Joseph M Tager


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Person Info

NAME

Joseph M

SURNAME

Tager

Publications in SciGraph latest 50 shown

  • 1999-04 Hugo and Ann Moser: A Unique Husband and Wife Team in NEUROCHEMICAL RESEARCH
  • 1994-07 Signals on proteins, intracellular targeting and inborn errors of organellar metabolism in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-05 Human alkyldihydroxyacetonephosphate synthase deficiency: A new peroxisomal disorder in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1994-01 Clinical and biochemical characteristics of peroxisomal disorders: an update in EUROPEAN JOURNAL OF PEDIATRICS
  • 1993-03 Pathogenesis of lysosomal storage disorders as illustrated by Gaucher disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992-11 PEROXISOMAL DYSFUNCTION IN A HETEROGENEOUS GROUP OF CHONDRODYSPLASIA PUNCTATA (CP) SYNDROMES in PEDIATRIC RESEARCH
  • 1992-07 X-linked adrenoleukodystrophy: Biochemical diagnosis and enzyme defect in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992-06 Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata — a complementation study in HUMAN GENETICS
  • 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
  • 1992-05 Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1992 Latency of Peroxisomal Enzymes in Digitonin-Permeabilized Cells: The Effect of ATP on Peroxisome Permeability in ADENINE NUCLEOTIDES IN CELLULAR ENERGY TRANSFER AND SIGNAL TRANSDUCTION
  • 1992 Sorting of Endogenous Proteins in Intestinal Epithelial Cells in ENDOCYTOSIS
  • 1992 Mannose Phosphate-Independent Membrane Association of Lysosomal Enzymes Occurs After Passage of the Golgi Complex in ENDOCYTOSIS
  • 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 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 Hair root diagnosis of Fabry's disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-04 Prenatal Diagnosis of Zellweger Syndrome by Direct Visualization of Peroxisomes in Chorionic Villus Fibroblasts by Immunofluorescence Microscopy in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989-03 Prenatal and perinatal diagnosis of peroxisomal disorders in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1989 Human Cytochrome c Oxidase Deficiencies; Structural and Functional Aspects in MOLECULAR BASIS OF MEMBRANE-ASSOCIATED DISEASES
  • 1989 Prenatal Diagnosis of Zellweger Syndrome by Direct Visualization of Peroxisomes in Chorionic Villus Fibroblasts by Immunofluorescence Microscopy in STUDIES IN INHERITED METABOLIC DISEASE
  • 1989 Control Analysis: Principles and Application to Experimental Practice in ORGANELLES IN EUKARYOTIC CELLS
  • 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
  • 1989 Functions, Biogenesis and Pathology of Peroxisomes in Man in ORGANELLES IN EUKARYOTIC CELLS
  • 1989 The Peroxisomal β-Oxidation Systems: Characteristics and (Dys) Functions in Man in MOLECULAR BASIS OF MEMBRANE-ASSOCIATED DISEASES
  • 1989 Prenatal and Perinatal Diagnosis of Peroxisomal Disorders in STUDIES IN INHERITED METABOLIC DISEASE
  • 1988-06 Cytochromec oxidase: Organ‐specific isoenzymes and deficiencies in JOURNAL OF INHERITED METABOLIC DISEASE
  • 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
  • 1988-06 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 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
  • 1988 Control Analysis of Cellular Metabolism: Application to Gluconeogenesis in Rat-Liver Cells in INTEGRATION OF MITOCHONDRIAL FUNCTION
  • 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 Intracellular Transport of Brush-Border and Lysosomal Enzymes in the Human Enterocyte in BIOMEMBRANES
  • 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
  • 1987-06 Generalized loss of peroxisomal functions in neonatal adrenoleukodystrophy: Implications for Pre- and postnatal detection and relationship to X-linked adrenoleukodystrophy in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1987-06 Cultured human muscle cells from controls and a Zellweger patient: Study on peroxisomes and peroxisomal functions in JOURNAL OF INHERITED METABOLIC DISEASE
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