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ALDH7A1 gene

Known as: AASA DEHYDROGENASE, ALDEHYDE DEHYDROGENASE 7 FAMILY, MEMBER A1, delta1-piperideine-6-carboxylate dehydrogenease 
 
National Institutes of Health

Papers overview

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Review
2011
Review
2011
Antiquitin (ATQ) deficiency is the main cause of pyridoxine dependent epilepsy characterized by early onset epileptic… Expand
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Highly Cited
2010
Highly Cited
2010
Pyridoxine-dependent epilepsy was recently shown to be due to mutations in the ALDH7A1 gene, which encodes antiquitin, an enzyme… Expand
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Highly Cited
2010
Highly Cited
2010
Mammalian ALDH7A1 is homologous to plant ALDH7B1, an enzyme that protects against various forms of stress, such as salinity… Expand
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Highly Cited
2010
Highly Cited
2010
Huntington disease (HD) is an inherited neurodegenerative disorder that initially affects the striatum and progressively the… Expand
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Highly Cited
2007
Highly Cited
2007
Patients with pyridoxine dependent epilepsy (PDE) present with early-onset seizures resistant to common anticonvulsants… Expand
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Highly Cited
2006
Highly Cited
2006
Despite extensive studies in eukaryotic aldehyde dehydrogenases, functional information about the ALDH7 antiquitin-like proteins… Expand
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Highly Cited
2006
Highly Cited
2006
We show here that children with pyridoxine-dependent seizures (PDS) have mutations in the ALDH7A1 gene, which encodes antiquitin… Expand
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Highly Cited
2006
Highly Cited
2006
John P. Castagna, University of Houston, and Shengjie Sun, Fusion Geophysical discuss a number of different methods for spectral… Expand
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Highly Cited
2004
Highly Cited
2004
Angus steers of known age (265 +/- 17 d) and parentage were used in a 2-yr study (yr 1, n = 40; yr 2, n = 45) to evaluate the… Expand
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Review
1998
Review
1998
Twelve aldehyde dehydrogenase (ALDH) genes have been identified in humans. These genes, located on different chromosomes, encode… Expand
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