Succinic semialdehyde dehydrogenase: biochemical-molecular-clinical disease mechanisms, redox regulation, and functional significance
about
Structural Basis for a Cofactor-dependent Oxidation Protection and Catalysis of Cyanobacterial Succinic Semialdehyde DehydrogenaseStructure and activity of the NAD(P)+-dependent succinate semialdehyde dehydrogenase YneI from Salmonella typhimuriumDisorders of GABA metabolism: SSADH and GABA-transaminase deficienciesAldehyde dehydrogenase inhibitors: a comprehensive review of the pharmacology, mechanism of action, substrate specificity, and clinical applicationThe Concise Guide to PHARMACOLOGY 2013/14: enzymes.The aldo-keto reductases (AKRs): Overview.Inherited disorders of gamma-aminobutyric acid metabolism and advances in ALDH5A1 mutation identification.Redox-switch regulatory mechanism of thiolase from Clostridium acetobutylicum.Quantitation of gamma-hydroxybutyric acid in dried blood spots: feasibility assessment for newborn screening of succinic semialdehyde dehydrogenase (SSADH) deficiency.RNA interference-mediated knockdown of the hydroxyacid-oxoacid transhydrogenase gene decreases thiamethoxam resistance in adults of the whitefly Bemisia tabaci.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Non-enzymatic chemistry enables 2-hydroxyglutarate-mediated activation of 2-oxoglutarate oxygenases.Defects in GABA metabolism affect selective autophagy pathways and are alleviated by mTOR inhibition.Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismTherapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.Kinetic and structural characterization for cofactor preference of succinic semialdehyde dehydrogenase from Streptococcus pyogenes.Evidence of redox imbalance in a patient with succinic semialdehyde dehydrogenase deficiencyEfficacy of vigabatrin intervention in a mild phenotypic expression of succinic semialdehyde dehydrogenase deficiency.A novel mutation of ALDH5A1 gene associated with succinic semialdehyde dehydrogenase deficiency.Linkage exclusion in Italian families with hereditary essential tremor.Modeling conformational redox-switch modulation of human succinic semialdehyde dehydrogenase.A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family.
P2860
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P2860
Succinic semialdehyde dehydrogenase: biochemical-molecular-clinical disease mechanisms, redox regulation, and functional significance
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Succinic semialdehyde dehydrog ...... n, and functional significance
@ast
Succinic semialdehyde dehydrog ...... n, and functional significance
@en
Succinic semialdehyde dehydrog ...... n, and functional significance
@nl
type
label
Succinic semialdehyde dehydrog ...... n, and functional significance
@ast
Succinic semialdehyde dehydrog ...... n, and functional significance
@en
Succinic semialdehyde dehydrog ...... n, and functional significance
@nl
prefLabel
Succinic semialdehyde dehydrog ...... n, and functional significance
@ast
Succinic semialdehyde dehydrog ...... n, and functional significance
@en
Succinic semialdehyde dehydrog ...... n, and functional significance
@nl
P2093
P2860
P356
P1476
Succinic semialdehyde dehydrog ...... n, and functional significance
@en
P2093
Cornelis Jakobs
K Michael Gibson
Kimmo Jensen
Kyung-Jin Kim
O Carter Snead
Patrizia Malaspina
Phillip L Pearl
P2860
P304
P356
10.1089/ARS.2010.3470
P407
P577
2011-08-01T00:00:00Z