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

Frontiers in cell and developmental biology, 2020-03, Vol.8, p.144-144

2020

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

Journal of neuroscience research, 2007-01, Vol.85 (1), p.58-72

2007

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Human peroxisomal disorders

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

2003

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Peroxisomes in zebrafish: distribution pattern and knockdown studies

Histochemistry and cell biology, 2010-07, Vol.134 (1), p.39-51

2010

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Mevalonate kinase is a cytosolic enzyme in humans

Journal of cell science, 2004-02, Vol.117 (Pt 4), p.631-639

2004

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Phosphomevalonate kinase is a cytosolic protein in humans

Journal of lipid research, 2004-04, Vol.45 (4), p.697-705

2004

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Expression of Calcium‐Sensing Receptor in Quail Granulosa Explants: A Key to Survival During Folliculogenesis

Anatomical record (Hoboken, N.J. : 2007), 2010-05, Vol.293 (5), p.890-899

2010

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

Human fertility (Cambridge, England), 2014-06, Vol.17 (2), p.90-98

2014

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

Biochimica et biophysica acta, 2015-02, Vol.1853 (2), p.285-298

2015

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Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

Molecular genetics and metabolism, 2004-03, Vol.81 (3), p.216-224

2004

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Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

Journal of inherited metabolic disease, 2015-01, Vol.38 (1), p.99-110

2015

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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

International journal of legal medicine, 2003-02, Vol.117 (1), p.2-9

2003

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

Mitochondrion, 2018-03, Vol.39, p.51-59

2018

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

Molecular genetics and metabolism, 2012-12, Vol.107 (4), p.735-747

2012

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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

Biochimie, 2011-05, Vol.93 (5), p.876-891

2011

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A Novel Disorder Caused by Defective Biosynthesis of N-Linked Oligosaccharides Due to Glucosidase I Deficiency

American journal of human genetics, 2000-06, Vol.66 (6), p.1744-1756

2000

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Peroxisome deficient aP2aPex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

Molecular genetics and metabolism, 2012-12, Vol.107 (4), p.735-747

2012

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Erratum: Expression of Calcium‐Sensing Receptor in Quail Granulosa Explants: A Key to Survival During Folliculogenesis

Anatomical record (Hoboken, N.J. : 2007), 2010-06, Vol.293 (6), p.1099-1099

2010

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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

American journal of human genetics, 2002-04, Vol.70 (4), p.1062-1068

2002

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Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

BMC clinical pathology, 2009-06, Vol.9 (4), p.4-4, Article 4

2009

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Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria

Kidney international, 1996-11, Vol.50 (5), p.1747-1752

1996

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Inverse Expression of Peroxisomes and Connexin-43 in the Granulosa Cells of the Quail Follicle

The journal of histochemistry and cytochemistry, 2000-02, Vol.48 (2), p.167-177

2000

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Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures

Journal of hepatology, 2000-03, Vol.32 (3), p.381-391

2000

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Peroxisomes during development and in distinct cell types

Advances in experimental medicine and biology, 2003, Vol.544, p.39

2003

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

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

Human peroxisomal disorders

Peroxisomes in zebrafish: distribution pattern and knockdown studies

Mevalonate kinase is a cytosolic enzyme in humans

Phosphomevalonate kinase is a cytosolic protein in humans

Expression of Calcium‐Sensing Receptor in Quail Granulosa Explants: A Key to Survival During Folliculogenesis

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

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

Human mevalonate pyrophosphate decarboxylase is localized in the cytosol

Inborn errors of metabolism in the biosynthesis and remodelling of phospholipids

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

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

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

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

A Novel Disorder Caused by Defective Biosynthesis of N-Linked Oligosaccharides Due to Glucosidase I Deficiency

Peroxisome deficient aP2aPex5 knockout mice display impaired white adipocyte and muscle function concomitant with reduced adrenergic tone

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: ThB and cholesterol biosynthesis in the liver

Erratum: Expression of Calcium‐Sensing Receptor in Quail Granulosa Explants: A Key to Survival During Folliculogenesis

A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: A novel type of primary hyperoxaluria

Inverse Expression of Peroxisomes and Connexin-43 in the Granulosa Cells of the Quail Follicle

Effects of extracellular matrix on the expression of peroxisomes in primary rat hepatocyte cultures

Peroxisomes during development and in distinct cell types

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