hydralazine 4-anisaldehyde hydrazone

Known as: HPAH 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2017
024619962017

Papers overview

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2014
2014
BACKGROUND Pulmonary arterial hypertension (PAH) is a lethal disease characterized by excessive proliferation of pulmonary… (More)
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2013
2013
4-Hydroxyphenylacetate 3-hydroxylases (HPAHs) of the two-component flavin-dependent monooxygenase family are attractive enzymes… (More)
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2011
2011
BACKGROUND: Hereditary pulmonary arterial hypertension(PAH) is usually caused by mutations in BMPR2. Mutations are found… (More)
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2007
2007
The interaction of the gram-negative phytopathogenic bacterium Xanthomonas campestris pv. vesicatoria with its host plants pepper… (More)
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2005
2005
p-Hydroxyphenylacetate (HPA) hydroxylase (HPAH) from Acinetobacter baumannii catalyzes hydroxylation of HPA to form 3,4… (More)
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2004
2004
Phenylketonuria (PKU) is an autosomal recessive metabolic disorder caused by a deficiency of phenylalanine hydroxylase (PAH). The… (More)
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2003
2003
Phenylalanine hydroxylase (PAH) is a multidomain tetrameric enzyme that displays positive cooperative substrate binding. This… (More)
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2001
2001
p-Hydroxyphenylacetate (HPA) hydroxylase (HPAH) was purified from Acinetobacter baumannii and shown to be a two-protein component… (More)
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1997
1997
The Klebsiella pneumoniae genes encoding the hydroxylase involved in the meta-cleavage pathway of 4-hydroxyphenylacetic acid (4… (More)
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1996
1996
Amino-terminal and carboxy-terminal deletion mutagenesis have been used to identify structurally and functionally critical… (More)
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