118 results on '"Roermund, Carlo W. T."'
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2. Maintenance of cellular vitamin B 6 levels and mitochondrial oxidative function depend on pyridoxal 5′-phosphate homeostasis protein
3. The Peroxisomal NAD Carrier from Arabidopsis Imports NAD in Exchange with AMP
4. Mutagenesis separates ATPase and thioesterase activities of the peroxisomal ABC transporter, Comatose
5. Maintenance of cellular vitamin B6 levels and mitochondrial oxidative function depend on pyridoxal 5'-phosphate homeostasis protein.
6. Peroxisomal NAD(H) Homeostasis in the Yeast Debaryomyces hansenii Depends on Two Redox Shuttles and the NAD + Carrier, Pmp47.
7. Intrinsic acyl-CoA thioesterase activity of a peroxisomal ATP binding cassette transporter is required for transport and metabolism of fatty acids
8. Peroxisomal ATP Uptake Is Provided by Two Adenine Nucleotide Transporters and the ABCD Transporters
9. The peroxisomal ABC transporter family
10. Peroxisomal Metabolite and Cofactor Transport in Humans
11. The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co‐imports CoASH into the peroxisome
12. The role of ELOVL1 in very long-chain fatty acid homeostasis and X-linked adrenoleukodystrophy
13. Plphp Deficiency: Clinical, Genetic, Biochemical, And Mechanistic Insights
14. Peroxisomes can oxidize medium‐ and long‐chain fatty acids through a pathway involving ABCD3 and HSD17B4
15. The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co‐imports CoASH into the peroxisome.
16. Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact
17. Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact
18. Regulation of Mitochondrial Respiration in Liver
19. Two NAD-linked redox shuttles maintain the peroxisomal redox balance in Saccharomyces cerevisiae
20. Peroxisomes can oxidize medium- and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4.
21. PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights.
22. ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism
23. Regulation of Mitochondrial Respiration in Liver
24. ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.
25. Peroxisomal fatty acid alpha- and beta-oxidation in health and disease: new insights
26. Peroxisomal Proteostasis Involves a Lon Family Protein That Functions as Protease and Chaperone
27. Identification and characterization of a complete carnitine biosynthesis pathway inCandida albicans
28. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters
29. Carnitine-Dependent Transport of Acetyl Coenzyme A in Candida albicans Is Essential for Growth on Nonfermentable Carbon Sources and Contributes to Biofilm Formation
30. Metabolite transport across the peroxisomal membrane
31. The peroxisomal ABC transporter family
32. The peroxisomal lumen in Saccharomyces cerevisiae is alkaline
33. Identification of a Peroxisomal ATP Carrier Required for Medium-Chain Fatty Acid β-Oxidation and Normal Peroxisome Proliferation in Saccharomyces cerevisiae
34. Transport of Activated Fatty Acids by the Peroxisomal ATP‐binding‐cassette Transporter Pxa2 in a Semi‐Intact Yeast Cell System
35. Cytosolic Aspartate Aminotransferase Encoded by the AAT2 Gene is Targeted to the Peroxisomes in Oleate-Grown Saccharomyces Cerevisiae
36. Peroxisomal Fatty Acid Uptake Mechanism in Saccharomyces cerevisiae.
37. Identification and characterization of a complete carnitine biosynthesis pathway in Candida albicans.
38. The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl-CoA esters.
39. Molecular characterization of carnitine-dependent transport of acetyl-CoA from peroxisomes to mitochondria in Saccharomyces cerevisiae and identification of a plasma membrane carnitine transporter, Agp2p.
40. Analysis of the control of citrulline synthesis in isolated rat-liver mitochondria.
41. Peroxisomal ß-oxidation of polyunsaturated fatty acids in Saccharomyces cerevisiae: isocitrate dehydrogenase provides NADPH for reduction of double bonds at even positions.
42. Factors determining the relative contribution of the adenine-nucleotide translocator and the ADP-regenerating system to the control of oxidative phosphorylation in isolated rat-liver mitochondria.
43. Properties of carbamoyl-phosphate synthetase (ammonia) in rat-liver mitochondria made permeable with toluene.
44. Carnitine-Dependent Transport of Acetyl Coenzyme A in Candida albicansIs Essential for Growth on Nonfermentable Carbon Sources and Contributes to Biofilm Formation
45. A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of Acyl-CoA oxidase (pseudo–Neonatal adrenoleukodystrophy)
46. A Lethal Defect of Mitochondrial and Peroxisomal Fission.
47. Human peroxisomal NAD + /NADH homeostasis is regulated by two independent NAD(H) shuttle systems.
48. Maintenance of cellular vitamin B 6 levels and mitochondrial oxidative function depend on pyridoxal 5'-phosphate homeostasis protein.
49. The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co-imports CoASH into the peroxisome.
50. Corrigendum to "Cardiolipin-deficient cells depend on anaplerotic pathways to ameliorate defective TCA cycle function" [Biochim. Biophys. Acta, Mol. Cell Biol. Lipids 1864/5(2019) 654-661].
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