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Sulforaphane treatment of autism spectrum disorder (ASD)

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (43), p.15550-15555

2014

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Role of ACSBG1 in Brain Lipid Metabolism and X-Linked Adrenoleukodystrophy Pathogenesis: Insights from a Knockout Mouse Model

Cells (Basel, Switzerland), 2024-10, Vol.13 (20), p.1687

2024

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Activation of the stress proteome as a mechanism for small molecule therapeutics

Human molecular genetics, 2012-10, Vol.21 (19), p.4237-4252

2012

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Hydroxyurea Improves Spatial Memory and Cognitive Plasticity in Mice and Has a Mild Effect on These Parameters in a Down Syndrome Mouse Model

Frontiers in aging neuroscience, 2019-05, Vol.11, p.96-96

2019

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Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

Annals of neurology, 2001-04, Vol.49 (4), p.512-517

2001

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Hydroxyurea attenuates oxidative, metabolic, and excitotoxic stress in rat hippocampal neurons and improves spatial memory in a mouse model of Alzheimer's disease

Neurobiology of aging, 2018-12, Vol.72, p.121-133

2018

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Participation of Two Members of the Very Long-chain Acyl-CoA Synthetase Family in Bile Acid Synthesis and Recycling

The Journal of biological chemistry, 2002-07, Vol.277 (27), p.24771-24779

2002

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SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes

Journal of neurology, 2012-07, Vol.259 (7), p.1440-1447

2012

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Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: A novel neonatal phenotype similar to peroxisomal biogenesis disorders

American journal of human genetics, 2002-06, Vol.70 (6), p.1520-1531

2002

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Adreno-leukodystrophy: Oxidative Stress of Mice and Men

Journal of neuropathology and experimental neurology, 2005-12, Vol.64 (12), p.1067-1079

2005

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Mouse Very Long-chain Acyl-CoA Synthetase in X-linked Adrenoleukodystrophy

The Journal of biological chemistry, 2002-08, Vol.277 (32), p.28765-28773

2002

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PEX11α Is Required for Peroxisome Proliferation in Response to 4-Phenylbutyrate but Is Dispensable for Peroxisome Proliferator-Activated Receptor Alpha-Mediated Peroxisome Proliferation

Molecular and Cellular Biology, 2002-12, Vol.22 (23), p.8226-8240

2002

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Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy

Nature medicine, 1998-11, Vol.4 (11), p.1261-1268

1998

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Role of Cyclic Nucleotides in Fetal Hemoglobin Induction in Cultured CD34 + Cells

Experimental hematology, 2006-09, Vol.34 (9), p.1150-1160

2006

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A Mouse Model for X-Linked Adrenoleukodystrophy

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (17), p.9366-9371

1997

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A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy

Human molecular genetics, 2003-05, Vol.12 (10), p.1145-1154

2003

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The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidation

The Journal of biological chemistry, 2003-11, Vol.278 (47), p.47070-47078

2003

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Potential Environmental and Host Participants in the Early White Matter Lesion of Adreno-Leukodystrophy: Morphologic Evidence for CD8 Cytotoxic T Cells, Cytolysis of Oligodendrocytes, and CD1-Mediated Lipid Antigen Presentation

Journal of neuropathology and experimental neurology, 2001-10, Vol.60 (10), p.1004-1019

2001

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The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage

Laboratory investigation, 2007-03, Vol.87 (3), p.261-272

2007

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X-linked adrenoleukodystrophy : Genes, mutations, and phenotypes

Neurochemical research, 1999, Vol.24 (4), p.521-535

1999

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Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations

The Journal of biological chemistry, 1998-07, Vol.273 (29), p.18210-18219

1998

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Pharmacological induction of peroxisomes in peroxisome biogenesis disorders

Annals of neurology, 2000-03, Vol.47 (3), p.286-296

2000

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Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders

American journal of human genetics, 2002-06, Vol.70 (6), p.1520-1531

2002

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One-Step Multiplex PCR Strategy for Identification of Mutations by SSCP and DNA Sequencing

BioTechniques, 2000-08, Vol.29 (2), p.234-236

2000

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X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases

Molecular genetics and metabolism, 2004-09, Vol.83 (1), p.117-127

2004

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Sulforaphane treatment of autism spectrum disorder (ASD)

Role of ACSBG1 in Brain Lipid Metabolism and X-Linked Adrenoleukodystrophy Pathogenesis: Insights from a Knockout Mouse Model

Activation of the stress proteome as a mechanism for small molecule therapeutics

Hydroxyurea Improves Spatial Memory and Cognitive Plasticity in Mice and Has a Mild Effect on These Parameters in a Down Syndrome Mouse Model

Adrenoleukodystrophy: Incidence, new mutation rate, and results of extended family screening

Hydroxyurea attenuates oxidative, metabolic, and excitotoxic stress in rat hippocampal neurons and improves spatial memory in a mouse model of Alzheimer's disease

Participation of Two Members of the Very Long-chain Acyl-CoA Synthetase Family in Bile Acid Synthesis and Recycling

SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: A novel neonatal phenotype similar to peroxisomal biogenesis disorders

Adreno-leukodystrophy: Oxidative Stress of Mice and Men

Mouse Very Long-chain Acyl-CoA Synthetase in X-linked Adrenoleukodystrophy

PEX11α Is Required for Peroxisome Proliferation in Response to 4-Phenylbutyrate but Is Dispensable for Peroxisome Proliferator-Activated Receptor Alpha-Mediated Peroxisome Proliferation

Gene redundancy and pharmacological gene therapy: Implications for X-linked adrenoleukodystrophy

Role of Cyclic Nucleotides in Fetal Hemoglobin Induction in Cultured CD34 + Cells

A Mouse Model for X-Linked Adrenoleukodystrophy

A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy

The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidation

Potential Environmental and Host Participants in the Early White Matter Lesion of Adreno-Leukodystrophy: Morphologic Evidence for CD8 Cytotoxic T Cells, Cytolysis of Oligodendrocytes, and CD1-Mediated Lipid Antigen Presentation

The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage

X-linked adrenoleukodystrophy : Genes, mutations, and phenotypes

Disruption of the Saccharomyces cerevisiae FAT1 gene decreases very long-chain fatty acyl-CoA synthetase activity and elevates intracellular very long-chain fatty acid concentrations

Pharmacological induction of peroxisomes in peroxisome biogenesis disorders

Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders

One-Step Multiplex PCR Strategy for Identification of Mutations by SSCP and DNA Sequencing

X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases

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