Carlo W T Van Roermund


Ontology type: schema:Person     


Person Info

NAME

Carlo W T

SURNAME

Van Roermund

Publications in SciGraph latest 50 shown

  • 2018-12 Systematic mapping of contact sites reveals tethers and a function for the peroxisome-mitochondria contact in NATURE COMMUNICATIONS
  • 2017-12 Two NAD-linked redox shuttles maintain the peroxisomal redox balance in Saccharomyces cerevisiae in SCIENTIFIC REPORTS
  • 2007-02 The peroxisomal ABC transporter family in PFLÜGERS ARCHIV - EUROPEAN JOURNAL OF PHYSIOLOGY
  • 2003-09 Fatty acid metabolism in Saccharomyces cerevisiae in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2003 Peroxisomal Fatty Acid Alpha-and Beta-Oxidation in Health and Disease: New insights in PEROXISOMAL DISORDERS AND REGULATION OF GENES
  • 1995-03 Phytanic acid oxidation in man: identification of a new enzyme catalysing the formation of 2-ketophytanic acid from 2-hydroxyphytanic acid and its deficiency in the Zellweger syndrome in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995-01 Measurement of peroxisomal fatty acid β-oxidation in cultured human skin fibroblasts in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995 Measurement of peroxisomal fatty acid β-oxidation in cultured human skin fibroblasts in DIAGNOSIS OF HUMAN PEROXISOMAL DISORDERS
  • 1992-07 X-linked adrenoleukodystrophy: Biochemical diagnosis and enzyme defect in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992-05 Bifunctional enzyme deficiency: Identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal β-oxidation of unknown aetiology by means of complementation analysis in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-05 Identification of pristanoyl-CoA oxidase and phytanic acid decarboxylation in peroxisomes and mitochondria from human liver: Implications for Zellweger syndrome in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-05 Di- and trihydroxycholestanaemia in twin sisters in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1991-03 Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: Aberrant subcellular localization in Zellweger syndrome in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-05 Di- and trihydroxycholestanoic acidaemia with hepatic failure in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-05 A bifunctional protein with deficient enzymic activity: Identification of a new peroxisomal disorder using novel methods to measure the peroxisomal β-oxidation enzyme activities in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1990-01 The inborn errors of peroxisomal β-oxidation: A review in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-12 Deficient oxidation of trihydroxycoprostanic acid in liver homogenates from patients with peroxisomal diseases in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989 The Peroxisomal β-Oxidation Systems: Characteristics and (Dys) Functions in Man in MOLECULAR BASIS OF MEMBRANE-ASSOCIATED DISEASES
  • 1988-06 Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: Correlation with pyridoxine responsiveness in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1988-06 Peroxisomes and peroxisomal functions in hyperpipecolic acidaemia in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1988-06 X-linked adrenoleukodystrophy: Identification of the primary defect at the level of a deficient peroxisomal very long chain fatty acyl-CoA synthetase using a newly developed method for the isolation of peroxisomes from skin fibroblasts in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1988 Diversity in Residual Alanine Glyoxylate Aminotransferase Activity in Hyperoxaluria Type I: Correlation with Pyridoxine Responsiveness in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988 Peroxisomes and Peroxisomal Functions in Hyperpipecolic Acidaemia in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988 X-Linked Adrenoleukodystrophy: Identification of the Primary Defect at the Level of a Deficient Peroxisomal Very Long Chain Fatty Acyl-CoA Synthetase Using a Newly Developed Method for the Isolation of Peroxisomes from Skin Fibroblasts in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988 Identification of the Enzymic Defect in X-Linked Adrenoleukodystrophy: Oxidation of Very Long Chain Fatty Acids is Deficient Due to an Impaired Ability of Peroxisomes to Activate Very Long Chain Fatty Acids in LIPID STORAGE DISORDERS
  • 1987-06 Peroxisomal fatty acid β-oxidation in human skin fibroblasts: X-linked adrenoleukodystrophy, a peroxisomal very long chain fatty acyl-CoA synthetase deficiency? in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-06 A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986 Regulation of Mitochondrial Respiration in Liver in MYOCARDIAL AND SKELETAL MUSCLE BIOENERGETICS
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