(Q28646251)

3 February 2017

title

Characterization of the human gene encoding alpha-aminoadipate aminotransferase (AADAT) (English)

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3 February 2017

2

Ankita Patel

1 reference

3 February 2017

Denise L. M. Goh

1

1 reference

3 February 2017

George H. Thomas

3

1 reference

3 February 2017

Gajja S. Salomons

4

1 reference

3 February 2017

Danielle S. M. Schor

5

1 reference

3 February 2017

Cornelis Jakobs

6

1 reference

3 February 2017

Michael T. Geraghty

7

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3 February 2017

publication date

1 July 2002

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Molecular Genetics and Metabolism

3 February 2017

published in

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3 February 2017

volume

76

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3 February 2017

issue

3

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3 February 2017

page(s)

172–180

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The degradation of hydroxy-L-lysine in liver via its phosphate ester

3 February 2017

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Lysine metabolism in the rat brain: the pipecolic acid-forming pathway

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Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia

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7 January 2021

Identification of the alpha-aminoadipic semialdehyde dehydrogenase-phosphopantetheinyl transferase gene, the human ortholog of the yeast LYS5 gene

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7 January 2021

Purification and properties of 2-aminoadipate: 2-oxoglutarate aminotransferase from bovine kidney

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7 January 2021

Alpha-aminoadipate aminotransferase of rat liver mitochondria

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7 January 2021

L-kynurenine aminotransferase and L-α-aminoadipate aminotransferase. I. Evidence for identity

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7 January 2021

Purification, characterization and identification of rat liver mitochondrial kynurenine aminotransferase with alpha-aminoadipate aminotransferase

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7 January 2021

Purification and Properties of α-Aminoadipate Aminotransferase from Rat Kidney

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7 January 2021

Purification and properties of alpha-aminoadipate aminotransferase from rat liver and kidney mitochondria

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7 January 2021

Cloning and functional expression of a soluble form of kynurenine/alpha-aminoadipate aminotransferase from rat kidney

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7 January 2021

Genomic organization and expression analysis of mouse kynurenine aminotransferase II, a possible factor in the pathophysiology of Huntington's disease

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7 January 2021

Characterisation of Saccharomyces cerevisiae ARO8 and ARO9 genes encoding aromatic aminotransferases I and II reveals a new aminotransferase subfamily

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7 January 2021

Phenylalanine- and tyrosine-auxotrophic mutants of Saccharomyces cerevisiae impaired in transamination

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7 January 2021

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

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7 January 2021

Molecular characterization of Saccharomyces cerevisiae Delta3, Delta2-enoyl-CoA isomerase

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7 January 2021

RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

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7 January 2021

Crystal structures of Escherichia coli aspartate aminotransferase in two conformations. Comparison of an unliganded open and two liganded closed forms

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7 January 2021

Cytotoxic effects of acidic and sulphur containing amino acids on the infant mouse central nervous system

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7 January 2021

Stereospecificity of the gliotoxic and anti-neurotoxic actions of alpha-aminoadipate

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7 January 2021

Glutamate-induced cellular injury in isolated chick embryo retina: Müller cell localization of initial effects

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7 January 2021

Treatment with vigabatrin may mimic alpha-aminoadipic aciduria

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7 January 2021

alpha-Aminoadipic aciduria and persistence of fetal haemoglobin in an oligophrenic child

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7 January 2021

Abnormal alpha-aminoadipic acid excretion in a newborn with a defect in platelet aggregation and antenatal cerebral haemorrhage

1 reference

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7 January 2021

10.1016/S1096-7192(02)00037-9

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017