Related references
Note: Only part of the references are listed.The Saccharomyces cerevisiae ABC subfamily D transporter Pxa1/Pxa2p co-imports CoASH into the peroxisome
Carlo W. T. van Roermund et al.
FEBS LETTERS (2021)
Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mouse
Pablo Ranea-Robles et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2020)
Metabolic interactions between peroxisomes and mitochondria with a special focus on acylcarnitine metabolism
Sander M. Houten et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2020)
Schnyder corneal dystrophy-associated UBIAD1 is defective in MK-4 synthesis and resists autophagy-mediated degradation[S]
Dong-Jae Jun et al.
JOURNAL OF LIPID RESEARCH (2020)
Deletion of 2-aminoadipic semialdehyde synthase limits metabolite accumulation in cell and mouse models for glutaric aciduria type 1
Joao Leandro et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2020)
Functional Peroxisomes Are Essential for Efficient Cholesterol Sensing and Synthesis
Khanichi N. Charles et al.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2020)
Peroxisomes can oxidize medium- and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4
Sara Violante et al.
FASEB JOURNAL (2019)
Germline deletion of Kriippel-like factor 14 does not increase risk of diet induced metabolic syndrome in male C57BL/6 mice
Carmen A. Argmann et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2017)
The Biochemistry and Physiology of Mitochondrial Fatty Acid beta-Oxidation and Its Genetic Disorders
Sander M. Houten et al.
ANNUAL REVIEW OF PHYSIOLOGY, VOL 78 (2016)
Compartmentation of Metabolism of the C12-, C9-, and C5-n-dicarboxylates in Rat Liver, Investigated by Mass Isotopomer Analysis ANAPLEROSIS FROM DODECANEDIOATE
Zhicheng Jin et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2015)
limma powers differential expression analyses for RNA-sequencing and microarray studies
Matthew E. Ritchie et al.
NUCLEIC ACIDS RESEARCH (2015)
Tissue-based map of the human proteome
Mathias Uhlen et al.
SCIENCE (2015)
Decreased carbon shunting from glucose toward oxidative metabolism in diet-induced ketotic rat brain
Yifan Zhang et al.
JOURNAL OF NEUROCHEMISTRY (2015)
A role for the human peroxisomal half-transporter ABCD3 in the oxidation of dicarboxylic acids
Carlo W. T. van Roermund et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2014)
Disturbances in cholesterol, bile acid and glucose metabolism in peroxisomal 3-ketoacylCoA thiolase B deficient mice fed diets containing high or low fat contents
Valerie Nicolas-Frances et al.
BIOCHIMIE (2014)
Regulation of peroxisomal lipid metabolism: The role of acyl-CoA and coenzyme A metabolizing enzymes
Mary C. Hunt et al.
BIOCHIMIE (2014)
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Yang Liao et al.
BIOINFORMATICS (2014)
voom: precision weights unlock linear model analysis tools for RNA-seq read counts
Charity W. Law et al.
GENOME BIOLOGY (2014)
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Michael I. Love et al.
GENOME BIOLOGY (2014)
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient
Sara Violante et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2013)
STAR: ultrafast universal RNA-seq aligner
Alexander Dobin et al.
BIOINFORMATICS (2013)
Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects
Sander M. Houten et al.
HUMAN MOLECULAR GENETICS (2013)
Carnitine supplementation attenuates myocardial lipid accumulation in long-chain acyl-CoA dehydrogenase knockout mice
Adrianus J. Bakermans et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2013)
Genome engineering using the CRISPR-Cas9 system
F. Ann Ran et al.
NATURE PROTOCOLS (2013)
The Peroxisomal Enzyme L-PBE Is Required to Prevent the Dietary Toxicity of Medium-Chain Fatty Acids
Jun Ding et al.
CELL REPORTS (2013)
Biochemical Competition Makes Fatty-Acid β-Oxidation Vulnerable to Substrate Overload
Karen van Eunen et al.
PLOS COMPUTATIONAL BIOLOGY (2013)
Peroxisomal L-bifunctional enzyme (Ehhadh) is essential for the production of medium-chain dicarboxylic acids
Sander M. Houten et al.
JOURNAL OF LIPID RESEARCH (2012)
Acadl-SNP based genotyping assay for long-chain acyl-CoA dehydrogenase deficient mice
Rita J. Luther et al.
MOLECULAR GENETICS AND METABOLISM (2012)
Fiji: an open-source platform for biological-image analysis
Johannes Schindelin et al.
NATURE METHODS (2012)
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
Marco Fidaleo et al.
BIOCHIMIE (2011)
Preparation and incubation of precision-cut liver and intestinal slices for application in drug metabolism and toxicity studies
Inge A. M. de Graaf et al.
NATURE PROTOCOLS (2010)
Improved reproducibility in preparing precision-cut liver tissue slices
Martina Zimmermann et al.
CYTOTECHNOLOGY (2009)
Triglyceride Synthesis in Epididymal Adipose Tissue CONTRIBUTION OF GLUCOSE AND NON-GLUCOSE CARBON SOURCES
Ilya R. Bederman et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Peroxisome Deficiency Causes a Complex Phenotype because of Hepatic SREBP/Insig Dysregulation Associated with Endoplasmic Reticulum Stress
Werner J. Kovacs et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Degradation of very long chain dicarboxylic polyunsaturated fatty acids in mouse hopatocytes, a peroxisomal process
Su Duy Nguyen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2008)
Coordinate induction of PPARα and SREBP2 in multifunctional protein 2 deficient mice
Katrin Martens et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS (2008)
Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidation
Malika Chegary et al.
MOLECULAR GENETICS AND METABOLISM (2008)
β-oxidation in hepatocyte cultures from mice with peroxisomal gene knockouts
Ruud Dirkx et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2007)
Localization of the pre-squalene segment of the isoprenoid biosynthetic pathway in mammalian peroxisomes
Werner J. Kovacs et al.
HISTOCHEMISTRY AND CELL BIOLOGY (2007)
Analysis of the mouse and human acyl-CoA thioesterase (ACOT) gene clusters shows that convergent, functional evolution results in a reduced number of human peroxisomal ACOTs
Mary C. Hunt et al.
FASEB JOURNAL (2006)
The identification of a succinyl-CoA thioesterase suggests a novel pathway for succinate production in peroxisomes
MAK Westin et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
A Subramanian et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Probing peroxisornal β-oxidation and the labelling of acetyl-CoA proxies with [1-13C]octanoate and [3-13C] octanoate in the perfused rat liver
T Kasumov et al.
BIOCHEMICAL JOURNAL (2005)
Precision-cut liver slices as a new model to study toxicity-induced hepatic stellate cell activation in a physiologic milieu
M van de Bovenkamp et al.
TOXICOLOGICAL SCIENCES (2005)
Phosphomevalonate kinase is a cytosolic protein in humans
S Hogenboom et al.
JOURNAL OF LIPID RESEARCH (2004)
Mevalonate kinase is a cytosolic enzyme in humans
S Hogenboom et al.
JOURNAL OF CELL SCIENCE (2004)
Disrupted blastocoele formation reveals a critical developmental role for long-chain acyl-CoA dehydrogenase
PS Berger et al.
MOLECULAR GENETICS AND METABOLISM (2004)
Disturbed cholesterol homeostasis in a peroxisome-deficient PEX2 knockout mouse model
WJ Kovacs et al.
MOLECULAR AND CELLULAR BIOLOGY (2004)
Identification of the peroxisomal β-oxidation enzymes involved in the degradation of long-chain dicarboxylic acids
S Ferdinandusse et al.
JOURNAL OF LIPID RESEARCH (2004)
Influence of diet on the modeling of adipose tissue triglycerides during growth
DZ Brunengraber et al.
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM (2003)
Characterization of an acyl-CoA thioesterase that functions as a major regulator of peroxisomal lipid metabolism
MC Hunt et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse
KB Cox et al.
HUMAN MOLECULAR GENETICS (2001)