Henk Van Den Bosch


Ontology type: schema:Person     


Person Info

NAME

Henk

SURNAME

Van Den Bosch

Publications in SciGraph latest 50 shown

  • 2002-01 Cytosolic phospholipase A2 and lipoxygenase are involved in cell cycle progression in neuroblastoma cells in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 2000-03 Alkyl-dihydroxyacetonephosphate synthase in CELL BIOCHEMISTRY AND BIOPHYSICS
  • 1999-01 Activation of mitogen-activated protein kinase and cytosolic phospholipase A2 by hydrogen peroxide in fibroblasts in LIPIDS
  • 1998-04 Induction of Secretory Phospholipase A2 Confirms the Systemic Inflammatory Nature of Adjuvant Arthritis in INFLAMMATION
  • 1996 Phospholipases A2 and the Production of Bioactive Lipids in MOLECULAR DYNAMICS OF BIOMEMBRANES
  • 1996 The Role of Peroxisomes in Ether Lipid Synthesis in PLATELET-ACTIVATING FACTOR AND RELATED LIPID MEDIATORS 2
  • 1995-12-01 Therapy with interleukin-2 induces the systemic release of phospholipase-A 2 in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 1995-09 Therapy with interleukin-2 induces the systemic release of phospholipase-A2 in CANCER IMMUNOLOGY, IMMUNOTHERAPY
  • 1995-01 Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1995 Measurement of dihydroxyacetone-phosphate acyltransferase (DHAPAT) in chorionic villous samples, blood cells and cultured cells in DIAGNOSIS OF HUMAN PEROXISOMAL DISORDERS
  • 1995 Regulation of 14 kDa Group II PLA2 in Rat Mesangial Cells in SIGNALLING MECHANISMS — FROM TRANSCRIPTION FACTORS TO OXIDATIVE STRESS
  • 1994-08 Contribution of group II phospholipase A2 to arachidonic acid release and prostaglandin synthesis by mesangial cells in INFLAMMATION RESEARCH
  • 1994 Phospholipases A2 and Prostaglandin Formation in Rat Glomerular Mesangial Cells in ESTERASES, LIPASES, AND PHOSPHOLIPASES
  • 1993-01 Cytokine regulation of Group II phospholipase A2 expression in glomerular mesangial cells in EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
  • 1992 The Induction of Cellular Group II Phospholipase A2 by Cytokines and its Prevention by Dexamethasone in NEUROBIOLOGY OF ESSENTIAL FATTY ACIDS
  • 1991-12 Studies on the selectivity of enzymes involved in platelet-activating factor formation in stimulated cells in LIPIDS
  • 1990-01 The inborn errors of peroxisomal β-oxidation: A review 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 Prenatal Diagnosis of Zellweger Syndrome by Direct Visualization of Peroxisomes in Chorionic Villus Fibroblasts by Immunofluorescence Microscopy in STUDIES IN INHERITED METABOLIC DISEASE
  • 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 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
  • 1988-12 Interaction of Sr2+ with Ca2+-induced Ca2+ release in mitochondria in JOURNAL OF BIOENERGETICS AND BIOMEMBRANES
  • 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 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
  • 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 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
  • 1987-03 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 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
  • 1986-12 Age-related differences in plasmalogen content of erythrocytes from patients with the cerebro-hepato-renal (Zellweger) syndrome: Implications for postnatal detection of the disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-10 Transfer of arachidonate from phosphatidylcholine to phosphatidylethanolamine and triacylglycerol in guinea pig alveolar macrophages in LIPIDS
  • 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
  • 1986-06 Deficiency of dihydroxyacetonephosphate acyltransferase and catalase-containing particles in patients with infantile refsum's disease in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-06 Infantile Refsum's disease: Biochemical findings suggesting multiple peroxisomal dysfunction in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-06 Pre- and postnatal diagnosis of the cerebrohepato-renal (Zellweger) syndrome via a simple method directly demonstrating the presence of absence of peroxisomes in cultured skin fibroblasts, amniocytes or chorionic villi fibroblasts in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1986-04 A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986-02 Impaired plasmalogen metabolism in infantile Refsum's disease in EUROPEAN JOURNAL OF PEDIATRICS
  • 1986 Some Properties of Membrane-Bound Phospholipases A2 in ENZYMES OF LIPID METABOLISM II
  • 1986 Deficiencies in Ether Glycerolipids and Their Biosynthesis in Inherited Peroxisomal Disorders in ENZYMES OF LIPID METABOLISM II
  • 1986 Pre- and Postnatal Diagnosis of the Cerebro-hepato-renal (Zellweger) Syndrome via a Simple Method Directly Demonstrating the Presence or Absence of Peroxisomes in Cultured Skin Fibroblasts, Amniocytes or Chorionic Villi Fibroblasts in PRACTICAL DEVELOPMENTS IN INHERITED METABOLIC DISEASE: DNA ANALYSIS, PHENYLKETONURIA AND SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

    [
      {
        "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "affiliation": [
          {
            "affiliation": {
              "id": "https://www.grid.ac/institutes/grid.5477.1", 
              "type": "Organization"
            }, 
            "isCurrent": true, 
            "type": "OrganizationRole"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.7177.6", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.6612.3", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.5132.5", 
            "type": "Organization"
          }, 
          {
            "id": "https://www.grid.ac/institutes/grid.266100.3", 
            "type": "Organization"
          }
        ], 
        "familyName": "Van Den Bosch", 
        "givenName": "Henk", 
        "id": "sg:person.01154226133.81", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01154226133.81"
        ], 
        "sdDataset": "persons", 
        "sdDatePublished": "2019-03-07T14:35", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-uberresearch-data-dimensions-researchers-20181010/20181011/dim_researchers/base/researchers_332.json", 
        "type": "Person"
      }
    ]
     

    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/person.01154226133.81'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/person.01154226133.81'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/person.01154226133.81'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/person.01154226133.81'


     

    This table displays all metadata directly associated to this object as RDF triples.

    24 TRIPLES      10 PREDICATES      15 URIs      7 LITERALS      2 BLANK NODES

    Subject Predicate Object
    1 sg:person.01154226133.81 schema:affiliation N8034424ffafd42a988b2ba10af41df97
    2 https://www.grid.ac/institutes/grid.266100.3
    3 https://www.grid.ac/institutes/grid.5132.5
    4 https://www.grid.ac/institutes/grid.6612.3
    5 https://www.grid.ac/institutes/grid.7177.6
    6 schema:familyName Van Den Bosch
    7 schema:givenName Henk
    8 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01154226133.81
    9 schema:sdDatePublished 2019-03-07T14:35
    10 schema:sdLicense https://scigraph.springernature.com/explorer/license/
    11 schema:sdPublisher Nc26131e1ae1649d1b315cfcb77276430
    12 sgo:license sg:explorer/license/
    13 sgo:sdDataset persons
    14 rdf:type schema:Person
    15 N8034424ffafd42a988b2ba10af41df97 schema:affiliation https://www.grid.ac/institutes/grid.5477.1
    16 sgo:isCurrent true
    17 rdf:type schema:OrganizationRole
    18 Nc26131e1ae1649d1b315cfcb77276430 schema:name Springer Nature - SN SciGraph project
    19 rdf:type schema:Organization
    20 https://www.grid.ac/institutes/grid.266100.3 schema:Organization
    21 https://www.grid.ac/institutes/grid.5132.5 schema:Organization
    22 https://www.grid.ac/institutes/grid.5477.1 schema:Organization
    23 https://www.grid.ac/institutes/grid.6612.3 schema:Organization
    24 https://www.grid.ac/institutes/grid.7177.6 schema:Organization
     




    Preview window. Press ESC to close (or click here)


    ...