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ASPA gene

Known as: AMINOACYLASE 2, ASPA, Canavan disease 
National Institutes of Health

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Aspartic Acid
Canavan Disease

Papers overview

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2015
2015
Catalytic cycle of aspartoacylase by the results of molecular dynamics and QM/MM simulations
2013
2013
Canavan Disease Mri and Mrs Findings: 3 Different Cases
Canavan disease is an autosomal recessively inherited severe progressive leukodystrophy and is rarely seen in nonJewish… 
2011
2011
[Deletion of the LIS1, ASPA, TRPV1 and CAMTA2 genes in region 17p13.3 in a patient with Miller-Dieker syndrome].
2009
2009
NON-JEWISH CHILD WITH CANAVAN DISEASE
Canavan disease (CD) is a rare autosomal recessive inherited disorder caused by a deficiency of aspartoacylase, which leads to… 
2006
2006
The Molecular Basis of Canavan Disease: Aspartoacylase Enzyme Characteristics
Abstract : Mutations in the gene for aspartoacylase (EC 3.5.1.15; ASPA), which catalyzes deacetylation of N-acetyl-L-aspartate… 
2001
2001
Cellular and developmental tissue distribution of NAA catabolic enzyme, aspartoacylase. Insights into NAA Function.
Methods Tissue harvest: Tissues from various regions of the rat brain, at key ages during postnatal development and maturation… 
2000
2000
MRUMRS of a Mouse Model for Canavan Disease
Introduction Canavan disease (CD) is an autosomal recessive leukodystrophy associated with spongy degeneration of the white… 
1984
1984
紡錘波自動分析装置 (ASPA) の製作と評価
1978
1978
Polymorphism of the cobalt-activated acylase in human tissues.
A method was elaborated for obtaining polyacrylamide gel zymograms of the cobalt-activated acylase after electrophoresis. Two…