Spectrophotometric Assay for Complex I of the Respiratory Chain in Tissue Samples and Cultured Fibroblasts von Janssen, Antoon J.M, Trijbels, Frans J.M, Sengers, Rob C.A, Smeitink, Jan A.M, van den Heuvel, Lambert P, Wintjes, Liesbeth T.M, Stoltenborg-Hogenkamp, Berendien J.M, Rodenburg, Richard J.T

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A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk von LIEVERS, Karin J. A, BOERS, Godfried H. J, VERHOEF, Petra, DEN HEIJER, Martin, KLUIJTMANS, Leo A. J, VAN DER PUT, Nathalie M. J, TRIJBELS, Frans J. M, BLOM, Henk J

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Measurement of the Energy-Generating Capacity of Human Muscle Mitochondria: Diagnostic Procedure and Application to Human Pathology von Janssen, Antoon J.M, Trijbels, Frans J.M, Sengers, Rob C.A, Wintjes, Liesbeth T.M, Ruitenbeek, Wim, Smeitink, Jan A.M, Morava, Eva, van Engelen, Baziel G.M, van den Heuvel, Lambert P, Rodenburg, Richard J.T

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Effect of the methylenetetrahydrofolate reductase 677C→T mutation on the relations among folate intake and plasma folate and homocysteine concentrations in a general population sam... von DE BREE, Angelika, VERSCHUREN, W. M, BJØRKE-MONSEN, Anne-Lise, VAN DER PUT, Nathalie M. J, HEIL, Sandra G, TRIJBELS, Frans J. M, BLOM, Henk J

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Cytochrome c oxidase biogenesis in a patient with a mutation in COX10 gene von Coenen, Marieke J. H., van den Heuvel, Lambert P., Ugalde, Cristina, ten Brinke, Marike, Nijtmans, Leo G. J., Trijbels, Frans J. M., Beblo, Skadi, Maier, Esther M., Muntau, Ania C., Smeitink, Jan A. M.

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Muscle 3243A→G mutation load and capacity of the mitochondrial energy-generating system von Janssen, Antoon J. M., Schuelke, Markus, Smeitink, Jan A. M., Trijbels, Frans J. M., Sengers, Rob C. A., Lucke, Barbara, Wintjes, Liesbeth T. M., Morava, Eva, van Engelen, Baziel G. M., Smits, Bart W., Hol, Frans A., Siers, Marloes H., Ter Laak, Henk, van der Knaap, Marjo S., Van Spronsen, Francjan J., Rodenburg, Richard J. T., van den Heuvel, Lambert P.

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Polymorphisms in the Transcobalamin Gene: Association with Plasma Homocysteine in Healthy Individuals and Vascular Disease Patients von Lievers, Karin J.A, Afman, Lydia A, Kluijtmans, Leo A.J, Boers, Godfried H.J, Verhoef, Petra, den Heijer, Martin, Trijbels, Frans J.M, Blom, Henk J

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Molecular beacons: a new approach for semiautomated mutation analysis von Giesendorf, Belinda A. J, Vet, Jacqueline A. M, Tyagi, Sanjay, Mensink, Ewald J. M. G, Trijbels, Frans J. M, Blom, Henk J

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Succinate in dystrophic white matter: A proton magnetic resonance spectroscopy finding characteristic for complex II deficiency von Brockmann, Knut, Bjornstad, Alf, Dechent, Peter, Korenke, Christoph G., Smeitink, Jan, Trijbels, J. M. Frans, Athanassopoulos, Sabine, Villagran, Rafael, Skjeldal, Ola H., Wilichowski, Ekkehard, Frahm, Jens, Hanefeld, Folker

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Coronary heart disease mortality, plasma homocysteine, and B-vitamins: a prospective study von de Bree, Angelika, Verschuren, W.Monique M., Blom, Henk J., Nadeau, Marie, Trijbels, Frans J.M., Kromhout, Daan

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The H475Y Polymorphism in the Glutamate Carboxypeptidase II Gene Increases Plasma Folate without Affecting the Risk for Neural Tube Defects in Humans von Afman, Lydia A., Trijbels, Frans J.M., Blom, Henk J.

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Human mitochondrial transmembrane metabolite carriers: tissue distribution and its implication for mitochondrial disorders von Huizing, M, Ruitenbeek, W, van den Heuvel, L P, Dolce, V, Iacobazzi, V, Smeitink, J A, Palmieri, F, Trijbels, J M

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Adenine nucleotide translocator 1 deficiency associated with Sengers syndrome von Jordens, Eric Z., Palmieri, Luigi, Huizing, Marjan, Van Den Heuvel, Lambert P., Sengers, Rob C. A., Dörner, Andrea, Ruitenbeek, Wim, Trijbels, Frans J., Valsson, Jullius, Sigfusson, Gunnlaugur, Palmieri, Ferdinando, Smeitink, Jan A. M.

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Thiopurine methyltransferase in acute lymphoblastic leukaemia: biochemical and molecular biological aspects von Brouwer, Connie, De Abreu, Ronney A., Keizer-Garritsen, Jenneke J., Lambooy, Lambert H.J., Ament, Kai, ter Riet, Patricia G.J.H., van Wering, Elisabeth R., Trijbels, Frans J.M., Veerman, Anjo J.P., Hoogerbrugge, Peter M., Bökkerink, Jos P.M.

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Thermolabile methylenetetrahydrofolate reductase in coronary artery disease von KLUIJTMANS, L. A. J, KASTELEIN, J. J. P, VERHEUGT, F. W. A, WILLEMS, F, BLOM, H. J, LINDEMANS, J, BOERS, G. H. J, HEIL, S. G, BRUSCHKE, A. V. G, JUKEMA, J. W, VAN DEN HEUVEL, L. P. W. J, TRIJBELS, F. J. M, BOERMA, G. J. M

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Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency von Coenen, Marieke J.H, Antonicka, Hana, Ugalde, Cristina, Sasarman, Florin, Rossi, Rainer, Heister, J.G.A.M. Angelien, Newbold, Robert F, Trijbels, Frans J.M.F, van den Heuvel, Lambert P, Shoubridge, Eric A, Smeitink, Jan A.M

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Monitoring of inosine monophosphate dehydrogenase activity in mononuclear cells of children with acute lymphoblastic leukemia: Enzymological and clinical aspects von Brouwer, Connie, Vermunt-de Koning, Diana G.M., Trueworthy, Robert C., ter Riet, Patricia G.J.H., Duley, John A., Trijbels, Frans J.M., Hoogerbrugge, Peter M., Bökkerink, Jos P.M., van Wering, Elisabeth R., De Abreu, Ronney A.

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Semiautomated DNA Mutation Analysis Using a Robotic Workstation and Molecular Beacons von Smit, Maarten L, Giesendorf, Belinda A.J, Vet, Jacqueline A.M, Trijbels, Frans J.M, Blom, Henk J

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Cystathionine β-synthase polymorphisms and hyperhomocysteinaemia: an association study von LIEVERS, Karin J. A, KLUIJTMANS, Leo A. J, HEIL, Sandra G, BOERS, Godfried H. J, VERHOEF, Petra, DEN HEIJER, Martin, TRIJBELS, Frans J. M, BLOM, Henk J

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Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida von van der Put, N.M.J., Trijbels, F.J.M., van den Heuvel, L.P., Blom, H.J., Steegers-Theunissen, R.P.M., Eskes, T.K.A.B., Mariman, E.C.M., den Heyer, M., Frosst, P., Rozen, R.

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