Andréw Schram


Ontology type: schema:Person     


Person Info

NAME

Andréw

SURNAME

Schram

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 Cytochromec oxidase: Organ‐specific isoenzymes and deficiencies 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
  • 1988-06 Bile acid analyses in “pseudo-Zellweger” syndrome; clues to the defect in peroxisomal β-oxidation in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1988 Complementation Analysis of Peroxisomal Diseases: Kinetics of Assembly of Peroxisomes After Fusion of Complementary Cell Lines from Patients Deficient in Peroxisomes in LIPID STORAGE DISORDERS
  • 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
  • 1988 Heterogeneity in Human Acid β-Glucosidase with Cellulose-Acetate Electrophoresis in LIPID STORAGE DISORDERS
  • 1988 Molecular Properties of Lysosomal Glucocerebrosidase in LIPID STORAGE DISORDERS
  • 1988 Parkinsonian Symptomatology in a Patient with Type I (Adult) Gaucher’s Disease in LIPID STORAGE DISORDERS
  • 1988 Bile Acid Analyses in “Pseudo-Zellweger” Syndrome; Clues to the Defect in Peroxisomal β-Oxidation in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988 Cytochrome c Oxidase: Organ-Specific Isoenzymes and Deficiencies in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988 Acid Sphingomyelinase from Human Urine: Purification and Characterisation in LIPID STORAGE DISORDERS
  • 1987-09 Infantile Refsum disease: an inherited peroxisomal disorder in EUROPEAN JOURNAL OF PEDIATRICS
  • 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
  • 1987-06 Prenatal diagnosis and confirmation of Infantile Refsum's disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-03 Zellweger syndrome: Biochemical procedures in diagnosis, prevention and treatment in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987 Complementation Analysis of Peroxisomal Diseases by Somatic Cell Fusion in PEROXISOMES IN BIOLOGY AND MEDICINE
  • 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
  • 1987 Peroxisomal Disorders: Biochemical Characteristics and Genetic Relationship Between the Different Diseases in HUMAN GENETICS
  • 1987-01 Ultrastructural localization of glucocerebrosidase in cultured Gaucher's disease fibroblasts by immunocytochemistry in JOURNAL OF NEUROLOGY
  • 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
  • 1986 Purification and Properties of Acid Sphingomyelinase from Human Urine in ENZYMES OF LIPID METABOLISM II
  • 1986 Impaired Maturation of Peroxisomal ß-oxidation Enzymes in Fibroblasts from Patients with the Zellweger Syndrome and Infantile Refsum Disease in ENZYMES OF LIPID METABOLISM II
  • 1986 Immunological Studies on Lysosomal Sphingomyelinase: Immunization Procedures, Properties of Polyclonal and Monoclonal Antibodies Obtained and Effect of Triton X-100 on Binding of Enzyme Activity in ENZYMES OF LIPID METABOLISM II
  • 1986 Molecular Forms, Biosynthesis and Maturation of Glucocerebrosidase, a Membrane-Associated Lysosomal Enzyme Deficient in Gaucher Disease 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
  • 1982-08 Genetic control of the conversion of dihydroflavonols into flavonols and anthocyanins in flowers of Petunia hybrida in PLANTA
  • 1981-03 Synthesis of malvidin and petunidin in pigmented tissue cultures ofPetunia hybrida in PROTOPLASMA
  • 1978-01 A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids in HUMAN GENETICS
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