The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesis

[1]  S. Ferdinandusse,et al.  The physiological functions of human peroxisomes. , 2022, Physiological reviews.

[2]  H. Waterham,et al.  Peroxisomal Metabolite and Cofactor Transport in Humans , 2021, Frontiers in Cell and Developmental Biology.

[3]  H. Waterham,et al.  Clinical, biochemical, and molecular characterization of mild (nonclassic) rhizomelic chondrodysplasia punctata , 2020, Journal of inherited metabolic disease.

[4]  G. Golderer,et al.  The TMEM189 gene encodes plasmanylethanolamine desaturase which introduces the characteristic vinyl ether double bond into plasmalogens , 2020, Proceedings of the National Academy of Sciences.

[5]  C. Argmann,et al.  Peroxisomes can oxidize medium‐ and long‐chain fatty acids through a pathway involving ABCD3 and HSD17B4 , 2018, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[6]  R. Wanders,et al.  Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophy. , 2017, Biochimica et biophysica acta. Molecular basis of disease.

[7]  Angela C. M. Luyf,et al.  Functional characterisation of peroxisomal β-oxidation disorders in fibroblasts using lipidomics , 2017, Journal of Inherited Metabolic Disease.

[8]  Angela C. M. Luyf,et al.  Lipidomic analysis of fibroblasts from Zellweger spectrum disorder patients identifies disease-specific phospholipid ratios[S] , 2016, Journal of Lipid Research.

[9]  R. Wanders,et al.  The Biochemistry and Physiology of Mitochondrial Fatty Acid β-Oxidation and Its Genetic Disorders. , 2016, Annual review of physiology.

[10]  J. Hiltunen,et al.  Peroxisomal Pex11 is a pore-forming protein homologous to TRPM channels. , 2016, Biochimica et biophysica acta.

[11]  A. Moser,et al.  A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3. , 2015, Human molecular genetics.

[12]  Feng Zhang,et al.  Genome engineering using CRISPR-Cas9 system. , 2015, Methods in molecular biology.

[13]  H. Waterham,et al.  A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acids. , 2014, Biochimica et biophysica acta.

[14]  C. Wiesinger,et al.  Impaired Very Long-chain Acyl-CoA β-Oxidation in Human X-linked Adrenoleukodystrophy Fibroblasts Is a Direct Consequence of ABCD1 Transporter Dysfunction* , 2013, The Journal of Biological Chemistry.

[15]  Günter P. Wagner,et al.  Measurement of mRNA abundance using RNA-seq data: RPKM measure is inconsistent among samples , 2012, Theory in Biosciences.

[16]  H. Waterham,et al.  Alkyl-Glycerol Rescues Plasmalogen Levels and Pathology of Ether-Phospholipid Deficient Mice , 2011, PloS one.

[17]  H. Waterham,et al.  Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation. , 2011, Biochimica et biophysica acta.

[18]  P. V. Van Veldhoven Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism[S] , 2010, Journal of Lipid Research.

[19]  R. Wanders,et al.  Biosynthesis of ether-phospholipids including plasmalogens, peroxisomes and human disease: new insights into an old problem , 2010 .

[20]  J. Reddy,et al.  Biochemical characterization of two functional human liver acyl-CoA oxidase isoforms 1a and 1b encoded by a single gene. , 2007, Biochemical and biophysical research communications.

[21]  J. Mandel,et al.  Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-adrenoleukodystrophy. , 2004, Human molecular genetics.

[22]  Jeffrey B. Cheng,et al.  Mammalian Wax Biosynthesis , 2004, Journal of Biological Chemistry.

[23]  S. Denis,et al.  Measurement of peroxisomal fatty acid β-oxidation in cultured human skin fibroblasts , 1995, Journal of Inherited Metabolic Disease.

[24]  G. Dacremont,et al.  Assay of plasmalogens and polyunsaturated fatty acids (PUFA) in erythrocytes and fibroblasts , 1995, Journal of Inherited Metabolic Disease.

[25]  R. Wanders,et al.  Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry. , 2003, Molecular genetics and metabolism.

[26]  R. Pauli,et al.  Natural history of rhizomelic chondrodysplasia punctata , 2003, American journal of medical genetics. Part A.

[27]  N. Nagan,et al.  Plasmalogens: biosynthesis and functions. , 2001, Progress in lipid research.

[28]  H. Tabak,et al.  Pex11p Plays a Primary Role in Medium-Chain Fatty Acid Oxidation, a Process That Affects Peroxisome Number and Size in Saccharomyces cerevisiae , 2000, The Journal of cell biology.

[29]  E. D. de Vet,et al.  Immunological localization and tissue distribution of alkyldihydroxyacetonephosphate synthase and deficiency of the enzyme in peroxisomal disorders. , 1997, European journal of biochemistry.

[30]  H. Hayashi,et al.  Fatty alcohol synthesis accompanied with chain elongation in liver peroxisomes. , 1997, Biochimica et biophysica acta.

[31]  T. Hashimoto,et al.  Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase. , 1996, Journal of biochemistry.

[32]  C. Rodrigues-Pousada,et al.  The ABC transporter proteins Pat1 and Pat2 are required for import of long‐chain fatty acids into peroxisomes of Saccharomyces cerevisiae. , 1996, The EMBO journal.

[33]  R. Wanders,et al.  Purification of peroxisomal acyl-CoA: dihydroxyacetonephosphate acyltransferase from human placenta. , 1994, Biochimica et biophysica acta.

[34]  J. Langeveld,et al.  Ether lipid synthesis: purification and identification of alkyl dihydroxyacetone phosphate synthase from guinea-pig liver. , 1993, Biochimica et biophysica acta.

[35]  H. Moser,et al.  Fatty alcohol accumulation in the autosomal recessive form of rhizomelic chondrodysplasia punctata. , 1993, Biochemical medicine and metabolic biology.

[36]  S. Eaton,et al.  Intermediates of peroxisomal β-oxidation. A study of the fatty acyl-CoA esters which accumulate during peroxisomal β-oxidation of [U-14C]hexadecanoate , 1990 .

[37]  R. Wanders,et al.  Plasmalogen biosynthesis in peroxisomal disorders: fatty alcohol versus alkylglycerol precursors. , 1988, Journal of lipid research.

[38]  C. Fiol,et al.  Properties of purified carnitine acyltransferases of mouse liver peroxisomes. , 1984, The Journal of biological chemistry.

[39]  J. Bremer,et al.  Chapter 5 Fatty acid oxidation and its regulation , 1984 .