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Characterization of the human mitochondrial aconitase gene (ACO2)
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scholarly article
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title
Characterization of the human mitochondrial aconitase gene (ACO2)
(English)
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main subject
Aconitase 2
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stated in
GOA release 2020-03-11
citrate metabolic process
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stated in
GOA release 2020-03-11
author
Richard Mayeux
series ordinal
6
object named as
R Mayeux
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Karen S. Marder
series ordinal
2
object named as
K Marder
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Greg Freyer
series ordinal
4
object named as
G Freyer
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J Graziano
series ordinal
3
object named as
J Graziano
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Kirk Wilhelmsen
series ordinal
7
object named as
K C Wilhelmsen
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D Mirel
series ordinal
1
object named as
D B Mirel
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author name string
Q Zhao
series ordinal
5
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language of work or name
English
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publication date
15 June 1998
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published in
Gene
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volume
213
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issue
1-2
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page(s)
205-18
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cites work
Ecogenetics of Parkinson's disease: 4-hydroxylation of debrisoquine
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The free radical hypothesis in idiopathic parkinsonism: evidence against it
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The density of [125I]-transferrin binding sites on perikarya of melanized neurons of the substantia nigra is decreased in Parkinson's disease.
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Molecular cloning of the yeast mitochondrial aconitase gene (ACO1) and evidence of a synergistic regulation of expression by glucose plus glutamate
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Reciprocal control of RNA-binding and aconitase activity in the regulation of the iron-responsive element binding protein: role of the iron-sulfur cluster
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Oxidative damage in neurodegenerative disease
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A regulated RNA binding protein also possesses aconitase activity
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Identification of a conserved and functional iron-responsive element in the 5'-untranslated region of mammalian mitochondrial aconitase
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A bacterial artificial chromosome-based framework contig map of human chromosome 22q.
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A double life: cytosolic aconitase as a regulatory RNA binding protein
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Regulating the fate of mRNA: the control of cellular iron metabolism
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The I.M.A.G.E. Consortium: an integrated molecular analysis of genomes and their expression
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A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study
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Dietary lipids and antioxidants in Parkinson's disease: a population-based, case-control study
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The frequency of idiopathic Parkinson's disease by age, ethnic group, and sex in northern Manhattan, 1988-1993
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Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
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The future of genetic studies of complex human diseases
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Structure of activated aconitase: formation of the [4Fe-4S] cluster in the crystal
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Binding of a cytosolic protein to the iron-responsive element of human ferritin messenger RNA
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Cloning of the cDNA encoding an RNA regulatory protein--the human iron-responsive element-binding protein
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Aconitase polymorphism in man
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Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease
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An expression-independent catalog of genes from human chromosome 22.
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A novel cytochrome P-450IID6 mutant gene associated with Parkinson's disease
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Diseases resulting from mitochondrial DNA point mutations
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Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13?
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Identifiers
DOI
10.1016/S0378-1119(98)00188-7
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PubMed ID
9630632
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