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How to engage the museum visitor in the ethic debate on the display of human remains: the Post Mortem exhibition as a case study
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Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids
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Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation
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Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilization
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Peroxisome deficient a P2-Pex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone
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A role for the peroxisomal 3-ketoacyl-CoA thiolase B enzyme in the control of PPAR alpha-mediated upregulation of SREBP-2 target genes in the liver
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Peroxisomes in zebrafish: distribution pattern and knockdown studies
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Expression of calcium-sensing receptor in quail granulosa explants: a key to survival during folliculogenesis
(2010) ANATOMICAL RECORD-ADVANCES IN INTEGRATIVE ANATOMY AND EVOLUTIONARY BIOLOGY. 293(5). p.890-899 -
- Journal Article
- A2
- open access
Mitochondrial mosaics in the liver of 3 infants with mtDNA defects
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Tissue distribution of peroxisomes in zebrafish
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S100B Expression in forensic brain trauma fatalities: a valuable tool?
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Ciliated bile duct epithelium in the liver of a Zellweger patient
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Ciliated bile duct epithelium in the liver of Zellweger patients
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Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver
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Immunohistochemical detection of interleukin-8 in human post-mortem skin for wound age determination
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Late-onset neuropathy and leukodystrophy revealing a peroxisomal biogenesis defect in two girls
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Human mevalonate pyrophosphate decarboxylase is localized in the cytosol
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Mevalonate kinase is a cytosolic enzyme in humans
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Phosphomevalonate kinase is a cytosolic protein in humans
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- Conference Paper
- C1
- open access
Peroxisome mosaics in patients : modulation of gene expression?
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Peroxisome mosaics
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- Conference Paper
- C3
- open access
Peroxisome mosaics revisited : follow-up of 10 patients
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Immunohistochemical demonstration of the amphetamine derivatives 3,4-methylenedioxymethamphetamine (MDMA) and 3,4-methylenedioxyamphetamine (MDA) in human post-mortem tissues
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Human peroxisomal disorders
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Modified peroxisomes in primary hepatocyte cultures.
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Simultaneous occurrence of a thyromediastinal muscle, a truncus bicaroticobrachialis, and a left superior vena cava
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Peroxisomes during development and in distinct cell types
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- Journal Article
- A1
- open access
Immunohistochemical demonstration of the amphetamine derivatives 3,4-methylenedioxymethamphetamine (MDMA) and 3,4-methylenedioxyamphetamine (MDA) in human post-mortem brain tissues and the pituitary gland
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Modulation of the peroxisomal gene expression pattern by dehydroepiandrosterone and vitamin D : therapeutic implications
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A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.
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A novel disorder in a newborn caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency
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A novel disorder caused by defective biosynthesis of N-linked oligosaccharides due to glucosidase I deficiency.
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Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures
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Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.
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Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution.
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Inverse expression of peroxisomes and connexin-43 in the granulosa cells of the quail follicle.
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Diagnosis and follow-up of a case of peroxisomal disorder with peroxisomal mosaicism.
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Clinical approach to inherited peroxisomal disorders: A series of 27 patients.
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Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease.
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Chondrodysplasia punctata with multiple congenital anomalies: a new syndrome?
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Maturation of the liver-specific peroxisome versus laminin, collagen IV and integrin expression.
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Klinische Anatomie en Embryologie aan de RU Gent. Gezond Onderwijs-8
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Biogenesis of peroxisomes in fetal liver
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Peroxisomes in avian and mammalian oocytes under treatment with polyunsaturated fatty acids: no evidence of peroxisome proliferator-activated receptor (PPAR) function
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Morphometry and AGT-immunoreactivity of hepatic peroxisomes: heterogeneity in primary hyperoxaluria type 1
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Heterogeneity in primary hyperoxaluria type 1: morphometry and AGT-immunoreactivity of hepatic peroxisomes
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Peroxisome mosaics in the liver of patients and the regulation of peroxisome expression in rat hepatocyte cultures
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Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria.
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Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: Clinical presentation, metabolic and histological findings.
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Long survival in a case of peroxisomal biogenesis disorder with peroxisome mosaicism in the liver.
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Hepatic peroxisomes in peroxisomal disorder patients and in the human fetus : contributions from immunocytochemistry
(1995) -
Diagnostic work-up of a peroxisomal patient
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Cell and tissue heterogeneity in peroxisomal patients
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Immunolocalization of a 43 kDA peroxisomal membrane protein in the liver of patients with generalized peroxisomal disorders
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PEROXISOME MOSAICISM IN THE LIVERS OF PEROXISOMAL DEFICIENCY PATIENTS.
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Immunocytochemical localization of peroxisomal proteins in human liver and kidney.
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Mosaicism of hepatic peroxisome distribution in peroxisomal patients
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Cytoplasmic catalase and ghost-like hepatic peroxisomes in a child with bone dysplasia and mental retardation
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Infantile Refsum-like phenotype in a boy with multiple peroxisomal defects but normal plasmalogen biosynthesis in fibroblasts
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Peroxisomal ghosts in human liver
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A new type of peroxisomal disorder with variable expression in liver and fibroblasts.
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CHARACTERIZATION OF HUMAN PEROXISOMAL MEMBRANE-PROTEINS.
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Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctata
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Immunocytochemische lokalisatie van peroxisomale eiwitten in de lever van operoxisomale eiwitten in de lever van peroxisomale patiënten: onderzoeksthema's in het Laboratorium voor Anatomie en Embryologie
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Cytoplasmic catalase but correct localization of four peroxisomal enzymes in the liver of a child with several peroxisomal dysfunctions
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Absence of peroxisomes in liver with normal peroxisomal functions in fibroblasts : a new peroxisomopathy
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Catalase-negative peroxisomes in human embryonic liver
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HUMAN LIVER PATHOLOGY IN PEROXISOMAL DISEASES - A REVIEW INCLUDING NOVEL DATA.
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Peroxisomal membrane ghosts
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Catalase deficient, giant hepatic peroxisomes containing four other enzymes in a child with bone dysplasia
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Catalase deficient, giant hepatic peroxisomes containing four other enzymes in a child with bone dysplasia
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Peroxisomal acyi-CoA oxidase immunocytochemistry in human liver. Limitations
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Peroxisomal ghosts in human liver
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Peroxisomal ghosts in human liver
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Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: A peroxisomal entity amenable to plasmapharesis
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Peroxisomal localization of the immunoreactive β-oxidation enzymes in a neonate with a β-oxidation defect : pathological observations in liver, adrenal cortex and kidney
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X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus
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Giant, catalase deficient hepatic peroxisomes in a child with bone dysplasia, impaired plasmogcn synthesis and phytanic acid storage
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Visualization of peroxisomes in archival human liver by catalase immunocytochemistry
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Liver pathology and immunocytochemistry in congenital peroxisomal diseases : a review
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- Journal Article
- A1
- open access
Different types of peroxisomes in human duodenal epithelium
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Post-mortem visualization of peroxisomes in rat and in human liver
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Immunocytochemical detection of peroxisomal β-oxidation enzymes in cryostat and paraffin sections of human post mortem liver
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Microscopic diagnosis in peroxisomal disorders. BIMDG Newsletter, 1997, 13, pp. 9-11.
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Regulation of peroxisome expression in embryonic rat liver and in cultured rat herpatocytes
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Hepatic Peroxisomes in 36 peroxisomal disorder patients.
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Histochemistry and Cytochemistry 1996, Proceedings of the Xth International Congress, Kyoto, Japan, T. Saito Ed., Acta Histochem. Cytochem., 1996, 29 Suppl., 294-295, figg.
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Liver cytochemistry in 36 peroxisomal disorder patients. J. Inher. Metab. Dis., 1996, 19, suppl. 1, 78.
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Peroxisomes in oocytes
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Peroxisomal acyl-CoA oxidase immunocytochemistry in human liver. Limitations. J. Inher. Metab. Dis., 15, p. 302, (1992).
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A new type of peroxisomal disorder with variable expression in liver and fibroblasts. Kon. Ned. Akademie van Wetenschappen. 'Peroxisomal disorders in relation to functions and biogenesis of peroxisomes', Colloquium Amsterdam 18-19 October, 1993.
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Heterogenität der Chondrodysplasia punctata. Verh. Dtsch. Ges. Path., 76, 465, (1992).
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Cell and Tissue heterogeneiry in peroxisomal patients. Kon. Ned. Akademie van Wetenschappen. 'Peroxisomal disorders in relation to functions and biogenesis of peroxisomes', Colloquium Amsterdam 18-19 October 1993.
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Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: A peroxisomal entity amenable to plasmapharesis. J. Inher. Metab. Dis., 15, 377-380, (1992).
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Neonatal seizures and severe hypotonia in a male infant suffering from a defect in peroxisomal b-oxidation. Neuromusc. Disorder, 2, 217-224, (1992), 10 figg.
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Neonatal adrenoleukodystrophy (NALD) with decreased docosahexaenoic acid C 22:6 CU 3: Follow up studies of a 9 year-old boy with prolonged survival. SSIEM 30th Annual Symposium, Leuven, 1992, 8-11 september, p. 155.