Search Results - Wanders, Ronald
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Mice with a deficiency in Peroxisomal Membrane Protein 4 (PXMP4) display mild changes in hepatic lipid metabolism by Blankestijn, Maaike (Author) , Bloks, Vincent W. (Author) , Struik, Dicky (Author) , Huijkman, Nicolette (Author) , Kloosterhuis, Niels (Author) , Wolters, Justina C. (Author) , Wanders, Ronald J. A. (Author) , Vaz, Frédéric M. (Author) , Islinger, Markus (Author) , Kuipers, Folkert (Author) , van de Sluis, Bart (Author) , Groen, Albert K. (Author) , Verkade, Henkjan J. (Author) , Jonker, Johan W. (Author) ,
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Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia by Vaz, Frédéric (Author) , McDermott, John H. (Author) , Alders, Mariëlle (Author) , Wortmann, Saskia Brigitte (Author) , Kölker, Stefan (Author) , Pras-Raves, Mia L. (Author) , Vervaart, Martin A. T. (Author) , van Lenthe, Henk (Author) , Luyf, Angela C. M. (Author) , Elfrink, Hyung L. (Author) , Metcalfe, Kay (Author) , Cuvertino, Sara (Author) , Clayton, Peter E. (Author) , Yarwood, Rebecca (Author) , Lowe, Martin P. (Author) , Lovell, Simon (Author) , Rogers, Richard Curtis (Author) , van Kampen, Antoine H. C. (Author) , Ruiter, Jos P. N. (Author) , Wanders, Ronald J. A. (Author) , Ferdinandusse, Sacha (Author) , van Weeghel, Michel (Author) , Engelen, Marc (Author) , Banka, Siddharth (Author) ,
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Cardiac-specific succinate dehydrogenase deficiency in Barth syndrome by Dudek, Jan (Author) , Cheng, I-Fen (Author) , Chowdhury, Arpita (Author) , Wozny, Katharina (Author) , Balleininger, Martina (Author) , Reinhold, Robert (Author) , Grunau, Silke (Author) , Callegari, Sylvie (Author) , Toischer, Karl (Author) , Wanders, Ronald JA (Author) , Hasenfuß, Gerd (Author) , Brügger, Britta (Author) , Guan, Kaomei (Author) , Rehling, Peter (Author) ,
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Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination by Silva, Tiago (Author) , Eira, Jessica (Author) , Lopes, André T. (Author) , Malheiro, Ana R. (Author) , Sousa, Vera (Author) , Luoma, Adrienne (Author) , Avila, Robin L. (Author) , Wanders, Ronald J. A. (Author) , Just, Wilhelm W. (Author) , Kirschner, Daniel A. (Author) , Sousa, Mónica M. (Author) , Brites, Pedro (Author) ,
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Peroxisomal alterations in Alzheimer’s disease by Kou, Jianqiu (Author) , Kovacs, Gabor G. (Author) , Höftberger, Romana (Author) , Kulik, Willem (Author) , Brodde, Alexander (Author) , Forss-Petter, Sonja (Author) , Hönigschnabl, Selma (Author) , Gleiss, Andreas (Author) , Brügger, Britta (Author) , Wanders, Ronald (Author) , Just, Wilhelm (Author) , Budka, Herbert (Author) , Jungwirth, Susanne (Author) , Fischer, Peter (Author) , Berger, Johannes (Author) ,
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A non-enzymatic function of 17β-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival by Rauschenberger, Katharina (Author) , Schöler, Katja (Author) , Sass, Jörn Oliver (Author) , Sauer, Sven (Author) , Djuric, Zdenka (Author) , Rumig, Cordula (Author) , Wolf, Nicole I. (Author) , Okun, Jürgen G. (Author) , Kölker, Stefan (Author) , Schwarz, Heinz (Author) , Fischer, Christine (Author) , Grziwa, Beate (Author) , Runz, Heiko (Author) , Nümann, Astrid (Author) , Shafqat, Naeem (Author) , Kavanagh, Kathryn L. (Author) , Hämmerling, Günter J. (Author) , Wanders, Ronald J. A. (Author) , Shield, Julian P. H. (Author) , Wendel, Udo (Author) , Stern, David (Author) , Nawroth, Peter Paul (Author) , Hoffmann, Georg F. (Author) , Bartram, Claus R. (Author) , Arnold, Bernd (Author) , Bierhaus, Angelika (Author) , Oppermann, Udo (Author) , Steinbeisser, Herbert (Author) , Zschocke, Johannes (Author) ,
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Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrum by Prietsch, Viola (Author) , Mayatepek, Ertan (Author) , Krastel, Hermann (Author) , Haas, Dorothea (Author) , Zundel, Dorothee (Author) , Waterham, Hans R. (Author) , Wanders, Ronald J. A. (Author) , Gibson, K. Michael (Author) , Hoffmann, Georg F. (Author) ,
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A method for quantitative acylcarnitine profiling in human skin fibroblasts using unlabelled palmitic acid: diagnosis of fatty acid oxidation disorders and differentiation between... by Okun, Jürgen G. (Author) , Kölker, Stefan (Author) , Schulze, Andreas (Author) , Kohlmüller, Dirk (Author) , Vill, Katharina (Author) , Lindner, Martin (Author) , Hoffmann, Georg F. (Author) , Wanders, Ronald J. A (Author) , Mayatepek, Ertan (Author) ,
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Alkyl-dihydroxyacetone phosphate synthase and dihydroxyacetone phosphate acyltransferase form a protein complex in peroxisomes by Biermann, Jan (Author) , Just, Wilhelm W. (Author) , Wanders, Ronald J. A. (Author) , Bosch, Henk van den (Author) ,
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Related Subjects
Acylcarnitine profiling
Aging
Barth syndrome
Beta-oxidation
ERAB
Gene regulation
HSD10
Human skin fibroblast
Medium-chain acyl-CoA dehydrogenase deficiency
Neurofibrillary tangles
Palmitic acid
Peroxisome
Peroxisomes
Plasmalogen
Tandem-mass spectrometry
VLCFA
apoptosis
cardiolipin
cerebellar atrophy
hyperimmunoglobulinemia D and periodic fever syndrome
mevalonate kinase deficiency
mevalonic aciduria
mitochondria
neurodegeneration
organic aciduria
respiratory chain
retinal dystrophy
succinate dehydrogenase