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C1ql1 expression in oligodendrocyte progenitor cells promotes oligodendrocyte differentiation. [PDF]

open access: yesFEBS J
Altunay ZM   +15 more
europepmc   +1 more source
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Purification and preliminary characterization of brain aspartoacylase

Archives of Biochemistry and Biophysics, 2003
Aspartoacylase catalyzes the deacetylation of N-acetylaspartic acid (NAA) in the brain to produce acetate and L-aspartate. An aspartoacylase deficiency, with concomitant accumulation of NAA, is responsible for Canavan disease, a lethal autosomal recessive disorder.
Roger A, Moore   +3 more
openaire   +4 more sources

Expression of aspartoacylase (ASPA) and Canavan disease

Gene, 2012
Canavan disease (CD) is a neurodegenerative disorder usually presenting in the first six months of life. CD patients can be identified via elevated levels of N-acetyl-l-aspartate in the pattern of urinary organic acids assessed by gas chromatography-mass spectrometry.
Sommer, Anke, Saß, Jörn-Oliver
openaire   +4 more sources

Modeling the Complete Catalytic Cycle of Aspartoacylase

The Journal of Physical Chemistry B, 2016
The complete catalytic cycle of aspartoacylase (ASPA), a zinc-dependent enzyme responsible for cleavage of N-acetyl-l-aspartate, is characterized by the methods of molecular modeling. The reaction energy profile connecting the enzyme-substrate (ES) and the enzyme-product (EP) complexes is constructed by the quantum mechanics/molecular mechanics (QM/MM)
Ekaterina D, Kots   +5 more
openaire   +2 more sources

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