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Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastoma

Cell death & disease, 2013-04, Vol.4 (4), p.e586-e586

2013

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The hematopoietic stem cell in chronic phase CML is characterized by a transcriptional profile resembling normal myeloid progenitor cells and reflecting loss of quiescence

Leukemia, 2009-05, Vol.23 (5), p.892-899

2009

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Demonstration of lanthanum in liver cells by energy‐dispersive X‐ray spectroscopy, electron energy loss spectroscopy and high‐resolution transmission electron microscopy

Journal of microscopy (Oxford), 2006-08, Vol.223 (2), p.133-139

2006

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Modulation of the peroxisomal gene expression pattern by dehydroepiandrosterone and vitamin D: therapeutic implications

Journal of endocrinology, 2002-12, Vol.175 (3), p.779-792

2002

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Mitochondrial Transmembrane Potential Changes Support the Concept of Mitochondrial Heterogeneity During Apoptosis

The journal of histochemistry and cytochemistry, 2001-10, Vol.49 (10), p.1277-1284

2001

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Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity

Cell death and differentiation, 2000-04, Vol.7 (4), p.331-337

2000

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511 INCREASED SHEAR STRESS ALONE CAN INDUCE HEPATIC PROLIFERATION IN NORMAL LIVERS

Journal of hepatology, 2008, Vol.48, p.S193-S193

2008

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WCN23-0641 TOWARDS STANDARDIZED HISTOLOGICAL ASSESSMENT CHRONIC INTERSTITIAL NEPHRITIS IN AGRICULTURAL COMMUNITIES: METHODS AND PITFALLS IN MICROSCOPIC DIAGNOSIS

Kidney international reports, 2023-03, Vol.8 (3), p.S122-S122

2023

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Peroxisomes in liver, heart, and kidney of mice fed a commercial fish oil preparation: original data and review on peroxisomal changes induced by high-fat diets

Journal of lipid research, 1994-07, Vol.35 (7), p.1241-1250

1994

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Clinical approach to inherited peroxisomal disorders: A series of 27 patients

Annals of neurology, 1998-11, Vol.44 (5), p.720-730

1998

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Cyclic Changes of the Canine Endometrial Surface: An Electron-Microscopic Study

Cells, tissues, organs, 2003, Vol.173 (1), p.46-53

2003

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Human peroxisomal disorders

Microscopy research and technique, 2003-06, Vol.61 (2), p.203-223

2003

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A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)

American journal of human genetics, 1988-03, Vol.42 (3), p.422-434

1988

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Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease

Neurology, 1998-11, Vol.51 (5), p.1427

1998

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Effect of Epidermal Growth Factor in Collagen Gel Cultures of Rat Hepatocytes

Toxicology in vitro, 1999-08, Vol.13 (4), p.579-585

1999

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Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator

The Journal of cell biology, 2005-04, Vol.169 (1), p.93-104

2005

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Heterogeneity of catalase staining in human hepatocellular peroxisomes

The journal of histochemistry and cytochemistry, 1989-03, Vol.37 (3), p.331-337

1989

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Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trials

Advances in experimental medicine and biology, 2003, Vol.544, p.369

2003

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Why study regulation of genes in inherited disorders?

Advances in experimental medicine and biology, 2003, Vol.544, p.1

Roels, Frank

2003

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Liver and chorion cytochemistry

Journal of inherited metabolic disease, 1995-01, Vol.18 (S1), p.155-171

1995

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Peroxisomal fatty acid alpha- and beta-oxidation in health and disease: new insights

Advances in experimental medicine and biology, 2003, Vol.544, p.293

2003

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Plasmalogens, docosahexaenoic acid and neurological disorders

Advances in experimental medicine and biology, 2003, Vol.544, p.335

2003

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Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution

Annals of neurology, 2000-01, Vol.47 (1), p.109-113

2000

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Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency

Virchows Archiv : an international journal of pathology, 2000-05, Vol.436 (5), p.459-465

2000

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Identification of PEX7 as the second gene involved in Refsum disease

Advances in experimental medicine and biology, 2003, Vol.544, p.69

2003

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Hox-C9 activates the intrinsic pathway of apoptosis and is associated with spontaneous regression in neuroblastoma

The hematopoietic stem cell in chronic phase CML is characterized by a transcriptional profile resembling normal myeloid progenitor cells and reflecting loss of quiescence

Demonstration of lanthanum in liver cells by energy‐dispersive X‐ray spectroscopy, electron energy loss spectroscopy and high‐resolution transmission electron microscopy

Modulation of the peroxisomal gene expression pattern by dehydroepiandrosterone and vitamin D: therapeutic implications

Mitochondrial Transmembrane Potential Changes Support the Concept of Mitochondrial Heterogeneity During Apoptosis

Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity

511 INCREASED SHEAR STRESS ALONE CAN INDUCE HEPATIC PROLIFERATION IN NORMAL LIVERS

WCN23-0641 TOWARDS STANDARDIZED HISTOLOGICAL ASSESSMENT CHRONIC INTERSTITIAL NEPHRITIS IN AGRICULTURAL COMMUNITIES: METHODS AND PITFALLS IN MICROSCOPIC DIAGNOSIS

Peroxisomes in liver, heart, and kidney of mice fed a commercial fish oil preparation: original data and review on peroxisomal changes induced by high-fat diets

Clinical approach to inherited peroxisomal disorders: A series of 27 patients

Cyclic Changes of the Canine Endometrial Surface: An Electron-Microscopic Study

Human peroxisomal disorders

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy)

Defective peroxisome biogenesis with a neuromuscular disorder resembling Werdnig-Hoffmann disease

Effect of Epidermal Growth Factor in Collagen Gel Cultures of Rat Hepatocytes

Phenylbutyrate up-regulates the adrenoleukodystrophy-related gene as a nonclassical peroxisome proliferator

Heterogeneity of catalase staining in human hepatocellular peroxisomes

Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trials

Why study regulation of genes in inherited disorders?

Liver and chorion cytochemistry

Peroxisomal fatty acid alpha- and beta-oxidation in health and disease: new insights

Plasmalogens, docosahexaenoic acid and neurological disorders

Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution

Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency

Identification of PEX7 as the second gene involved in Refsum disease

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