Identification and characterization of new long chain acyl-CoA dehydrogenases (Q24337104)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21237683%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

Identification and characterization of new long chain acyl-CoA dehydrogenases (English)

1 reference

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Acyl-CoA dehydrogenase family member 11

20 January 2020

main subject

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Acyl-CoA dehydrogenase family member 9

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Acyl-CoA dehydrogenase medium chain

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Acyl-CoA dehydrogenase family member 10

1 reference

author

Al-Walid Mohsen

3

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20 January 2020

Jerry Vockley

8

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20 January 2020

6

Paul P Van Veldhoven

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20 January 2020

author name string

Miao He

1

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20 January 2020

Zhengtong Pei

2

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20 January 2020

Paul Watkins

4

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20 January 2020

Geoffrey Murdoch

5

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20 January 2020

Regina Ensenauer

7

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20 January 2020

language of work or name

English

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publication date

17 December 2010

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Molecular Genetics and Metabolism

20 January 2020

published in

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20 January 2020

volume

102

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20 January 2020

issue

4

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20 January 2020

page(s)

418-429

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Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I

20 January 2020

cites work

1 reference

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Evidence for Physical Association of Mitochondrial Fatty Acid Oxidation and Oxidative Phosphorylation Complexes

19 March 2017

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A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency

19 March 2017

1 reference

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Proteomic analysis of rat liver peroxisome: presence of peroxisome-specific isozyme of Lon protease

19 March 2017

1 reference

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Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients

19 March 2017

1 reference

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

19 March 2017

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A novel approach to the characterization of substrate specificity in short/branched chain Acyl-CoA dehydrogenase

19 March 2017

1 reference

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Global survey of organ and organelle protein expression in mouse: combined proteomic and transcriptomic profiling

19 March 2017

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Peroxisomal beta-oxidation of 2-methyl-branched acyl-CoA esters: stereospecific recognition of the 2S-methyl compounds by trihydroxycoprostanoyl-CoA oxidase and pristanoyl-CoA oxidase

19 March 2017

1 reference

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Mitochondrial regulation of neuronal plasticity

19 March 2017

1 reference

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Alternative splicing: new insights from global analyses

27 September 2017

1 reference

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Modulation by phenylacetate of early estrogen-mediated events in MCF-7 breast cancer cells

27 September 2017

1 reference

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Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3073726

Cloning and characterization of a human cDNA ACAD10 mapped to chromosome 12q24.1.

27 September 2017

1 reference

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Why is carbon from some polyunsaturates extensively recycled into lipid synthesis?

27 September 2017

1 reference

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Defects of mitochondrial beta-oxidation: a growing group of disorders.

27 September 2017

1 reference

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Peroxisomal fatty acid alpha- and beta-oxidation in humans: enzymology, peroxisomal metabolite transporters and peroxisomal diseases

27 September 2017

1 reference

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Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies

27 September 2017

1 reference

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Changes in the fatty acid composition of cerebrosides and sulfatides of human nervous tissue with age

30 May 2018

1 reference

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The variant human isovaleryl-CoA dehydrogenase gene responsible for type II isovaleric acidemia determines an RNA splicing error, leading to the deletion of the entire second coding exon and the production of a truncated precursor protein that inter

30 May 2018

1 reference

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Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB gene

30 May 2018

1 reference

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Pilot study of combination transcriptional modulation therapy with sodium phenylbutyrate and 5-azacytidine in patients with acute myeloid leukemia or myelodysplastic syndrome.

29 November 2018

1 reference

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Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency

29 November 2018

1 reference

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Mechanisms of cytotoxicity induced by horseradish peroxidase/indole-3-acetic acid gene therapy

29 November 2018

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Identification and purification of a peroxisomal branched chain fatty acyl-CoA oxidase

29 November 2018

1 reference

12 December 2020

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Identification of the molecular defects responsible for the various genotypes of isovaleric acidemia

1 reference

12 December 2020

Clinical and neurophysiologic response of myopathy and neuropathy in long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency to oral prednisone

1 reference

12 December 2020

Human long chain, very long chain and medium chain acyl-CoA dehydrogenases are specific for the S-enantiomer of 2- methylpentadecanoyl-CoA

1 reference

12 December 2020

Identification of the catalytic residue of human short/branched chain acyl-CoA dehydrogenase by in vitro mutagenesis

1 reference

12 December 2020

IBR3, a novel peroxisomal acyl-CoA dehydrogenase-like protein required for indole-3-butyric acid response

1 reference

12 December 2020

10.1016/J.YMGME.2010.12.005

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21237683%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21237683%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

PubMed publication ID

21237683

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