Topography of very-long-chain-fatty-acid-activating activity in peroxisomes from rat liver.

Por Lageweg, W, Tager, J M, Wanders, R J
Publicado em 1991

Increased plasma malondialdehyde associated with cerebellar structural defects

Por Ramaekers, V, Bosman, B, Jansen, G, Wanders, R
Publicado em 1997

A new defect of peroxisomal function involving pristanic acid: a case report

Por McLean, B, Allen, J, Ferdinandusse, S, Wanders, R
Publicado em 2002

Incidence and molecular mechanism of aberrant splicing owing to a G→C splice acceptor site mutation causing Smith-Lemli-Opitz syndrome

Por WATERHAM, H, OOSTHEIM, W, ROMEIJN, G, WANDERS, R, HENNEKAM, R
Publicado em 2000

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy

Por van Geel, B. M, Assies, J., Wanders, R., Barth, P.
Publicado em 1997

Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients.

Por Kamijo, T, Wanders, R J, Saudubray, J M, Aoyama, T, Komiyama, A, Hashimoto, T
Publicado em 1994

Novel genotype of mevalonic aciduria with fatalities in premature siblings

Por Raupp, P, Varady, E, Duran, M, Wanders, R, Waterham, H, Houten, S
Publicado em 2004

Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits.

Por Ushikubo, S., Aoyama, T., Kamijo, T., Wanders, R. J., Rinaldo, P., Vockley, J., Hashimoto, T.
Publicado em 1996

Peroxisomal and mitochondrial carnitine acetyltransferases of Saccharomyces cerevisiae are encoded by a single gene.

Por Elgersma, Y, van Roermund, C W, Wanders, R J, Tabak, H F
Publicado em 1995

Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect.

Por Shimozawa, N, Suzuki, Y, Orii, T, Moser, A, Moser, H W, Wanders, R J
Publicado em 1993

The membrane of peroxisomes in Saccharomyces cerevisiae is impermeable to NAD(H) and acetyl-CoA under in vivo conditions.

Por van Roermund, C W, Elgersma, Y, Singh, N, Wanders, R J, Tabak, H F
Publicado em 1995

Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA an...

Por IJlst, L, Ruiter, J P, Hoovers, J M, Jakobs, M E, Wanders, R J
Publicado em 1996

Molecular basis of hepatic carnitine palmitoyltransferase I deficiency.

Por IJlst, L, Mandel, H, Oostheim, W, Ruiter, J P, Gutman, A, Wanders, R J
Publicado em 1998

PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders.

Por Liu, Y, Björkman, J, Urquhart, A, Wanders, R J, Crane, D I, Gould, S J
Publicado em 1999

High tolerance for oral galactose in classical galactosaemia: dietary implications

Por Bosch, A, Bakker, H, de B, Wenniger-Pri... L J M, Wanders, R, Wijburg, F
Publicado em 2004

Rhizomelic chondrodysplasia punctata with isolated DHAP-AT deficiency.

Por Barr, D G, Kirk, J M, al Howasi, M, Wanders, R J, Schutgens, R B
Publicado em 1993

A new peroxisomal disorder with fetal and neonatal adrenal insufficiency.

Por Vanhole, C, de Zegher, F, Casaer, P, Devlieger, H, Wanders, R J, Vanhove, G, Jaeken, J
Publicado em 1994

Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil"

Por van Geel, B M, Assies, J, Haverkort, E, Koelman, J, Verbeeten, B, Wanders, R, Barth, P
Publicado em 1999

Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carni...

Por van Roermund, C W, Hettema, E H, van den Berg, M, Tabak, H F, Wanders, R J
Publicado em 1999

High-affinity binding of very-long-chain fatty acyl-CoA esters to the peroxisomal non-specific lipid-transfer protein (sterol carrier protein-2).

Por Dansen, T B, Westerman, J, Wouters, F S, Wanders, R J, van Hoek, A, Gadella, T W, Wirtz, K W
Publicado em 1999