Andréw Schram

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Publications in SciGraph latest 50 shown

  • 1989 Genetic Heterogeneity in Inherited Disorders with a Generalized Impairment of Peroxisomal Functions: Visualization by Immunofluorescence Microscopy of Peroxisome Assembly After Somatic Cell Fusion of Complementary Cell Lines in MOLECULAR BASIS OF MEMBRANE-ASSOCIATED DISEASES
  • 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 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 A genetic disorder due to the deficiency of the peroxisomal β-oxidation enzyme 3-oxoacyl-CoA thiolase in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987 Glucocerebrosidase, a Membrane-Associated Lysosomal Enzyme Deficient in Gaucher Disease in CELLS, MEMBRANES, AND DISEASE, INCLUDING RENAL
  • 1987 Biochemical Analysis in Peroxisomal Disorders in PEROXISOMES IN BIOLOGY AND MEDICINE
  • 1986-08 Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal β-oxidation enzyme proteins in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986 Forms of Glucocerebrosidase Present in Tissues and Urine in ENZYMES OF LIPID METABOLISM II
  • 1984 Immunological Approaches to the Diagnosis of Lysosomal Storage Diseases and Heterozygote Detection in SCREENING AND MANAGEMENT OF POTENTIALLY TREATABLE GENETIC METABOLIC DISORDERS
  • 1983-11 Chalcone isomerase in flowers of mutants of Petunia hybrida in PLANTA
  • 1983-06 The genetic control of the enzyme UDP-glucose: 3-0-flavonoïd-glucosyltransferase in flowers of Petunia hybrida in THEORETICAL AND APPLIED GENETICS
  • 1981-03 Synthesis of malvidin and petunidin in pigmented tissue cultures ofPetunia hybrida in PROTOPLASMA
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