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Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

The Journal of clinical investigation, 2002-07, Vol.110 (2), p.259-269

2002

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Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts

Journal of lipid research, 1998-01, Vol.39 (1), p.66-74

1998

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Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders

Molecular genetics and metabolism, 2007-12, Vol.92 (4), p.346-350

2007

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2-Methylbutyryl-coenzyme A dehydrogenase deficiency : A new inborn error of L-isoleucine metabolism

Pediatric research, 2000-06, Vol.47 (6), p.830-833

2000

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Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening

Pediatric research, 2006-09, Vol.60 (3), p.315-320

2006

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Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans

Molecular genetics and metabolism, 2002-09, Vol.77 (1), p.68-79

2002

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Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

Clinica chimica acta, 2001-10, Vol.312 (1), p.55-67

2001

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Detection of gene defects in branched-chain amino acid metabolism by tandem mass spectrometry of carnitine esters produced by cultured fibroblasts

Methods in enzymology, 2000, Vol.324, p.424

2000

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Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated α-fetoprotein and cystic renal changes

Prenatal diagnosis, 2001-10, Vol.21 (10), p.856-859

2001

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Recent Developments in the Investigation of Inherited Metabolic Disorders Using Cultured Human Cells

Molecular Genetics and Metabolism, 1999-10, Vol.68 (2), p.243-257

1999

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Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism

Molecular genetics and metabolism, 1998-12, Vol.65 (4), p.264-271

1998

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Evidence for a Short-Chain Carnitine–Acylcarnitine Translocase in Mitochondria Specifically Related to the Metabolism of Branched-Chain Amino Acids

Molecular genetics and metabolism, 2000-01, Vol.69 (1), p.69-75

2000

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Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

The Journal of clinical investigation, 2002-07, Vol.110 (2), p.259-269

2002

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Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family

Molecular genetics and metabolism, 2001-05, Vol.73 (1), p.64-70

2001

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Methylmalonic Semialdehyde Dehydrogenase Deficiency: Psychomotor Delay and Methylmalonic Aciduria without Metabolic Decompensation

Molecular genetics and metabolism, 1998-09, Vol.65 (1), p.35-43

1998

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Methylmalonic aciduria in pregnancy: A case report

American journal of obstetrics and gynecology, 1995-03, Vol.172 (3), p.1057-1059

1995

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Identification of Two Novel Mutations in the Hypoglycemic Phenotype of Very Long Chain Acyl-CoA Dehydrogenase Deficiency

Biochemical and biophysical research communications, 1999-10, Vol.264 (2), p.483-487

1999

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Automated analysis for free and short-chain acylcarnitine in plasma with a centrifugal analyzer

Clinical chemistry (Baltimore, Md.), 1992-11, Vol.38 (11), p.2215-2220

1992

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From Poachers to Protectors: Engaging Local Communities in Solutions to Illegal Wildlife Trade

Conservation letters, 2017-05, Vol.10 (3), p.367-374

2017

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Differential regulation of CD103 (αE integrin) expression in human dendritic cells by retinoic acid and Toll‐like receptor ligands

Journal of leukocyte biology, 2017-05, Vol.101 (5), p.1169-1180

2017

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Sensitivity and engineered resistance of myeloid leukemia cells to BRD9 inhibition

Nature chemical biology, 2016-09, Vol.12 (9), p.672-679

2016

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Retinoic acid-induced expression of CD103 in human DCs is dependent on p38 MAPK signaling and NFAT1c

The Journal of immunology (1950), 2019-05, Vol.202 (1_Supplement), p.59-59.16

2019

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A Synthetic Hydrogel, VitroGel ® ORGANOID-3, Improves Immune Cell-Epithelial Interactions in a Tissue Chip Co-Culture Model of Human Gastric Organoids and Dendritic Cells

Frontiers in pharmacology, 2021-09, Vol.12, p.707891-707891

2021

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p38 MAPK signaling mediates retinoic acid‐induced CD103 expression in human dendritic cells

Immunology, 2020-11, Vol.161 (3), p.230-244

2020

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Does the consumption of caloric and non-caloric beverages with a meal affect energy intake?

Appetite, 2005-04, Vol.44 (2), p.187-193

2005

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Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

Phytanic acid and pristanic acid are oxidized by sequential peroxisomal and mitochondrial reactions in cultured fibroblasts

Choice of oils for essential fat supplements can enhance production of abnormal metabolites in fat oxidation disorders

2-Methylbutyryl-coenzyme A dehydrogenase deficiency : A new inborn error of L-isoleucine metabolism

Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening

Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans

Oxidation of unsaturated fatty acids by human fibroblasts with very-long-chain acyl-CoA dehydrogenase deficiency: aspects of substrate specificity and correlation with clinical phenotype

Detection of gene defects in branched-chain amino acid metabolism by tandem mass spectrometry of carnitine esters produced by cultured fibroblasts

Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: association with elevated α-fetoprotein and cystic renal changes

Recent Developments in the Investigation of Inherited Metabolic Disorders Using Cultured Human Cells

Isolated Isobutyryl-CoA Dehydrogenase Deficiency: An Unrecognized Defect in Human Valine Metabolism

Evidence for a Short-Chain Carnitine–Acylcarnitine Translocase in Mitochondria Specifically Related to the Metabolism of Branched-Chain Amino Acids

Treatment of cardiomyopathy and rhabdomyolysis in long-chain fat oxidation disorders using an anaplerotic odd-chain triglyceride

Carnitine/Acylcarnitine Translocase Deficiency (Neonatal Phenotype): Successful Prenatal and Postmortem Diagnosis Associated with a Novel Mutation in a Single Family

Methylmalonic Semialdehyde Dehydrogenase Deficiency: Psychomotor Delay and Methylmalonic Aciduria without Metabolic Decompensation

Methylmalonic aciduria in pregnancy: A case report

Identification of Two Novel Mutations in the Hypoglycemic Phenotype of Very Long Chain Acyl-CoA Dehydrogenase Deficiency

Automated analysis for free and short-chain acylcarnitine in plasma with a centrifugal analyzer

From Poachers to Protectors: Engaging Local Communities in Solutions to Illegal Wildlife Trade

Differential regulation of CD103 (αE integrin) expression in human dendritic cells by retinoic acid and Toll‐like receptor ligands

Sensitivity and engineered resistance of myeloid leukemia cells to BRD9 inhibition

Retinoic acid-induced expression of CD103 in human DCs is dependent on p38 MAPK signaling and NFAT1c

A Synthetic Hydrogel, VitroGel ® ORGANOID-3, Improves Immune Cell-Epithelial Interactions in a Tissue Chip Co-Culture Model of Human Gastric Organoids and Dendritic Cells

p38 MAPK signaling mediates retinoic acid‐induced CD103 expression in human dendritic cells

Does the consumption of caloric and non-caloric beverages with a meal affect energy intake?

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