List of works - Marc Espeel

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents

scientific article

A role for the peroxisomal 3-ketoacyl-CoA thiolase B enzyme in the control of PPARα-mediated upregulation of SREBP-2 target genes in the liver.

scientific article published on 23 February 2011

Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilization.

scientific article published on 31 March 2014

Expression of calcium-sensing receptor in quail granulosa explants: a key to survival during folliculogenesis

scientific article published in May 2010

Fine structure of the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (Crustacea, Mysidacea)

scientific article published on 01 November 1985

Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

scientific article

Human peroxisomal disorders ⬇️

scientific article published on June 1, 2003

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

scientific article published on 25 January 2003

Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

scientific article

Mevalonate kinase is a cytosolic enzyme in humans

scientific article

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation

scientific article published on 20 November 2014

Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites

scientific article published on 30 August 2017

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

scientific article

Modified peroxisomes in primary hepatocyte cultures.

scientific article

Morphogenesis during molting of the setae in the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (crustacea, mysidacea)

scientific article published on 01 January 1986

Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver

scientific article published in January 2007

Peroxisome deficient aP2-Pex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

scientific article published on 22 October 2012

Peroxisome mosaics.

scientific article

Peroxisomes during development and in distinct cell types.

scientific article published on January 2003

Peroxisomes in zebrafish: distribution pattern and knockdown studies

scientific article published on 17 June 2010

Phosphomevalonate kinase is a cytosolic protein in humans

scientific article

Slc25a17 Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic Acid

scientific article published on 24 March 2020

List of works by Marc Espeel

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents

A role for the peroxisomal 3-ketoacyl-CoA thiolase B enzyme in the control of PPARα-mediated upregulation of SREBP-2 target genes in the liver.

Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilization.

Expression of calcium-sensing receptor in quail granulosa explants: a key to survival during folliculogenesis

Fine structure of the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (Crustacea, Mysidacea)

Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

Human peroxisomal disorders ⬇️

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

Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

Mevalonate kinase is a cytosolic enzyme in humans

Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferation

Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolites

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

Modified peroxisomes in primary hepatocyte cultures.

Morphogenesis during molting of the setae in the statocyst sensilla of the mysid shrimp Neomysis integer (Leach, 1814) (crustacea, mysidacea)

Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver

Peroxisome deficient aP2-Pex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

Peroxisome mosaics.

Peroxisomes during development and in distinct cell types.

Peroxisomes in zebrafish: distribution pattern and knockdown studies

Phosphomevalonate kinase is a cytosolic protein in humans

Slc25a17 Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic Acid