Neurotransmitter alterations in embryonic succinate semialdehyde dehydrogenase (SSADH) deficiency suggest a heightened excitatory state during development
about
Succinic semialdehyde dehydrogenase: biochemical-molecular-clinical disease mechanisms, redox regulation, and functional significancePhenotype of GABA-transaminase deficiency.A new case of GABA transaminase deficiency facilitated by proton MR spectroscopy.Novel QTL at chromosome 6p22 for alcohol consumption: Implications for the genetic liability of alcohol use disorders.Thirty years beyond discovery--clinical trials in succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism.Effect of gene dosage on single-cell hippocampal electrophysiology in a murine model of SSADH deficiency (gamma-hydroxybutyric aciduria).Plasticity of postsynaptic, but not presynaptic, GABAB receptors in SSADH deficient mice.'Succinic semialdehyde dehydrogenase deficiency: phenotype evolution in an adolescent patient at 20-year follow-up'.Decreased GABA-A binding on FMZ-PET in succinic semialdehyde dehydrogenase deficiency.Biomarkers in a Taurine Trial for Succinic Semialdehyde Dehydrogenase Deficiency.Quantitation of gamma-hydroxybutyric acid in dried blood spots: feasibility assessment for newborn screening of succinic semialdehyde dehydrogenase (SSADH) deficiency.Succinic semialdehyde dehydrogenase deficiency (SSADHD): Pathophysiological complexity and multifactorial trait associations in a rare monogenic disorder of GABA metabolismDifferential protein profile in zebrafish (Danio rerio) brain under the joint exposure of methyl parathion and cadmium.mTOR inhibitors rescue premature lethality and attenuate dysregulation of GABAergic/glutamatergic transcription in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.Correlation of blood biomarkers with age informs pathomechanisms in succinic semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism.Gamma-Hydroxybutyrate (GHB) Content in Hair Samples Correlates Negatively with Age in Succinic Semialdehyde Dehydrogenase Deficiency.Succinic semialdehyde dehydrogenase deficiency, a disorder of GABA metabolism: an update on pharmacological and enzyme-replacement therapeutic strategies.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
Neurotransmitter alterations in embryonic succinate semialdehyde dehydrogenase (SSADH) deficiency suggest a heightened excitatory state during development
description
2008 nî lūn-bûn
@nan
2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Neurotransmitter alterations i ...... atory state during development
@ast
Neurotransmitter alterations i ...... atory state during development
@en
type
label
Neurotransmitter alterations i ...... atory state during development
@ast
Neurotransmitter alterations i ...... atory state during development
@en
prefLabel
Neurotransmitter alterations i ...... atory state during development
@ast
Neurotransmitter alterations i ...... atory state during development
@en
P2093
P2860
P356
P1476
Neurotransmitter alterations i ...... atory state during development
@en
P2093
Cornelis Jakobs
Eduard Struys
Elizabeth Hager
Erwin E W Jansen
K Michael Gibson
O Carter Snead
P2860
P2888
P356
10.1186/1471-213X-8-112
P577
2008-11-28T00:00:00Z
P5875
P6179
1025678914