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Marc Espeel

Showing results (11-20 of 21) with videos related to

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Advances in Experimental Medicine and Biology|January 10, 2004
Modified peroxisomes in primary hepatocyte culturesMarianne Depreter, Tracy Walker, Sonja Beken, et al.
Journal of Neuroscience Research|November 1, 2006
Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liverOlga Krysko, Leen Hulshagen, Anneleen Janssen, et al.
Human Fertility (Cambridge, England)|April 2, 2014
Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilizationAraceli Diez-Fraile, Tim Lammens, Kelly Tilleman, et al.
Journal of Inherited Metabolic Disease|September 3, 2014
Inborn errors of metabolism in the biosynthesis and remodelling of phospholipidsSaskia B Wortmann, Marc Espeel, Ligia Almeida, et al.
Frontiers in Cell and Developmental Biology|April 9, 2020
<i>Slc25a17</i> Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic AcidPaul P Van Veldhoven, Evelyn de Schryver, Stephen G Young, et al.
Biochimica Et Biophysica Acta|December 3, 2014
Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferationAnnelies Peeters, Abhijit Babaji Shinde, Ruud Dirkx, et al.
BMC Clinical Pathology|June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defectsFrank Roels, Patrick Verloo, François Eyskens, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Mitochondrion|September 4, 2017
Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolitesAbhijit Babaji Shinde, Ritesh Kumar Baboota, Simone Denis, et al.
Biochimie|March 1, 2011
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 liverMarco Fidaleo, Ségolène Arnauld, Marie-Claude Clémencet, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Advances in Experimental Medicine and Biology|January 10, 2004
Modified peroxisomes in primary hepatocyte culturesMarianne Depreter, Tracy Walker, Sonja Beken, et al.
Journal of Neuroscience Research|November 1, 2006
Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liverOlga Krysko, Leen Hulshagen, Anneleen Janssen, et al.
Human Fertility (Cambridge, England)|April 2, 2014
Age-associated differential microRNA levels in human follicular fluid reveal pathways potentially determining fertility and success of in vitro fertilizationAraceli Diez-Fraile, Tim Lammens, Kelly Tilleman, et al.
Journal of Inherited Metabolic Disease|September 3, 2014
Inborn errors of metabolism in the biosynthesis and remodelling of phospholipidsSaskia B Wortmann, Marc Espeel, Ligia Almeida, et al.
Frontiers in Cell and Developmental Biology|April 9, 2020
<i>Slc25a17</i> Gene Trapped Mice: PMP34 Plays a Role in the Peroxisomal Degradation of Phytanic and Pristanic AcidPaul P Van Veldhoven, Evelyn de Schryver, Stephen G Young, et al.
Biochimica Et Biophysica Acta|December 3, 2014
Mitochondria in peroxisome-deficient hepatocytes exhibit impaired respiration, depleted DNA, and PGC-1α independent proliferationAnnelies Peeters, Abhijit Babaji Shinde, Ruud Dirkx, et al.
BMC Clinical Pathology|June 9, 2009
Mitochondrial mosaics in the liver of 3 infants with mtDNA defectsFrank Roels, Patrick Verloo, François Eyskens, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Mitochondrion|September 4, 2017
Mitochondrial disruption in peroxisome deficient cells is hepatocyte selective but is not mediated by common hepatic peroxisomal metabolitesAbhijit Babaji Shinde, Ritesh Kumar Baboota, Simone Denis, et al.
Biochimie|March 1, 2011
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 liverMarco Fidaleo, Ségolène Arnauld, Marie-Claude Clémencet, et al.
Pageof 3