransen, et al.
Journal of Neuropathology and Experimental Neurology
|
April 10, 2002
The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation
M Baes, P Gressens, S Huyghe, et al.
Page
of 15